Sodium-Glucose Co-Transporter 2 Inhibitors and the Risk of Genitourinary Infections at HbA1c ≥10%: A Population Health-Based Retrospective Review.

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2024-07-29 DOI:10.1177/10600280241264585
Bryce Ashby, Marina Kawaguchi-Suzuki, Yvette Grando Holman, Jackie Harris, Rachel Chlasta, Ryan Wargo
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Abstract

Background: Sodium-glucose co-transporter 2 inhibitors (SGLT2i) are first-line treatment for type 2 diabetes. Evidence has shown a 3- to 5-fold increase in the risk of genitourinary infections with their use due to inhibition of renal glucose reabsorption, resulting in glucosuria. Increased glucosuria is thought to increase the risk of genitourinary infections at a greater degree in patients with a significantly elevated HbA1c (≥10%), and initiation of SGLT2i is often delayed in these patients. While a limited body of evidence exists indicating that A1c level is not an independent risk factor for SGLT2i-induced genitourinary infection, pragmatically this concern remains a barrier to SGLT2i utilization.

Objective: Evaluate the real-world genitourinary (GU) infection rate in patients receiving SGLT2i with a baseline HbA1c ≥10% compared to patients with a baseline HbA1c <10%.

Methods: This retrospective cohort study evaluated data from 5542 adult patients treated between January 2013 and January 2023, who were prescribed an SGLT2i. Data collected included sex, age, race/ethnicity, renal function, date of SGLT2i start, number of SGLT2i orders, name and dose of SGLT2i, HbA1c, and a predetermined set of diagnosis codes related to bacterial and fungal genitourinary infections. The primary outcome was the overall GU infection rate after SGLT2i initiation within groups of baseline HbA1c of ≥10% and <10%, and the secondary outcome was total GU infections within these same groups.

Results: The primary outcome was equivalent between those with HbA1c <10% and HbA1c ≥10% (0.0064 ± 0.0565 vs 0.0030 ± 0.0303 infection per month [mean ± standard deviation]; P < 0.0001 for both lower and upper bounds). There was no statistically significant difference in total GU infections between the same groups (0.027 ± 0.21 vs 0.015 ± 0.14, P = 0.11). Female gender and prior recurrent infection were associated with increased GU infection after SGLT2i.

Conclusion and relevance: A baseline HbA1c ≥ 10% was not significantly associated with an increased risk of GU infection following the initiation of SGLT2i compared to those with a baseline HbA1c of <10%.

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钠-葡萄糖共转运体 2 抑制剂与 HbA1c≥10% 时泌尿生殖系统感染的风险:基于人群健康的回顾性研究。
背景:钠-葡萄糖协同转运体 2 抑制剂(SGLT2i)是治疗 2 型糖尿病的一线药物。有证据显示,由于抑制了肾脏葡萄糖重吸收,导致葡萄糖尿,使用该药物后泌尿生殖系统感染的风险会增加 3 到 5 倍。在 HbA1c 显著升高(≥10%)的患者中,葡萄糖尿的增加被认为会更大程度地增加泌尿生殖系统感染的风险,因此这些患者通常会延迟开始使用 SGLT2i。虽然有有限的证据表明 A1c 水平不是 SGLT2i 引起泌尿生殖系统感染的独立风险因素,但在实际应用中,这种担忧仍是使用 SGLT2i 的障碍:评估基线 HbA1c≥10% 的 SGLT2i 患者与基线 HbA1c 患者相比的泌尿生殖系统(GU)感染率:这项回顾性队列研究评估了 2013 年 1 月至 2023 年 1 月期间接受 SGLT2i 治疗的 5542 名成年患者的数据。收集的数据包括性别、年龄、种族/民族、肾功能、开始使用 SGLT2i 的日期、SGLT2i 订单数量、SGLT2i 的名称和剂量、HbA1c 以及一组与细菌和真菌泌尿生殖系统感染相关的预定诊断代码。主要结果是基线 HbA1c≥10% 组和结果组开始使用 SGLT2i 后的总泌尿生殖系统感染率:HbA1c P < 0.0001(下限和上限)的组别之间的主要结果相同。同组间的 GU 感染总数差异无统计学意义(0.027 ± 0.21 vs 0.015 ± 0.14,P = 0.11)。女性性别和既往复发感染与 SGLT2i 治疗后 GU 感染增加有关:与基线 HbA1c≥10% 的患者相比,基线 HbA1c≥10% 的患者在使用 SGLT2i 后发生 GU 感染的风险并没有明显增加。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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