Department of Oncology and Metabolism, University of Sheffield, Sheffield, UK.
Institute of Translational Genomics, Helmholtz Zentrum München - German Research Center for Environmental Health, Neuherberg, Germany.
Calcif Tissue Int. 2021 Sep;109(3):257-276. doi: 10.1007/s00223-020-00702-6. Epub 2020 May 11.
Congruent, low-friction relative movement between the articulating elements of a synovial joint is an essential pre-requisite for sustained, efficient, function. Where disorders of joint formation or maintenance exist, mechanical overloading and osteoarthritis (OA) follow. The heritable component of OA accounts for ~ 50% of susceptible risk. Although almost 100 genetic risk loci for OA have now been identified, and the epidemiological relationship between joint development, joint shape and osteoarthritis is well established, we still have only a limited understanding of the contribution that genetic variation makes to joint shape and how this modulates OA risk. In this article, a brief overview of synovial joint development and its genetic regulation is followed by a review of current knowledge on the genetic epidemiology of established joint shape disorders and common shape variation. A summary of current genetic epidemiology of OA is also given, together with current evidence on the genetic overlap between shape variation and OA. Finally, the established genetic risk loci for both joint shape and osteoarthritis are discussed.
滑液关节的关节结构之间的协调、低摩擦相对运动是持续、高效功能的基本前提。在关节形成或维持方面存在障碍时,会发生机械性过载和骨关节炎(OA)。OA 的遗传成分占易感风险的约 50%。尽管现在已经确定了近 100 个 OA 的遗传风险位点,并且关节发育、关节形状和骨关节炎之间的流行病学关系已经确立,但我们对遗传变异对关节形状的贡献以及这种贡献如何调节 OA 风险的理解仍然有限。在本文中,简要概述了滑液关节的发育及其遗传调控,随后回顾了已确立的关节形状障碍和常见形状变异的遗传流行病学的现有知识。还总结了 OA 的遗传流行病学现状,以及形状变化与 OA 之间遗传重叠的现有证据。最后,讨论了关节形状和骨关节炎的既定遗传风险位点。