Diagnostics

15 pages, 2595 KiB

Open AccessReview

Computer-Aided Evaluation of Interstitial Lung Diseases

by Davide Colombi, Maurizio Marvisi, Sara Ramponi, Laura Balzarini, Chiara Mancini, Gianluca Milanese, Mario Silva, Nicola Sverzellati, Mario Uccelli and Francesco Ferrozzi

Diagnostics 2025, 15(7), 943; https://doi.org/10.3390/diagnostics15070943 - 7 Apr 2025

Viewed by 332

Abstract

The approach for the diagnosis and treatment of interstitial lung diseases (ILDs) has changed in recent years, mainly for the identification of new entities, such as interstitial lung abnormalities (ILAs) and progressive pulmonary fibrosis (PPF). Clinicians and radiologists are facing new challenges for [...] Read more.

The approach for the diagnosis and treatment of interstitial lung diseases (ILDs) has changed in recent years, mainly for the identification of new entities, such as interstitial lung abnormalities (ILAs) and progressive pulmonary fibrosis (PPF). Clinicians and radiologists are facing new challenges for the screening, diagnosis, prognosis, and follow-up of ILDs. The detection and classification of ILAs or the identification of fibrosis progression at high-resolution computed tomography (HRCT) is difficult, with high inter-reader variability, particularly for non-expert radiologists. In the last few years, various software has been developed for ILD evaluation at HRCT, with excellent results, equal to or more reliable than humans. AI tools can classify ILDs, quantify the extent, analyze the features hidden from the human eye, predict prognosis, and evaluate the progression of the disease. More advanced tools can incorporate clinical and radiological data to obtain personalized prognosis, with the potential ability to steer treatment decisions. To step forward and implement in daily practice such tools, more collaboration is required to collect more homogeneous clinical and radiological data; furthermore, more robust, prospective trials, with the new AI-derived biomarkers compared with each other, are needed to demonstrate the real reliability of the computer-aided evaluation of ILDs. Full article

(This article belongs to the Special Issue Recent Advances in Radiomics in Medical Imaging)

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18 pages, 945 KiB

Open AccessReview

Myocardial Infarction with Nonobstructive Coronary Arteries (MINOCA): Current Insights into Pathophysiology, Diagnosis, and Management

by Chiara Tognola, Alessandro Maloberti, Marisa Varrenti, Patrizio Mazzone, Cristina Giannattasio and Fabrizio Guarracini

Diagnostics 2025, 15(7), 942; https://doi.org/10.3390/diagnostics15070942 - 7 Apr 2025

Viewed by 1681

Abstract

Myocardial infarction with nonobstructive coronary arteries (MINOCA) is an increasingly recognized clinical entity characterized by myocardial injury in the absence of a significant coronary artery obstruction. MINOCA encompasses a diverse range of pathophysiological mechanisms, including coronary plaque disruption, coronary vasospasm, coronary microvascular dysfunction, [...] Read more.

Myocardial infarction with nonobstructive coronary arteries (MINOCA) is an increasingly recognized clinical entity characterized by myocardial injury in the absence of a significant coronary artery obstruction. MINOCA encompasses a diverse range of pathophysiological mechanisms, including coronary plaque disruption, coronary vasospasm, coronary microvascular dysfunction, thromboembolism, and spontaneous coronary artery dissection. A systematic diagnostic approach is essential to identify the underlying etiology and guide appropriate management strategies. Advanced imaging techniques, particularly cardiac magnetic resonance, play a pivotal role in distinguishing ischemic from non-ischemic myocardial injury and refining prognosis. Despite growing awareness, standardized treatment protocols remain limited, with current management largely extrapolated from strategies used in obstructive coronary artery disease. Notably, MINOCA is significantly more prevalent in women, emphasizing the need to understand sex-related differences in its pathophysiology, presentation, and clinical outcomes. This narrative review offers a comprehensive and up-to-date overview of MINOCA, including a dedicated chapter on sex-related considerations. It integrates recent advancements and highlights the importance of personalized management strategies. Full article

(This article belongs to the Special Issue Advances in the Diagnosis and Management of Cardiovascular Diseases)

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21 pages, 667 KiB

Open AccessReview

Impact of Drugs Used in Intensive Care on Routine Coagulation Testing

by Joffrey Feriel, Marjorie A. Goujon, Miki Desez and François Depasse

Diagnostics 2025, 15(7), 941; https://doi.org/10.3390/diagnostics15070941 - 7 Apr 2025

Viewed by 407

Abstract

Coagulation testing is commonly used in the intensive care unit (ICU) to monitor and manage the hemostatic balance, assess bleeding risk, and guide anticoagulant therapy. Routine tests used for this purpose include prothrombin time, activated partial thromboplastin time, fibrinogen, and anti-Xa assays. Some [...] Read more.

Coagulation testing is commonly used in the intensive care unit (ICU) to monitor and manage the hemostatic balance, assess bleeding risk, and guide anticoagulant therapy. Routine tests used for this purpose include prothrombin time, activated partial thromboplastin time, fibrinogen, and anti-Xa assays. Some of the drugs commonly used in critically ill patients may influence coagulation assays by interacting in vitro with reagents or in vivo with coagulation pathways, thus altering the coagulation cascade and the fibrinolytic pathway. While the pharmacological effects of drugs on coagulation are usually documented, to our knowledge, no comprehensive review article has been published to date. In this review, we have conducted a critical analysis of the literature to define: (1) the impact of hydroxocobalamin, intravenous lipid emulsion, and propofol on chromogenic assays; (2) the impact of PEGylated compounds, emicizumab, recombinant activated factor VII, antibiotics, and sugammadex on chronometric assays; (3) the challenges associated with bridging anticoagulation in the ICU as well as the effect of N-acetylcystein, serotonin reuptake inhibitors, and tramadol on the hemostasis system. For each drug, we specify the routine coagulation assay that is impacted, whether this is linked to an in vitro interference or an in vivo effect, and the potential consequences on patient management. Full article

(This article belongs to the Section Clinical Laboratory Medicine)

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31 pages, 382 KiB

Open AccessReview

Emerging Biomarkers and Electrochemical Biosensors for Early Detection of Premature Coronary Artery Disease

by Nanthini Mageswaran, Sarah Husnaini Zainal, Nurul Izzaty Hassan, Nurul Huda Abd Karim and Noor Akmal Shareela Ismail

Diagnostics 2025, 15(7), 940; https://doi.org/10.3390/diagnostics15070940 - 7 Apr 2025

Viewed by 368

Abstract

Coronary artery disease (CAD) is one of the primary causes of morbidity and death worldwide. Premature CAD (pCAD) is the term used to describe the 3–10% of CAD occurrences that occur in people under 45 worldwide. Diagnostic difficulties arise from the different risk [...] Read more.

Coronary artery disease (CAD) is one of the primary causes of morbidity and death worldwide. Premature CAD (pCAD) is the term used to describe the 3–10% of CAD occurrences that occur in people under 45 worldwide. Diagnostic difficulties arise from the different risk factor profiles of pCAD and late-onset CAD. Better cardiovascular risk prediction in younger populations has been made possible by the development of biomarker detection tools. This can be applied to a diagnostic tool, including electrochemical biosensors, which have been predicted to be instrumental because of their adaptability for point-of-care applications for quicker diagnoses. These biosensors provide efficient, scalable, and reasonably priced solutions for the quick identification and tracking of CAD. Multiplex biomarker detection has been adopted as a viable approach for early diagnosis and risk assessment due to the constraints of using a single biomarker for pCAD diagnosis. Thus, this study looks at current developments in biosensing technology and discusses established and new cardiac biomarker panels for pCAD identification. Full article

(This article belongs to the Collection Diagnostic Sensors)

21 pages, 779 KiB

Open AccessSystematic Review

The Use of Artificial Intelligence for Skin Cancer Detection in Asia—A Systematic Review

by Xue Ling Ang and Choon Chiat Oh

Diagnostics 2025, 15(7), 939; https://doi.org/10.3390/diagnostics15070939 - 7 Apr 2025

Viewed by 559

Abstract

Background: Artificial intelligence (AI) developed for skin cancer recognition has been shown to have comparable or superior performance to dermatologists. However, it is uncertain if current AI models trained predominantly with lighter Fitzpatrick skin types can be effectively adapted for Asian populations. [...] Read more.

