You are currently on the new version of our website. Access the old version .

37 Results Found

  • Review
  • Open Access
6 Citations
4,707 Views
29 Pages

An Update in Cystic Fibrosis-Related Diabetes in Children and Adolescents

  • Dana-Teodora Anton-Păduraru,
  • Alina Mariela Murgu,
  • Mădălina Andreea Donos,
  • Felicia Trofin,
  • Alice Nicoleta Azoicăi,
  • Paula Popovici,
  • Aurelian Bogdan Stana,
  • Ionela Gheorghiescu and
  • Laura Mihaela Trandafir

30 November 2023

This paper delineates several aspects of cystic fibrosis-related diabetes (CFRD)—a common complication of cystic fibrosis (CF). CFRD exhibits a predilection for older individuals with CF, yet it also extends its influence on children and adoles...

  • Article
  • Open Access
4 Citations
2,492 Views
9 Pages

Cystic Fibrosis-Related Diabetes in Poland

  • Marta Rachel,
  • Marek Biesiadecki and
  • Sabina Galiniak

Cystic fibrosis (CF) is the most common autosomal recessive inherited monogenic disease in Caucasians. As medical technology progresses and the quality of patient care improves, the survival time of patients with CF has increased, which results in mo...

  • Review
  • Open Access
22 Citations
7,689 Views
16 Pages

Cystic Fibrosis-Related Diabetes (CFRD): Overview of Associated Genetic Factors

  • Fernanda Iafusco,
  • Giovanna Maione,
  • Francesco Maria Rosanio,
  • Enza Mozzillo,
  • Adriana Franzese and
  • Nadia Tinto

Cystic fibrosis (CF) is the most common autosomal recessive disease in the Caucasian population and is caused by mutations in the CF transmembrane conductance regulator (CFTR) gene that encodes for a chloride/bicarbonate channel expressed on the memb...

  • Article
  • Open Access
983 Views
11 Pages

Prevalence and Characteristics of Patients with Cystic Fibrosis-Related Diabetes in Croatia

  • Lora Stanka Kirigin Biloš,
  • Maja Baretić,
  • Andrea Vukić Dugac,
  • Krešimir Schoenwald,
  • Ivan Bambir,
  • Duška Tješić Drinković,
  • Nevena Krnić and
  • Velimir Altabas

20 May 2025

This study investigated the prevalence of cystic fibrosis-related diabetes (CFRD) in the Croatian cystic fibrosis (CF) population, the age at diagnosis, insulin requirements, and the relationship between age at diagnosis and other clinical parameters...

  • Systematic Review
  • Open Access
5 Citations
3,680 Views
15 Pages

Screening Methods for Diagnosing Cystic Fibrosis-Related Diabetes: A Network Meta-Analysis of Diagnostic Accuracy Studies

  • Vera Dóra Izsák,
  • Alexandra Soós,
  • Zsolt Szakács,
  • Péter Hegyi,
  • Márk Félix Juhász,
  • Orsolya Varannai,
  • Ágnes Rita Martonosi,
  • Mária Földi,
  • Alexandra Kozma and
  • Andrea Párniczky
  • + 2 authors

31 March 2021

Background: Cystic fibrosis-related diabetes (CFRD) has become more common due to higher life expectancy with cystic fibrosis. Early recognition and prompt treatment of CFRD leads to improved outcomes. Methods: We performed a network meta-analysis (N...

  • Article
  • Open Access
544 Views
13 Pages

Role of Matsuda Index in Identifying Patients at Risk for Cystic Fibrosis-Related Diabetes Development

  • Serpil Albayrak,
  • Elif Arık,
  • Özlem Keskin,
  • Murat Karaoğlan,
  • Mehmet Keskin,
  • Gaye İnal,
  • Mahmut Cesur,
  • Ercan Küçükosmanoğlu and
  • Ahmet Yıldırım

18 November 2025

Background: Cystic fibrosis-related diabetes (CFRD) is a frequent comorbidity in individuals with cystic fibrosis (CF). While insulin secretion defects are the primary mechanism in CFRD pathophysiology, insulin resistance may contribute as an additio...

