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代谢相关脂肪性肝病与心血管疾病风险。

Metabolic dysfunction-associated steatotic liver disease and risk of cardiovascular disease.

机构信息

Department of Preventive Medicine, Yonsei University College of Medicine, Seoul, South Korea.

Institute for Innovation in Digital Healthcare, Yonsei University, Seoul, South Korea.

出版信息

Gut. 2024 Feb 23;73(3):533-540. doi: 10.1136/gutjnl-2023-331003.


DOI:10.1136/gutjnl-2023-331003
PMID:37907259
Abstract

OBJECTIVE: We explored clinical implications of the new definition of metabolic dysfunction-associated steatotic liver disease (MASLD) by assessing its prevalence and associated cardiovascular disease (CVD) risk. DESIGN: From nationwide health screening data, we identified 9 775 066 adults aged 20-79 who underwent health examination in 2009. Participants were categorised into four mutually exclusive groups: (1) MASLD; (2) MASLD with increased alcohol intake (MetALD); (3) MASLD with other combined aetiology (the three collectively referred to as MASLD/related steatotic liver disease (SLD)); and (4) no MASLD/related SLD. SLD was determined by fatty liver index ≥30. The primary outcome was CVD event, defined as a composite of myocardial infarction, ischaemic stroke, heart failure or cardiovascular death. RESULTS: The prevalence of MASLD, MetALD and MASLD with other combined aetiology was 27.5%, 4.4% and 1.5%, respectively. A total of 8 808 494 participants without prior CVD were followed up for a median of 12.3 years, during which 272 863 CVD events occurred. The cumulative incidence and multivariable-adjusted risk of CVD were higher in participants with MASLD/related SLD than in those without (HR 1.38 (95% CI 1.37 to 1.39)). Multivariable-adjusted HR (95% CI) of CVD events was 1.39 (1.38 to 1.40) for MASLD, 1.28 (1.26 to 1.30) for MetALD and 1.30 (1.26 to 1.34) for MASLD with other combined aetiology compared to the absence of any of these conditions. CVD risk was also higher in participants with metabolic dysfunction-associated fatty liver disease or non-alcoholic fatty liver disease than in those without the respective condition. CONCLUSION: Over one-third of Korean adults have MASLD/related SLD and bear a high CVD risk.

摘要

目的:通过评估新的代谢功能障碍相关脂肪性肝病(MASLD)定义的临床意义,我们探讨了其流行程度及其与心血管疾病(CVD)风险的关联。

设计:我们从全国性健康筛查数据中,确定了 9775066 名年龄在 20-79 岁之间在 2009 年接受体检的成年人。将参与者分为四个互斥的组别:(1)MASLD;(2)MASLD 伴饮酒增加(MetALD);(3)MASLD 伴其他合并病因(三者统称为 MASLD/相关脂肪性肝病(SLD));(4)无 MASLD/相关 SLD。通过脂肪性肝病指数≥30 来确定 SLD。主要结局为 CVD 事件,定义为心肌梗死、缺血性中风、心力衰竭或心血管死亡的综合。

结果:MASLD、MetALD 和 MASLD 伴其他合并病因的患病率分别为 27.5%、4.4%和 1.5%。共有 8808494 名无既往 CVD 的参与者中位随访 12.3 年,期间发生了 272863 例 CVD 事件。与无 MASLD/相关 SLD 的参与者相比,MASLD/相关 SLD 患者的累积发病率和多变量校正后 CVD 风险更高(HR 1.38[95%CI 1.37 至 1.39])。多变量校正后的 HR(95%CI)为 MASLD 患者的 CVD 事件为 1.39(1.38 至 1.40),MetALD 患者为 1.28(1.26 至 1.30),MASLD 伴其他合并病因患者为 1.30(1.26 至 1.34),与这些情况均不相关的患者相比。与无代谢功能障碍相关的脂肪性肝病或非酒精性脂肪性肝病的患者相比,患有这些疾病的患者的 CVD 风险也更高。

结论:超过三分之一的韩国成年人患有 MASLD/相关 SLD,且 CVD 风险较高。

相似文献

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[3]
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[4]
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[5]
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Int J Hypertens. 2025-8-25

[2]
MAFLD: A Comprehensive Review of the Link Between Metabolic Dysfunction and Cardiovascular Risk.

Hepat Med. 2025-8-19

[3]
Impact of smoking and physical activity on cardiovascular outcomes in type 2 diabetes across steatotic liver disease categories.

Sci Rep. 2025-8-23

[4]
Attributable burden of steatotic liver disease on cardiovascular outcomes in Asia.

JHEP Rep. 2025-6-6

[5]
The role of irregular eating behaviors in metabolic dysfunction-associated steatotic liver disease: evidence from a multicenter cross-sectional study in China.

J Transl Med. 2025-8-2

[6]
Guideline-directed medical strategies for the co-management of heart failure and metabolic dysfunction-associated steatotic liver disease.

Commun Med (Lond). 2025-7-28

[7]
Pathogenesis and management of metabolic dysfunction-associated steatohepatitis-related hepatocellular carcinoma: a narrative review.

Ewha Med J. 2024-10

[8]
Association of metabolic dysfunction-associated steatotic liver disease and steatosis-associated fibrosis estimator with subclinical coronary atherosclerosis: observation cohort study.

Sci Rep. 2025-7-10

[9]
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J Gastroenterol. 2025-7-7

[10]
Pioglitazone with SGLT2 inhibitors or GLP-1 receptor agonists in patients with type 2 diabetes and non-alcoholic fatty liver disease: could the combinations of an old friend with new players yield better outcomes?

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