Background: Artificial intelligence (AI) developed for skin cancer recognition has been shown to have comparable or superior performance to dermatologists. However, it is uncertain if current AI models trained predominantly with lighter Fitzpatrick skin types can be effectively adapted for Asian populations. Objectives: A systematic review was performed to summarize the existing use of artificial intelligence for skin cancer detection in Asian populations. Methods: Systematic search was conducted on PubMed and EMBASE for articles published regarding the use of artificial intelligence for skin cancer detection amongst Asian populations. Information regarding study characteristics, AI model characteristics, and outcomes was collected. Conclusions: Current studies show optimistic results in utilizing AI for skin cancer detection in Asia. However, the comparison of image recognition abilities might not be a true representation of the diagnostic abilities of AI versus dermatologists in the real-world setting. To ensure appropriate implementation, maximize the potential of AI, and improve the transferability of AI models across various Asian genotypes and skin cancers, it is crucial to focus on prospective, real-world-based practice, as well as the expansion and diversification of existing Asian databases used for training and validation. Full article

(This article belongs to the Special Issue Artificial Intelligence in Dermatology)

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11 pages, 2878 KiB

Open AccessCase Report

Metastatic Renal Cell Carcinoma Presenting a Maxillary Mucosal Lesion as a First Visible Sign of Disease: A Case Report and Review of Literature

by Umma Habiba, Abu Faem Mohammad Almas Chowdhury, Rafiz Ahmed, Saiyka S. Chowdhury, Raihanul Ferdoush, Koki Ise, Harun ur Rashid, Zillur Rahman, Zen-ichi Tanei, Shinya Tanaka and Asad-Uz Zaman

Diagnostics 2025, 15(7), 938; https://doi.org/10.3390/diagnostics15070938 - 7 Apr 2025

Viewed by 938

Abstract

Background and Clinical Significance: Renal cell carcinoma (RCC) is the third most common cancer that metastasizes to the oral and maxillofacial region following breast and lung cancers. Metastatic involvement in the oral cavity is rare and can present as a diagnostic challenge due [...] Read more.

Background and Clinical Significance: Renal cell carcinoma (RCC) is the third most common cancer that metastasizes to the oral and maxillofacial region following breast and lung cancers. Metastatic involvement in the oral cavity is rare and can present as a diagnostic challenge due to non-specific clinical features that mimic other benign or malignant conditions. The limited information available regarding oral metastasis of RCC highlights the importance of recognizing this uncommon presentation. Case Presentation: A 50-year-old female presented with a painful swelling in the buccal and palatal mucosa of the right maxilla that progressively enlarged over several months. Initially, this lesion was diagnosed clinically as a pyogenic granuloma. However, given the lesion’s continued growth and unusual presentation, a biopsy was performed. Histopathological examination confirmed the lesion as metastatic renal clear-cell carcinoma (ccRCC), with immunohistochemical analysis verifying the renal origin. Further diagnostic tests, including a computed tomography (CT) urogram, chest CT, and bone scintigraphy, revealed additional metastases in the left adrenal gland, lungs, and bone. Conclusions: This case is notable because the oral lesion was the first visible sign of RCC, making it a rare presentation of metastatic RCC. This underscores the importance of thorough history taking, detailed clinical evaluations, and considering rare metastatic conditions in the differential diagnosis of oral swellings. Additionally, this case reinforces the significance of routine cancer screenings for early detection of undiagnosed cancer. We also updated a previous literature review of metastatic RCC to the head and neck region, covering cases until 2023. Full article

(This article belongs to the Section Medical Imaging and Theranostics)

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15 pages, 2292 KiB

Open AccessArticle

Novel Usefulness of M2BPGi for Predicting Severity and Clinical Outcomes in Hospitalized COVID-19 Patients

by Mikyoung Park, Mina Hur, Hanah Kim, Chae Hoon Lee, Jong Ho Lee, Hyung Woo Kim, Minjeong Nam and Seungho Lee

Diagnostics 2025, 15(7), 937; https://doi.org/10.3390/diagnostics15070937 - 6 Apr 2025

Viewed by 399

Abstract

Background/Objectives: Mac-2 binding protein glycosylation isomer (M2BPGi) is a novel biomarker for liver fibrosis, and its prognostic role has never been explored in coronavirus disease 2019 (COVID-19). We compared the M2BPGi level simultaneously with age, severe/critical disease, the sequential organ failure assessment (SOFA) [...] Read more.

Background/Objectives: Mac-2 binding protein glycosylation isomer (M2BPGi) is a novel biomarker for liver fibrosis, and its prognostic role has never been explored in coronavirus disease 2019 (COVID-19). We compared the M2BPGi level simultaneously with age, severe/critical disease, the sequential organ failure assessment (SOFA) score, and the National Early Warning Score 2 (NEWS2) in a total of 53 hospitalized patients with COVID-19 (mild/moderate [n = 15] and severe/critical [n = 38]). Methods: M2BPGi levels were measured using the HISCL M2BPGi assay (Sysmex, Kobe, Japan) in an HISCL-5000 analyzer (Sysmex), and clinical outcomes were analyzed according to M2BPGi and the clinical variables, using the receiver operating characteristic (ROC) curve, Kaplan–Meier survival, and Cox proportional hazards regression analyses. Results: M2BPGi levels differed significantly according to disease severity, 30-day mortality, and 60-day mortality (p = 0.045, 0.011, and 0.002, respectively). In the ROC curve analysis, the M2BPGi, age, SOFA score, and NEWS2, except for severe/critical disease, significantly predicted clinical outcomes (all p < 0.01). In the survival analysis, the hazard ratios of M2BPGi added to each clinical variable were higher than that of each clinical variable alone, and M2BPGi was the only independent prognostic factor for the mortality. Conclusions: This study demonstrated that M2BPGi may be a useful biomarker for assessing disease severity and clinical outcomes in hospitalized COVID-19 patients. Combined with conventional clinical assessment, M2BPGi would provide objective and valuable information for prognosis prediction in these critically ill patients. Further studies are warranted to extend its utility in other clinical settings. Full article

(This article belongs to the Special Issue Biochemical Testing Applications in Clinical Diagnosis)

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11 pages, 915 KiB

Open AccessArticle

Backward Walking as a Marker of Mobility and Disability in Multiple Sclerosis: A Cross-Sectional Analysis

by Meral Seferoğlu, Abdulkadir Tunç, Ali Özhan Sıvacı, Samed Öncel, Tuğba Düztaban, Hamide Dikilitaş, Abdul Samed Görgül and Muhammed Furkan Öztürkci

Diagnostics 2025, 15(7), 936; https://doi.org/10.3390/diagnostics15070936 - 6 Apr 2025

Viewed by 397

Abstract

Background: Mobility impairments in multiple sclerosis (MS) significantly affect quality of life. This study evaluated the clinical utility and sensitivity of the Backward Timed 25-Foot Walk Test (B-T25FW) and its associations with key clinical measures in MS. Methods: A cross-sectional study was [...] Read more.

Background: Mobility impairments in multiple sclerosis (MS) significantly affect quality of life. This study evaluated the clinical utility and sensitivity of the Backward Timed 25-Foot Walk Test (B-T25FW) and its associations with key clinical measures in MS. Methods: A cross-sectional study was conducted with 129 ambulatory patients with MS from two centers. Disability (Expanded Disability Status Scale, EDSS), cognition (Symbol Digit Modalities Test, SDMT), manual dexterity (Nine-Hole Peg Test, 9HPT), fatigue, and forward and backward walking were assessed. Correlation and receiver operating characteristic (ROC) analyses were performed. Results: The participants included in the study were 76% female, with a mean age of 38 years, and the majority were diagnosed with relapsing–remitting MS (86.8%). Backward and forward walking times significantly correlated with key clinical measures, including the EDSS, SDMT, and 9HPT. Backward walking times showed moderate correlations with EDSS (r = 0.469) and weaker but significant correlations with 9HPT (r = 0.452) and disease duration (r = 0.245). Both walking tests were negatively correlated with SDMT scores. For prognostic purposes, forward walking exhibited slightly higher predictive power compared to backward walking. Conclusions: The B-T25FW is a clinically relevant, practical, and sensitive tool for assessing mobility impairments in individuals with MS. Its integration into clinical practice could complement forward walking assessments, enhancing disease monitoring and guiding interventions. Future research should validate its longitudinal utility. Full article

(This article belongs to the Section Clinical Diagnosis and Prognosis)

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32 pages, 1152 KiB

Open AccessReview

Current Concepts in Gastroparesis and Gastric Neuromuscular Disorders—Pathophysiology, Diagnosis, and Management

by Jennifer Dimino and Braden Kuo

Diagnostics 2025, 15(7), 935; https://doi.org/10.3390/diagnostics15070935 - 5 Apr 2025

Viewed by 1493

Abstract

Upper gastrointestinal concerns including gastroparesis-like symptoms affect a large portion of the population, and determining the culprit condition can be difficult due to largely shared symptoms, clinical course, pathophysiology, and treatment pathways. The understanding of gastric neuromuscular disorders (GNDs) is emerging as a [...] Read more.