  • Review
  • Open Access
8 Citations
2,884 Views
18 Pages

Oxidative Stress Biomarkers in Cystic Fibrosis and Cystic Fibrosis-Related Diabetes in Children: A Literature Review

  • Anca Daniela Pinzaru,
  • Cristina Maria Mihai,
  • Tatiana Chisnoiu,
  • Alexandru Cosmin Pantazi,
  • Vasile Valeriu Lupu,
  • Mustafa Ali Kassim Kassim,
  • Ancuta Lupu,
  • Elena Grosan,
  • Ahmed Zaki Naji Al Jumaili and
  • Ileana Ion
  • + 2 authors

29 September 2023

The most common inherited condition that results in death, particularly in those of Caucasian heritage, is cystic fibrosis (CF). Of all the young adults diagnosed with cystic fibrosis, 20% will develop hyperglycemia as a complication, later classifie...

  • Article
  • Open Access
20 Citations
8,356 Views
23 Pages

FOXO1 Content Is Reduced in Cystic Fibrosis and Increases with IGF-I Treatment

  • Arianna Smerieri,
  • Luisa Montanini,
  • Luigi Maiuri,
  • Sergio Bernasconi and
  • Maria E. Street

8 October 2014

Cystic fibrosis-related diabetes is to date the most frequent complication in cystic fibrosis (CF). The mechanisms underlying this condition are not well understood, and a possible role of insulin resistance is debated. We investigated insulin signal...

  • Article
  • Open Access
729 Views
13 Pages

Nutritional and Morphofunctional Assessment in a Cohort of Adults Living with Cystic Fibrosis with or Without Pancreatic Exocrine and/or Endocrine Involvement

  • Ana Piñar-Gutiérrez,
  • José Luis Pereira-Cunill,
  • Andrés Jiménez-Sánchez,
  • Silvia García-Rey,
  • María del Carmen Roque-Cuéllar,
  • Antonio J. Martínez-Ortega,
  • Irene González-Navarro,
  • Esther Quintana-Gallego,
  • Ángeles Pizarro and
  • Pedro Pablo García-Luna
  • + 2 authors

20 June 2025

Objectives: To describe the results of nutritional and morphofunctional assessment in a cohort of adults with cystic fibrosis; to evaluate differences in nutritional status between patients with and without exocrine and/or endocrine pancreatic involv...

  • Review
  • Open Access
6 Citations
2,710 Views
13 Pages

14 March 2024

Cystic fibrosis-related diabetes (CFRD) is the most common comorbidity in patients with cystic fibrosis (CF). CFRD has been correlated with important clinical outcomes, including poor nutrition, reduced pulmonary function, and earlier mortality. Howe...

  • Article
  • Open Access
3 Citations
2,603 Views
12 Pages

Evaluation of Insulin Secretion and Continuous Glucose Monitoring in Patients with Cystic Fibrosis After Initiation of Transmembrane Conductance Regulator Modulator: A 52-Week Prospective Study

  • Ane Bayona,
  • Edurne Lecumberri Pascual,
  • Saioa Vicente,
  • Luis Maíz,
  • Ana Morales,
  • Adelaida Lamas,
  • Cristina Sánchez Rodríguez,
  • Rosa Yelmo,
  • María Martín-Frías and
  • Lía Nattero-Chávez
  • + 2 authors

24 October 2024

Introduction: Limited studies have explored the impact of cystic fibrosis (CF) transmembrane conductance regulator (CFTR) modulators on glucose tolerance and insulin secretion in patients with CF, yielding varied results. This study aims to assess al...

  • Article
  • Open Access
9 Citations
3,625 Views
9 Pages

12 November 2021

Objective: Cystic fibrosis-related diabetes (CFRD) affects up to half of the people with cystic fibrosis (CF) by adulthood. CFRD is primarily caused by pancreatic dysfunction that leads to insufficient insulin release and/or insulin resistance. Exocr...

  • Review
  • Open Access
12 Citations
5,869 Views
18 Pages

Evolving Nutritional Needs in Cystic Fibrosis

  • Theresa Frantzen,
  • Sara Barsky,
  • Geralyn LaVecchia,
  • Michelle Marowitz and
  • Janice Wang

22 June 2023

The course of cystic fibrosis (CF) as a nutritional illness is diverging since the introduction of highly effective modulator therapy, leading to more heterogeneous phenotypes of the disease despite CF genetic mutations that portend worse prognosis....

  • Article
  • Open Access
4 Citations
2,545 Views
12 Pages

Continuous Glucose Monitoring as an Additional Tool in Early Cystic Fibrosis-Related Diabetes Monitoring and in Evaluation of Short-Term Sitagliptin Response

  • Fernando Sebastian-Valles,
  • José Alfonso Arranz Martín,
  • Rosa María Girón,
  • Carolina Knott-Torcal,
  • Miguel Antonio Sampedro-Nuñez,
  • Jose Carlos Martin-Adan,
  • Jessica Jiménez-Díaz and
  • Mónica Marazuela

Cystic fibrosis-related diabetes (CFRD) is a complication associated with a negative prognosis in patients with cystic fibrosis (CF). Although the oral glucose tolerance test (OGTT) is the widely recommended screening test for CFRD diagnosis, continu...

