D'Silva Kristin M, Cromer Sara Jane, Yu Elaine W, Fischer Michael, Kim Seoyoung C
Division of Pharmacoepidemiology and Pharmacoeconomics, Brigham and Women's Hospital, Boston, MA, USA.
Division of Rheumatology, Allergy, and Immunology, Massachusetts General Hospital, Boston, MA, USA.
J Bone Miner Res. 2021 Jan;36(1):52-60. doi: 10.1002/jbmr.4174. Epub 2020 Nov 2.
Zoledronic acid (ZA) is an effective agent in osteoporosis and malignancy-related bone disease but may be associated with increased risk of atrial fibrillation (AF), although current studies disagree on this risk. To examine the risk of incident AF among patients receiving ZA compared with denosumab in the first year of treatment, we performed a new-user, active comparator cohort study including privately insured Americans between January 1, 2010, and June 30, 2019. Individuals aged ≥50 years without known arrhythmia or advanced kidney disease who initiated ZA were 1:1 propensity score (PS)-matched to individuals initiating denosumab in separate osteoporosis and malignancy cohorts. The primary outcome was incident diagnosis of AF (≥1 inpatient or ≥2 outpatient diagnostic codes) over 1 year. Secondary outcomes included stroke/transient ischemic attack (TIA) and nonvertebral fracture. In the osteoporosis cohort (n = 16,235 pairs), mean age was 71 years, and 93% were female. There was higher risk of AF with ZA compared with denosumab over 1 year (incidence rate [IR] = 18.6 versus 14.9 per 1000 person-years; hazard ratio [HR] = 1.25; 95% confidence interval [CI] 1.04 to 1.50). In the malignancy cohort (n = 7732 pairs), mean age was 70 years, and 66% were female. There was a numerically higher, albeit not statistically significant, risk of AF with ZA compared with denosumab over 1 year (IR = 46.9 versus 39.0 per 1000 person-years; HR = 1.19; 95% CI 1.00 to 1.43; p = 0.06). No difference in stroke/TIA rates occurred. In the malignancy cohort, ZA was less effective than denosumab at preventing nonvertebral fractures (HR = 1.32; 95% CI 1.01 to 1.74). Compared with denosumab, ZA treatment for osteoporosis and possibly for malignancy-related bone disease is associated with modestly increased risk of incident AF in the first year of treatment. © 2020 American Society for Bone and Mineral Research (ASBMR).
唑来膦酸(ZA)是治疗骨质疏松症和恶性肿瘤相关骨病的有效药物,但可能会增加心房颤动(AF)的风险,尽管目前的研究对此风险存在分歧。为了研究在治疗的第一年,接受ZA治疗的患者与接受地诺单抗治疗的患者相比发生AF的风险,我们进行了一项新用户、活性对照队列研究,纳入了2010年1月1日至2019年6月30日期间有私人保险的美国人。年龄≥50岁且无已知心律失常或晚期肾病的开始使用ZA的个体,在单独的骨质疏松症和恶性肿瘤队列中,按1:1倾向评分(PS)与开始使用地诺单抗的个体进行匹配。主要结局是1年内AF的确诊(≥1次住院或≥2次门诊诊断代码)。次要结局包括中风/短暂性脑缺血发作(TIA)和非椎体骨折。在骨质疏松症队列(n = 16,235对)中,平均年龄为71岁,93%为女性。与地诺单抗相比,ZA在1年内发生AF的风险更高(发病率[IR]=每1000人年18.6例对14.9例;风险比[HR]=1.25;95%置信区间[CI]1.04至1.50)。在恶性肿瘤队列(n = 7732对)中,平均年龄为70岁,66%为女性。与地诺单抗相比,ZA在1年内发生AF的风险在数值上更高,尽管无统计学意义(IR =每1000人年46.9例对39.0例;HR = 1.19;95%CI 1.00至1.43;p = 0.06)。中风/TIA发生率无差异。在恶性肿瘤队列中,ZA在预防非椎体骨折方面不如地诺单抗有效(HR = 1.32;95%CI 1.01至1.74)。与地诺单抗相比,ZA用于治疗骨质疏松症以及可能用于治疗恶性肿瘤相关骨病,在治疗的第一年发生AF的风险会适度增加。©2020美国骨与矿物质研究学会(ASBMR)