Upper gastrointestinal concerns including gastroparesis-like symptoms affect a large portion of the population, and determining the culprit condition can be difficult due to largely shared symptoms, clinical course, pathophysiology, and treatment pathways. The understanding of gastric neuromuscular disorders (GNDs) is emerging as a heterogeneous group encompassing conditions from gastroparesis to functional dyspepsia with chronic nausea, early satiety, bloating, or abdominal pain, irrespective of gastric emptying. This article aims to review the current concepts in gastroparesis and GNDs including pathophysiology, diagnosis, and management. While some established standards in their diagnosis and management exist, a number of novel diagnostics are becoming available. Durable therapeutic options are notably limited for such common conditions with chronic and debilitating symptoms, and neuromodulators may play a key role in symptom control, which has been previously under-recognized and underutilized. Advances in both pharmacologic treatment targets as well as noninvasive and invasive interventions and devices show promise in improving the experience of patients with gastroparesis-like symptoms. At this time, treatment of GNDs requires comprehensive multidisciplinary care from providers to achieve successful treatment outcomes. Full article

(This article belongs to the Special Issue Functional Gastrointestinal Disorders (FGIDs): Diagnosis and Pathophysiology, Second Edition)

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13 pages, 1067 KiB

Open AccessArticle

A Comparative Analysis of the Clinical Application of a Novel Helicobacter pylori Serum Antibody Typing Test and the ¹³C-Urea Breath Test

by Chonghui Hu, Zhipeng Zhao, Dong Zhu, Runqing Li, Xuan Jiang, Yutang Ren, Xin Ma and Xiuying Zhao

Diagnostics 2025, 15(7), 934; https://doi.org/10.3390/diagnostics15070934 - 5 Apr 2025

Viewed by 425

Abstract

Background/Objectives: To compare and analyze the application of a Helicobacter pylori (H. pylori, Hp) serum antibody typing test (Hp-sATT) and the ¹³C-urea breath test (¹³C-UBT) in the diagnosis of Hp infection against an empirical therapy background. Methods [...] Read more.

Background/Objectives: To compare and analyze the application of a Helicobacter pylori (H. pylori, Hp) serum antibody typing test (Hp-sATT) and the ¹³C-urea breath test (¹³C-UBT) in the diagnosis of Hp infection against an empirical therapy background. Methods: The detection of Hp-sATT using a combination of the quantum dot immunofluorescence method and the ¹³C-UBT was carried out in 237 patients who visited the Department of Gastroenterology at Beijing Tsinghua Changgung Hospital. The diagnostic consistency and correlation with gastric lesions of the two detection methods were analyzed by integrating the detection results, clinical information, and special staining of Hp in histopathological tissues (SS-Hp). Results: For the ¹³C-UBT, 104 (43.88%) cases were positive and 133 (56.12%) were negative. Positive results were found in 127 (53.59%) patients by using the Hp-sATT, with 67 (28.27%) cases of Type I Hp infection and 60 (25.32%) cases of Type II Hp infection. The consistency analysis between the Hp-sATT and ¹³C-UBT for all the patients showed a Kappa value of 0.339 (p < 0.001); the consistency analysis between the Hp-sATT and the 127 patients with SS-Hp showed a Kappa value of 0.427 (p < 0.001); and the consistency analysis between the ¹³C-UBT and the 127 patients with SS-Hp indicated a Kappa value of 0.621 (p < 0.001). However, in 191 patients without a history of Hp eradication, the consistency analysis results for the three methods improved, with Kappa values of 0.467 (p < 0.001) and 0.457 (p < 0.001) for the Hp-sATT with the ¹³C-UBT and SS-Hp, respectively, and 0.646 (p < 0.001) for the ¹³C-UBT with SS-Hp. In addition, a positive correlation was found between the signal values of anti-urease antibodies and the Delta Over Baseline (DOB) values of the ¹³C-UBT. The results also indicated that Hp-infected patients exhibited more pronounced gastric lesions, while cases with Type I Hp infection did not. Conclusions: In patients without a history of Hp eradication, the consistency between the Hp-sATT and ¹³C-UBT is moderate. However, Hp eradication therapy can reduce the consistency of the test results. When screening for Hp infection using the Hp-sATT, it is necessary to consider the patient’s history of Hp eradication. Full article

(This article belongs to the Special Issue Advances in the Diagnosis of Gastrointestinal Diseases—2nd Edition)

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12 pages, 454 KiB

Open AccessReview

Impact of Adequate Disinfection Techniques for Ultrasound-Guided Injections in Musculoskeletal Rehabilitation: A Scoping Review

by Angelo Alito, Alessandro de Sire, Marco Di Gesù, Enrico Buccheri, Daniele Borzelli, Rita Chiaramonte, Umile Giuseppe Longo, Antonio Ammendolia, Michele Vecchio and Daniele Bruschetta

Diagnostics 2025, 15(7), 933; https://doi.org/10.3390/diagnostics15070933 - 5 Apr 2025

Viewed by 477

Abstract

Background: Interventional physiatry is a branch of medicine that uses minimally invasive ultrasound-guided techniques for diagnosis and treatment in the musculoskeletal system. The aim of this scoping review is to investigate the sterilisation techniques used and the rate of infection with ultrasound-guided [...] Read more.

Background: Interventional physiatry is a branch of medicine that uses minimally invasive ultrasound-guided techniques for diagnosis and treatment in the musculoskeletal system. The aim of this scoping review is to investigate the sterilisation techniques used and the rate of infection with ultrasound-guided injections. Methods: PubMed was searched up to 30 September 2024 using the following search terms (“Ultrasound, Interventional”[mesh]) AND “Injections, Intra-Articular”[mesh]; “Ultrasound-guided intra-articular injection”. The inclusion criteria were randomised clinical trials, written in English, involving US-guided mini-invaexercissive procedures. Results: The search identified a total of 256 potentially relevant publications. After screening for duplication, inclusion, and exclusion criteria, 105 articles were eligible for data extraction. In 51 studies, the method of skin disinfection was not specified, 18 RCT reported a ’sterile condition’, 9 studies used povidone–iodine solution, 5 used alcohol, and 2 used chlorhexidine 0.5%. In 64 trials, the method of probe preparation was not specified, 11 trials described the use of sterile gel, 10 trials reported the use of a probe cover, sterile pad, or barrier, and 2 trials reported the use of chlorhexidine 0.5%; 41 studies reported mild adverse events and 4 serious adverse events. Conclusions: Taken together, the findings of this scoping review did not show a clear relationship between current sterilisation protocols and the prevention of the microbial contamination of the probes or the patient’s skin. The variation in protocols highlights the need for standardised guidelines and more rigorous studies to accurately determine the most effective disinfection practices. Full article

(This article belongs to the Section Medical Imaging and Theranostics)

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18 pages, 725 KiB

Open AccessReview

Endoscopic Full Thickness Resection Device (FTRD^®) for the Management of Gastrointestinal Lesions: Current Evidence and Future Perspectives

by Magdalini Manti, Apostolis Papaefthymiou, Spyridon Dritsas, Nikolaos Kamperidis, Ioannis S. Papanikolaou, Konstantina Paraskeva, Antonio Facciorusso, Konstantinos Triantafyllou, Vasilios Papadopoulos, Georgios Tziatzios and Paraskevas Gkolfakis

Diagnostics 2025, 15(7), 932; https://doi.org/10.3390/diagnostics15070932 - 4 Apr 2025

Viewed by 382

Abstract

Endoscopic full-thickness resection (EFTR) has emerged as a transformative technique for managing gastrointestinal (GI) lesions, previously deemed unsuitable for endoscopic removal. Unlike conventional endoscopic resection methods, such as endoscopic mucosal resection (EMR) and endoscopic submucosal dissection (ESD), EFTR enables en bloc excision of [...] Read more.

