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Aging processes and the development of osteoarthritis

机译:衰老过程与骨关节炎的发展

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Purpose of Review: Aging is a primary risk factor for the development of osteoarthritis and the understanding of how aging processes contribute to the development of osteoarthritis is an important area of active research. The most recent literature in this area was reviewed in order to update investigators on the status of the field. Recent Findings: The field is beginning to move beyond a cartilage focus to include other joint tissues relevant to osteoarthritis such as ligaments, meniscus, and bone. Synovitis also appears to play a role in osteoarthritis but has not been a focus of aging studies. Studies in small animals, including mice and rats, demonstrate age-related changes that can contribute to osteoarthritis and show that animal age is a key factor to be considered in interpreting the results of studies using surgically induced models of osteoarthritis. There is accumulating evidence that cellular processes such as damage-induced cell senescence contribute to osteoarthritis and a growing body of literature on the role of epigenetic regulation of gene expression in aging and osteoarthritis. Summary: Not all osteoarthritis is due to aging processes in joint tissues, but the age-related changes being discovered certainly could play a major contributing role.
机译:审查目的:衰老是骨关节炎发展的主要风险因素,了解衰老过程如何促进骨关节炎的发展是活跃研究的重要领域。审查了该领域的最新文献,以使研究人员了解该领域的状况。最新发现:该领域开始超越软骨的关注范围,包括与骨关节炎相关的其他关节组织,例如韧带,半月板和骨骼。滑膜炎似乎在骨关节炎中也起作用,但尚未成为衰老研究的重点。在包括小鼠和大鼠在内的小动物中进行的研究表明,年龄相关的变化可能会导致骨关节炎,并且表明动物年龄是在使用外科手术诱发的骨关节炎模型解释研究结果时要考虑的关键因素。越来越多的证据表明,诸如损伤诱导的细胞衰老之类的细胞过程促成骨关节炎,并且表观遗传调控基因表达在衰老和骨关节炎中的作用的文献越来越多。简介:并非所有的骨关节炎都归因于关节组织的衰老过程,但是被发现的与年龄相关的变化当然可以起主要作用。

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