赛马鲁肽
医学
杜拉鲁肽
荟萃分析
安慰剂
内科学
恶心
糖尿病
2型糖尿病
2型糖尿病
中止
利拉鲁肽
胃肠病学
艾塞那肽
内分泌学
替代医学
病理
作者
Aihua Li,Xiaorong Su,Shanshan Hu,Yong Wang
标识
DOI:10.1016/j.diabres.2023.110605
摘要
Abstract
Objectives
To investigate the efficacy and safety of oral semaglutide 7 and 14 mg, the only orally delivered glucagon-like peptide-1 (GLP-1) receptor agonist tablet approved for type 2 diabetes mellitus (T2DM) patients. Methods
Search several databases for randomized controlled trials (RCTs) of oral semaglutide in patients with T2DM from inception through May 31, 2021. The primary outcomes included change from baseline in hemoglobin A1c (HbA1c) and body weight. Risk ratios (RR), mean differences (MD), and 95% confidence intervals (CI) were calculated to evaluate the outcomes. Results
This meta-analysis included 11 RCTs with a total of 9821 patients. Compared with placebo, semaglutide 7 and 14 mg reduced HbA1c by 1.06% (95% CI, 0.81–1.30) and 1.10% (95% CI, 0.88–1.31), respectively. While in comparison with other antidiabetic agents, semaglutide 7 and 14 mg reduced HbA1c by 0.26% (95% CI, 0.15–0.38) and 0.38% (95%CI, 0.31–0.45). Both doses of semaglutide could significantly reduce body weight. Semaglutide 14 mg did increase the incidence of medication discontinuation and gastrointestinal events (nausea, vomiting and diarrhea). Conclusion
Once-daily semaglutide 7 and 14 mg can significantly lowered HbA1c and body weight in patients with T2DM, and this effect increases with dose. Significantly, more gastrointestinal events occurred with semaglutide 14 mg.
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