Suppr超能文献

钠-葡萄糖协同转运蛋白2抑制剂与老年2型糖尿病患者发生泌尿生殖系统感染的风险

Sodium-glucose cotransporter-2 inhibitors and risk for genitourinary infections in older adults with type 2 diabetes.

作者信息

Varshney Navya, Billups Sarah J, Saseen Joseph J, Fixen Cy W

机构信息

Department of Pharmacy, Johns Hopkins Health System, Baltimore, MD, USA.

University of Colorado Skaggs School of Pharmacy and Pharmaceutical Sciences; University of Colorado School of Medicine, Aurora, CO, USA.

出版信息

Ther Adv Drug Saf. 2021 Mar 29;12:2042098621997703. doi: 10.1177/2042098621997703. eCollection 2021.

Abstract

BACKGROUND AND AIMS

Although landmark clinical trials have demonstrated an increased risk for genitourinary infection (GUI) after initiation of sodium-glucose cotransporter-2 inhibitor (SGLT2i) therapy that led to an FDA label warning, real world findings have been inconsistent and evidence specifically in older adults is lacking. The objective of the study was to examine the incidence of GUI in patients aged 65 years or older initiated on SGLT2i compared with glucagon-like peptide-1 receptor agonist (GLP1-RA) therapy at a large academic health system.

METHODS

A retrospective population-based cohort study was conducted using electronic health records of patients aged 65 years and older with a diagnosis of type 2 diabetes mellitus. Patients newly initiated on SGLT2i or GLP1-RA therapy with estimated glomerular filtration rate (eGFR) ⩾30 mL/min per 1.73 m² and active within the health system for at least 1 year prior to initiation were included. We compared the incidence of inpatient, emergency room, or outpatient diagnosis of GUI (bacterial and mycotic) within 6 months of SGLT2i or GLP1-RA initiation. A chi-square or Fisher's exact test were used to analyze between-group differences for categorical variables, while a -test was used for continuous variables. A Cox proportional hazards model was used to estimate the impact of confounding variables on the primary outcome.

RESULTS

One hundred and thirty-three patients were initiated on SGLT2i therapy and 341 patients newly initiated on GLP1-RA therapy. After adjusting for differences in age, A1c, body mass index, eGFR, race and sex, there was no statistically significant difference in GUI incidence within 6 months of SGLT2i GLP1-RA initiation (3.8% 6.5%, adjusted hazard ratio: 0.784, 95% confidence interval 0.260-2.367).

CONCLUSION

We found no increased risk of composite GUI within 6 months of initiating SGLT2i compared with GLP1-RA therapy. These real-world data in older adults add to previous findings, which suggest no increased risk of urinary tract infection with SGLT2i initiation.

PLAIN LANGUAGE SUMMARY

A class of antidiabetic medications and risk for genitourinary infections in older adults with type 2 diabetesOlder adults with type 2 diabetes often benefit from a class of antidiabetic medications known as sodium-glucose cotransporter-2 inhibitors (SGLT2is) which help to lower blood glucose, decrease risk for cardiovascular disease and prevent kidney disease progression. However, there is concern that these medications may increase risk for urinary tract infections and/or genital fungal infections in older adults based on clinical trial evidence. Our study evaluated the real-world occurrence of these safety events in patients aged 65 years or older who were newly started on these medications. We compared these patients with a group of patients newly started on an alternative class of antidiabetic agents which are not expected to increase risk for infections, known as glucagon-like peptide-1 receptor agonists (GLP1-RA). In our study, we included 133 patients who started an SGLT2i and 341 patients who started a GLP1-RA at a large teaching hospital. We evaluated the occurrence of infection up to 6 months after initiation of these mediations. We found no significant difference in infection rate between these two groups. We conclude in the study that the use of SGLT2i in older adults was not associated with increased risk for urinary tract infections or genital fungal infections when compared with GLP1-RA use.

摘要

背景与目的

尽管具有里程碑意义的临床试验已证明,启动钠-葡萄糖协同转运蛋白2抑制剂(SGLT2i)治疗后泌尿生殖系统感染(GUI)风险增加,这导致了美国食品药品监督管理局(FDA)的标签警告,但实际研究结果并不一致,且缺乏针对老年人的具体证据。本研究的目的是在一个大型学术医疗系统中,比较65岁及以上开始使用SGLT2i的患者与胰高血糖素样肽-1受体激动剂(GLP1-RA)治疗的患者中GUI的发生率。

方法

采用65岁及以上2型糖尿病患者的电子健康记录进行一项基于人群的回顾性队列研究。纳入新开始使用SGLT2i或GLP1-RA治疗、估计肾小球滤过率(eGFR)≥30 mL/(min·1.73 m²)且在开始治疗前在医疗系统内至少活跃1年的患者。我们比较了开始使用SGLT2i或GLP1-RA后6个月内住院、急诊或门诊诊断的GUI(细菌和真菌)发生率。采用卡方检验或Fisher精确检验分析分类变量的组间差异,连续变量则采用t检验。使用Cox比例风险模型估计混杂变量对主要结局的影响。

结果

133例患者开始使用SGLT2i治疗,341例患者新开始使用GLP1-RA治疗。在调整年龄、糖化血红蛋白、体重指数、eGFR、种族和性别差异后,开始使用SGLT2i与GLP1-RA后6个月内的GUI发生率无统计学显著差异(3.8%对6.5%,调整后风险比:0.784,95%置信区间0.260 - 2.367)。

结论

我们发现,与GLP1-RA治疗相比,开始使用SGLT2i后6个月内复合GUI风险没有增加。这些老年人的实际数据补充了先前的研究结果,表明开始使用SGLT2i不会增加尿路感染风险。

通俗易懂的总结

一类抗糖尿病药物与2型糖尿病老年人的泌尿生殖系统感染风险2型糖尿病老年人通常受益于一类称为钠-葡萄糖协同转运蛋白2抑制剂(SGLT2i)的抗糖尿病药物,这类药物有助于降低血糖、降低心血管疾病风险并预防肾脏疾病进展。然而,根据临床试验证据,人们担心这些药物可能会增加老年人尿路感染和/或生殖器真菌感染的风险。我们的研究评估了65岁及以上新开始使用这些药物的患者中这些安全事件的实际发生率。我们将这些患者与一组新开始使用另一类预计不会增加感染风险的抗糖尿病药物(称为胰高血糖素样肽-1受体激动剂(GLP1-RA))的患者进行了比较。在我们的研究中,我们纳入了一家大型教学医院中133例开始使用SGLT2i的患者和341例开始使用GLP1-RA的患者。我们评估了这些药物开始使用后长达6个月的感染发生率。我们发现这两组之间的感染率没有显著差异。我们在研究中得出结论,与使用GLP1-RA相比,老年人使用SGLT2i与尿路感染或生殖器真菌感染风险增加无关。

相似文献

引用本文的文献

本文引用的文献

1
12. Older Adults: .12. 老年人: 。
Diabetes Care. 2021 Jan;44(Suppl 1):S168-S179. doi: 10.2337/dc21-S012.
2
9. Pharmacologic Approaches to Glycemic Treatment: .9. 血糖治疗的药物学方法: 。
Diabetes Care. 2021 Jan;44(Suppl 1):S111-S124. doi: 10.2337/dc21-S009.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验