Rodríguez-Martín Sara, Barreira-Hernández Diana, Mazzucchelli Ramón, Gil Miguel, García-Lledó Alberto, Izquierdo-Esteban Laura, Pérez-Gómez Ana, Rodríguez-Miguel Antonio, De Abajo Francisco J
Department of Biomedical Sciences (Pharmacology), University of Alcalá (IRYCIS), Alcalá de Henares, Spain.
Rheumatology Department, University Hospital "Fundación Alcorcón", Madrid, Spain.
Front Pharmacol. 2023 May 26;14:1197238. doi: 10.3389/fphar.2023.1197238. eCollection 2023.
Bisphosphonates have been reported to increase the risk of atrial fibrillation. Therefore, it is conceivable that they may increase the risk of cardioembolic ischemic stroke (IS). However, most epidemiological studies carried out thus far have not shown an increased risk of IS, though none separated by the main pathophysiologic IS subtype (cardioembolic and non-cardioembolic) which may be crucial. In this study, we tested the hypothesis that the use of oral bisphosphonates increases specifically the risk of cardioembolic IS, and explored the effect of treatment duration, as well as the potential interaction between oral bisphosphonates and calcium supplements and anticoagulants. We performed a case-control study nested in a cohort of patients aged 40-99 years, using the Spanish primary healthcare database BIFAP, over the period 2002-2015. Incident cases of IS were identified and classified as cardioembolic or non-cardioembolic. Five controls per case were randomly selected, matched for age, sex, and index date (first recording of IS) using an incidence-density sampling. The association of IS (overall and by subtype) with the use of oral bisphosphonates within the last year before index date was assessed by computing the adjusted odds ratios (AOR) and their 95% CI using a conditional logistic regression. Only initiators of oral bisphosphonates were considered. A total of 13,781 incident cases of IS and 65,909 controls were included. The mean age was 74.5 (SD ± 12.4) years and 51.6% were male. Among cases, 3.15% were current users of oral bisphosphonates, while among controls they were 2.62%, yielding an AOR of 1.15 (95% CI:1.01-1.30). Of all cases, 4,568 (33.1%) were classified as cardioembolic IS (matched with 21,697 controls) and 9,213 (66.9%) as non-cardioembolic IS (matched with 44,212 controls) yielding an AOR of 1.35 (95% CI:1.10-1.66) and 1.03 (95% CI: 0.88-1.21), respectively. The association with cardioembolic IS was clearly duration-dependent (AOR≤1 year = 1.10; 95% CI:0.82-1.49; AOR>1-3 years = 1.41; 95% CI:1.01-1.97; AOR>3 years = 1.81; 95% CI:1.25-2.62; for trend = 0.001) and completely blunted by anticoagulants, even in long-term users (AOR>1 year = 0.59; 0.30-1.16). An interaction between oral bisphosphonates and calcium supplements was suggested. The use of oral bisphosphonates increases specifically the odds of cardioembolic IS, in a duration-dependent manner, while leaves materially unaffected the odds of non-cardioembolic IS.
据报道,双膦酸盐会增加心房颤动的风险。因此,可以想象它们可能会增加心源性栓塞性缺血性卒中(IS)的风险。然而,迄今为止进行的大多数流行病学研究并未显示IS风险增加,尽管没有一项研究按主要病理生理IS亚型(心源性栓塞性和非心源性栓塞性)进行区分,而这可能至关重要。在本研究中,我们检验了口服双膦酸盐的使用会特别增加心源性栓塞性IS风险这一假设,并探讨了治疗持续时间的影响,以及口服双膦酸盐与钙补充剂和抗凝剂之间的潜在相互作用。我们在2002年至2015年期间,利用西班牙初级医疗保健数据库BIFAP,对40至99岁的患者队列进行了一项巢式病例对照研究。确定IS的发病病例并将其分类为心源性栓塞性或非心源性栓塞性。每个病例随机选择5名对照,采用发病密度抽样方法按年龄、性别和索引日期(IS的首次记录)进行匹配。通过使用条件逻辑回归计算调整后的优势比(AOR)及其95%置信区间,评估索引日期前最后一年内IS(总体和按亚型)与口服双膦酸盐使用之间的关联。仅考虑口服双膦酸盐的起始使用者。总共纳入了13781例IS发病病例和65909名对照。平均年龄为74.5(标准差±12.4)岁,51.6%为男性。在病例中,3.15%为口服双膦酸盐的当前使用者,而在对照中为2.62%,AOR为1.15(95%置信区间:1.01 - 1.30)。在所有病例中,4568例(33.1%)被分类为心源性栓塞性IS(与21697名对照匹配),9213例(66.9%)为非心源性栓塞性IS(与44212名对照匹配),AOR分别为1.35(95%置信区间:1.10 - 1.66)和1.03(95%置信区间:0.88 - 1.21)。与心源性栓塞性IS的关联明显呈持续时间依赖性(AOR≤1年 = 1.10;95%置信区间:0.82 - 1.49;AOR>1 - 3年 = 1.41;95%置信区间:1.01 - 1.97;AOR>3年 = 1.81;95%置信区间:1.25 - 2.62;趋势P = 0.001),并且即使在长期使用者中也完全被抗凝剂抵消(AOR>1年 = 0.59;0.30 - 1.16)。提示口服双膦酸盐与钙补充剂之间存在相互作用。口服双膦酸盐的使用特别以持续时间依赖的方式增加心源性栓塞性IS的几率,而对非心源性栓塞性IS的几率基本没有影响。
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