替尔泊肽对成人低密度脂蛋白胆固醇水平的影响:一项系统评价
Effects of Tirzepatide on Low-Density Lipoprotein Cholesterol Levels in Adults: A Systematic Review.
作者信息
Hong Isaac, Hidalgo Ramos Roberto A, Dufner Krieger Sebastián, Secades Daniela, Ortiz Marcelo, Moya Porras Luis F, Piedra Pacheco Ana L, Esquivel Jose E
机构信息
Faculty of Medicine, University of Costa Rica, San José, CRI.
Department of Endocrinology, Hospital San Juan de Dios, San José, CRI.
出版信息
Cureus. 2025 Jul 20;17(7):e88390. doi: 10.7759/cureus.88390. eCollection 2025 Jul.
Tirzepatide, a dual agonist of the glucose-dependent insulinotropic polypeptide and glucagon-like peptide-1 receptors, is recognized for its effectiveness in regulating glucose levels and promoting weight loss. This systematic review aims to evaluate the current evidence on the impact of tirzepatide on low-density lipoprotein (LDL) cholesterol levels in adult patients (i.e., individuals 18 years and older). A comprehensive search was conducted in the PubMed, EMBASE, and Web of Science databases through June 26, 2025, following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. Eligible studies included randomized controlled trials and observational studies in adults that reported LDL levels before and after receiving tirzepatide. The quality assessment was done using the Risk of Bias 2 tool (RoB 2, Cochrane Collaboration, London, UK) and the Risk of Bias in Non-randomized Studies of Interventions (ROBINS-I). This review found that high doses of tirzepatide were associated with moderate reductions in LDL cholesterol levels, accompanied by a 19% reduction and improvements in LDL particle size. However, the findings revealed heterogeneity, with younger individuals (i.e., those 64 years and younger) exhibiting larger reductions in LDL levels compared to older individuals (i.e., those 65 years and older). Observational studies also reported heterogeneous results, limited by confounding factors and co-interventions. Overall, tirzepatide may decrease LDL cholesterol and improve its lipid profile characteristics, especially at high doses (15 mg) and in individuals with metabolic risk factors; however, variability across studies and short follow-up periods limits the ability to draw definitive conclusions. Further research is needed to establish the role of tirzepatide in controlling LDL levels and reducing cardiovascular risk.
替尔泊肽是一种葡萄糖依赖性促胰岛素多肽和胰高血糖素样肽-1受体的双重激动剂,因其在调节血糖水平和促进体重减轻方面的有效性而受到认可。本系统评价旨在评估目前关于替尔泊肽对成年患者(即18岁及以上个体)低密度脂蛋白(LDL)胆固醇水平影响的证据。按照系统评价和Meta分析的首选报告项目(PRISMA)指南,于2025年6月26日前在PubMed、EMBASE和科学网数据库中进行了全面检索。符合条件的研究包括成人的随机对照试验和观察性研究,这些研究报告了接受替尔泊肽前后的LDL水平。使用偏倚风险2工具(RoB 2,英国伦敦Cochrane协作网)和干预性非随机研究中的偏倚风险(ROBINS-I)进行质量评估。本评价发现,高剂量替尔泊肽与LDL胆固醇水平适度降低有关,同时LDL颗粒大小降低19%且有所改善。然而,研究结果显示存在异质性,与老年个体(即65岁及以上者)相比,年轻个体(即64岁及以下者)的LDL水平降低幅度更大。观察性研究也报告了异质性结果,受到混杂因素和联合干预的限制。总体而言,替尔泊肽可能会降低LDL胆固醇并改善其脂质谱特征,尤其是在高剂量(15 mg)时以及在有代谢危险因素的个体中;然而,研究之间的变异性和较短的随访期限制了得出明确结论的能力。需要进一步研究以确定替尔泊肽在控制LDL水平和降低心血管风险方面的作用。
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