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替尔泊肽 15 mg 是否为 2 型糖尿病的首选治疗策略?一项荟萃分析和试验序列分析。

Is tirzepatide 15 mg the preferred treatment strategy for type 2 diabetes? A meta-analysis and trial-sequence-analysis.

机构信息

College of Chinese Medicine, Hunan University of Chinese Medicine, Changsha, Hunan, China.

出版信息

Eur Rev Med Pharmacol Sci. 2023 Aug;27(15):7164-7179. doi: 10.26355/eurrev_202308_33290.

Abstract

OBJECTIVE

The study aims to evaluate tirzepatide's efficacy and safety in treating type 2 diabetes by meta-analysis and trial-sequential-analysis (TSA).

MATERIALS AND METHODS

Eight databases were searched for clinical trials on tirzepatide for type 2 diabetes with a time limit of November 2022. Revman5.3 and TSA 0.9.5.10 Beta were selected for meta-analysis and TSA.

RESULTS

Compared with placebo, the meta-analysis demonstrated that tirzepatide 15 mg reduced hemoglobin-type-A1C (HbA1c) (p<0.00001), fasting-serum-glucose (FSG) (p<0.00001), and weight (p<0.00001). Compared with insulin, tirzepatide 15 mg reduced HbA1c (p<0.00001), FSG (p<0.00007), and weight (p<0.00001). Compared with glucagon-like-peptide-1 receptor-agonist (GLP-1 RA), tirzepatide 15 mg reduced HbA1c (p=0.00004), FSG (p=0.001), and weight (p<0.00001). In safety endpoints, the meta-analysis revealed that adverse events (AEs) of placebo, insulin and GLP-1 RA were comparable to tirzepatide 15 mg. The total AEs (p=0.02) and gastrointestinal (GI) AEs (p=0.03) were higher in tirzepatide 15 mg than in the placebo, while hypoglycemia (<54 mg/dl) was comparable. The major adverse cardiovascular events-4 (MACE-4) (p=0.03) and hypoglycemia (<54 mg/dl) (p<0.00001) of tirzepatide 15 mg were lower when compared to insulin, while total AEs (p=0.03) were increased. Compared with GLP-1 RA, tirzepatide 15 mg was comparable in safety endpoints in total AEs and GI AEs, while hypoglycemia (<54 mg/dl) (p=0.04) was higher. TSA indicated that HgA1c, FSG, and weight benefits were conclusive. In safety endpoints, only MACE-4 and hypoglycemia (<54 mg/dl) of Tirzepatide 15 mg vs. Insulin were conclusive. Harbord regression of AEs suggested no evident publication bias (p=0.618).

CONCLUSIONS

Tirzepatide 15 mg reduced HbA1c and weight more effectively than placebo, insulin, and GLP-1 RA. Total AEs were higher than placebo and insulin but comparable to GLP-1 RA. Tirzepatide 15 mg is a kind of optimal strategy to treat type 2 diabetes. However, there is a need to focus on GI AEs.

摘要

目的

通过荟萃分析和序贯分析(TSA)评估替西帕肽治疗 2 型糖尿病的疗效和安全性。

材料和方法

检索了截至 2022 年 11 月有关替西帕肽治疗 2 型糖尿病的临床试验的 8 个数据库。选择 Revman5.3 和 TSA 0.9.5.10 Beta 进行荟萃分析和 TSA。

结果

与安慰剂相比,荟萃分析表明替西帕肽 15mg 降低了糖化血红蛋白(HbA1c)(p<0.00001)、空腹血清葡萄糖(FSG)(p<0.00001)和体重(p<0.00001)。与胰岛素相比,替西帕肽 15mg 降低了 HbA1c(p<0.00001)、FSG(p<0.00007)和体重(p<0.00001)。与胰高血糖素样肽-1 受体激动剂(GLP-1RA)相比,替西帕肽 15mg 降低了 HbA1c(p=0.00004)、FSG(p=0.001)和体重(p<0.00001)。在安全性终点方面,荟萃分析显示安慰剂、胰岛素和 GLP-1RA 的不良事件(AE)与替西帕肽 15mg 相当。替西帕肽 15mg 的总 AE(p=0.02)和胃肠道(GI)AE(p=0.03)高于安慰剂,而低血糖(<54mg/dl)则相当。替西帕肽 15mg 的主要不良心血管事件-4(MACE-4)(p=0.03)和低血糖(<54mg/dl)(p<0.00001)低于胰岛素,而总 AE(p=0.03)增加。与 GLP-1RA 相比,替西帕肽 15mg 在总 AE 和 GI AE 方面的安全性终点相当,而低血糖(<54mg/dl)(p=0.04)较高。TSA 表明,HgA1c、FSG 和体重获益是结论性的。在安全性终点方面,只有替西帕肽 15mg 与胰岛素相比的 MACE-4 和低血糖(<54mg/dl)是结论性的。AE 的 Harbord 回归表明不存在明显的发表偏倚(p=0.618)。

结论

替西帕肽 15mg 降低 HbA1c 和体重的效果优于安慰剂、胰岛素和 GLP-1RA。总 AE 高于安慰剂和胰岛素,但与 GLP-1RA 相当。替西帕肽 15mg 是治疗 2 型糖尿病的一种理想策略。然而,需要关注 GI AE。

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