Endoscopic full-thickness resection (EFTR) has emerged as a transformative technique for managing gastrointestinal (GI) lesions, previously deemed unsuitable for endoscopic removal. Unlike conventional endoscopic resection methods, such as endoscopic mucosal resection (EMR) and endoscopic submucosal dissection (ESD), EFTR enables en bloc excision of both intraluminal and subepithelial lesions by resecting all layers of the GI wall, followed by defect closure to prevent complications. The introduction of the full-thickness resection device (FTRD^®) has significantly enhanced the feasibility and safety of EFTR, particularly in the colon and upper GI tract, with increasing adoption worldwide. This review provides a comprehensive analysis of FTRD^®, focusing on its clinical applications, procedural methodology, and comparative efficacy against other endoscopic resection techniques. The indications and contraindications for EFTR are explored, highlighting its utility in treating non-lifting adenomas, subepithelial tumours, and T1 carcinomas without lymph node involvement. This review synthesizes current clinical data and FTRD^® advantages. Despite its strengths, EFTR via FTRD^® incorporates challenges such as limitations in lesion size, procedural complexity, and potential adverse events. Strategies for overcoming these challenges, including hybrid techniques and modifications in procedural approach, are examined. The review also emphasizes the need for further research to optimize surveillance strategies and determine the long-term clinical impact of EFTR in GI lesion management. By integrating recent evidence, this paper provides valuable insights into the evolving role of EFTR in therapeutic endoscopy. Full article

(This article belongs to the Special Issue Diagnosis and Prognosis of Abdominal Diseases)

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12 pages, 813 KiB

Open AccessArticle

Telomere Length and Genetic Variations in Acquired Pediatric Aplastic Anemia: A Flow-FISH Study in Korean Patients

by Yuna Hong, Jong-Mi Lee, Chaeyeon Lee, Duyeon Na, Jin Jung, Ari Ahn, Jae Won Yoo, Jae Wook Lee, Nack-Gyun Chung, Myungshin Kim and Yonggoo Kim

Diagnostics 2025, 15(7), 931; https://doi.org/10.3390/diagnostics15070931 - 4 Apr 2025

Viewed by 335

Abstract

Background: Aplastic anemia (AA) is a rare bone marrow failure syndrome characterized by notably short telomere length, which is associated with treatment responses. In this study, we measured telomere lengths in Korean pediatric AA patients using flow-fluorescence in situ hybridization (Flow-FISH) and [...] Read more.

Background: Aplastic anemia (AA) is a rare bone marrow failure syndrome characterized by notably short telomere length, which is associated with treatment responses. In this study, we measured telomere lengths in Korean pediatric AA patients using flow-fluorescence in situ hybridization (Flow-FISH) and explored their shortening in relation to disease characteristics, genetic conditions and patient outcomes. Methods: We analyzed peripheral blood samples from 75 AA patients and 101 healthy controls. Telomere lengths were measured using Flow-FISH, and relative telomere length (RTL) and delta RTL assessments were conducted. Genetic evaluations included karyotyping, chromosome breakage tests and clinical exome sequencing (CES) to identify inherited bone marrow failure syndrome (IBMFS)-associated genetic variants. Results: Telomere lengths in AA patients were significantly lower than those of age-adjusted healthy controls. Patients receiving immunosuppressive therapy tended to have long telomeres, as indicated by high delta RTL values. Patients with genetic abnormalities, including karyotype abnormalities (n = 2) and genetic variants (n = 11) such as carrier genes of IBMFS or variants of unclear significance, showed significantly short telomere lengths. Conclusions: This study reinforces the importance of telomere length as a biomarker in acquired AA. Utilizing Flow-FISH, we were able to accurately measure telomere lengths and establish confidence in this method as an appropriate laboratory test. We found significant reduction in telomere lengths in AA patients, and importantly, longer telomeres were correlated with better outcomes in immunosuppressive therapy. Additionally, our genetic analysis underscored the relevance of variants in IBMFS-associated genes to the pathophysiology of short telomeres. Full article

(This article belongs to the Section Pathology and Molecular Diagnostics)

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12 pages, 3173 KiB

Open AccessArticle

Information Extraction from Lumbar Spine MRI Radiology Reports Using GPT4: Accuracy and Benchmarking Against Research-Grade Comprehensive Scoring

by Katharina Ziegeler, Virginie Kreutzinger, Michelle W. Tong, Cynthia T. Chin, Emma Bahroos, Po-Hung Wu, Noah Bonnheim, Aaron J. Fields, Jeffrey C. Lotz, Thomas M. Link and Sharmila Majumdar

Diagnostics 2025, 15(7), 930; https://doi.org/10.3390/diagnostics15070930 - 4 Apr 2025

Viewed by 412

Abstract

Background/Objectives: This study aimed to create a pipeline for standardized data extraction from lumbar-spine MRI radiology reports using a large language model (LLM) and assess the agreement of the extracted data with research-grade semi-quantitative scoring. Methods: We included a subset of [...] Read more.

Background/Objectives: This study aimed to create a pipeline for standardized data extraction from lumbar-spine MRI radiology reports using a large language model (LLM) and assess the agreement of the extracted data with research-grade semi-quantitative scoring. Methods: We included a subset of data from a multi-site NIH-funded cohort study of chronic low back pain (cLBP) participants. After initial prompt development, a secure application programming interface (API) deployment of OpenAIs GPT-4 was used to extract different classes of pathology from the clinical radiology report. Unsupervised UMAP and agglomerative clustering of the pathology terms’ embeddings provided insight into model comprehension for optimized prompt design. Model extraction was benchmarked against human extraction (gold standard) with F1 scores and false-positive and false-negative rates (FPR/FNR). Then, an expert MSK radiologist provided comprehensive research-grade scores of the images, and agreement with report-extracted data was calculated using Cohen’s kappa. Results: Data from 230 patients with cLBP were included (mean age 53.2 years, 54% women). The overall model performance for extracting data from clinical reports was excellent, with a mean F1 score of 0.96 across pathologies. The mean FPR was marginally higher than the FNR (5.1% vs. 3.0%). Agreement with comprehensive scoring was moderate (kappa 0.424), and the underreporting of lateral recess stenosis (FNR 63.6%) and overreporting of disc pathology (FPR 42.7%) were noted. Conclusions: LLMs can accurately extract highly detailed information on lumbar spine imaging pathologies from radiology reports. Moderate agreement between the LLM and comprehensive scores underscores the need for less subjective, machine-based data extraction from imaging. Full article

(This article belongs to the Special Issue AI in Radiology and Nuclear Medicine: Challenges and Opportunities)

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20 pages, 1932 KiB

Open AccessArticle

A Distillation Approach to Transformer-Based Medical Image Classification with Limited Data

by Aynur Sevinc, Murat Ucan and Buket Kaya

Diagnostics 2025, 15(7), 929; https://doi.org/10.3390/diagnostics15070929 - 4 Apr 2025

Viewed by 479

Abstract

Background/Objectives: Although transformer-based deep learning architectures are preferred in many hybrid architectures due to their flexibility, they generally perform poorly on image classification tasks with small datasets. An important improvement in performance when transformer architectures work with limited data is the use [...] Read more.

Background/Objectives: Although transformer-based deep learning architectures are preferred in many hybrid architectures due to their flexibility, they generally perform poorly on image classification tasks with small datasets. An important improvement in performance when transformer architectures work with limited data is the use of distillation techniques. The impact of distillation techniques on classification accuracy in transformer-based models has not yet been extensively investigated. Methods: This study investigates the impact of distillation techniques on the classification performance of transformer-based deep learning architectures trained on limited data. We use transformer-based models ViTx32 and ViTx16 without distillation and DeiT and BeiT with distillation. A four-class dataset of brain MRI images is used for training and testing. Results: Our experiments show that the DeiT and BeiT architectures with distillation achieve performance gains of 2.2% and 1%, respectively, compared to ViTx16. A more detailed analysis shows that the distillation techniques improve the detection of non-patient individuals by about 4%. Our study also includes a detailed analysis of the training times for each architecture. Conclusions: The results of the experiments show that using distillation techniques in transformer-based deep learning models can significantly improve classification accuracy when working with limited data. Based on these findings, we recommend the use of transformer-based models with distillation, especially in medical applications and other areas where flexible models are developed with limited data. Full article

(This article belongs to the Special Issue AI and Big Data in Healthcare)

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13 pages, 258 KiB

Open AccessArticle

Usefulness of the CDC/AAP and the EFP/AAP Criteria to Detect Subclinical Atherosclerosis in Subjects with Diabetes and Severe Periodontal Disease

by Greicy C. Montenegro-González, Carlos Bea, F. Javier Ampudia-Blasco, Herminia González-Navarro, José T. Real, Maria Peñarrocha-Diago and Sergio Martínez-Hervás

Diagnostics 2025, 15(7), 928; https://doi.org/10.3390/diagnostics15070928 - 4 Apr 2025

Viewed by 383

Abstract

Background/Objectives: Periodontitis is an inflammatory disease associated with many systemic disorders such as diabetes and cardiovascular disease. The aim was to evaluate the usefulness of the CDC/AAP and the EFP/AAP criteria to detect subclinical atherosclerosis in subjects with diabetes and severe periodontal [...] Read more.

