Yalçın Nazif, Aktaş Selman, Uyar Seyit, Koca Nizameddin
Department of Internal Medicine, Bursa Faculty of Medicine, University of Health Sciences, Bursa City Training and Research Hospital, Bursa 16009, Türkiye.
Department of Biostatistics, Hamidiye Faculty of Medicine, University of Health Sciences, Istanbul 34396, Türkiye.
Life (Basel). 2025 Apr 29;15(5):722. doi: 10.3390/life15050722.
: Cardiovascular disease (CVD) is a leading cause of mortality in Type 2 diabetes mellitus (T2DM). Sodium-glucose co-transporter 2 (SGLT2) inhibitors are known to provide cardioprotective effects, but their influence on validated cardiovascular risk models remains underexplored. This study assessed the impact of SGLT2 inhibitors on cardiovascular risk scores, metabolic parameters, and laboratory profiles over six months. : This study was conducted on 152 T2DM patients initiating SGLT2 inhibitors. Cardiovascular risk was evaluated using the SCORE2-DM model at baseline and after six months. Generalized Estimating Equation (GEE) analysis assessed temporal risk stratification changes. Metabolic parameters and laboratory profiles were analyzed using repeated-measures ANOVA. : Cardiovascular risk scores decreased significantly, i.e., from 21.68 to 17.43 ( < 0.001). Systolic and diastolic blood pressure were reduced by 9.21 mmHg and 6.16 mmHg, respectively ( < 0.001). BMI declined by 1.27 kg/m ( < 0.001), and HbA1c decreased by 1.38% ( < 0.001). Triglyceride levels dropped by 22.91 mg/dL ( < 0.001), while renal parameters remained stable. The GEE analysis confirmed significant shifts to lower cardiovascular risk categories (β = -0.777, < 0.001), with comparable efficacy between empagliflozin and dapagliflozin ( = 0.922). : SGLT2 inhibitor therapy significantly reduces cardiovascular risk and improves metabolic and laboratory parameters in T2DM patients. These findings highlight the importance of integrating SGLT2 inhibitors into comprehensive cardiometabolic management strategies.
心血管疾病(CVD)是2型糖尿病(T2DM)患者死亡的主要原因。已知钠-葡萄糖协同转运蛋白2(SGLT2)抑制剂具有心脏保护作用,但其对经过验证的心血管风险模型的影响仍未得到充分研究。本研究评估了SGLT2抑制剂在六个月内对心血管风险评分、代谢参数和实验室指标的影响。
本研究对152例开始使用SGLT2抑制剂的T2DM患者进行。在基线和六个月后使用SCORE2-DM模型评估心血管风险。采用广义估计方程(GEE)分析评估时间风险分层变化。使用重复测量方差分析对代谢参数和实验室指标进行分析。
心血管风险评分显著降低,即从21.68降至17.43(P<0.001)。收缩压和舒张压分别降低了9.21 mmHg和6.16 mmHg(P<0.001)。体重指数(BMI)下降了1.27 kg/m²(P<0.001),糖化血红蛋白(HbA1c)下降了1.38%(P<0.001)。甘油三酯水平下降了22.91 mg/dL(P<0.001),而肾脏参数保持稳定。GEE分析证实心血管风险类别显著向较低风险转变(β=-0.777,P<0.001),恩格列净和达格列净的疗效相当(P=0.922)。
SGLT2抑制剂治疗可显著降低T2DM患者的心血管风险,并改善代谢和实验室参数。这些发现凸显了将SGLT2抑制剂纳入综合心脏代谢管理策略的重要性。