Department of Medicine, Fleischer Institute for Diabetes and Metabolism (FIDAM), Einstein Institute for Aging Research, Einstein-Sinai Diabetes Research Center (ES-DRC), Albert Einstein College of Medicine, New York City, NY (P.M., F.V., S.S.J., A.L., G.S.).
ASL Avellino, Italy (P.M., A.P., S.F.).
Hypertension. 2022 Aug;79(8):1633-1643. doi: 10.1161/HYPERTENSIONAHA.122.19586. Epub 2022 Jun 15.
Frailty is a multidimensional condition often diagnosed in older adults with hypertension and diabetes, and both these conditions are associated with endothelial dysfunction and oxidative stress. We investigated the functional role of the SGLT2 (sodium glucose cotransporter 2) inhibitor empagliflozin in frail diabetic and hypertensive older adults.
We studied the effects of empagliflozin in consecutive hypertensive and diabetic older patients with frailty presenting at the ASL (local health unit of the Italian Ministry of Health) of Avellino, Italy, from March 2021 to January 2022. Moreover, we performed in vitro experiments in human endothelial cells to measure cell viability, permeability, mitochondrial Ca, and oxidative stress.
We evaluated 407 patients; 325 frail elders with diabetes successfully completed the study. We propensity-score matched 75 patients treated with empagliflozin and 75 with no empagliflozin. We observed a correlation between glycemia and Montreal Cognitive Assessment (MoCA) score and between glycemia and 5-meter gait speed (5mGS). At 3-month follow-up, we detected a significant improvement in the MoCA score and in the 5mGS in patients receiving empagliflozin compared with non-treated subjects. Mechanistically, we demonstrate that empagliflozin significantly reduces mitochondrial Ca overload and reactive oxygen species production triggered by high glucose in human endothelial cells, attenuates cellular permeability, and improves cell viability in response to oxidative stress.
Taken together, our data indicate that empagliflozin reduces frailty in diabetic and hypertensive patients, most likely by decreasing the mitochondrial generation of reactive oxygen species in endothelial cells.
衰弱是一种常见于患有高血压和糖尿病的老年患者的多维病症,这两种病症都与内皮功能障碍和氧化应激有关。我们研究了 SGLT2(钠-葡萄糖共转运蛋白 2)抑制剂恩格列净在衰弱的糖尿病和高血压老年患者中的作用。
我们研究了恩格列净对意大利阿韦利诺 ASL(意大利卫生部地方卫生单位)连续就诊的衰弱的高血压和糖尿病老年患者的影响。此外,我们在人内皮细胞中进行了体外实验,以测量细胞活力、通透性、线粒体 Ca 和氧化应激。
我们评估了 407 名患者;325 名患有糖尿病的衰弱老年人成功完成了研究。我们对 75 名接受恩格列净治疗的患者和 75 名未接受恩格列净治疗的患者进行了倾向评分匹配。我们观察到血糖与蒙特利尔认知评估(MoCA)评分之间以及血糖与 5 米步行速度(5mGS)之间存在相关性。在 3 个月随访时,我们发现接受恩格列净治疗的患者的 MoCA 评分和 5mGS 显著改善,而未接受治疗的患者则没有改善。在机制上,我们证明恩格列净显著降低了高葡萄糖引起的人内皮细胞中线粒体 Ca 过载和活性氧的产生,减轻了细胞通透性,并改善了细胞对氧化应激的活力。
综上所述,我们的数据表明,恩格列净可降低糖尿病和高血压患者的衰弱程度,这很可能是通过减少内皮细胞中线粒体产生的活性氧来实现的。