Background/Objectives: Periodontitis is an inflammatory disease associated with many systemic disorders such as diabetes and cardiovascular disease. The aim was to evaluate the usefulness of the CDC/AAP and the EFP/AAP criteria to detect subclinical atherosclerosis in subjects with diabetes and severe periodontal disease. Methods: This was a cross-sectional study. Atheroma plaque was evaluated by high-resolution carotid and femoral ultrasonography. A dental examination protocol was implemented by a trained periodontist. A full-mouth periodontal clinical examination was carried out at six sites by automated computerized Florida Probe Periodontal Probing. Periodontal disease was defined by CDC/AAP and EFP/AAP criteria. Results: In total, 98 patients were included (60.2% women), of which 50% had diabetes. Subjects with diabetes showed a high prevalence of severe cases of periodontal disease. Both criteria were useful to detect the presence of atheroma plaque only in the presence of diabetes. However, the CDC/AAP criteria had higher correlation with atheroma plaques than EFP/AAP criteria (r = 0.522 vs. r = 0.369, p < 0.001). Conclusions: The CDC/AAP and the EFP/AAP criteria are a useful tool to identify subclinical atherosclerosis in subjects with severe periodontal disease and diabetes. These results show the potential role of the oral healthcare team in the dental office for the identification of subjects with diabetes at risk of developing cardiovascular disease. Full article

(This article belongs to the Special Issue Periodontal Disease: Diagnosis and Management)

17 pages, 1193 KiB

Open AccessArticle

Evaluating the Nuclear Reaction Optimization (NRO) Algorithm for Gene Selection in Cancer Classification

by Shahad Alkamli and Hala Alshamlan

Diagnostics 2025, 15(7), 927; https://doi.org/10.3390/diagnostics15070927 - 3 Apr 2025

Viewed by 394

Abstract

Background/Objectives: Cancer classification using microarray datasets presents a significant challenge due to their extremely high dimensionality. This complexity necessitates advanced optimization methods for effective gene selection. Methods: This study introduces and evaluates the Nuclear Reaction Optimization (NRO)—drawing inspiration from nuclear fission [...] Read more.

Background/Objectives: Cancer classification using microarray datasets presents a significant challenge due to their extremely high dimensionality. This complexity necessitates advanced optimization methods for effective gene selection. Methods: This study introduces and evaluates the Nuclear Reaction Optimization (NRO)—drawing inspiration from nuclear fission and fusion—for identifying informative gene subsets in six benchmark cancer microarray datasets. Employed as a standalone approach without prior dimensionality reduction, NRO was assessed using both Support Vector Machine (SVM) and k-Nearest Neighbors (k-NN). Leave-One-Out Cross-Validation (LOOCV) was used to rigorously evaluate classification accuracy and the relevance of the selected genes. Results: Experimental results show that NRO achieved high classification accuracy, particularly when used with SVM. In select datasets, it outperformed several state-of-the-art optimization algorithms. However, due to the absence of additional dimensionality reduction techniques, the number of selected genes remains relatively high. Comparative analysis with Harris Hawks Optimization (HHO), Artificial Bee Colony (ABC), Particle Swarm Optimization (PSO), and Firefly Algorithm (FFA) shows that while NRO delivers competitive performance, it does not consistently outperform all methods across datasets. Conclusions: The study concludes that NRO is a promising gene selection approach, particularly effective in certain datasets, and suggests that future work should explore hybrid models and feature reduction techniques to further enhance its accuracy and efficiency. Full article

(This article belongs to the Special Issue Advancing Clinical Diagnosis with Artificial Intelligence: Applications, Challenges, and Future Directions)

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10 pages, 1526 KiB

Open AccessArticle

The Application and Validity of a New Composite Radiographic Index for Patients with Osteonecrosis of the Jaws

by Zafeiroula Yfanti, Sotirios Tetradis, Nikolaos G. Nikitakis, Konstantina Eleni Alexiou, Emmanouil Vardas, Christos Angelopoulos and Kostas Tsiklakis

Diagnostics 2025, 15(7), 926; https://doi.org/10.3390/diagnostics15070926 - 3 Apr 2025

Viewed by 305

Abstract

Background/Objectives: This study aims to determine the validity of a recently developed and published index (the modified Composite Radiographic Index—CRIm) as an indicator of disease gravity and progression in the CBCT scans of patients with medication-related osteonecrosis of the jaw (MRONJ) and [...] Read more.

Background/Objectives: This study aims to determine the validity of a recently developed and published index (the modified Composite Radiographic Index—CRIm) as an indicator of disease gravity and progression in the CBCT scans of patients with medication-related osteonecrosis of the jaw (MRONJ) and to detect possible correlations between the radiologic findings and clinical staging of the disease. Methods: This study included 43 MRONJ patients with CBCT scans from the School of Dentistry of National and Kapodistrian University of Athens, approved by the Research Ethics Committee. Clinical staging (0–3) was provided based on AAOMS 2022 guidelines. A total of 52 CBCT scans were analyzed, with maxillae and mandibles evaluated separately when both were involved. Two independent observers assessed eight radiologic features, including lytic changes, sclerosis, periosteal reaction, sequestration, non-healing extraction sockets, and other findings (sinus involvement, inferior alveolar canal involvement, and jaw fracture). The CRIm was applied to quantify osseous changes, scoring each feature (0 (absent), 1 (localized/single), 2 (extensive/multiple)), yielding a range of 0–12. For the statistical analysis, Fisher’s exact test and Spearman’s correlation coefficient were used. Results: Clinical Stage 1 consisted of 19 jaws, Stage 2 consisted of 16 jaws, and Stage 3 consisted of 17 jaws. No affected jaws were recorded with Stage 0. A statistically significant correlation between the clinical stage and lytic changes, sequestration, and inferior alveolar canal involvement was found (p-value < 0.05). Extensive lytic changes, sclerosis, sequestration, periosteal bone formation, and inferior alveolar canal involvement were mostly observed in clinical Stage 3. Furthermore, a statistically significant correlation between clinical stage and CRIm classification was found (rho = 0.446; p-value < 0.001). Conclusions: The CRIm tends to increase as the clinical stages of MRONJ advance, suggesting a correlation between them. Full article

(This article belongs to the Section Medical Imaging and Theranostics)

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16 pages, 2246 KiB

Open AccessSystematic Review

The Anatomy of the Stylohyoid Chain: A Systematic Review with Meta-Analysis

by George Triantafyllou, Ioannis Paschopoulos, Fabrice Duparc, George Tsakotos, Panagiotis Papadopoulos-Manolarakis and Maria Piagkou

Diagnostics 2025, 15(7), 925; https://doi.org/10.3390/diagnostics15070925 - 3 Apr 2025

Viewed by 396

Abstract

Background: The temporal bone’s styloid process (SP) is an important structure that extends from the skull base to the parapharyngeal space. The stylohyoid ligament (SHL) attaches it to the hyoid bone. The SP and SHL are considered the stylohyoid chain (SHC) components. [...] Read more.

Background: The temporal bone’s styloid process (SP) is an important structure that extends from the skull base to the parapharyngeal space. The stylohyoid ligament (SHL) attaches it to the hyoid bone. The SP and SHL are considered the stylohyoid chain (SHC) components. The SP’s close relationship with vital head and neck structures has important clinical implications. Specifically, SP and SHC variants are linked with clinical conditions. Therefore, adequate knowledge of these variations is of paramount importance. Methods: Using the latest guidelines, a systematic literature review was performed in four online databases (PubMed, Google Scholar, Scopus, and Web of Science) to identify studies referring to the SP’s typical anatomy and possible SHC morphological variants. The meta-analysis was conducted using R programming software to calculate the prevalence of typical anatomy and possible variants and the pooled mean length of the SP. Results: A total of 104 studies were included, with a total sample of 136,010 heminecks. The typical SP (under 30 mm) was estimated to have a pooled prevalence of 74.97%. SP elongation was observed in 25.03%. The subgroup analysis identified significant differences based on the study type, with computed tomography (CT) studies having the highest pooled prevalence. The SP length was calculated to have a pooled mean of 28.91 mm. For SHC ossification, the pseudo-articulated type was identified to have a pooled prevalence of 4.39%, and that of the segmented type was detected to be 3.89%. The geographical distribution and study type affected the estimated pooled prevalence. Conclusions: The current evidence-based systematic review with meta-analysis investigated the SHC’s typical anatomy and possible variants. The elongated SP pooled prevalence of 25.03% indicates that it is not a rare variant, and CT is the optimal method to investigate such a variant. These details demonstrated by the current meta-analysis could be of importance for clinicians. Full article

(This article belongs to the Special Issue Clinical Anatomy and Diagnosis in 2025)

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8 pages, 28576 KiB

Open AccessCase Report

An Incidental Finding of Appendiceal Gastrointestinal Stromal Tumor with Abundant Skeinoid Fibers: A Rare Case Report with Insights from a Comprehensive Literature Review

by Yu Liu, Yaomin Chen, Asra Feroze and Zhiyan Fu

Diagnostics 2025, 15(7), 924; https://doi.org/10.3390/diagnostics15070924 - 3 Apr 2025

Viewed by 309

Abstract

Background and Clinical Significance: Gastrointestinal stromal tumors (GISTs) are the most common mesenchymal tumors of the gastrointestinal tract but are exceedingly rare in the appendix, with only 20 cases reported in the literature. Due to their rarity, clinical behavior, histopathologic features, and management [...] Read more.

