Saixian Shi, Xiaofeng Li, Ye Chen, Jiahao Li, Yan Dai
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Use R 4.3.2 software to conduct network meta-analysis for drug category comparison.</p><p><strong>Results: </strong>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.</p><p><strong>Conclusion: </strong>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. 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引用次数: 0
摘要
目的:为2型糖尿病(T2DM)合并心血管疾病(CVD)患者心血管获益药物的选择提供循证依据。方法:全面检索PubMed、Embase、Web of Science、Cochrane Library和Clinical trials .gov网站自成立至2023年12月13日的所有相关文献,并选择符合预先设定的纳入和排除标准的随机对照试验(RCTs)。使用Cochrane偏倚风险评估工具评价纳入文献的质量。使用r4.3.2软件进行网络meta分析,进行药品品类比较。结果:共纳入24项大规模随机对照试验(RCTs),包括19项干预措施,共纳入172 803例患者。网络荟萃分析结果显示:GLP1RA (OR 0.89, 95% CI 0.81-0.97)和SGLT2i (OR 0.91, 95% CI 0.83-0.99)可降低主要心血管不良事件(MACE)的发生,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)降低了心力衰竭住院的发生率,GLP1RA (OR 0.88, 95% CI 0.81-0.97)和SGLT2i (OR 0.89, 95% CI 0.80-0.97)降低了全因死亡的发生率。结论:在新降糖药物类别的比较中,GLP1RA和SGLT2i降低T2DM合并CVD患者的MACE、心血管死亡率和全因死亡率,疗效无显著差异,且DPP4i不逊于安慰剂。只有GLP1RA降低了非致死性卒中的风险,只有SGLT2i降低了HHF的风险。
Cardiovascular Therapy Benefits of Novel Antidiabetic Drugs in Patients With Type 2 Diabetes Mellitus Complicated With Cardiovascular Disease: A Network Meta-Analysis.
Objective: Provide an evidence-based basis for the selection of cardiovascular benefit drugs in Type 2 diabetes mellitus (T2DM) patients with cardiovascular disease (CVD).
Methods: 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.
Results: 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.
Conclusion: 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.
期刊介绍:
Journal of Diabetes (JDB) devotes itself to diabetes research, therapeutics, and education. It aims to involve researchers and practitioners in a dialogue between East and West via all aspects of epidemiology, etiology, pathogenesis, management, complications and prevention of diabetes, including the molecular, biochemical, and physiological aspects of diabetes. The Editorial team is international with a unique mix of Asian and Western participation.
The Editors welcome submissions in form of original research articles, images, novel case reports and correspondence, and will solicit reviews, point-counterpoint, commentaries, editorials, news highlights, and educational content.