  • Article
  • Open Access
3 Citations
1,748 Views
9 Pages

One-Year Effect of Elexacaftor/Tezacaftor/Ivacaftor Therapy on HbA1c Levels and Insulin Requirement in Patients with Insulin-Dependent Cystic Fibrosis-Related Diabetes: A Retrospective Observational Study

  • Marta Bassi,
  • Marina Francesca Strati,
  • Gaia Spiandorello,
  • Marta Scalas,
  • Federico Cresta,
  • Maria Grazia Calevo,
  • Giuseppe d’Annunzio,
  • Carlo Castellani,
  • Nicola Minuto and
  • Rosaria Casciaro
  • + 1 author

16 October 2024

Introduction: The impact of ETI therapy on pulmonary function and nutritional status has been widely studied; the literature on the possible outcomes on glycemic control and insulin requirement in patients affected by CFRD is controversial. Aim: The...

  • Review
  • Open Access
24 Citations
5,404 Views
11 Pages

Future Comorbidities in an Aging Cystic Fibrosis Population

  • Javier Humberto Ticona,
  • Nicole Lapinel and
  • Janice Wang

31 May 2023

Cystic fibrosis (CF) is an autosomal recessive disease due to mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. With the advent of highly effective modulator therapy targeting the abnormal CFTR protein, people with CF...

  • Review
  • Open Access
2 Citations
1,892 Views
19 Pages

People with diabetes are at increased risk of developing lung infections and have more severe complications. However, the link between these risks and outcomes is unknown. These trends are also seen in people with chronic lung diseases, including cys...

  • Brief Report
  • Open Access
1 Citations
2,391 Views
6 Pages

Oral Glucose Tolerance Testing Using Candy: A Sweet Solution to Improve Screening in Children with Cystic Fibrosis?

  • Caroline Weeks,
  • Sarah Jackson,
  • Nadir Demirel,
  • Janelle Olson,
  • Vicki Dean,
  • Caitlin Pyrz and
  • Ana L. Creo

31 July 2023

Introduction: Oral glucose tolerance testing is recommended for all children with CF older than 9 years, yet compliance remains poor across centers. Methods: We performed a small pilot study assessing the glycemic curves and participant satisfaction...

  • Feature Paper
  • Review
  • Open Access
985 Views
14 Pages

Evolving Cystic Fibrosis Care: Lung Immunology and Emerging Health Challenges in the Era of CFTR Modulators

  • Giuseppe Fabio Parisi,
  • Maria Papale,
  • Giulia Pecora,
  • Santiago Presti,
  • Monica Tosto,
  • Enza Mulé,
  • Vittorio Ornato,
  • Donatella Aloisio and
  • Salvatore Leonardi

16 October 2025

The introduction of CFTR modulators has dramatically shifted the clinical management of cystic fibrosis (CF) from a life-limiting pediatric condition to a chronic disease with broader health implications. This review explores the impact of these adva...

  • Article
  • Open Access
2 Citations
2,108 Views
16 Pages

Distribution of OGTT-Related Variables in Patients with Cystic Fibrosis from Puberty to Adulthood: An Italian Multicenter Study

  • Andrea Foppiani,
  • Fabiana Ciciriello,
  • Arianna Bisogno,
  • Silvia Bricchi,
  • Carla Colombo,
  • Federico Alghisi,
  • Vincenzina Lucidi,
  • Maria Ausilia Catena,
  • Mariacristina Lucanto and
  • Alberto Battezzati
  • + 2 authors

3 March 2023

Background: Insulin secretion and glucose tolerance is annually assessed in patients with cystic fibrosis (PwCF) through oral glucose tolerance tests (OGTTs) as a screening measure for cystic fibrosis-related diabetes. We aimed to describe the distri...

  • Review
  • Open Access
15 Citations
9,924 Views
11 Pages

Low Glycaemic Index Dietary Interventions in Youth with Cystic Fibrosis: A Systematic Review and Discussion of the Clinical Implications

  • Ben W. R. Balzer,
  • Christie L. Graham,
  • Maria E. Craig,
  • Hiran Selvadurai,
  • Kim C. Donaghue,
  • Jennie C. Brand-Miller and
  • Kate S. Steinbeck

18 April 2012

A systematic review was conducted to assess what is known about the effect of low glycaemic index (GI) diets on glycaemic control, weight and quality of life in youth with cystic fibrosis (CF). Eligibility criteria were systematic reviews, randomised...

