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代谢功能障碍相关脂肪性肝病和脂肪变性相关纤维化评估指标与亚临床冠状动脉粥样硬化的关联:观察性队列研究

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

作者信息

Jeong Joonho, Han Seungbong, Park Gyung-Min, Park Sangwoo, Jeon Young-Jee, Lim Soyeoun, Kwon Woon Jung, Choi Seong Hoon, Park Neung Hwa

机构信息

Division of Hepatology, Department of Internal Medicine, Ulsan University Hospital, University of Ulsan College of Medicine, Ulsan, Republic of Korea.

Department of Biostatistics, College of Medicine, Korea University, Goryeodae-ro 73, Anam-dong, Seongbuk-gu, Seoul, 02841, Republic of Korea.

出版信息

Sci Rep. 2025 Jul 10;15(1):24953. doi: 10.1038/s41598-025-10380-9.


DOI:10.1038/s41598-025-10380-9
PMID:40640424
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12246488/
Abstract

Previous population-based studies have demonstrated differences in cardiovascular events according to the new classification of steatotic liver disease (SLD). However, detailed data on coronary artery status have not been presented. We aimed to investigate the association between subtypes of SLD and coronary artery status using findings from coronary computed tomography angiography (CCTA). We analyzed 8622 asymptomatic individuals without coronary artery disease (CAD) who underwent both abdominal ultrasonography and CCTA. Study participants were divided into four groups: 934 in the no SLD without cardiometabolic (CM) criteria group, 4811 in the no SLD with CM criteria group, 2494 in the metabolic dysfunction-associated steatotic liver disease (MASLD) group, and 252 in the MASLD with increased alcohol intake (Met-ALD) group. Obstructive CAD was defined as coronary arterial stenosis ≥ 50%. Compared with the no SLD without CM group, the no SLD with CM, MASLD, and Met-ALD groups were significantly associated with any coronary plaque (multivariable-adjusted OR 2.05 [95% CI 1.67-2.52], 2.71 [2.18-3.35], and 2.36 [1.69-3.31], respectively); calcified plaques (1.97 [1.59-2.43], 2.54 [2.04-3.16], and 2.10 [1.49-2.96], respectively); non-calcified plaques (2.04 [1.28-3.25], 2.42 [1.51-3.89], and 3.26 [1.73-6.13], respectively); and obstructive CAD (2.57 [1.53-4.32], 3.64 [2.15-6.16], and 3.51 [1.73-7.10], respectively) (p for all < 0.05). In addition, the inverse probability of treatment weighting (IPTW) analyses showed similar ORs for coronary plaques and obstructive CAD. Additionally, higher steatosis-associated fibrosis estimator (SAFE) was strongly associated with all atherosclerotic plaques and obstructive CAD. This association remained significant after multivariable adjustment and IPTW analyses. Subtypes of SLD had significant, yet different strengths of associations with subclinical coronary atherosclerosis. SAFE score classification effectively stratified the distinct associations with subclinical atherosclerosis in subjects with MASLD.

摘要

以往基于人群的研究表明,根据脂肪性肝病(SLD)的新分类,心血管事件存在差异。然而,尚未提供有关冠状动脉状况的详细数据。我们旨在利用冠状动脉计算机断层扫描血管造影(CCTA)的结果,研究SLD亚型与冠状动脉状况之间的关联。我们分析了8622名无症状且无冠状动脉疾病(CAD)的个体,这些个体同时接受了腹部超声检查和CCTA。研究参与者被分为四组:无SLD且无心脏代谢(CM)标准组934人,无SLD且有CM标准组4811人,代谢功能障碍相关脂肪性肝病(MASLD)组2494人,以及饮酒量增加的MASLD(Met-ALD)组252人。阻塞性CAD定义为冠状动脉狭窄≥50%。与无SLD且无CM组相比,无SLD且有CM组、MASLD组和Met-ALD组与任何冠状动脉斑块(多变量调整后的OR分别为2.05 [95%CI 1.67 - 2.52]、2.71 [2.18 - 3.35]和2.36 [1.69 - 3.31])、钙化斑块(分别为1.97 [1.59 - 2.43]、2.54 [2.04 - 3.16]和2.10 [1.49 - 2.96])、非钙化斑块(分别为2.04 [1.28 - 3.25]、2.42 [1.5

