钠-葡萄糖共转运蛋白-2抑制剂与2型糖尿病心血管结局:一项系统综述

Z. Nasr, Fatemeh Jalali, D. Ahmed, K. Wilby
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摘要

钠-葡萄糖共转运蛋白- 2 (SGLT2)抑制剂是一类新型的抗糖尿病药物,已被证明可以降低血压、血糖和体重。然而,这些药物的长期心血管(CV)安全性影响仍不清楚。本系统综述旨在评估与SGLT2抑制剂长期心血管安全性相关的现有临床试验证据。检索数据库EMBASE和MEDLINE。纳入了评估SGLT2抑制剂与安慰剂或抗糖尿病药物的CV安全性的随机对照试验。两名研究者独立提取研究数据并完成偏倚风险评估(序列生成、分配隐藏、盲法、不完整结果数据或选择性结果报告和其他偏倚)。结果包括CV死亡、心肌梗死和中风。电子检索共确定了464项研究,另有14项研究来自其他来源。全文综述后纳入16项随机临床试验。所有研究都报告了至少一种预先定义的结局(心血管死亡、心肌梗死和卒中)。SGLT2抑制剂组报告了19例CV死亡,安慰剂组或其他比较组报告了10例CV死亡;在达格列净组中数值更高。SGLT2抑制剂组的CV事件数量高于其他组。偏倚风险评估的结果好坏参半,16项研究中有6项(37.5%)的总体质量评估被认为不明确。研究结果显示,服用SGLT2抑制剂的患者确实会出现CV结果,但临床意义尚不清楚。这些结果可以被认为是假设产生,因为研究受到不足的权力和/或随访时间的限制。在这些新药被广泛应用于临床实践之前,需要进一步的纵向研究来评估它们的有效性和安全性。
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Sodium-glucose cotransporter-2 inhibitors and cardiovascular outcomes in type 2 diabetes mellitus: A systematic review
Sodium-glucose cotransporter - 2 (SGLT2) inhibitors are a novel class of anti-diabetics proven to reduce blood pressure, blood glucose and body weight. However, the long-term cardiovascular (CV) safety implications of these agents remain unclear. This systematic review aimed to evaluate the available clinical trial evidence pertaining to long-term cardiovascular safety of SGLT2 inhibitors. The databases EMBASE and MEDLINE were searched. Randomized controlled trials assessing CV safety of SGLT2 inhibitors compared with placebo or anti-diabetic medications were included. Two investigators independently extracted study data and completed risk of bias assessments (sequence generation, allocation concealment, blinding, incomplete outcome data, or selective outcome reporting and other biases). Outcomes included CV death, myocardial infarction, and stroke. A total of 464 studies were identified in the electronic search and 14 from other sources. Sixteen randomized clinical trials were included after full-text review. All studies reported at least one of the pre-defined outcomes (CV death, myocardial infarction, and stroke). Nineteen CV deaths were reported in SGLT2 inhibitors groups versus 10 CV deaths in placebo or other comparator arms; numerically higher in the dapagliflozin arms. The number of CV events was numerically higher in SGLT2 inhibitor groups than in other arms. Risk of bias assessment showed mixed results, with overall quality assessments deemed unclear for 6 of 16 studies (37.5%). Findings showed CV outcomes do occur in patients taking SGLT2 inhibitors yet the clinical significance remains unclear. These results can be considered hypothesis generating, as studies were limited by inadequate power and/or follow-up time. Future longitudinal studies are needed to further assess the efficacy and safety profiles of these new agents before they become widely adopted in clinical practice.
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