  • Article
  • Open Access
18 Citations
4,072 Views
10 Pages

Feasibility and Efficacy of Telehealth-Based Resistance Exercise Training in Adolescents with Cystic Fibrosis and Glucose Intolerance

  • Clifton J. Holmes,
  • Susan B. Racette,
  • Leslie Symonds,
  • Ana Maria Arbeláez,
  • Chao Cao and
  • Andrea Granados

The aims of this study were to (1) determine the feasibility of a home-based resistance exercise training (RET) program in patients with cystic fibrosis and impaired glucose tolerance using virtual personal training and (2) observe the effects comple...

  • Article
  • Open Access
4 Citations
3,060 Views
10 Pages

The Relation between Vitamin D Level and Lung Clearance Index in Cystic Fibrosis—A Pilot Study

  • Mihaela Dediu,
  • Ioana Mihaiela Ciuca,
  • Liviu Laurentiu Pop and
  • Daniela Iacob

Background: Life expectancy has increased in cystic fibrosis (CF) patients; however, the rate of mortality is still high, and in a majority of cases, the cause of death is due to respiratory deterioration. Vitamin D plays an important role in immunit...

  • Review
  • Open Access
13 Citations
3,993 Views
14 Pages

Reproductive Counseling and Care in Cystic Fibrosis: A Multidisciplinary Approach for a New Therapeutic Era

  • Julie McGlynn,
  • Joan K. DeCelie-Germana,
  • Catherine Kier and
  • Elinor Langfelder-Schwind

12 July 2023

With the advent of highly effective modulator therapies, many people with cystic fibrosis (CF) are living longer, healthier lives. Pregnancy rates for women with CF more than doubled between 2019 and 2021, reflecting increases in both planned and unp...

  • Review
  • Open Access
56 Citations
10,478 Views
23 Pages

15 March 2023

Elexacaftor/Tezacaftor/Ivacaftor (ELX/TEZ/IVA) is a new CFTR (Cystic Fibrosis Transmembrane Conductance Regulator) modulator treatment, used over the last few years, which has shown an improvement in different clinical outcomes in patients with cysti...

  • Article
  • Open Access
5 Citations
2,414 Views
12 Pages

(1) Background: In cystic fibrosis (CF), the oral glucose tolerance test (OGTT) is recommended from 10 years old annually to screen and diagnose cystic fibrosis-related diabetes (CFRD). Alternative OGTT characteristics (glucose curve shape, time to g...

  • Review
  • Open Access
4 Citations
838 Views
5 Pages

Pleiotropic Effect of Vitamin D in Cystic Fibrosis

  • Teresa Grzelak and
  • Klaudia Mikołajczyk

15 August 2018

Cystic fibrosis (CF) is the most common recessively autosomally and inherited disorder in the Caucasian population. It is incurable, multi-systemic disease with progressive course. CF is caused by CFTR gene mutation, the product of which is Cystic Fi...

  • Article
  • Open Access
2 Citations
3,208 Views
11 Pages

DNAJB11 Mutation in ADPKD Patients: Clinical Characteristics in a Monocentric Cohort

  • Valeria Aiello,
  • Francesca Ciurli,
  • Amalia Conti,
  • Carlotta Pia Cristalli,
  • Sarah Lerario,
  • Francesca Montanari,
  • Nicola Sciascia,
  • Gisella Vischini,
  • Benedetta Fabbrizio and
  • Irene Capelli
  • + 6 authors

19 December 2023

Autosomal Dominant Polycystic Kidney Disease (ADPKD) is a late-onset cilia-related disorder, characterized by progressive cystic enlargement of the kidneys. It is genetically heterogeneous with PKD1 and PKD2 pathogenic variants identified in approxim...

  • Review
  • Open Access
46 Citations
6,300 Views
22 Pages

Genistein—Opportunities Related to an Interesting Molecule of Natural Origin

  • Ewa Garbiec,
  • Judyta Cielecka-Piontek,
  • Magdalena Kowalówka,
  • Magdalena Hołubiec and
  • Przemysław Zalewski

26 January 2022

Nowadays, increasingly more attention is being paid to a holistic approach to health, in which diet contributes to disease prevention. There is growing interest in functional food that not only provides basic nutrition but has also been demonstrated...