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e0e/12246488/9fc5ee1782b6/41598_2025_10380_Fig2a_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e0e/12246488/33d741247720/41598_2025_10380_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e0e/12246488/9fc5ee1782b6/41598_2025_10380_Fig2a_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e0e/12246488/33d741247720/41598_2025_10380_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e0e/12246488/9fc5ee1782b6/41598_2025_10380_Fig2a_HTML.jpg

相似文献

[1]
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

[2]
Steatotic Liver Disease as a Risk Enhancer in the Presence of Metabolic Syndrome.

Eur J Prev Cardiol. 2025-6-12

[3]
Differential impact of lipoprotein(a) on subclinical coronary atherosclerosis in asymptomatic individuals with and without diabetes mellitus.

Sci Rep. 2025-7-1

[4]
Prevalence, severity and determinants of steatotic liver disease among individuals with metabolic and alcohol risk from the community.

J Hepatol. 2025-7-4

[5]
Cause-specific mortality in patients with steatotic liver disease in the United States.

J Hepatol. 2025-5-24

[6]
Prevalence and outcomes of steatotic liver disease subtypes in older adults.

Hepatol Commun. 2025-6-30

[7]
Incremental predictive value of liver fat fraction based on spectral detector CT for major adverse cardiovascular events in T2DM patients with suspected coronary artery disease.

Cardiovasc Diabetol. 2025-4-2

[8]
All-cause and cause-specific mortality in patients with chronic hepatitis B and concurrent steatotic liver disease.

J Hepatol. 2024-12-14

[9]
Impact of metabolic dysfunction severity in steatotic liver disease and its interaction with liver fibrosis on all-cause mortality and multiple hepatic and extra-hepatic outcomes.

Metabolism. 2025-9

[10]
The Significance of the Presence of Gilbert's Syndrome in Patients With Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD): A Retrospective Cohort Study.

Cureus. 2025-5-30

本文引用的文献

[1]
Prognostic value of metabolic dysfunction-associated steatotic liver disease over coronary computed tomography angiography findings: comparison with no-alcoholic fatty liver disease.

Cardiovasc Diabetol. 2024-5-10

[2]
Impact of MASLD and MetALD on clinical outcomes: A meta-analysis of preliminary evidence.

Liver Int. 2024-8

[3]
Steatotic liver disease and its newly proposed sub-classifications correlate with progression of the coronary artery calcium score.

PLoS One. 2024

[4]
Steatotic liver disease predicts cardiovascular disease and advanced liver fibrosis: A community-dwelling cohort study with 20-year follow-up.

Metabolism. 2024-4

[5]
The association of metabolic dysfunction-associated steatotic liver disease (MASLD) with the risk of myocardial infarction: a systematic review and meta-analysis.

Ann Med. 2024-12

[6]
MASLD: a systemic metabolic disorder with cardiovascular and malignant complications.

Gut. 2024-3-7

[7]
Mortality in metabolic dysfunction-associated steatotic liver disease: A nationwide population-based cohort study.

Metabolism. 2024-3

[8]
Steatotic liver disease, MASLD and risk of chronic kidney disease.

Diabetes Metab. 2024-1

[9]
Global survey of stigma among physicians and patients with nonalcoholic fatty liver disease.

J Hepatol. 2024-3

[10]
Metabolic dysfunction-associated steatotic liver disease increases the risk of incident cardiovascular disease: a nationwide cohort study.

EClinicalMedicine. 2023-10-28

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