医学
艾塞那肽
内科学
超重
荟萃分析
血压
安慰剂
元回归
置信区间
随机对照试验
人口
糖尿病
减肥
2型糖尿病
内分泌学
肥胖
病理
替代医学
环境卫生
作者
Hon Jen Wong,Keith Zhi Xian Toh,Yao Hao Teo,Yao Neng Teo,Mark Y. Chan,Leonard L.L. Yeo,Pei Chia Eng,Benjamin Yong‐Qiang Tan,Xin Zhou,Qing Yang,Mayank Dalakoti,Ching‐Hui Sia
标识
DOI:10.1097/hjh.0000000000003903
摘要
Introduction: Glucagon-like peptide-1 receptor agonists are novel medications with proven efficacy in treating type 2 diabetes mellitus, and are increasingly being used for weight loss. They may potentially have benefit in treating metabolic disorders; however, evidence is sparse with regards to treating high blood pressure (BP). We performed a systematic review, meta-analysis and meta-regression investigating the efficacy of GLP-1 RAs in lowering BP in obese or overweight patients. Methods: Three electronic databases (PubMed, EMBASE, and CENTRAL) were systematically searched for randomized controlled trials (RCTs) published from inception to 13 February 2024. Pair-wise meta-analysis and random effects meta-regression models were utilized. Fixed effects meta-regression was used to unify treatment effects across different GLP-1 RA doses. Results: We included a total of 30 RCTs with a combined population of 37 072 patients. GLP-1 RAs demonstrated a mean systolic BP (SBP) reduction of −3.37 mmHg [95% confidence interval (CI) −3.95 to −2.80] and a mean diastolic BP (DBP) reduction of −1.05 mmHg (95% CI −1.46 to −0.65) compared with placebo. This effect was consistent across subgroups for diabetic status, formulation of GLP-1 RA, follow-up duration and route of administration for both SBP and DBP, with the exception of subgroups investigating exenatide. Meta-regression suggested no significant correlation between BP reduction and baseline characteristics such as age, percentage of male patients, HbA1c, weight, BMI, and percentage of patients with hypertension. Conclusion: Our meta-analysis suggests significant BP reduction benefits from GLP-1 RA use in obese or overweight patients, consistent across diabetic status, duration of treatment, and across route of administration.
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