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作 者:倪乙洪 王正博 刘权 毛莉[3] 陈璐璐 NI Yihong;WANG Zhengbo;LIU Quan;MAO Li;CHEN Lulu(Nanjing Medical University, Nanjing 211166, China;Nanjing First Hospital, Nanjing 210006, China;Huai’an First People’s Hospital, Huai’an 223300, China)
机构地区:[1]南京医科大学,江苏南京211166 [2]南京市第一医院,江苏南京210006 [3]淮安市第一人民医院,江苏淮安223300
出 处:《中国骨质疏松杂志》2020年第8期1207-1211,共5页Chinese Journal of Osteoporosis
基 金:国家自然科学基金(81500682);中国博士后科学基金(2018M642279);江苏省博士后科研资助计划。
摘 要:越来越多的研究认为衰老是许多年龄相关疾病的最大危险因素,认为抑制衰老可延迟多种慢性病的出现或降低其严重程度,老年骨质疏松症常与这些衰老相关疾病共存。临床前研究和动物实验发现,随着衰老,骨微环境中的衰老细胞增加,衰老相关的促炎性分泌蛋白产生增多,导致骨吸收增加和骨形成减少。而消除衰老细胞或抑制促炎性分泌蛋白的产生可预防年龄相关的骨丢失。本文就细胞衰老对老年骨质疏松症的影响作分析总结,综述近年来研究进展,以期为老年骨质疏松症的研究与治疗提供参考。A number of studies suggest that aging is the greatest risk factor for many age-related diseases.It is believed that inhibition of aging can delay the appearence or reduce the severity of many chronic diseases.Osteoporosis is often associated with these aging-related diseases.Preclinical studies and animal experiments have found that with aging,senescent cells in the bone microenvironment increase,which can produce senescence-associated secretory phenotype,resultsing in increased bone resorption and decreased bone formation.Elimination of senescent cells or inhibition of the production of pro-inflammatory secretory proteins prevents age-related bone loss.In this paper,we analyze the effects of cell senescence on age-related osteoporosisand summarize the research progress in recent years,aiming to provide reference for the research and treatment of age-related osteoporosis.
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