Chang Kai-Chun, Su Tung-Hung, Wu Cho-Kai, Huang Shang-Chin, Tseng Tai-Chung, Hong Chun-Ming, Hsu Shih-Jer, Liu Chen-Hua, Yang Hung-Chih, Liu Chun-Jen, Kao Jia-Horng
Division of Cardiology, Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan.
Division of Gastroenterology and Hepatology, Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan.
Eur J Heart Fail. 2025 Mar;27(3):512-520. doi: 10.1002/ejhf.3567. Epub 2025 Jan 8.
AIMS: Metabolic dysfunction-associated steatotic liver disease (MASLD), defined by steatotic liver disease (SLD) and cardiometabolic factors, is increasing in prevalence, but its association with heart failure (HF) is unclear. METHODS AND RESULTS: Patients with SLD without a history of HF from 2006 to 2021 were retrospectively included and were classified into MASLD and non-MASLD groups that were followed longitudinally. The primary outcome was the new development of HF, which was sub-classified by echocardiography. Multivariable and propensity score matching analyses were conducted to adjust for confounding factors. Overall, 26 676 patients with SLD were included, with a median age of 51 years and 71% classified as MASLD. During a median follow-up of 6 years, 429 (1.61%) patients developed HF, and 76% were HF with preserved ejection fraction (HFpEF). The risk of HF was significantly higher in patients with MASLD than in those without (sub-distribution hazard ratio [SHR] 2.59, 95% confidence interval [CI] 1.84-3.64) after adjustment of competing mortality. There was a dose-dependent increase in HF risks in patients with more cardiometabolic risk factors (SHR 1.12, 95% CI 1.04-1.22). MASLD was also associated with higher risk of HF-related hospitalization (SHR 2.30, 95% CI 1.31-4.04) and specifically, the risk of HFpEF (SHR 1.91, 95% CI 1.27-2.86). In propensity score-matched cohorts, MASLD was also associated with a 2.52-fold higher risk of HF. CONCLUSION: In patients with SLD, those with MASLD show a higher risk of HF, specifically HFpEF. Future studies are warranted to validate the association between HF and MASLD.
目的:代谢功能障碍相关脂肪性肝病(MASLD)由脂肪性肝病(SLD)和心脏代谢因素定义,其患病率正在上升,但其与心力衰竭(HF)的关联尚不清楚。 方法与结果:回顾性纳入2006年至2021年无HF病史的SLD患者,并分为MASLD组和非MASLD组,进行纵向随访。主要结局是HF的新发情况,通过超声心动图进行亚分类。进行多变量和倾向评分匹配分析以调整混杂因素。总体而言,纳入了26676例SLD患者,中位年龄为51岁,71%被归类为MASLD。在中位随访6年期间,429例(1.61%)患者发生HF,其中76%为射血分数保留的HF(HFpEF)。调整竞争死亡率后,MASLD患者发生HF的风险显著高于非MASLD患者(亚分布风险比[SHR]2.59,95%置信区间[CI]1.84 - 3.64)。心脏代谢风险因素越多的患者发生HF的风险呈剂量依赖性增加(SHR 1.12,95% CI 1.04 - 1.22)。MASLD还与HF相关住院的较高风险相关(SHR 2.30,95% CI 1.31 - 4.04),具体而言,与HFpEF的风险相关(SHR 1.91,95% CI 1.27 - 2.86)。在倾向评分匹配队列中,MASLD也与HF风险高2.52倍相关。 结论:在SLD患者中,患有MASLD的患者发生HF的风险更高,尤其是HFpEF。未来有必要开展研究以验证HF与MASLD之间的关联。
Cardiovasc Diabetol. 2024-11-1
Lipids Health Dis. 2025-3-20
bioRxiv. 2025-5-21