Bangalore Sripal, Parkar Sanobar, Grossman Ehud, Messerli Franz H
Department of Medicine, Division of Cardiology, St. Luke's-Roosevelt Hospital and Columbia University College of Physicians and Surgeons, New York, NY, USA.
Am J Cardiol. 2007 Oct 15;100(8):1254-62. doi: 10.1016/j.amjcard.2007.05.057. Epub 2007 Aug 10.
Beta blockers used for the treatment of hypertension may be associated with increased risk for new-onset diabetes mellitus (DM). A search of Medline, PubMed, and EMBASE was conducted for randomized controlled trials of patients taking beta blockers as first-line therapy for hypertension with data on new-onset DM and follow-up for > or =1 year. Twelve studies evaluating 94,492 patients fulfilled the inclusion criteria. Beta-blocker therapy resulted in a 22% increased risk for new-onset DM (relative risk 1.22, 95% confidence interval [CI] 1.12 to 1.33) compared with nondiuretic antihypertensive agents. A higher baseline fasting glucose level (odds ratio [OR] 1.01, 95% CI 1.00 to 1.02, p = 0.004) and greater systolic (OR 1.05, 95% CI 1.05 to 1.08, p = 0.001) and diastolic (OR 1.06, 95% CI 1.01 to 1.10, p = 0.011) blood pressure differences between the 2 treatment modalities were significant univariate predictors of new-onset DM. Multivariate meta-regression analysis showed that a higher baseline body mass index (OR 1.17, 95% CI 1.01 to 1.33, p = 0.034) was a significant predictor of new-onset DM. The risk for DM was greater with atenolol, in the elderly, and in studies in which beta blockers were less efficacious antihypertensive agents and increased exponentially with increased duration on beta blockers. For the secondary end points, beta blockers resulted in a 15% increased risk for stroke, with no benefit for the end point of death or myocardial infarction. In conclusion, beta blockers are associated with an increased risk for new-onset DM, with no benefit for the end point of death or myocardial infarction and with a 15% increased risk for stroke compared with other agents. This risk was greater in patients with higher baseline body mass indexes and higher baseline fasting glucose levels and in studies in which beta blockers were less efficacious antihypertensive agents compared with other treatments.
用于治疗高血压的β受体阻滞剂可能与新发糖尿病(DM)风险增加有关。检索了Medline、PubMed和EMBASE,以查找将β受体阻滞剂作为高血压一线治疗药物的患者的随机对照试验,试验需包含新发DM的数据且随访时间≥1年。12项评估94492例患者的研究符合纳入标准。与非利尿剂抗高血压药物相比,β受体阻滞剂治疗使新发DM风险增加22%(相对风险1.22,95%置信区间[CI]为1.12至1.33)。较高的基线空腹血糖水平(比值比[OR]1.01,95%CI为1.00至1.02,p = 0.004)以及两种治疗方式之间较大的收缩压差异(OR 1.05,95%CI为1.05至1.08,p = 0.001)和舒张压差异(OR 1.06,95%CI为1.01至1.10,p = 0.011)是新发DM的显著单变量预测因素。多变量meta回归分析显示,较高的基线体重指数(OR 1.17,95%CI为1.01至1.33,p = 0.034)是新发DM的显著预测因素。阿替洛尔、老年患者以及β受体阻滞剂作为抗高血压药物疗效较差的研究中,DM风险更高,且随着β受体阻滞剂使用时间延长呈指数增加。对于次要终点,β受体阻滞剂使中风风险增加15%,对死亡或心肌梗死终点无益处。总之,与其他药物相比,β受体阻滞剂与新发DM风险增加有关,对死亡或心肌梗死终点无益处,且使中风风险增加15%。在基线体重指数较高、基线空腹血糖水平较高的患者以及β受体阻滞剂作为抗高血压药物疗效低于其他治疗的研究中,这种风险更大。