IF 2.4 4区 医学 Q1 MEDICINE, GENERAL & INTERNAL
Frederick Berro Rivera, Marielle Nicole Cabusas Chin, Polyn Luz S Pine, Monica Marie Jadena Ruyeras, Danica Janine Cabahug Galang, Keshia Marice Gandionco, Benna Lynn Faye D Morales, Zackaree Michael V Climaco, Nathan Ross Baoy Bantayan, John Vincent Magalong, Gerard Francis Mangubat, Kenneth Ong
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引用次数: 0

摘要

背景:胰高血糖素样肽-1受体激动剂(GLP-1RAs)对血脂成分的影响尚不明确。我们旨在量化 GLP1-RAs 的降脂效果:截至 2023 年 1 月,我们对 GLP-1RA 治疗的安慰剂对照随机对照试验 (RCT) 进行了全面的数据库检索。对数据进行提取和质量评估,采用随机效应模型进行稳健的统计分析,确定以毫克/分升(mg/dl)为单位的加权平均差(MD)和95%置信区间(CI)的结果。主要终点是低密度脂蛋白胆固醇(LDL-C)的平均差异。次要终点是总胆固醇 (TC)、甘油三酯、高密度脂蛋白-C (HLD-C) 和极低密度脂蛋白-C (VLDL-C) 的平均差异。为考虑协变量,进行了分组分析和元回归:与安慰剂相比,GLP-1RAs 可适度降低 LDL-C(MD -2.93,95% CI (-5.01, -0.85),P = 0.01)。无论治疗时间长短,治疗效果都是一致的;12 周或更短 MD:-5.39,95% CI (-10.36,-0.42),P = 0.03 vs >12 周 MD:-2.39,95% CI (-4.70,-0.007),P = 0.04,P 交互作用 0.28)。GLP-1RA 可使血脂降低 7 毫克/分升。甘油三酯(MD = -7.19,95% CI (-15.01, 0.62],P = 0.07)和 VLDL-C ∼ 4 mg/dl(MD = -3.99,95%,CI (-8.73, 0.75),P = 0.10)没有明显降低。此外,GLP-1RA 并未增加 HDL-C(MD = -0.12,95% CI (-0.73, 0.49],P = 0.69)。回归分析表明,体重的平均变化不影响对低密度脂蛋白胆固醇(tau2 = 28.38,I2 = 99.83,R2 = 0.0,P = 0.67)和总胆固醇(tau2 = 93.6,I2 = 99.86,R2 = 0.0,P = 0.92)的治疗效果:结论:与安慰剂相比,服用GLP-1RA的患者可适度降低低密度脂蛋白胆固醇和总胆固醇。结论:与安慰剂相比,GLP-1RA 可适度降低患者的 LDL-C 和 TC,但 GLP-1RA 并未降低甘油三酯和 VLDL-C。GLP-1RA没有增加高密度脂蛋白胆固醇。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Glucagon-like peptide 1 receptor agonists modestly reduced low-density lipoprotein cholesterol and total cholesterol levels independent of weight reduction: a meta-analysis and meta-regression of placebo controlled randomized controlled trials.

Background: The effects of glucagon-like peptide-1 receptor agonists (GLP-1RAs) on lipid components are unclear. We aim to quantify the lipid lowering effects of GLP1-RAs.

Methods: A comprehensive database search for placebo-controlled randomized controlled trials (RCTs) on GLP-1RA treatment was conducted until January 2023. Data extraction and quality assessment were performed, and outcomes were analyzed using a random-effects model to calculate weighted mean differences (MDs) in milligrams per deciliter (mg/dl) and 95% confidence intervals (CIs). The primary endpoint was the mean difference in low-density lipoprotein cholesterol (LDL-C). Secondary endpoints included total cholesterol (TC), triglycerides, high density lipoprotein-C (HLD-C), and very low-density lipoprotein-C (VLDL-C). Subgroup analyses and meta-regression accounted for covariates.

Results: GLP-1RAs modestly reduced LDL-C (MD -2.93, 95% CI (-5.01, -0.85), p = 0.01), consistent across treatment durations: ≤12 weeks (MD: -5.39, 95% CI (-10.36, -0.42), p = 0.03) and >12 weeks (MD: -2.39, 95% CI (-4.70, -0.007), p = 0.04). GLP-1RA reduced TC by ∼7 mg/dl. There was no significant reduction in triglycerides (MD = -7.19, 95% CI (-15.01, 0.62), p = 0.07) or VLDL-C (MD = -3.99, 95%, CI (-8.73, 0.75), p = 0.10). GLP-1RA did not increase HDL-C (MD = -0.12, 95% CI (-0.73, 0.49), p = 0.69). Weight change did not influence LDL-C (tau2 = 28.38, I2 = 99.83, R2 = 0.0, p = 0.67) or TC (tau2 = 93.6, I2 = 99.86, R2 = 0.0, p = 0.92).

Conclusion: GLP-1RA treatment modestly decreased LDL-C and TC but did not significantly affect triglycerides, VLDL-C, or HDL-C.

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来源期刊
Current Medical Research and Opinion
Current Medical Research and Opinion 医学-医学:内科
CiteScore
4.40
自引率
4.30%
发文量
247
审稿时长
3-8 weeks
期刊介绍: Current Medical Research and Opinion is a MEDLINE-indexed, peer-reviewed, international journal for the rapid publication of original research on new and existing drugs and therapies, Phase II-IV studies, and post-marketing investigations. Equivalence, safety and efficacy/effectiveness studies are especially encouraged. Preclinical, Phase I, pharmacoeconomic, outcomes and quality of life studies may also be considered if there is clear clinical relevance
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