Cho Yongin, Shin Sung-Hee, Park Min-Ae, Suh Young Ju, Park Sojeong, Jang Ji-Hun, Kim Dae-Young, Kim So Hun
Department of Endocrinology and Metabolism, Inha University College of Medicine, Incheon, Republic of Korea.
Department of Cardiology, Inha University College of Medicine, Incheon, Republic of Korea.
PLoS One. 2025 Feb 7;20(2):e0314454. doi: 10.1371/journal.pone.0314454. eCollection 2025.
Sodium glucose cotransporter 2 (SGLT2) inhibitors improve clinical outcomes in several populations including type 2 diabetes (T2D), chronic renal insufficiency, and heart failure (HF). However, limited data exist on their effects on atrial fibrillation (AF).
We conducted a retrospective cohort study using the National Health Insurance Service database. A total of 4,771 patients with T2D and AF who were newly prescribed SGLT2 inhibitors or DPP4 inhibitors were selected and matched in a 1:2 ratio by propensity score with 37 confounding variables. We assessed the effect of SGLT2 inhibitors on the composite outcome of either HF hospitalization or death.
Over a median follow-up of 31 months, patients on SGLT2 inhibitors were associated with a lower risk of hospitalizations for HF or mortality compared to those on DPP4 inhibitors (HR 0.61; 95% CI 0.44-0.85; P = 0.004). SGLT2 inhibitor use was also associated with a lower risk of mortality (HR 0.61; 95% CI 0.39-0.94; P = 0.025) and CV mortality (HR 0.43; 95% CI 0.21-0.86; P = 0.018), but not of MI (HR 1.22 [95% CI 0.72-2.09]; P = 0.461) or stroke (HR 1.00 [95% CI 0.75-1.33]; P = 0.980). The incidence of hospitalizations for HF, although statistically insignificant, tended to be lower in the SGLT2 inhibitor group (HR 0.63 [95% CI 0.39-1.02]; P = 0.062).
In a nationwide cohort of patients with T2D and AF, SGLT2 inhibitor was associated with a lower risk of mortality, which may suggest that SGLT2 inhibitors may be considered as the first-line antidiabetic medication in patients with T2D and AF.
钠-葡萄糖协同转运蛋白2(SGLT2)抑制剂可改善包括2型糖尿病(T2D)、慢性肾功能不全和心力衰竭(HF)在内的多种人群的临床结局。然而,关于其对心房颤动(AF)影响的数据有限。
我们使用国民健康保险服务数据库进行了一项回顾性队列研究。总共选取了4771例新开具SGLT2抑制剂或二肽基肽酶4(DPP4)抑制剂的T2D合并AF患者,并根据倾向得分按1:2的比例与37个混杂变量进行匹配。我们评估了SGLT2抑制剂对HF住院或死亡这一复合结局的影响。
在中位随访31个月期间,与使用DPP4抑制剂的患者相比,使用SGLT2抑制剂的患者发生HF住院或死亡的风险较低(风险比[HR]为0.61;95%置信区间[CI]为0.44 - 0.85;P = 0.004)。使用SGLT2抑制剂还与较低的死亡风险(HR 0.61;95% CI 0.39 - 0.94;P = 0.025)和心血管死亡风险(HR 0.43;95% CI 0.21 - 0.86;P = 0.018)相关,但与心肌梗死(MI)(HR 1.22[95% CI 0.72 - 2.09];P = 0.461)或中风(HR 1.00[95% CI 0.75 - 1.33];P = 0.980)无关。HF住院的发生率在SGLT2抑制剂组中虽无统计学意义,但有降低趋势(HR 0.63[95% CI 0.39 - 1.02];P = 0.062)。
在全国范围内的T2D合并AF患者队列中,SGLT2抑制剂与较低的死亡风险相关,这可能表明SGLT2抑制剂可被视为T2D合并AF患者的一线抗糖尿病药物。