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与使用双膦酸盐和其他抗骨质疏松药物相关的心房颤动风险:一项队列研究。

Risk of atrial fibrillation associated with use of bisphosphonates and other drugs against osteoporosis: a cohort study.

机构信息

Department of Endocrinology and Metabolism C, Aarhus University Hospital, Tage Hansens Gade 2, 8000 Arhus C, Denmark.

出版信息

Calcif Tissue Int. 2010 May;86(5):335-42. doi: 10.1007/s00223-010-9349-0. Epub 2010 Mar 23.

Abstract

We studied the association between bisphosphonate use and risk of atrial fibrillation or flutter and the effect of confounders such as heart and lung disease in a nationwide retrospective cohort from Denmark. All users of bisphosphonates and other drugs against osteoporosis between 1996 and 2006 (n = 103,562) were the exposed group and three age- and gender-matched controls from the general population (n = 310,683) were the nonexposed group. The main outcome measure was atrial fibrillation or atrial flutter. Before initiation of treatment against osteoporosis, no excess of atrial fibrillation or flutter was present for any drug except for etidronate (OR = 1.22, 95% CI 1.15-1.29). After initiation of treatment, raloxifene was not associated with any excess risk of atrial fibrillation (OR = 0.98, 95% CI 0.72-1.33). Etidronate (HR = 1.08, 95% CI 1.02-1.14) and alendronate (HR = 1.09, 95% CI 1.00-1.20) were associated with an excess risk of atrial fibrillation after treatment start if statistical adjustments were made for cardiovascular disease. However, this association disappeared upon statistical adjustment for chronic obstructive pulmonary disease (COPD) (etidronate HR = 1.04, 95% CI 0.98-1.10; alendronate HR = 1.05, 95% CI 0.96-1.15). In patients using etidronate (12.5% vs. 3.8%) and alendronate (11.4% vs. 4.6%) major differences were present in prevalence of COPD at start of treatment compared to matched controls. In conclusion, oral bisphosphonates do not seem to be associated with an excess risk of atrial fibrillation. Any excess risk seen in prior studies may be due to confounding from COPD.

摘要

我们在丹麦进行了一项全国性的回顾性队列研究,旨在研究双膦酸盐的使用与心房颤动或心房扑动的风险之间的关系,以及心脏病和肺部疾病等混杂因素的影响。1996 年至 2006 年间使用双膦酸盐和其他骨质疏松症药物的所有患者(n=103562)为暴露组,从普通人群中随机选择年龄和性别相匹配的 310683 人作为非暴露组。主要观察指标为心房颤动或心房扑动。在开始骨质疏松症治疗之前,除了依替膦酸外,没有任何药物会导致心房颤动或心房扑动的风险增加(OR=1.22,95%CI 1.15-1.29)。开始治疗后,雷洛昔芬与任何心房颤动风险增加无关(OR=0.98,95%CI 0.72-1.33)。依替膦酸(HR=1.08,95%CI 1.02-1.14)和阿仑膦酸钠(HR=1.09,95%CI 1.00-1.20)在治疗开始后与心房颤动风险增加相关,如果对心血管疾病进行统计学调整。然而,当对慢性阻塞性肺疾病(COPD)进行统计学调整时,这种关联消失(依替膦酸 HR=1.04,95%CI 0.98-1.10;阿仑膦酸钠 HR=1.05,95%CI 0.96-1.15)。在使用依替膦酸(12.5%vs.3.8%)和阿仑膦酸钠(11.4%vs.4.6%)的患者中,治疗开始时 COPD 的患病率与匹配对照组相比存在显著差异。总之,口服双膦酸盐似乎与心房颤动风险增加无关。以前研究中观察到的任何风险增加可能是由于 COPD 造成的混杂。

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