SGLT2 抑制剂的使用和心脏结局在2型糖尿病与肝硬化2型糖尿病
Mu-Chi Chung1,2,3, Tung-Min Yu1, Laing-You Wu4
1Division of Nephrology, Department of Medicine, Taichung Veterans General Hospital, Taichung, Taiwan.
JAMA network open
|February 23, 2026
概括
与二二酶-4抑制剂 (DPP4is) 相比,-葡萄糖共运输体-2抑制剂 (SGLT2is) 在患有肝硬化的2型糖尿病患者中显著降低了,心血管和肝脏问题的风险. SGLT2is提供心脏和肝脏的保护.
科学领域:
- 心脏病学 心脏病学
- 腎臟病學 (nephrology) 是一種醫學專業.
- 肝病学 肝病学是一种肝病学.
- 内分泌学 在内分泌学.
背景情况:
- 2型糖尿病 (T2D) 和肝硬化经常同时存在,对健康构成重大风险.
- 患有这两种疾病的患者面临脏和心血管并发症的风险增加.
- 对这一群体进行最佳的抗糖尿病治疗仍未得到充分研究.
研究的目的:
- 为了评估-葡萄糖配运输体-2 抑制剂 (SGLT2i) 与二二酶-4 抑制剂 (DPP4i) 的相关性,使用.
- 评估对结局,心血管事件和肝脏衰竭的影响.
- 分析T2D和肝硬化同时发生的患者的这些影响.
主要方法:
- 使用台湾国家医疗保险数据库 (2016年5月 - 2023年12月) 进行全国性回顾性队列研究.
- 包括T2D和肝硬化发病的成年人,开始SGLT2is或DPP4is.
- 使用治疗权重的逆概率来平衡基线特征.
主要成果:
- 与DPP4is相比,SGLT2i治疗与末期病 (ESKD) (aHR,0.34) 和急性损伤 (AKI) (aHR,0.66) 的风险显著降低.
- 此外,SGLT2i的使用也显著降低了主要不良心血管事件 (MACE) 的风险 (aHR,0.67),全因死亡率 (aHR,0.58),以及肝脏衰竭的风险 (aHR,0.65).
- 该研究包括24,259名患者,平均随访时间为2.3年.
结论:
- 与T2D和肝硬化患者的DPP4抑制剂相比,SGLT2抑制剂显示脏,心血管和肝脏不良结果的风险明显较低.
- 这些发现表明,SGLT2在这种高风险人群中具有显著的心脏,脏和肝脏保护益处.
- 在患有肝硬化并存的患者中,SGLT2is代表了管理T2D的潜在优越治疗选择.
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