  • Review
  • Open Access
16 Citations
6,451 Views
15 Pages

16 February 2023

The pancreas represents an important organ that has not been comprehensively studied in many fields. To fill this gap, many models have been generated, and traditional models have shown good performance in addressing pancreatic-related diseases, but...

  • Review
  • Open Access
35 Citations
33,542 Views
22 Pages

Causes of Exocrine Pancreatic Insufficiency Other Than Chronic Pancreatitis

  • Lumír Kunovský,
  • Petr Dítě,
  • Petr Jabandžiev,
  • Michal Eid,
  • Karolina Poredská,
  • Jitka Vaculová,
  • Dana Sochorová,
  • Pavel Janeček,
  • Pavla Tesaříková and
  • Zdeněk Kala
  • + 3 authors

10 December 2021

Exocrine pancreatic insufficiency (EPI), an important cause of maldigestion and malnutrition, results from primary pancreatic disease or is secondary to impaired exocrine pancreatic function. Although chronic pancreatitis is the most common cause of...

  • Review
  • Open Access
2,702 Views
25 Pages

Evolution and Prognostic Variables of Cystic Fibrosis in Children and Young Adults: A Narrative Review

  • Mădălina Andreea Donos,
  • Elena Țarcă,
  • Elena Cojocaru,
  • Viorel Țarcă,
  • Lăcrămioara Ionela Butnariu,
  • Valentin Bernic,
  • Paula Popovici,
  • Solange Tamara Roșu,
  • Mihaela Camelia Tîrnovanu and
  • Laura Mihaela Trandafir
  • + 1 author

Introduction: Cystic fibrosis (CF) is a genetic condition affecting several organs and systems, including the pancreas, colon, respiratory system, and reproductive system. The detection of a growing number of CFTR variants and genotypes has contribut...

  • Review
  • Open Access
61 Citations
7,264 Views
17 Pages

10 November 2020

Chronic inflammatory diseases are considered to be one of the biggest threats to human health. Most prescribed pharmaceutical drugs aiming to treat these diseases are characterized by side-effects and negatively affect therapy adherence. Finding alte...

  • Article
  • Open Access
28 Citations
14,188 Views
13 Pages

1 February 2025

Introduction: Glucagon-like peptide-1 receptor agonists (GLP-1 RAs) are commonly prescribed for the management of type 2 diabetes mellitus (T2DM). However, the potential connection between GLP-1 RAs and the risk of pancreatitis presents a complex and...

  • Review
  • Open Access
25 Citations
22,337 Views
16 Pages

5 January 2022

Vitamin K2 activates vitamin K-dependent proteins that support many biological functions, such as bone mineralization, the inhibition of vascular stiffness, the improvement of endothelial function, the maintenance of strong teeth, brain development,...

  • Article
  • Open Access
2 Citations
2,023 Views
12 Pages

Polymorphisms of the Vitamin D Binding Protein (VDBP) and Free Vitamin D in Patients with Cystic Fibrosis

  • Paula Quesada-Colloto,
  • Noelia Avello-Llano,
  • Ruth García-Romero,
  • María Garriga-García,
  • Marina Álvarez-Beltrán,
  • Ana Isabel Reyes-Domínguez,
  • Ana Estefanía Fernández-Lorenzo,
  • Helena Gil-Peña,
  • Carlos Gómez-Alonso and
  • David González-Jiménez
  • + 8 authors

11 November 2024

Objectives/Background: Vitamin D-binding protein (VDBP) and free vitamin D are new markers that are being studied as a possible markers of vitamin D status. The main aim of our study was to analyze the VDBP genotype and quantify the levels of free vi...

  • Article
  • Open Access
39 Citations
5,448 Views
12 Pages

First Wave of COVID-19 in French Patients with Cystic Fibrosis

  • Harriet Corvol,
  • Sandra de Miranda,
  • Lydie Lemonnier,
  • Astrid Kemgang,
  • Martine Reynaud Gaubert,
  • Raphael Chiron,
  • Marie-Laure Dalphin,
  • Isabelle Durieu,
  • Jean-Christophe Dubus and
  • Pierre-Régis Burgel
  • + 7 authors

10 November 2020

Viral infections are known to lead to serious respiratory complications in cystic fibrosis (CF) patients. Hypothesizing that CF patients were a population at high risk for severe respiratory complications from SARS-CoV-2 infection, we conducted a nat...