Gray Shelly L, LaCroix Andrea Z, Larson Joseph, Robbins John, Cauley Jane A, Manson JoAnn E, Chen Zhao
School of Pharmacy, University of Washington, Box 357630, Seattle, WA 98195, USA.
Arch Intern Med. 2010 May 10;170(9):765-71. doi: 10.1001/archinternmed.2010.94.
Proton pump inhibitor (PPI) medications have been inconsistently shown to be associated with osteoporotic fractures. We examined the association of PPI use with bone outcomes (fracture, bone mineral density [BMD]).
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.
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.
Use of PPIs was not associated with hip fractures but was modestly associated with clinical spine, forearm or wrist, and total fractures.
质子泵抑制剂(PPI)药物与骨质疏松性骨折的关联尚不明确。我们研究了PPI使用与骨骼结局(骨折、骨矿物质密度[BMD])之间的关联。
这项前瞻性分析纳入了161806名年龄在50至79岁之间、无髋部骨折病史的绝经后女性,她们参与了女性健康倡议(WHI)观察性研究和临床试验,平均(标准差)随访7.8(1.6)年。对130487名信息完整的女性进行了分析。药物信息在面对面访谈(基线、第3年)期间直接从药瓶中获取。主要结局指标为自我报告的骨折(髋部[经判定]、临床脊柱、前臂或腕部以及总骨折),对于一个子样本(3个骨密度测量部位),为BMD的3年变化。
在1005126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例临床脊柱骨折以及21247例总骨折。当前使用PPI的多变量调整风险比,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),前臂或腕部骨折为1.26(95%CI,1.05 - 1.51),总骨折为1.25(95%CI,1.15 - 1.36)。基线时,PPI使用者和非使用者的BMD测量值无差异。使用PPI仅对髋部3年BMD变化有微小影响(P = 0.05),但对其他部位无影响。
使用PPI与髋部骨折无关,但与临床脊柱、前臂或腕部骨折以及总骨折有适度关联。