Efficacy and Safety of Oral Semaglutide in the Treatment of Type 2 Diabetes: A Meta-Analysis

Lin Zhang BS, Zixin Hua BS, Zhenwei Fang MS, Juanjuan Wei MS, Yang Lin PhD
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Abstract

This study aims to systematically review the efficacy and safety of oral semaglutide in the treatment of type 2 diabetes mellitus (T2DM) and provide a basis for the rational use of the drug in clinical practice. From the database's inception until February 2023, a systematic search was conducted in PubMed, Embase, the Cochrane Library, Web of Science, China National Knowledge Infrastructure, Wanfang Database, and China Science and Technology Journal Database to identify randomized controlled trials (RCTs) comparing the efficacy of oral semaglutide at dosages of 3, 7, and 14 mg (trial group) against placebo or other positive control drugs (control group) for the treatment of T2DM. Following literature screening and data extraction, the bias risk assessment tool in the Cochrane reviewer handbook 5.1.0 was used to evaluate the literature quality. Meta-analysis was carried out with RevMan 5.4 software. A total of 10 RCTs with 9541 patients were included. The meta-analysis results revealed that compared with placebo or positive control drugs (empagliflozin, sitagliptin, liraglutide, and dulaglutide), oral semaglutide significantly reduced the hemoglobin A1c (HbA1c) in patients (compared to placebo, 3 mg [MD = −0.61%, 95% CI (−0.89, −0.34)], 7 mg [MD = −1.12%, 95% CI (−1.45, −0.79)], 14 mg [MD = −1.08%, 95% CI (−1.32, −0.85)]; compared to positive control drugs (7 mg [MD = −0.26%, 95% CI (−0.38, −0.15)], 14 mg [MD = −0.37%, 95% CI (−0.52, −0.23)]). Oral semaglutide also showed certain advantages over placebo or positive control drugs in terms of weight loss, HbA1c reduction achievement rate, fasting plasma glucose level, and body mass index with overall dose-dependent efficacy. The incidence of nausea, diarrhea, and vomiting caused by oral semaglutide was higher than that of the placebo or positive control drugs, and the incidence of appetite decrease or constipation was higher than that of the placebo. Severe or symptomatic hypoglycemic episodes were reduced compared to positive control drugs. Oral semaglutide has definite clinical benefits of reducing blood glucose, body weight, reducing the risk of hypoglycemia, and with good safety.

口服塞马鲁肽治疗 2 型糖尿病的有效性和安全性:元分析。
本研究旨在系统回顾口服塞马鲁肽治疗2型糖尿病(T2DM)的疗效和安全性,为临床合理用药提供依据。自数据库建立起至2023年2月,在PubMed、Embase、Cochrane图书馆、Web of Science、中国国家知识基础设施、万方数据库和中国科技期刊数据库中进行了系统检索,以确定比较3、7和14毫克剂量口服塞马鲁肽(试验组)与安慰剂或其他阳性对照药物(对照组)治疗T2DM疗效的随机对照试验(RCT)。在进行文献筛选和数据提取后,采用 Cochrane 审稿人手册 5.1.0 中的偏倚风险评估工具对文献质量进行评估。荟萃分析采用 RevMan 5.4 软件进行。共纳入了 10 项 RCT,9541 名患者。荟萃分析结果显示,与安慰剂或阳性对照药物(恩格列净、西格列汀、利拉鲁肽和度拉鲁肽)相比,口服司马鲁肽可显著降低患者的血红蛋白 A1c(HbA1c)(与安慰剂相比,3 毫克 [MD = -0.61%,95% CI (-0.89, -0.34)], 7 mg [MD = -1.12%, 95% CI (-1.45, -0.79)], 14 mg [MD = -1.08%, 95% CI (-1.32, -0.85)];与阳性对照药物相比(7 mg [MD = -0.26%, 95% CI (-0.38, -0.15)],14 mg [MD = -0.37%, 95% CI (-0.52, -0.23)])。与安慰剂或阳性对照药物相比,口服塞马鲁肽在体重减轻、HbA1c降低成功率、空腹血浆葡萄糖水平和体重指数方面也显示出一定的优势,总体疗效呈剂量依赖性。口服塞马鲁肽引起恶心、腹泻和呕吐的发生率高于安慰剂或阳性对照药物,食欲下降或便秘的发生率高于安慰剂。与阳性对照药物相比,严重或有症状的低血糖发作有所减少。口服塞马鲁肽在降低血糖、体重、减少低血糖风险方面具有明确的临床疗效,而且安全性良好。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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