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Proton pump inhibitor use, hip fracture, and change in bone mineral density in postmenopausal women: Results from the women's health initiative

机译:绝经后妇女使用质子泵抑制剂,髋部骨折和骨矿物质密度变化:妇女健康倡议的结果

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摘要

Background: Proton pump inhibitor (PPI) medications have been inconsistently shown to be associated with osteoporotic fractures. We examined the association of PPI usewith bone outcomes (fracture, bone mineral density [BMD]). Methods: This prospective analysis included 161 806 postmenopausal women 50 to 79 years old, without history of hip fracture, enrolled in the Women's Health Initiative (WHI) Observational Study and Clinical Trials with a mean (SD) follow-up of 7.8 (1.6) years. Analyses were conducted for 130 487 women with complete information. Medication information was taken directly from drug containers during in-person interviews (baseline, year 3). The main outcome measures were self-reported fractures (hip [adjudicated] , clinical spine, forearm or wrist, and total fractures) and for a subsample (3 densitometry sites), 3-year change in BMD. Results: During 1 005 126 person-years of follow-up, 1500 hip fractures, 4881 forearm or wrist fractures, 2315 clinical spine fractures, and 21 247 total fractures occurred. The multivariate-adjusted hazard ratios for current PPI use were 1.00 (95% confidence interval [CI], 0.71-1.40) for hip fracture, 1.47 (95% CI, 1.18-1.82) for clinical spine fracture, 1.26 (95% CI, 1.05-1.51) for forearm or wrist fracture, and 1.25 (95% CI, 1.15-1.36) for total fractures. The BMD measurements did not vary between PPI users and nonusers at baseline. Use of PPIs was associated with only a marginal effect on 3-year BMD change at the hip (P=.05) but not at other sites. Conclusion: Use of PPIs was not associated with hip fractures but wasmodestly associated with clinical spine, forearm or wrist, and total fractures. ©2010 American Medical Association. All rights reserved.
机译:背景:质子泵抑制剂(PPI)药物已不一致地显示与骨质疏松性骨折有关。我们检查了PPI使用与骨结局(骨折,骨矿物质密度[BMD])之间的关系。方法:这项前瞻性分析纳入了161806名50至79岁的绝经后妇女,没有髋部骨折史,参加了妇女健康倡议(WHI)观察研究和临床试验,平均随访(SD)7.8(1.6)年份。对130 487名妇女进行了分析,并提供了完整的信息。药物信息是在面对面访问(基线,第3年)时直接从药品容器中获取的。主要预后指标为自我报告的骨折(髋关节[已判定],临床脊柱,前臂或腕部骨折,以及全部骨折)和子样本(3个光密度测定部位)的BMD改变3年。结果:在1 005 126人年的随访期间,发生了1500例髋部骨折,4881例前臂或腕部骨折,2315例临床脊柱骨折和21 247例总骨折。当前使用PPI的多因素调整后的危险比,髋部骨折为1.00(95%置信区间[CI],0.71-1.40),临床脊柱骨折为1.47(95%CI,1.18-1.82),1.26(95%CI,前臂或腕部骨折为1.05-1.51),全部骨折为1.25(95%CI,1.15-1.36)。在基线时,PPI用户和非用户之间的BMD测量没有变化。使用PPI仅与髋部3年BMD变化的边际效应相关(P = .05),而与其他部位无关。结论:PPI的使用与髋部骨折无关,而与临床脊柱,前臂或腕部以及全骨折有关。 ©2010美国医学会。版权所有。

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