{"title":"钠-葡萄糖共转运蛋白2抑制剂与严重尿路感染:队列研究的真实meta分析。","authors":"Mohammed Aboukaoud, Yocheved Morhi, Ester Osher","doi":"10.1177/10600280241312432","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>There is limited knowledge about severe urinary tract infections associated with SGLT2i, despite this being the basis for the Food and Drug Administration (FDA) warning. We aim to provide real-world evidence to clarify this relationship further.</p><p><strong>Data source: </strong>A literature review was performed in PubMed and Embase for cohort studies published up to August 2024 using PICO-consistent terms.</p><p><strong>Study selection and data extraction: </strong>Cohort studies in English involving new users of SGLT2i that compare SGLT2i with glucagon-like receptor agonists (GLP-1RA), DPP4i, and other glucose-lowering medications and report severe urinary tract infection (UTI).</p><p><strong>Data synthesis: </strong>The random-effect model determined the odds ratio (OR) and 95% confidence interval (CI) for severe UTI. Subgroup analysis and meta-regression were used to identify sources of heterogeneity. In 11 cohort studies involving 679 617 individuals with type 2 diabetes mellitus and a median age of 64 (interquartile range [IQR] = 56-72) and 42% (IQR = 39%-51%) females, it was found that the use of SGLT2i was associated with a reduced risk of severe UTI compared with both composite glucose-lowering medications (OR = 0.73, 95% CI = 0.60-0.88) and DPP4i (OR = 0.48, 95% CI = 0.43-0.54). There was no significant difference in the risk compared with GLP-1RA (OR = 0.94, 95% CI = 0.78-1.14).</p><p><strong>Relevance to patient care and clinical practice: </strong>The lack of increased risk for severe UTI reassures physicians when assessing benefit-risk to continue SGLT2i after a severe UTI. This may enhance patient adherence and improve diabetes management. Furthermore, our findings show no significant risk increase in chronic kidney disease (CKD) patients who would benefit significantly from SGLT2i.</p><p><strong>Conclusion: </strong>SGLT2i does not appear to pose a greater risk of severe UTI than other oral glucose-lowering medications. This contributes to the existing literature on UTI, accounting for the event's severity. However, more data are needed to assess the potential association between SGLT2i and life-threatening UTI events.</p>","PeriodicalId":7933,"journal":{"name":"Annals of Pharmacotherapy","volume":" ","pages":"10600280241312432"},"PeriodicalIF":2.3000,"publicationDate":"2025-01-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Sodium-Glucose Co-Transporter 2 Inhibitors and Severe Urinary Tract Infections: Real-World Meta-Analysis of Cohort Studies.\",\"authors\":\"Mohammed Aboukaoud, Yocheved Morhi, Ester Osher\",\"doi\":\"10.1177/10600280241312432\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objective: </strong>There is limited knowledge about severe urinary tract infections associated with SGLT2i, despite this being the basis for the Food and Drug Administration (FDA) warning. We aim to provide real-world evidence to clarify this relationship further.</p><p><strong>Data source: </strong>A literature review was performed in PubMed and Embase for cohort studies published up to August 2024 using PICO-consistent terms.</p><p><strong>Study selection and data extraction: </strong>Cohort studies in English involving new users of SGLT2i that compare SGLT2i with glucagon-like receptor agonists (GLP-1RA), DPP4i, and other glucose-lowering medications and report severe urinary tract infection (UTI).</p><p><strong>Data synthesis: </strong>The random-effect model determined the odds ratio (OR) and 95% confidence interval (CI) for severe UTI. Subgroup analysis and meta-regression were used to identify sources of heterogeneity. In 11 cohort studies involving 679 617 individuals with type 2 diabetes mellitus and a median age of 64 (interquartile range [IQR] = 56-72) and 42% (IQR = 39%-51%) females, it was found that the use of SGLT2i was associated with a reduced risk of severe UTI compared with both composite glucose-lowering medications (OR = 0.73, 95% CI = 0.60-0.88) and DPP4i (OR = 0.48, 95% CI = 0.43-0.54). There was no significant difference in the risk compared with GLP-1RA (OR = 0.94, 95% CI = 0.78-1.14).