Metabolic‐associated fatty liver disease in relation to site‐specific and multiple‐site subclinical atherosclerosis

Author:

Wang Xinyu1ORCID,Zhang Ruosu1,Man Sailimai123ORCID,Lv Jun145,Yu Canqing145,Yin Jianchun6,Wang Xiaona7,Deng Yuhan28,Wang Bo234,Li Liming145,Pang Yuanjie15ORCID

Affiliation:

1. Department of Epidemiology & Biostatistics, School of Public Health Peking University Beijing China

2. Meinian Institute of Health Beijing China

3. Peking University Health Science Center Meinian Public Health Institute Beijing China

4. Peking University Center for Public Health and Epidemic Preparedness and Response Beijing China

5. Key Laboratory of Epidemiology of Major Diseases Ministry of Education, Peking University Beijing China

6. MJ Health Care Group Shanghai China

7. Beijing MJ Health Check‐up Center Beijing China

8. Department of Social Medicine and Health Education, School of Public Health Peking University Beijing China

Abstract

AbstractBackground & AimsNon‐alcoholic fatty liver disease (NAFLD) and the newly proposed metabolic‐associated fatty liver disease (MAFLD) were each associated with subclinical atherosclerosis. However, there is limited evidence on risk of atherosclerosis in individuals who meet the criteria for one but not the other. We aimed to investigate the associations of MAFLD or NAFLD status with site‐specific and multiple‐site atherosclerosis.MethodsThis is a prospective cohort study involving 4524 adults within the MJ health check‐up cohort. Logistic regression model was used to estimate odds ratios (ORs) and confidence intervals (CIs) for subclinical atherosclerosis (elevated carotid intima‐media thickness [CIMT], carotid plaque [CP], coronary artery calcification [CAC] and retinal atherosclerosis [RA]) associated with MAFLD or NAFLD status, MAFLD subtypes and fibrosis status.ResultsMAFLD was associated with higher risks of elevated CIMT, CP, CAC and RA (OR: 1.41 [95% CI 1.18–1.68], 1.23 [1.02–1.48], 1.60 [1.24–2.08], and 1.79 [1.28–2.52], respectively), whereas NAFLD per se did not increase risk of atherosclerosis except for elevated CIMT. Individuals who met both definitions or the definition for MAFLD but not NAFLD had higher risk of subclinical atherosclerosis. Among MAFLD subtypes, MAFLD with diabetes had the highest risk of subclinical atherosclerosis, but the associations did not differ by fibrosis status. Stronger positive associations were observed of MAFLD with multiple‐site than single‐site atherosclerosis.ConclusionsIn Chinese adults, MAFLD was associated with subclinical atherosclerosis, with stronger associations for multiple‐site atherosclerosis. More attention should be paid to MAFLD with diabetes, and MAFLD might be a better predictor for atherosclerotic disease than NAFLD.

Funder

China Postdoctoral Science Foundation

Fundamental Research Funds for the Central Universities

Ministry of Science and Technology of the People's Republic of China

Publisher

Wiley

Subject

Hepatology

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