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A Model-Based Meta-Analysis of 24 Antihyperglycemic Drugs for Type 2 Diabetes: Comparison of Treatment Effects at Therapeutic Doses

机译:24型糖尿病24种抗血糖药物的基于模型的荟萃分析:治疗剂量治疗效果的比较

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Model-based meta-analysis was used to compare glycemic control, weight changes, and hypoglycemia risk across 24 antihyperglycemic drugs used to treat type 2 diabetes. Electronic searches identified 229 randomized controlled studies comprising 121,914 patients. To ensure fair and unbiased treatment comparisons, the analyses adjusted for important differences between studies, including duration of treatment, baseline glycated hemoglobin, and drug dosages. At the approved doses, glycemic control was typically greatest with glucagon-like peptide 1 receptor agonists (GLP-1RAs), and least with dipeptidyl peptidase-4 (DPP-4) inhibitors. Weight loss was highly variable across GLP-1RAs but was similar across sodium-glucose cotransporter 2 (SGLT2) inhibitors. Large weight increases were observed with sulfonylureas and thiazolidinediones. Hypoglycemia risk was highest with sulfonylureas, although gliclazide was notably lower. Hypoglycemia risk for DPP-4 inhibitors, SGLT2 inhibitors, and thiazolidinediones was generally very low but increased slightly for both GLP-1RAs and metformin. In summary, important differences between and within drug classes were identified.
机译:基于模型的荟萃分析用于比较血糖控制,体重变化和用于治疗2型糖尿病的抗血糖药物的低血糖风险。电子搜索确定了229项随机对照研究,包括121,914名患者。为了确保公平和无偏见的治疗比较,分析调整了研究之间的重要差异,包括治疗持续时间,基线糖化血红蛋白和药物剂量。在经批准的剂量上,血糖控制通常与胰高血糖素肽1受体激动剂(GLP-1RAS)最大,并且至少用二肽基肽酶-4(DPP-4)抑制剂。在GLP-1RAS上减轻体重率高度变化,但在钠葡萄糖Cotroanger 2(SGLT2)抑制剂上具有相似。用磺酰脲和噻唑烷二酮观察到大量增加。磺脲类的低血糖风险最高,但Gliclazide显着降低。 DPP-4抑制剂,SGLT2抑制剂和噻唑烷基的低血糖风险通常非常低,但GLP-1RAS和二甲双胍略微增加。总之,确定了药物课程之间的重要差异。

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