</p><p><strong>Relevance to patient care and clinical practice: </strong>The lack of increased risk for severe UTI reassures physicians when assessing benefit-risk to continue SGLT2i after a severe UTI. This may enhance patient adherence and improve diabetes management. Furthermore, our findings show no significant risk increase in chronic kidney disease (CKD) patients who would benefit significantly from SGLT2i.</p><p><strong>Conclusion: </strong>SGLT2i does not appear to pose a greater risk of severe UTI than other oral glucose-lowering medications. This contributes to the existing literature on UTI, accounting for the event's severity. 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引用次数: 0
摘要
目的:尽管这是美国食品和药物管理局(FDA)警告的基础,但关于SGLT2i相关的严重尿路感染的知识有限。我们的目标是提供真实世界的证据来进一步阐明这种关系。数据来源:在PubMed和Embase中对截至2024年8月发表的使用pico一致术语的队列研究进行了文献综述。研究选择和数据提取:涉及SGLT2i新使用者的英语队列研究,将SGLT2i与胰高血糖素样受体激动剂(GLP-1RA)、DPP4i和其他降糖药物进行比较,并报告严重尿路感染(UTI)。数据综合:随机效应模型确定了严重UTI的优势比(OR)和95%置信区间(CI)。采用亚组分析和元回归来确定异质性的来源。在11项队列研究中,涉及679617例2型糖尿病患者,中位年龄为64岁(四分位数间距[IQR] = 56-72), 42% (IQR = 39%-51%)为女性,结果发现,与复合降糖药物(OR = 0.73, 95% CI = 0.60-0.88)和DPP4i (OR = 0.48, 95% CI = 0.43-0.54)相比,使用SGLT2i可降低严重UTI的风险。与GLP-1RA相比,风险无显著差异(OR = 0.94, 95% CI = 0.78-1.14)。与患者护理和临床实践的相关性:严重尿路感染的风险不增加,使医生在评估严重尿路感染后继续进行SGLT2i的获益-风险时感到放心。这可能会提高患者的依从性并改善糖尿病的管理。此外,我们的研究结果显示,从SGLT2i中获益的慢性肾脏疾病(CKD)患者的风险没有显著增加。结论:SGLT2i似乎不会比其他口服降糖药物带来更大的严重尿路感染风险。这有助于现有的UTI文献,说明事件的严重性。然而,需要更多的数据来评估SGLT2i与危及生命的UTI事件之间的潜在关联。
Sodium-Glucose Co-Transporter 2 Inhibitors and Severe Urinary Tract Infections: Real-World Meta-Analysis of Cohort Studies.
Objective: There is limited knowledge about severe urinary tract infections associated with SGLT2i, despite this being the basis for the Food and Drug Administration (FDA) warning. We aim to provide real-world evidence to clarify this relationship further.
Data source: A literature review was performed in PubMed and Embase for cohort studies published up to August 2024 using PICO-consistent terms.
Study selection and data extraction: Cohort studies in English involving new users of SGLT2i that compare SGLT2i with glucagon-like receptor agonists (GLP-1RA), DPP4i, and other glucose-lowering medications and report severe urinary tract infection (UTI).
Data synthesis: The random-effect model determined the odds ratio (OR) and 95% confidence interval (CI) for severe UTI. Subgroup analysis and meta-regression were used to identify sources of heterogeneity. In 11 cohort studies involving 679 617 individuals with type 2 diabetes mellitus and a median age of 64 (interquartile range [IQR] = 56-72) and 42% (IQR = 39%-51%) females, it was found that the use of SGLT2i was associated with a reduced risk of severe UTI compared with both composite glucose-lowering medications (OR = 0.73, 95% CI = 0.60-0.88) and DPP4i (OR = 0.48, 95% CI = 0.43-0.54). There was no significant difference in the risk compared with GLP-1RA (OR = 0.94, 95% CI = 0.78-1.14).
Relevance to patient care and clinical practice: The lack of increased risk for severe UTI reassures physicians when assessing benefit-risk to continue SGLT2i after a severe UTI. This may enhance patient adherence and improve diabetes management. Furthermore, our findings show no significant risk increase in chronic kidney disease (CKD) patients who would benefit significantly from SGLT2i.
Conclusion: SGLT2i does not appear to pose a greater risk of severe UTI than other oral glucose-lowering medications. This contributes to the existing literature on UTI, accounting for the event's severity. However, more data are needed to assess the potential association between SGLT2i and life-threatening UTI events.
期刊介绍:
Annals of Pharmacotherapy (AOP) is a peer-reviewed journal that advances pharmacotherapy throughout the world by publishing high-quality research and review articles to achieve the most desired health outcomes.The articles provide cutting-edge information about the most efficient, safe and cost-effective pharmacotherapy for the treatment and prevention of various illnesses. This journal is a member of the Committee on Publication Ethics (COPE). Average time from submission to first decision: 14 days