Background and Clinical Significance: Gastrointestinal stromal tumors (GISTs) are the most common mesenchymal tumors of the gastrointestinal tract but are exceedingly rare in the appendix, with only 20 cases reported in the literature. Due to their rarity, clinical behavior, histopathologic features, and management of appendiceal GISTs remain poorly understood. Case Presentation: We present the case of a 74-year-old man who underwent a right hemicolectomy for colonic adenocarcinoma, during which an incidental 1.2 cm appendiceal GIST was discovered. Histopathological examination revealed spindle cell morphology with abundant skeinoid fibers (SF), minimal mitotic activity (<1/50 HPF), and no nuclear atypia. Immunohistochemical staining confirmed positivity for CD117, DOG1, and CD34. The tumor was classified as low risk based on its size and mitotic count, and the patient remained recurrence-free at a 4-month follow-up. Conclusions: Our case expands the limited literature on appendiceal GISTs by demonstrating their histopathological and immunohistochemical features, favorable prognostic outcomes, and potential for incidental detection during surgeries for unrelated conditions. However, additional studies are needed to further elucidate their molecular characteristics and overall clinical behavior. Full article

(This article belongs to the Section Pathology and Molecular Diagnostics)

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16 pages, 970 KiB

Open AccessArticle

Analytical Validation of MyProstateScore 2.0

by Jacob I. Meyers, Tabea M. Schatz, Cameron J. Seitz, Rachel Botbyl, Bradley S. Moore, Bill G. Crafts, John R. Kitchen and Spencer Heaton

Diagnostics 2025, 15(7), 923; https://doi.org/10.3390/diagnostics15070923 - 3 Apr 2025

Viewed by 435

Abstract

Background/Objectives: Prostate cancer (PCa) is a leading cause of cancer-related deaths among men, with early detection playing a crucial role in improving outcomes. MyProstateScore 2.0 (MPS2), a novel urinary biomarker test, predicts clinically significant PCa to reduce invasive biopsy procedures. This study [...] Read more.

Background/Objectives: Prostate cancer (PCa) is a leading cause of cancer-related deaths among men, with early detection playing a crucial role in improving outcomes. MyProstateScore 2.0 (MPS2), a novel urinary biomarker test, predicts clinically significant PCa to reduce invasive biopsy procedures. This study evaluates the analytical performance of MPS2 using both a post-digital rectal exam (DRE) and non-DRE urine samples. Methods: We assessed the reproducibility, precision, and detection limits of the eighteen MPS2 analytes. Analytical parameters including the linear range, upper and lower limits of quantification (ULOQ and LLOQ), and interference from substances commonly present in urine were evaluated. The reproducibility of the MPS2 scores was evaluated across post-DRE and non-DRE clinical urine samples. Results: MPS2 analytes demonstrated high linearity (R² ≥ 0.975) across defined quantification ranges, with PCR efficiencies of 97–105%. The limits of detection (LOD) ranged from 40 to 160 copies/reaction, while the ULOQ was determined to be 10⁶–10⁷ copies/reaction for each analyte. Precision studies showed intra-run, inter-run, and inter-instrument standard deviations ≤0.5 Crt. Among the 12 potential interfering substances, only whole blood affected the performance of MPS2. The reproducibility of the MPS2 scores was consistent across post-DRE and non-DRE urine samples, meeting the acceptance criteria. Conclusions: The analytical validation confirms that MPS2 is robust and reliable in detecting biomarkers for clinically significant PCa. These findings, coupled with previous clinical validations, support the clinical use of MPS2 as a non-invasive diagnostic tool. Full article

(This article belongs to the Section Clinical Laboratory Medicine)

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13 pages, 586 KiB

Open AccessBrief Report

Identification of Coronary Morphological Damage in Patients with Chronic Inflammatory Rheumatic Diseases

by Elena Heras-Recuero, Juan Antonio Martínez-López, Macarena Garbayo-Bugeda, Álvaro Castrillo-Capilla, Teresa Blázquez-Sánchez, Arantxa Torres-Roselló, Antia García-Fernández, Javier Llorca, Raquel Largo, Juan Antonio Franco-Peláez, José Tuñón and Miguel Ángel González-Gay

Diagnostics 2025, 15(7), 922; https://doi.org/10.3390/diagnostics15070922 - 2 Apr 2025

Viewed by 353

Abstract

Objective: Patients with chronic inflammatory rheumatic diseases (CIRDs) have a higher incidence of coronary artery disease (CAD) due to accelerated atherogenesis. This study aimed to assess the extent and location of CAD lesions in CIRD patients compared to non-CIRD patients. Methods: A retrospective [...] Read more.

Objective: Patients with chronic inflammatory rheumatic diseases (CIRDs) have a higher incidence of coronary artery disease (CAD) due to accelerated atherogenesis. This study aimed to assess the extent and location of CAD lesions in CIRD patients compared to non-CIRD patients. Methods: A retrospective study was conducted on CIRD patients (rheumatoid arthritis, ankylosing spondylitis, and psoriatic arthritis) who underwent coronary angiography at Hospital Fundación Jiménez Díaz (Madrid, Spain) between 2018 and 2022. For each CIRD patient, at least two frequency-matched controls were selected based on sex, age (±2 years), diabetic status, and clinical indication for coronary angiography. The indications for coronary angiography in both groups were chronic coronary syndrome and acute coronary syndrome with or without ST elevation. Results: A total of 66 CIRD patients were included, with 42 (63.6%) women, and a median age of 66.6 years (range: 58.3–75.2). Compared to the controls, CIRD patients had a higher number of affected coronary arteries (2.03 vs. 1.56, p = 0.03). The mid-anterior descending artery and the right posterior descending artery were more frequently involved in CIRD patients than in controls (odds ratio [OR] of 2.45 and 3.53, respectively, p ≤ 0.02 for both comparisons). The frequency of coronary calcification was higher in CIRD patients, though the difference did not reach statistical significance (5 of 66 in CIRD patients vs. 3 of 140 in non-CIRD controls, OR of 3.74, p = 0.06). Revascularization was more commonly performed in patients with CIRD (50 of 66 vs. 85 of 140 in those without CIRD (OR: 2.02 [95% CI: 1.01–4.18]; p = 0.03). Conclusions: Patients with CIRD exhibit more extensive CAD, with a higher propensity for involvement inthe mid-anterior descending and right posterior descending arteries compared to patients without CIRD. These findings highlight the need for closer cardiovascular monitoring and early risk stratification in CIRD patients to improve the detection and management of CAD. Full article

(This article belongs to the Special Issue Diagnosis, Prognosis and Management of Cardiovascular Disease in Patients with Rheumatic Conditions)

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20 pages, 31191 KiB

Open AccessGuidelines

Best Practices for the Use of High-Frequency Ultrasound to Guide Esthetic Filler Injections—Part 3: Lower Third of the Face

by Roberta Vasconcelos-Berg, Stella Desyatnikova, Paula Bonavia, Alexander Navarini, Maria Cristina Chammas and Rosa Sigrist

Diagnostics 2025, 15(7), 921; https://doi.org/10.3390/diagnostics15070921 - 2 Apr 2025

Viewed by 540

Abstract

Background: The lower third of the face plays a crucial role in overall facial harmony, and age-related volume loss in areas such as the pre-jowl region, labiomental folds, and lips can significantly impact esthetic appearance. High-resolution ultrasound is helpful for identifying key structures, [...] Read more.

Background: The lower third of the face plays a crucial role in overall facial harmony, and age-related volume loss in areas such as the pre-jowl region, labiomental folds, and lips can significantly impact esthetic appearance. High-resolution ultrasound is helpful for identifying key structures, such as the facial artery, parotid gland, and masseter muscle, which are critical to avoid during filler injections. Objectives: This article, the final installment in a three-part series on ultrasound-guided facial injections, provides an in-depth analysis of the sonographic anatomy of the lower face, including the mandibular, marionette, and chin regions. Methods: This article outlines step-by-step techniques for ultrasound-guided filler procedures, with a focus on the importance of pre- and intra-procedural scanning to ensure safe and accurate filler placement. Results: By employing techniques like “scan before injecting” and “scan while injecting”, injectors aim to reduce risks such as vascular occlusion, muscle injection, and skin necrosis. Discussion: The use of ultrasound guidance in these regions enhances both esthetic outcomes and patient safety, providing optimal results while minimizing complications. With continued advancements, ultrasound-guided injections will become increasingly precise, enabling more targeted and safer treatments in the lower face. Full article

(This article belongs to the Special Issue Ultrasound in the Diagnosis and Management of Skin Diseases)

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19 pages, 5166 KiB

Open AccessArticle

Federated Learning-Based CNN Models for Orthodontic Skeletal Classification and Diagnosis

by Demet Süer Tümen and Mehmet Nergiz

Diagnostics 2025, 15(7), 920; https://doi.org/10.3390/diagnostics15070920 - 2 Apr 2025

Viewed by 441

Abstract

Background/Objectives: Accurate skeletal classification is essential for orthodontic diagnosis. This study evaluates the effectiveness of federated convolutional neural network (CNN) models for skeletal classification using cephalometric images from the ISBI and Dicle datasets. This research aims to evaluate the effectiveness of federated learning [...] Read more.

