Gao Yaqian, Yao Jianjun, Liu Suyi, Yin Song, Jia Zhenyu, Huang Yueqing, Zhao Chunhua, He Dingliu
Departments of General Medicine, The Affiliated Suzhou Hospital of Nanjing Medical University, Suzhou Municipal Hospital, Suzhou, Jiangsu, China.
Departments of General Medicine, The Huangqiao Subdistrict Community Health Service Center of Xiangcheng District, Suzhou, Jiangsu, China.
Front Endocrinol (Lausanne). 2025 Jun 18;16:1585725. doi: 10.3389/fendo.2025.1585725. eCollection 2025.
OBJECTIVE: While metabolic-associated fatty liver disease (MAFLD) has been associated with individual cardiometabolic diseases (CMDs), its role in the dynamic progression to cardiometabolic multimorbidity (CMM) remains unclear. We investigated the association of MAFLD, its severity and subtypes with CMM in individuals with no or one CMD at baseline. METHODS: This prospective cohort study involved 386,651 individuals (344,415 without and 42,236 with a single CMD at baseline) from the UK Biobank. MAFLD was defined as the presence of hepatic steatosis plus overweight/obesity, type 2 diabetes (T2D), or metabolic abnormalities. CMM was defined as the coexistence of two or more CMDs in the same person, including T2D, coronary heart disease (CHD) and stroke. Cox proportional hazard models and multistate models were performed to estimate the hazard ratios (HRs) and 95% confidence intervals (95% CIs). RESULTS: During a median follow-up of 13.85 years, 4,622 new-onset CMM cases emerged among participants free of CMD at baseline. MAFLD was significantly associated with an increased risk of incident CMM (adjusted HR: 2.78, 95% CI: 2.60-2.96). Multistate models showed that MAFLD adversely affected most transitions from baseline to single CMDs and then to CMM. Among the single-CMD participants, the adjusted HRs of incident CMM in the MAFLD group were 1.21 (95% CI: 1.13-1.31) for T2D patients, 1.90 (1.75-2.05) for CHD patients, and 1.65 (1.45-1.87) for stroke patients, respectively. CONCLUSION: MAFLD independently elevated the risk of incident CMM, regardless of the baseline CMD status. These findings emphasize the necessity of targeted MAFLD interventions for CMM prevention.
目的:虽然代谢相关脂肪性肝病(MAFLD)已与个体心血管代谢疾病(CMD)相关联,但其在向心血管代谢多重疾病(CMM)动态进展中的作用仍不清楚。我们调查了基线时无CMD或仅有1种CMD的个体中MAFLD及其严重程度和亚型与CMM的关联。 方法:这项前瞻性队列研究纳入了英国生物银行的386,651名个体(344,415名基线时无CMD,42,236名有1种CMD)。MAFLD定义为存在肝脂肪变性加超重/肥胖、2型糖尿病(T2D)或代谢异常。CMM定义为同一人同时存在两种或更多种CMD,包括T2D、冠心病(CHD)和中风。采用Cox比例风险模型和多状态模型来估计风险比(HR)和95%置信区间(95%CI)。 结果:在中位随访13.85年期间,基线时无CMD的参与者中出现了4622例新发CMM病例。MAFLD与CMM发病风险增加显著相关(校正HR:2.78,95%CI:2.60 - 2.96)。多状态模型显示,MAFLD对从基线到单一CMD再到CMM的大多数转变产生不利影响。在单一CMD参与者中,MAFLD组CMM发病的校正HR分别为:T2D患者1.21(95%CI:1.13 - 1.31),CHD患者1.90(1.75 - 2.05),中风患者1.65(1.45 - 1.87)。 结论:无论基线CMD状态如何,MAFLD都会独立增加CMM发病风险。这些发现强调了针对MAFLD进行干预以预防CMM的必要性。
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