Ambulatory blood pressure monitoring strengthens the cardiovascular signal of GLP-1RA: a meta-analysis of blood pressure and weight mediation

医学 狼牙棒 血压 动态血压 内科学 回廊的 心脏病学 危险系数 随机对照试验 2型糖尿病 临床试验 置信区间 减肥 糖尿病 不利影响 重量变化 收缩 混淆 重症监护医学 急诊医学 血流动力学
作者
Nicolás F Renna,Eliel Ivan Ramirez,Matias Fernando Arrupe,Jesica Magalí Ramirez,Nicolás F Renna
出处
期刊:Journal of Hypertension [Lippincott Williams & Wilkins]
标识
DOI:10.1097/hjh.0000000000004158
摘要

Background: GLP-1 receptor agonists (GLP-1RA) and dual GLP-1/GIP agonists reduce cardiovascular events in patients with type 2 diabetes and obesity. The extent to which these benefits are mediated by blood pressure (BP) reduction vs. weight loss, especially in hypertensive patients, remains unclear. Methods: We conducted a systematic review and meta-analysis of randomized controlled trials published from January 2015 to April 2025 evaluating GLP-1RA or dual agonists. Eligible trials reported major adverse cardiovascular events (MACE) and changes in SBP and/or weight. Random-effects meta-analyses and meta-regressions were used to assess associations between MACE and reductions in BP or weight. Subgroup analyses were performed according to BP measurement method (clinical vs. ambulatory). Results: Twenty-one trials including 145 322 participants were analyzed. GLP-1RA significantly reduced MACE (pooled hazard ratio 0.86; 95% confidence interval 0.81–0.91). Meta-regression revealed that both SBP and weight reductions were independently associated with MACE risk reduction, with BP reduction showing a stronger relationship in trials using ambulatory BP monitoring. Conclusion: The cardiovascular benefits of GLP-1RA are likely influenced by both BP and weight reductions. Ambulatory BP monitoring strengthens the observed association between BP control and cardiovascular outcomes, although causality cannot be definitively established. These findings support the use of GLP-1RA in individuals with hypertension, including those with resistant phenotypes.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
liguanyu1078完成签到,获得积分10
刚刚
001完成签到,获得积分10
1秒前
鸢雨情笺完成签到,获得积分10
1秒前
尊敬的小凡完成签到,获得积分10
1秒前
娃哈哈完成签到,获得积分10
2秒前
andre20完成签到 ,获得积分10
3秒前
缥缈云朵完成签到,获得积分10
3秒前
Sampson完成签到,获得积分10
3秒前
落后的小伙完成签到,获得积分10
4秒前
lxhhh完成签到,获得积分10
4秒前
醉清风完成签到 ,获得积分10
4秒前
5秒前
中华牌老阿姨完成签到,获得积分10
5秒前
秋秋完成签到,获得积分10
6秒前
jfw完成签到 ,获得积分10
7秒前
SCI硬通货完成签到 ,获得积分10
10秒前
11秒前
枫糖叶落完成签到,获得积分10
11秒前
大雪完成签到 ,获得积分10
12秒前
尼古拉斯完成签到,获得积分10
12秒前
小巧的白竹完成签到,获得积分10
13秒前
adoudoo完成签到,获得积分10
14秒前
希希完成签到 ,获得积分10
14秒前
苏silence发布了新的文献求助10
15秒前
沫荔完成签到 ,获得积分10
16秒前
拾个勤天完成签到,获得积分10
16秒前
科研通AI6.2应助此间无人采纳,获得10
17秒前
季冬十五完成签到,获得积分10
18秒前
青衫完成签到 ,获得积分10
18秒前
为为的小耳朵完成签到 ,获得积分10
18秒前
Galahad_14完成签到,获得积分10
19秒前
优秀念柏完成签到,获得积分10
21秒前
光亮向真完成签到,获得积分10
22秒前
Julie完成签到 ,获得积分0
22秒前
Nole应助小刘吖采纳,获得10
25秒前
Dorren完成签到,获得积分10
25秒前
dan完成签到 ,获得积分10
25秒前
whuhustwit完成签到,获得积分10
26秒前
科研混子完成签到 ,获得积分10
29秒前
靓丽战斗机完成签到 ,获得积分10
29秒前
高分求助中
Principles of Economics, 11th Edition 10000
University Physics with Modern Physics, 16th edition 10000
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Development of a Bridge Weigh-In-Motion System: A technology to convert the bridge response to the passage of traffic into data on vehicle configurations, speeds, times of travel and weights 1000
ズームレンズの光学設計に関する研究 800
Fundamentals of Pharmaceutical and Biologics Regulations: A Global Perspective, Second Edition 700
Matrix Methods in Data Mining and Pattern Recognition Second Edition 610
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7282488
求助须知:如何正确求助?哪些是违规求助? 8903239
关于积分的说明 18834053
捐赠科研通 6953287
什么是DOI,文献DOI怎么找? 3207575
关于科研通互助平台的介绍 2377861
邀请新用户注册赠送积分活动 2182761