Assessing the translational value of animal models in developing pain-targeting therapies for clinical osteoarthritis

Abstract Osteoarthritis (OA) is a highly prevalent and disabling disease, with pain as its most debilitating symptom. Despite extensive preclinical research, no therapy has successfully translated from animal models into routine clinical use. Commonly used animal models (e.g., acute, surgically, or chemically induced OA in young, single-sex animals) often fail to reflect the chronic and multifactorial human condition, which is often seen in older, postmenopausal women with comorbidities and mixed nociceptive–neuropathic pain. This review aims to identify animal models and pain assessment methods for predicting drug efficacy in OA pain management and to examine the translational gap, focusing on pain as a primary endpoint in animal and human clinical studies. Ultimately, we emphasize the need for phenotype-specific, clinically relevant models to improve translational validity and accelerate the development of effective OA pain therapies.

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Publication Details

Journal
Communications Medicine
Published
2026-10-08
DOI
https://doi.org/10.1038/s43856-026-01926-7
Primary Topic
Osteoarthritis Treatment and Mechanisms
Type
article
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article

Assessing the translational value of animal models in developing pain-targeting therapies for clinical osteoarthritis

Nico Sollmann, Carmen Corciulo, Jaqueline Lourdes Rios, Ali Mobasheri et al.
Communications Medicine
Osteoarthritis Treatment and Mechanisms
article

Assessing the translational value of animal models in developing pain-targeting therapies for clinical osteoarthritis

Nico Sollmann, Carmen Corciulo, Jaqueline Lourdes Rios, Ali Mobasheri, Rosa Maria Nothnagel, Gina Lisignoli, Alexandra Stubelius, Luminita Simion Labusca, Cecilia Aulin, Lucienne Angela Vonk, Sylvia Nürnberger, Christos Kontogiorgis, Carla Cunha, Martijn Van den Bosch
article en

Abstract

Abstract Osteoarthritis (OA) is a highly prevalent and disabling disease, with pain as its most debilitating symptom. Despite extensive preclinical research, no therapy has successfully translated from animal models into routine clinical use. Commonly used animal models (e.g., acute, surgically, or chemically induced OA in young, single-sex animals) often fail to reflect the chronic and multifactorial human condition, which is often seen in older, postmenopausal women with comorbidities and mixed nociceptive–neuropathic pain. This review aims to identify animal models and pain assessment methods for predicting drug efficacy in OA pain management and to examine the translational gap, focusing on pain as a primary endpoint in animal and human clinical studies. Ultimately, we emphasize the need for phenotype-specific, clinically relevant models to improve translational validity and accelerate the development of effective OA pain therapies.

Communications MedicineVol. 6(1)
Openalex Percentile: Top 12%
Osteoarthritis Treatment and Mechanisms
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