Background/Objectives: Accurate skeletal classification is essential for orthodontic diagnosis. This study evaluates the effectiveness of federated convolutional neural network (CNN) models for skeletal classification using cephalometric images from the ISBI and Dicle datasets. This research aims to evaluate the effectiveness of federated learning (FL) for orthodontic skeletal classification by comparing its performance against centralized learning (CL) and local learning (LL). The objective is to determine whether FL can achieve competitive performance while preserving data privacy and enabling collaborative model training across multiple institutions. Methods: The DenseNet121 model and its augmented versions, incorporating channel attention, spatial attention, squeeze and excitation, and spatial pyramid pooling blocks, are proposed and adapted for the study. Models are evaluated on the ISBI and Dicle datasets using accuracy, sensitivity, and specificity metrics, with performance gains benchmarked across CL, LL, and FL frameworks. Results: Accuracy improvements exceed 26% compared to the baseline model on FL framework. The DenseNet121_SA model, augmented with spatial pyramid pooling blocks, achieves a 20.86% performance gain over LL settings on the ISBI dataset. Similarly, the DenseNet121_SA model, augmented with spatial attention, and DenseNet121_SA_SE model, augmented with spatial attention and squeeze and excitation, obtain 16.58% and 15.22% by not sacrificing performance loss with respect to CL. The inclusion of the Dicle dataset provides additional validation for the models. Conclusions: Federated CNN models exhibit significant promise for orthodontic skeletal classification. These models demonstrate the potential of FL to enhance collaborative model training while preserving data privacy. This approach represents a step forward in leveraging precise orthodontic diagnostics technology by enabling a data-secure collaborative artificial intelligence among various orthodontic clinics. Full article

(This article belongs to the Special Issue Artificial Intelligence in the Diagnostics of Dental Diseases, 2nd Edition)

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25 pages, 5530 KiB

Open AccessReview

Ultrasound of Bile Ducts—An Update on Measurements, Reference Values, and Their Influencing Factors

by Claudia Lucius, Anja Flückiger, Jennifer Meier, Kathleen Möller, Christian Jenssen, Barbara Braden, Michael Kallenbach, Benjamin Misselwitz, Christian Nolsøe, Michael Sienz, Constantinos Zervides and Christoph Frank Dietrich

Diagnostics 2025, 15(7), 919; https://doi.org/10.3390/diagnostics15070919 - 2 Apr 2025

Viewed by 567

Abstract

Objective: To provide an overview of the technique and normal values of ultrasound studies of the bile system based on the published literature. Methods: A literature search for ultrasound studies with measurements of the bile ducts in healthy subjects was performed. Relevant data [...] Read more.

Objective: To provide an overview of the technique and normal values of ultrasound studies of the bile system based on the published literature. Methods: A literature search for ultrasound studies with measurements of the bile ducts in healthy subjects was performed. Relevant data published between 1975 and end of 2024 were extracted, discussed, and complemented with the own experiences of the authors. The clinical implications are presented and discussed. Results: For the diameter of the common bile duct, reference values between 5 and 9 mm have been published. The main influencing factors are age and history of cholecystectomy, and other factors to be considered are discussed here. The cut-off for the common bile duct wall is set at 1.5 mm. The literature on measurements of intrahepatic bile ducts is scarce. A diameter of <2–3 mm can be considered normal. The method of ultrasound examination is presented here, as well as a comparison with other imaging methods and their clinical implications. Conclusions: Standardized measurement techniques and normal values in the context of influencing factors are crucial for the ultrasound examination of the bile system. Full article

(This article belongs to the Special Issue Imaging Diagnosis in Abdomen, 2nd Edition)

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12 pages, 1495 KiB

Open AccessArticle

Phenotypes and Genotypes of Children with Vitamin D-Dependent Rickets Type 1A: A Single Tertiary Pediatric Center in Vietnam

by Thi Anh Thuong Tran, Tran Minh Dien, Ngoc Lan Nguyen, Khanh Ngoc Nguyen, Thi Bich Ngoc Can, Bui Phuong Thao, Nguyen Thi Thuy Hong, Van Khanh Tran, Thinh Huy Tran, Ngo Xuan Khoa, Nguyen Thi Kim Lien, Nguyen Thien Tao, Huy Hoang Nguyen and Chi Dung Vu

Diagnostics 2025, 15(7), 918; https://doi.org/10.3390/diagnostics15070918 - 2 Apr 2025

Viewed by 418

Abstract

Background: Vitamin D-dependent rickets type 1A (VDDR1A) is a rare autosomal recessive disorder caused by mutations in the CYP27B1 gene, leading to a deficiency in active vitamin D (1,25-dihydroxyvitamin D). This study examines the genotypic and phenotypic characteristics of VDDR1A in Vietnamese [...] Read more.

Background: Vitamin D-dependent rickets type 1A (VDDR1A) is a rare autosomal recessive disorder caused by mutations in the CYP27B1 gene, leading to a deficiency in active vitamin D (1,25-dihydroxyvitamin D). This study examines the genotypic and phenotypic characteristics of VDDR1A in Vietnamese children. Patients and Methods: A retrospective analysis was conducted on 19 Vietnamese children diagnosed with VDDR1A. Clinical, radiological, biochemical, and molecular data were collected. Rickets Severity Scores (RSSs), biochemical parameters, and height standard deviation scores (HtSDSs) were used to assess the severity of the condition. Results: The study included 19 children from 17 families (ten males and nine females). The median age of rickets diagnosis was 19.2 months, while with VDDR1A, the median time of diagnosis was 7.5 months. Common symptoms among the children included thickened wrists and ankles (19/19), genu varum or genu valgum (18/19), failure to thrive (18/19), rachitic rosary (12/19), and delayed walking (11/19). The radiographic features showed that all children had cupping, splaying, and fraying, twelve children had rachitic rosary, and six exhibited pseudofractures. The biochemical findings showed severe hypocalcemia, normal or mildly low serum phosphate, elevated alkaline phosphatase and parathyroid hormone levels, and normal serum 25-hydroxyvitamin D levels. Genetic analysis identified biallelic CYP27B1 variants, including one known pathogenic frameshift mutation, c.1319_1325dup p.(Phe443Profs*24), one novel likely pathogenic missense variant, c.616C>T p.(Arg206Cys), and one novel pathogenic frameshift mutation, c.96_97del p.(Ala33Thrfs*299). The c.1319_1325dup p.(Phe443Profs*24) variant was the most common, present in 18 out of 19 children. Conclusions: The children with VDDR1A in this study presented with growth failure and skeletal deformities. Key findings included severe hypocalcemia, elevated alkaline phosphatase and parathyroid hormone levels, normal or elevated 25(OH)D, and high RSSs. Predominant frameshift mutations in CYP27B1, especially c.1319_1325dup, highlighted the importance of early genetic diagnosis for optimal management. Additionally, two novel CYP27B1 variants were identified, expanding the known mutation spectrum of VDDR1A. Full article

(This article belongs to the Special Issue Diagnosis and Management of Metabolic Bone Diseases: 2nd Edition)

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10 pages, 1230 KiB

Open AccessArticle

Surgical Management of Sacral Bone Tumors: A Retrospective Analysis of Outcomes, Complications, and Survival

by Chiara Cini, Emanuela Asunis, Cristiana Griffoni, Gisberto Evangelisti, Giuseppe Tedesco, Riccardo Ghermandi, Marco Girolami, Valerio Pipola, Silvia Terzi, Giovanni Barbanti Brodano, Stefano Bandiera, Stefano Boriani and Alessandro Gasbarrini

Diagnostics 2025, 15(7), 917; https://doi.org/10.3390/diagnostics15070917 - 2 Apr 2025

Viewed by 322

Abstract

Background: Primary malignant bone tumors are exceedingly rare, with an incidence of 0.5 to 1 per million, and sacral localization is even more uncommon, representing only 1–3.5% of these tumors. These malignancies are often diagnosed late due to their asymptomatic nature until [...] Read more.

