The role of genetic factors and monocyte-to-osteoclast differentiation in the pathogenesis of Charcot neuroarthropathy.

Diabetes Res Clin Pract

University of Gdańsk, Faculty of Biology, Department of Medical Biology and Genetics, Wita Stwosza 59, 80-308 Gdańsk, Poland. Electronic address:

Published: August 2020

AI Article Synopsis

  • Charcot neuroarthropathy is a progressive condition in diabetic patients that leads to bone destruction in the foot and joint disorganization.
  • Current prevention and treatment lack effectiveness, and there's no reliable way to identify at-risk diabetic patients.
  • The review explores the condition's history, symptoms, potential genetic markers, and recent research on monocyte-to-osteoclast differentiation in its development.

Article Abstract

Charcot neuroarthropathy is a chronic, progressive condition of the skeletal system that affects some patients with diabetic neuropathy. It results in progressive destruction of bones of the foot and disorganisation of pedal joints and ligaments. Effective prevention and treatment for Charcot neuroarthropathy remain a challenge. Currently, there are no reliable repeatable markers to identify patients with diabetes who are at higher risk of developing Charcot neuroarthropathy. The pathogenesis underlying the development of Charcot neuroarthropathy also remains unclear. In this review, we provide an overview of the history, prevalence, symptoms, risk factors, diagnostics and treatment of Charcot neuroarthropathy. We also discuss the potential for OPG and RANKL gene variants to act as predictive markers for the development of Charcot neuroarthropathy. Finally, we summarise the latest research on the role of monocyte-to-osteoclast differentiation in the development of acute Charcot neuroarthropathy.

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Source
http://dx.doi.org/10.1016/j.diabres.2020.108337DOI Listing

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