Bone Disorder Therapeutics: Novel Drug Candidates and Treatment Strategies

A special issue of Pharmaceuticals (ISSN 1424-8247). This special issue belongs to the section "Pharmacology".

Deadline for manuscript submissions: closed (31 January 2025) | Viewed by 1198

Special Issue Editor


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Guest Editor
Orthopedic Research Laboratory, Hôpital du Sacré-Coeur de Montréal, Université de Montréal, Montréal, QC H4J 1C5, Canada
Interests: osteoarthritis; drug delivery; gene delivery; biomaterials
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Special Issue Information

Dear Colleagues,

Bone disorders represent a significant global health burden, characterized by a diverse range of pathologies affecting bone structure and function. The development of innovative drug candidates and therapies to address these conditions remains a critical unmet medical need. This Special Issue aims to highlight cutting-edge research focused on the discovery, preclinical development, and clinical translation of promising therapeutic approaches for bone disorders.

We invite contributions that explore a wide spectrum of therapeutic modalities, including small molecules, biologics, gene therapies, and cell-based therapies. Potential topics of interest include, but are not limited to, the following:

  • Novel drug targets and mechanisms of action;
  • Formulation and delivery strategies;
  • Preclinical efficacy and safety studies;
  • Clinical trial design and outcomes;
  • Biomarkers for disease progression and therapeutic response.

By fostering collaboration and knowledge exchange among researchers in academia, industry, and clinical settings, this Special Issue seeks to accelerate the development of effective treatments for patients with bone disorders.

Dr. Mahdi Rahimi
Guest Editor

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Keywords

  • bone health
  • osteoporosis
  • arthritis
  • osteoarthritis
  • bone cancer
  • regeneration
  • repair
  • metabolism
  • gene therapy
  • cell therapy

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Published Papers (1 paper)

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Research

18 pages, 1706 KiB  
Article
Development of a Medication-Related Osteonecrosis of the Jaw Prediction Model Using the FDA Adverse Event Reporting System Database and Machine Learning
by Shinya Toriumi, Komei Shimokawa, Munehiro Yamamoto and Yoshihiro Uesawa
Pharmaceuticals 2025, 18(3), 423; https://doi.org/10.3390/ph18030423 - 17 Mar 2025
Cited by 1 | Viewed by 912
Abstract
Background: Medication-related osteonecrosis of the jaw (MRONJ) is a rare but serious adverse event. Herein, we conducted a quantitative structure–activity relationship analysis using the U.S. Food and Drug Administration Adverse Drug Reaction Database System (FAERS) and machine learning to construct a drug prediction [...] Read more.
Background: Medication-related osteonecrosis of the jaw (MRONJ) is a rare but serious adverse event. Herein, we conducted a quantitative structure–activity relationship analysis using the U.S. Food and Drug Administration Adverse Drug Reaction Database System (FAERS) and machine learning to construct a drug prediction model for MRONJ induction based solely on chemical structure information. Methods: A total of 4815 drugs from FAERS were evaluated, including 70 and 139 MRONJ-positive and MRONJ-negative drugs, respectively, identified based on reporting odds ratios, Fisher’s exact tests, and ≥100 total adverse event reports. Then, we calculated 326 chemical structure descriptors for each drug and compared three supervised learning algorithms (random forest, gradient boosting, and artificial neural networks). We also compared the number of chemical structure descriptors (5, 6, 7, 8, 9, 10, 20, and 30 descriptors). Results: We indicated that the MRONJ prediction model using an artificial neural network algorithm and eight descriptors achieved the highest validation receiver operating characteristic curve value of 0.778. Notably, the total polar surface area (ASA_P) was among the top-ranking descriptors, and MRONJ-positive drugs such as bisphosphonates and anticancer drugs showed high values. Our final model demonstrated a balanced accuracy of 0.693 and a specificity of 0.852. Conclusions: In this study, our MRONJ-inducing drug prediction model identified drugs with polar surface area properties as potential causes of MRONJ. This study demonstrates a promising approach for predicting MRONJ risk, which could enhance drug safety assessment and streamline drug screening in clinical and preclinical settings. Full article
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