Suppr超能文献

真实世界数据中钠-葡萄糖共转运蛋白 2 抑制剂相关糖尿病酮症酸中毒的流行情况:系统评价和荟萃分析。

Prevalence of sodium-glucose transporter 2 inhibitor-associated diabetic ketoacidosis in real-world data: A systematic review and meta-analysis.

出版信息

J Am Pharm Assoc (2003). 2024 Jan-Feb;64(1):9-26.e6. doi: 10.1016/j.japh.2023.10.010. Epub 2023 Oct 14.

Abstract

BACKGROUND

The U.S. Food and Drug Administration (FDA) revised the labels of sodium-glucose transporter 2 (SGLT2) inhibitors in December 2015 to inform users regarding the risk of diabetic ketoacidosis (DKA). As more drugs of this class are approved and their indications are expanded, this serious adverse effect has been increasingly reported.

OBJECTIVE

This review evaluated observational studies to inform the prevalence of SGLT2-inhibitor-associated DKA compared with other antihyperglycemic agents.

METHODS

A systematic review was conducted in PubMed and EMBASE until 19 July 2022 (PROSPERO: CRD42022385425). We included published retrospective cohort active comparator/new user (ACNU) and prevalent new user studies assessing SGLT2-inhibitor-associated DKA prevalence in adult patients with type 2 diabetes mellitus (T2DM) against active comparators. We excluded studies which lacked 1:1 propensity score matching. The JBI Checklist for Cohort Studies guided the risk-of-bias assessments. Meta-analysis was conducted based on the inverse variance method in R software.

RESULTS

Sixteen studies with a sample of 2,956,100 nonunique patients met the inclusion criteria. Most studies were conducted in North America (n = 9) and adopted the ACNU design (n = 15). Meta-analysis of 14 studies identified 33% higher DKA risk associated with SGLT2 inhibitors (HR = 1.33, 95% CI: 1.14-1.55, P < 0.01). Meta-regression analysis identified the study location (P = 0.02), analysis principle (P < 0.001), exclusion of chronic comorbidities (P = 0.007), and canagliflozin (P = 0.04) as significant moderator variables.

CONCLUSIONS

Despite limitations related to heterogeneity, generalizability, and misclassification, the results of this study show that SGLT2 inhibitors increase the prevalence of DKA among adult T2DM patients in the real world. The findings supplement evidence from randomized controlled trials (RCTs) and call for continued vigilance.

摘要

背景

美国食品和药物管理局(FDA)于 2015 年 12 月修订了钠-葡萄糖协同转运蛋白 2(SGLT2)抑制剂的标签,以告知使用者糖尿病酮症酸中毒(DKA)的风险。随着该类药物的批准数量增加和适应证扩大,这种严重的不良反应报告也越来越多。

目的

本综述评估了观察性研究,以报告 SGLT2 抑制剂相关 DKA 与其他抗高血糖药物相比的发生率。

方法

在 PubMed 和 EMBASE 中进行了系统综述,检索时间截至 2022 年 7 月 19 日(PROSPERO:CRD42022385425)。我们纳入了评估成人 2 型糖尿病患者 SGLT2 抑制剂相关 DKA 发生率的已发表回顾性队列活性对照/新使用者(ACNU)和现患新使用者研究,这些研究的活性对照为其他药物。我们排除了缺乏 1:1 倾向评分匹配的研究。JBI 队列研究清单指导了偏倚风险评估。采用 R 软件中的逆方差法进行荟萃分析。

结果

纳入了 16 项研究,共计 2956100 名非唯一患者,符合纳入标准。大多数研究(n=9)在北美进行,采用 ACNU 设计(n=15)。对 14 项研究的荟萃分析显示,SGLT2 抑制剂相关 DKA 风险增加 33%(HR=1.33,95%CI:1.14-1.55,P<0.01)。Meta 回归分析确定了研究地点(P=0.02)、分析原理(P<0.001)、排除慢性合并症(P=0.007)和卡格列净(P=0.04)是显著的调节变量。

结论

尽管存在异质性、可推广性和分类错误相关的局限性,但本研究结果表明,SGLT2 抑制剂会增加真实世界中成年 2 型糖尿病患者 DKA 的发生率。这些发现补充了随机对照试验(RCT)的证据,并呼吁持续关注。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验