Bonten Tobias N, Plaizier Chiara E I, Snoep Jaap-Jan D, Stijnen Theo, Dekkers Olaf M, van der Bom Johanna G
Department of Clinical Epidemiology, Leiden University Medical Center, Leiden, The Netherlands.
Br J Clin Pharmacol. 2014 Nov;78(5):940-9. doi: 10.1111/bcp.12404.
Platelets play an important role in cardiovascular disease, and β-blockers are often prescribed for cardiovascular disease prevention. β-Blockers may directly affect platelet aggregation, because β-adrenergic receptors are present on platelets. There is uncertainty about the existence and magnitude of an effect of β-blockers on platelet aggregation. The aim of this study was to perform a systematic review and meta-analysis of the effect of β-blockers on platelet aggregation.
MEDLINE and EMBASE were searched until April 2014. Two reviewers independently performed data extraction and risk of bias assessment. Type of β-blocker, population, treatment duration and platelet aggregation were extracted. Standardized mean differences were calculated for each study and pooled in a random-effects meta-analysis.
We retrieved 31 studies (28 clinical trials and three observational studies). β-Blockers decreased platelet aggregation (standardized mean difference -0.54, 95% confidence interval -0.85 to -0.24, P < 0.0001). This corresponds to a reduction of 13% (95% confidence interval 8-17%). Nonselective lipophilic β-blockers decreased platelet aggregation more than selective nonlipophilic β-blockers.
Clinically used β-blockers significantly reduce platelet aggregation. Nonselective lipophilic β-blockers seem to reduce platelet aggregation more effectively than selective nonlipophilic β-blockers. These findings may help to explain why some β-blockers are more effective than others in preventing cardiovascular disease.
血小板在心血管疾病中发挥重要作用,β受体阻滞剂常用于预防心血管疾病。β受体阻滞剂可能直接影响血小板聚集,因为血小板上存在β肾上腺素能受体。β受体阻滞剂对血小板聚集的影响的存在及程度尚不确定。本研究的目的是对β受体阻滞剂对血小板聚集的影响进行系统评价和荟萃分析。
检索MEDLINE和EMBASE直至2014年4月。两名研究者独立进行数据提取和偏倚风险评估。提取β受体阻滞剂类型、人群、治疗持续时间和血小板聚集情况。计算每项研究的标准化均数差,并汇总进行随机效应荟萃分析。
我们检索到31项研究(28项临床试验和3项观察性研究)。β受体阻滞剂降低了血小板聚集(标准化均数差-0.54,95%置信区间-0.85至-0.24,P<0.0001)。这相当于降低了13%(95%置信区间8-17%)。非选择性亲脂性β受体阻滞剂比选择性非亲脂性β受体阻滞剂更能降低血小板聚集。
临床使用的β受体阻滞剂显著降低血小板聚集。非选择性亲脂性β受体阻滞剂似乎比选择性非亲脂性β受体阻滞剂更有效地降低血小板聚集。这些发现可能有助于解释为什么某些β受体阻滞剂在预防心血管疾病方面比其他药物更有效。