Background: Primary malignant bone tumors are exceedingly rare, with an incidence of 0.5 to 1 per million, and sacral localization is even more uncommon, representing only 1–3.5% of these tumors. These malignancies are often diagnosed late due to their asymptomatic nature until they present as large, advanced intrapelvic tumors. Management is complicated by the need for precise surgical intervention and the consideration of adjuvant therapies based on tumor histology and patient factors. Methods: We conducted a single-center, retrospective analysis of patients who underwent complete, partial, or hemisacrectomy for primary malignant bone tumors or recurrent sacral metastases. Excluded were patients with metastatic disease not necessitating sacrectomy. Data collected included demographics, clinical characteristics, tumor types, resection status, adjuvant therapies, recurrence, metastasis, and complications. Surgical approaches were categorized as posterior, anterior, or combined anterior–posterior. The primary outcomes were overall survival and disease-free survival, while the secondary outcomes focused on complication rates and functional outcomes. Results: The study included 19 patients (7 females, 12 males) with a mean age of 48.9 years at the time of surgery. Primary malignancies were present in 90% of patients. Surgical approaches varied: 20% underwent double access and 5% anterior access only, and the remainder had posterior approaches. High partial sacrectomy (above S3) was performed in 20%, while low sacrectomy (at or below S3) was performed in 80%. Complete resection with clean margins (R0) was achieved in 65% of cases, while 35% had R1 resections with microscopic tumor remnants. Root resection was necessary in 25% of patients. Local recurrence occurred in 25% of patients, with two requiring reoperation and neurological sacrifice. Distant metastases were observed in 20% of cases. Postoperative complications affected 60% of patients. The most common issues were surgical wound dehiscence with delayed healing (35%) and visceral changes affecting the bowel and urination (25%). No mechanical complications were reported. Conclusions: Sacrectomy remains a challenging procedure with substantial morbidity and variability in outcomes. The choice of surgical approach—posterior, anterior, or combined—depends on tumor location and extent. While posterior-only approaches are often preferred for lower sacral lesions, combined approaches may be necessary for more extensive tumors. Survival and disease-free survival rates are influenced by resection margins and the biological behavior of the tumor. Wide-margin resections (R0) are associated with lower local recurrence rates but do not eliminate the risk of distant metastases. Full article

(This article belongs to the Special Issue Diagnosis and Management of Soft Tissue and Bone Tumors)

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15 pages, 1743 KiB

Open AccessArticle

Identification of Eye Diseases Through Deep Learning

by Elena Acevedo, Dinora Orantes, Marco Acevedo and Ricardo Carreño

Diagnostics 2025, 15(7), 916; https://doi.org/10.3390/diagnostics15070916 - 2 Apr 2025

Viewed by 505

Abstract

Background: Ocular diseases have been a severe problem worldwide, specifically in underdeveloped countries that do not have enough technology or economy to treat them. It would be beneficial to have software with low installation complexity and ease of use, allowing high efficacy [...] Read more.

Background: Ocular diseases have been a severe problem worldwide, specifically in underdeveloped countries that do not have enough technology or economy to treat them. It would be beneficial to have software with low installation complexity and ease of use, allowing high efficacy in diagnosing eye diseases. This study aims to design and implement an algorithm based on deep learning to classify ocular diseases with high precision. Methods: This work describes digital image processing techniques for the easier handling of eye images; in particular, blur filters were used. The Canny filter was also applied to obtain the edges that allow the difference between the analyzed diseases. Once the images were pre-processed, a convolutional neural network of our own design was applied to perform the classification task. The validation algorithm used in this work was the hold-out algorithm (80–20). The metrics used to evaluate our proposal were the confusion matrix, accuracy, recall precision, and F1-score. Results: The dataset has five classes, namely, normal, cataract, diabetic retinopathy, glaucoma, and other retina diseases. The network architecture consists of 11 layers, including three convolutional layers, three max pooling layers, one batch normalization layer, one flattening layer, two hidden layers, and one output layer. This model resulted in 97% efficiency across all metrics. Conclusions: With the individual analysis of each metric, it can be observed that the proposed algorithm is capable of differentiating, first, images of healthy eyes from diseased ones and, second, adequately classifying eye diseases. Full article

(This article belongs to the Special Issue Updates on the Diagnosis and Management of Retinal Diseases)

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13 pages, 1052 KiB

Open AccessArticle

Sex Bias in Frailty Screening: A Cross-Sectional Analysis of PRISMA-7 and the Clinical Frailty Scale in Primary Care

by Christian J. Wiedermann, Verena Barbieri, Dietmar Ausserhofer, Adolf Engl, Giuliano Piccoliori and Angelika Mahlknecht

Diagnostics 2025, 15(7), 915; https://doi.org/10.3390/diagnostics15070915 - 2 Apr 2025

Viewed by 305

Abstract

Background/Objectives: Frailty screening is essential in primary care for the early identification of vulnerable older adults. PRISMA-7 is a widely used screening tool, but Item 2 (“Are you male?”) introduces potential sex bias and overestimates frailty in men. PRISMA-6, a modified version [...] Read more.

Background/Objectives: Frailty screening is essential in primary care for the early identification of vulnerable older adults. PRISMA-7 is a widely used screening tool, but Item 2 (“Are you male?”) introduces potential sex bias and overestimates frailty in men. PRISMA-6, a modified version that excludes Item 2, might provide a more equitable alternative. This study evaluates PRISMA-6’s alignment with the Clinical Frailty Scale (CFS) and its impact on sex-specific frailty classification. Methods: A cross-sectional study was conducted in 142 general practices across South Tyrol, including 9190 general practice patients aged ≥75 years. Frailty was assessed using PRISMA-7, PRISMA-6, and the CFS. Correlations between tools were calculated using Kendall’s Tau-b, whereas Fisher’s z-test was used to compare differences in alignment. The frailty prevalence and odds ratios were stratified according to sex and age. Results: PRISMA-6 showed a stronger correlation with the CFS (τ = 0.492) than PRISMA-7 (τ = 0.308, z = −10.2, p < 0.001). This effect was pronounced in men (z = −9.8, p < 0.001), whereas no difference was observed in women (z = 0.00, p = 1.000). PRISMA-6 reduced the frailty detection rate in men and was more closely aligned with the CFS. Conclusions: PRISMA-6 demonstrated improved alignment with the CFS and reduced sex bias compared to PRISMA-7. However, its use as a screening tool for men requires prospective validation in diverse settings. PRISMA-6 shows promise as a reliable and equitable frailty screening tool and should be considered for use in future studies, particularly in primary care settings, while awaiting further prospective validation. Full article

(This article belongs to the Special Issue Risk Factors for Frailty in Older Adults)

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Open AccessArticle

Mesopancreas—Anatomical Insights and Its Implications for Diagnosis and Clinical and Surgical Practice

by Florin-Mihail Filipoiu, Georgian-Theodor Badea, Mihaly Enyedi, Ștefan Oprea, Zoran-Florin Filipoiu and Daniela-Elena Gheoca Mutu

Diagnostics 2025, 15(7), 914; https://doi.org/10.3390/diagnostics15070914 - 2 Apr 2025

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Abstract

Background: The concept of mesopancreas is frequently discussed in the surgical literature as the neural pathway for metastatic spread in pancreatic head cancer. It generally refers to a retro-pancreatic plane that should be resected to reduce the incidence of regional metastases. However, this [...] Read more.

Background: The concept of mesopancreas is frequently discussed in the surgical literature as the neural pathway for metastatic spread in pancreatic head cancer. It generally refers to a retro-pancreatic plane that should be resected to reduce the incidence of regional metastases. However, this concept remains poorly defined, both embryologically and anatomically. Our objective was to establish a clear embryological and anatomical definition of the mesopancreas, making anatomical data more applicable in surgical practice. Methods: We examined seven cadavers (5 males, 2 females, aged 62–71) with no medical or surgical history, preserved in 9% formalin at Carol Davila University’s Anatomy Department. Regional dissections were performed in successive planes, highlighting the celiac ganglia and the associated network of neural connections that comprise the mesopancreas. Results: Our study defines the “mesopancreas” as remnants of primordial mesenteries that coalesced into the Treitz fascia. We identified its functional components as nerve fibers linking the celiac ganglia and superior mesenteric plexus to the pancreas, along with vascular structures, lymphatics, and connective and adipose tissue. These components likely contribute to regional metastasis in pancreatic head cancer. While resection of the mesopancreas could help prevent metastasis, its complex anatomy and proximity to major vessels pose significant surgical challenges. Conclusions: Based on our findings, we propose a plausible definition for the term “mesopancreas”. It encompasses the structures that originated as part of the primordial mesenteries, which subsequently coalesced, resulting in the formation of the Treitz fascia. In essence, the mesopancreas is the functional content of a former mesentery. Full article

(This article belongs to the Special Issue Abdominal Diseases: Diagnosis, Treatment and Management)

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Diagnostics, Volume 15, Issue 7 (April-1 2025) – 151 articles

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