Qian Zhiyu, Song Jonathan, Jones Alyssa, Tao Brian, Xiao Boyuan, Labban Muhieddine, Dagnino Filippo, Stelzl Daniel, Zurl Hanna, Cole Alexander P, Trinh Quoc-Dien, Lerner Lori B
Department of Urological Surgery, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
Center for Surgery and Public Health, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
Urol Pract. 2025 Jan;12(1):131-137. doi: 10.1097/UPJ.0000000000000698. Epub 2024 Aug 30.
We investigated the risk of UTIs and complex UTIs associated with SGLT2 (sodium-glucose cotransporter-2) inhibitors in men, emphasizing older men at higher risk for voiding dysfunction.
Utilizing a pharmacovigilance case-noncase design, we analyzed VigiBase reports from 1967 to 2022 among male patients. VigiBase is a comprehensive global database for drug safety. Disproportionality analysis, which compares the frequency of reported adverse events for specific drugs against other drugs, was conducted using reporting odds ratio (ROR) and empirical Bayes estimator (EBE). Age was stratified at 65 years as a threshold for increased susceptibility to male voiding dysfunctions. Sensitivity analyses were performed to compare SGLT2 inhibitor with other diabetes medications and years 2013 to 2022.
There were 484 UTIs (ROR 6.75 [95% CI: 6.17-7.39]; EBE 6.78) and 165 complex UTIs (ROR 8.09 [95% CI: 6.94-9.43]; EBE 8.60). In men under 65, there were 178 UTIs (ROR 6.82 [95% CI: 5.88-7.91]; EBE 6.99) and 65 complex UTIs (ROR 7.30 [95% CI: 5.71-9.32]; EBE 7.90). In men 65 and over, we found 153 UTIs (ROR 5.11 [95% CI: 4.35-5.99]; EBE 5.44) and 59 complex UTIs (ROR 8.79 [95% CI: 6.79-11.37]; EBE 9.60). Sensitivity analyses consistently showed significant signals.
This study suggests an elevated risk for both UTIs and complex UTIs in men taking SGLT2 inhibitors, with a more pronounced risk for complex UTI in older men who may have benign prostatic hyperplasia-related voiding dysfunction. These findings highlight the need for a balanced approach in prescribing SGLT2 inhibitors, particularly in populations potentially more susceptible to UTIs.
我们调查了男性使用钠-葡萄糖协同转运蛋白2(SGLT2)抑制剂相关的尿路感染(UTIs)及复杂性UTIs风险,重点关注排尿功能障碍风险较高的老年男性。
采用药物警戒病例-非病例设计,我们分析了1967年至2022年男性患者的VigiBase报告。VigiBase是一个全面的全球药物安全数据库。使用报告比值比(ROR)和经验贝叶斯估计器(EBE)进行不成比例分析,该分析比较特定药物报告的不良事件频率与其他药物。年龄以65岁为界分层,作为男性排尿功能障碍易感性增加的阈值。进行敏感性分析以比较SGLT2抑制剂与其他糖尿病药物以及2013年至2022年的数据。
共有484例UTIs(ROR 6.75 [95% CI:6.17 - 7.39];EBE 6.78)和165例复杂性UTIs(ROR 8.09 [95% CI:6.94 - 9.43];EBE 8.60)。在65岁以下男性中,有178例UTIs(ROR 6.82 [95% CI:5.88 - 7.91];EBE 6.99)和65例复杂性UTIs(ROR 7.30 [95% CI:5.71 - 9.32];EBE 7.90)。在65岁及以上男性中,我们发现153例UTIs(ROR 5.11 [95% CI:4.35 - 5.99];EBE 5.44)和59例复杂性UTIs(ROR 8.79 [95% CI:6.79 - 11.37];EBE 9.60)。敏感性分析一致显示出显著信号。
本研究表明,服用SGLT2抑制剂的男性发生UTIs和复杂性UTIs的风险升高,对于可能患有良性前列腺增生相关排尿功能障碍的老年男性,发生复杂性UTI的风险更为明显。这些发现凸显了在开具SGLT2抑制剂处方时采用平衡方法的必要性,特别是在可能更易发生UTIs的人群中。