Shi Saixian, Li Xiaofeng, Chen Ye, Li Jiahao, Dai Yan
School of Pharmacy, Southwest Medical University, Luzhou, Sichuan Province, China.
Pangang Xichang Hospital, Xichang, Sichuan Province, China.
J Diabetes. 2025 Jan;17(1):e70044. doi: 10.1111/1753-0407.70044.
Provide an evidence-based basis for the selection of cardiovascular benefit drugs in Type 2 diabetes mellitus (T2DM) patients with cardiovascular disease (CVD).
Conduct a comprehensive search of all relevant literature from PubMed, Embase, Web of Science, Cochrane Library, and Clinical Trials.gov from their establishment until December 13, 2023, and select randomized controlled trials (RCTs) that meet the pre-established inclusion and exclusion criteria. Use the Cochrane bias risk assessment tool to evaluate the quality of the included literature. Use R 4.3.2 software to conduct network meta-analysis for drug category comparison.
A total of 24 large-scale randomized controlled trials (RCTs) were included, including 19 intervention measures, and 172 803 patients participated in the study. The results of the network meta-analysis show that: GLP1RA (OR 0.89, 95% CI 0.81-0.97) and SGLT2i (OR 0.91, 95% CI 0.83-0.99) can reduce the occurrence of major adverse cardiovascular events (MACE), GLP1RA (OR 0.88, 95% CI 0.79-0.97) and SGLT2i (OR 0.89, 95% CI 0.81-0.99) reduced the risk of cardiovascular death. SGLT2i (OR 0.68, 95% CI 0.62-0.75) reduced the occurrence of hospitalization for heart failure, GLP1RA (OR 0.88, 95% CI 0.81-0.97) and SGLT2i (OR 0.89, 95% CI 0.80-0.97) reduced the occurrence of all-cause death.
In the comparison of new hypoglycemic drug classes, GLP1RA and SGLT2i reduced MACE, cardiovascular mortality and all-cause mortality in T2DM patients with CVD, with no significant difference in efficacy, and DPP4i was noninferior to placebo. Only GLP1RA reduced the risk of nonfatal stroke, and only SGLT2i reduced the risk of HHF.
为2型糖尿病(T2DM)合并心血管疾病(CVD)患者选择心血管获益药物提供循证依据。
全面检索PubMed、Embase、Web of Science、Cochrane图书馆和Clinical Trials.gov自建立至2023年12月13日的所有相关文献,选择符合预先设定的纳入和排除标准的随机对照试验(RCT)。使用Cochrane偏倚风险评估工具评估纳入文献的质量。使用R 4.3.2软件对药物类别进行网状Meta分析。
共纳入24项大规模随机对照试验(RCT),包括19种干预措施,172803例患者参与研究。网状Meta分析结果显示:胰高血糖素样肽-1受体激动剂(GLP1RA,比值比[OR]0.89,95%置信区间[CI]0.81-0.97)和钠-葡萄糖协同转运蛋白2抑制剂(SGLT2i,OR 0.91,95%CI 0.83-0.99)可降低主要不良心血管事件(MACE)的发生风险;GLP1RA(OR 0.88,95%CI 0.79-0.97)和SGLT2i(OR 0.89,95%CI 0.81-0.99)可降低心血管死亡风险。SGLT2i(OR 0.68,95%CI 0.62-0.75)可降低心力衰竭住院发生率;GLP1RA(OR 0.88,95%CI 从0.81-0.97)和SGLT2i(OR 0.89,95%CI 0.80-0.97)可降低全因死亡发生率。
在新型降糖药物类别比较中,GLP1RA和SGLT2i可降低T2DM合并CVD患者的MACE、心血管死亡率和全因死亡率,但疗效无显著差异,二肽基肽酶-4抑制剂(DPP4i)不劣于安慰剂。仅GLP1RA可降低非致死性卒中风险,仅SGLT2i可降低心力衰竭住院风险。