{"title":"A Review on the Relationship between Aspirin and Bone Health","authors":"K. Chin","doi":"10.1155/2017/3710959","DOIUrl":null,"url":null,"abstract":"Aspirin is a cyclooxygenase inhibitor commonly used in primary prevention of cardiovascular diseases and cancers. Its users are elderly population susceptible to osteoporosis. It also inhibits the synthesis of prostaglandin E2 essential in bone remodeling. This prompts the question whether it can influence bone health among users. This review aimed to summarize the current literature on the use of aspirin on bone health. A literature search on experimental and clinical evidence on the effects of aspirin on bone health was performed using major scientific databases. In vitro studies showed that aspirin could enhance the survival of bone marrow mesenchymal stem cells, the progenitors of osteoblasts, and stimulate the differentiation of preosteoblasts. Aspirin also inhibited the nuclear factor kappa-B (NFκB) pathway and decreased the expression of receptor activator of NFκB ligand, thus suppressing the formation of osteoclast. Aspirin could prevent bone loss in animal models of osteoporosis. Despite a positive effect on bone mineral density, the limited human epidemiological studies revealed that aspirin could not reduce fracture risk. A study even suggested that the use of aspirin increased fracture risk. As a conclusion, aspirin may increase bone mineral density but its effect on fracture prevention is inconclusive. More data are needed to determine the effects of aspirin and bone health in human.","PeriodicalId":45384,"journal":{"name":"Journal of Osteoporosis","volume":null,"pages":null},"PeriodicalIF":1.1000,"publicationDate":"2017-01-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"32","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Osteoporosis","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1155/2017/3710959","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"ORTHOPEDICS","Score":null,"Total":0}
引用次数: 32
Abstract
Aspirin is a cyclooxygenase inhibitor commonly used in primary prevention of cardiovascular diseases and cancers. Its users are elderly population susceptible to osteoporosis. It also inhibits the synthesis of prostaglandin E2 essential in bone remodeling. This prompts the question whether it can influence bone health among users. This review aimed to summarize the current literature on the use of aspirin on bone health. A literature search on experimental and clinical evidence on the effects of aspirin on bone health was performed using major scientific databases. In vitro studies showed that aspirin could enhance the survival of bone marrow mesenchymal stem cells, the progenitors of osteoblasts, and stimulate the differentiation of preosteoblasts. Aspirin also inhibited the nuclear factor kappa-B (NFκB) pathway and decreased the expression of receptor activator of NFκB ligand, thus suppressing the formation of osteoclast. Aspirin could prevent bone loss in animal models of osteoporosis. Despite a positive effect on bone mineral density, the limited human epidemiological studies revealed that aspirin could not reduce fracture risk. A study even suggested that the use of aspirin increased fracture risk. As a conclusion, aspirin may increase bone mineral density but its effect on fracture prevention is inconclusive. More data are needed to determine the effects of aspirin and bone health in human.
阿司匹林是一种环氧化酶抑制剂,常用于心血管疾病和癌症的一级预防。其使用者为易患骨质疏松症的老年人群。它还能抑制骨重塑所必需的前列腺素E2的合成。这引发了一个问题,即它是否会影响使用者的骨骼健康。本文综述了阿司匹林对骨骼健康的影响。利用主要的科学数据库对阿司匹林对骨骼健康影响的实验和临床证据进行文献检索。体外研究表明,阿司匹林能提高成骨细胞的祖细胞骨髓间充质干细胞的存活率,刺激成骨前细胞的分化。阿司匹林还能抑制核因子κ b (NFκB)通路,降低NFκB配体受体激活因子的表达,从而抑制破骨细胞的形成。阿司匹林可预防骨质疏松动物模型骨质流失。尽管阿司匹林对骨密度有积极作用,但有限的人类流行病学研究显示阿司匹林不能降低骨折风险。一项研究甚至表明,服用阿司匹林会增加骨折的风险。因此,阿司匹林可增加骨密度,但对骨折的预防作用尚无定论。还需要更多的数据来确定阿司匹林对人体骨骼健康的影响。