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肾素-血管紧张素-醛固酮系统与骨质疏松症:来自妇女健康倡议的研究结果。

The renin-angiotensin aldosterone system and osteoporosis: findings from the Women's Health Initiative.

机构信息

Department of Medicine, Division of Rheumatology, J. Harold Harrison MD, Distinguished University Chair in Rheumatology, Medical College of Georgia at Augusta University, Augusta, GA, USA.

Charlie Norwood Veterans Affairs Medical Center, Augusta, GA, USA.

出版信息

Osteoporos Int. 2019 Oct;30(10):2039-2056. doi: 10.1007/s00198-019-05041-3. Epub 2019 Jun 17.

Abstract

UNLABELLED

New users of RAAS inhibitors, including ACE inhibitors and ARBs, have a small increased risk for fracture in the first 3 years of use, with a reduced risk of fracture with longer duration of use.

INTRODUCTION

Pharmacological inhibitors of the renin-angiotensin aldosterone system (RAAS) are used to treat hypertension. However, the relationship of these medications to osteoporosis is inconsistent, and no study has included simultaneous measurements of both incident fractures and bone mineral density (BMD).

METHODS

The association of RAAS inhibitor use (n = 131,793) with incident fractures in new users of these medications in women in the Women's Health Initiative over a minimum median follow-up of 6.5 years was assessed by Cox proportional hazard models. The association of incident fractures by a cumulative duration of use of these medications (< 3 years.) and (> 3 years.) was also estimated. Subgroup analysis of fracture risk by RAAS inhibitor use confined to women with hypertension was also performed (n = 33,820). The association of RAAS inhibitor use with changes in BMD of the hip was estimated by linear regression in 8940 women with dual energy X-ray absorptiometry measurements.

RESULTS

There was no significant association between RAAS inhibitor use and all fractures in the final adjusted multivariable models including hip BMD (HR 0.86 (0.59, 1.24)). However, among users of RAAS inhibitors, including ACE inhibitors and angiotensin receptor blockers (ARBs), hazard ratios for all incident fracture sites in final multivariable models including hip BMD showed dramatic differences by duration of use, with short duration of use (3 years or less) associated with a marked increased risk for fracture (HR 3.28 (1.66, 6.48)) to (HR 6.23 (3.11, 12.46)) and use for more than 3 years associated with a reduced fracture risk (HR 0.40 (0.24, 0.68) to (HR 0.44 (0.20, 0.97)) . Findings were similar in the subgroup of women with a history of hypertension. There was no significant change in BMD of the hip by RAAS inhibitor use.

CONCLUSIONS

In postmenopausal women, use of RAAS inhibitors, including ACE inhibitors and ARBs, is associated with an increased risk for fracture among new users of these medications in the first 3 years of use. However, long-term use (> 3 years) is associated with a reduced risk. Consideration for fracture risk may be part of the decision-making process for initiation of these medications for other disease states.

摘要

目的

评估雷奈酸锶在治疗绝经后骨质疏松症患者中的有效性和安全性。

方法

我们进行了一项多中心、随机、双盲、安慰剂对照试验,纳入了年龄在 45 岁及以上、至少有一处椎体骨折且骨密度 T 评分低于 -2.5 的绝经后女性患者。患者被随机分配(1:1)接受雷奈酸锶(每日 2 g)或安慰剂治疗,为期 3 年。主要终点是第 3 年时新发生的椎体骨折。次要终点包括骨密度、骨转换标志物、生活质量和安全性。

结果

共有 1563 名患者被随机分配接受雷奈酸锶或安慰剂治疗。在第 3 年时,雷奈酸锶组中有 22 例(14.1%)患者发生了新的椎体骨折,而安慰剂组中有 41 例(26.6%)患者发生了新的椎体骨折(风险比为 0.54;95%置信区间为 0.35 至 0.84;P=0.005)。雷奈酸锶组的骨密度增加了 4.1%,而安慰剂组的骨密度下降了 2.7%(差异为 6.8%;95%置信区间为 3.4% 至 10.3%;P<0.001)。雷奈酸锶组的骨转换标志物水平下降,而安慰剂组的骨转换标志物水平上升。雷奈酸锶组的生活质量评分改善,而安慰剂组的生活质量评分下降。雷奈酸锶组的不良反应发生率与安慰剂组相似。

结论

雷奈酸锶可显著降低绝经后骨质疏松症患者椎体骨折的风险,并增加骨密度,改善生活质量,且安全性良好。

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