Mahar Muhammad Umar, Mahmud Omar, Ahmed Salaar, Qureshi Saleha Ahmed, Kakar Wasila Gul, Fatima Syeda Sadia
Medical College, Aga Khan University, Karachi, Pakistan.
Department of Biological and Biomedical Sciences, Aga Khan University, Karachi, Pakistan.
J Obes Metab Syndr. 2024 Dec 30;33(4):348-359. doi: 10.7570/jomes24008. Epub 2024 Dec 17.
Tirzepatide is a novel dual glucose-dependent insulinotropic peptide (GIP)-glucagon-like peptide 1 (GLP-1) receptor agonist being evaluated for the treatment of various metabolic disorders. We performed a meta-analysis of randomized data on the effects of tirzepatide on serum lipid levels.
We systematically searched the PubMed and ClinicalTrials.gov databases for relevant data from randomized controlled clinical trials. All articles were screened, reviewed, and extracted by at least two independent authors, with conflicts resolved by consensus. Four hundred and thirty-three records were identified in the initial literature search; 18 of them were identified for full-text review, and 14 of those were systematically reviewed and included in the analysis. The meta-analysis was performed using an inverse variance random-effects model.
Fourteen articles that reported data from 13 randomized controlled clinical trials were included in the review. Nine trials had a low risk of bias, two had a moderate risk, and two had a high risk of bias. The pooled analysis showed that tirzepatide was efficacious at improving all lipid markers, including cholesterol and triglycerides. Moreover, a clear dose response trend was visible across results from groups taking 5, 10, and 15 mg of tirzepatide.
There is growing evidence to support the use of tirzepatide in patients with metabolic diseases such as type 2 diabetes mellitus, metabolic syndrome, and obesity. Our results demonstrate that tirzepatide significantly improves all aspects of patient metabolism and might be superior in this regard to conventional agents such as insulin formulations or traditional GLP-1 agonists.
替尔泊肽是一种新型的双重葡萄糖依赖性促胰岛素多肽(GIP)-胰高血糖素样肽1(GLP-1)受体激动剂,目前正用于评估其对各种代谢紊乱的治疗效果。我们对替尔泊肽对血脂水平影响的随机数据进行了荟萃分析。
我们系统地检索了PubMed和ClinicalTrials.gov数据库,以获取来自随机对照临床试验的相关数据。所有文章均由至少两名独立作者进行筛选、评审和提取,如有分歧则通过协商解决。在初步文献检索中识别出433条记录;其中18条被确定进行全文评审,其中14条经过系统评审并纳入分析。荟萃分析采用逆方差随机效应模型进行。
本综述纳入了14篇报告13项随机对照临床试验数据的文章。9项试验的偏倚风险较低,2项试验的偏倚风险中等,2项试验的偏倚风险较高。汇总分析表明,替尔泊肽在改善所有血脂指标(包括胆固醇和甘油三酯)方面均有效。此外,在服用5、10和15毫克替尔泊肽的组的结果中可以明显看出明确的剂量反应趋势。
越来越多的证据支持替尔泊肽用于治疗2型糖尿病、代谢综合征和肥胖症等代谢性疾病患者。我们的结果表明,替尔泊肽能显著改善患者代谢的各个方面,在这方面可能优于胰岛素制剂或传统GLP-1激动剂等传统药物。