The University of Southampton
University of Southampton Institutional Repository

Comparative associations of nonalcoholic fatty liver disease and metabolic dysfunction-associated fatty liver disease with coronary artery calcification: a cross-sectional and longitudinal cohort study

Comparative associations of nonalcoholic fatty liver disease and metabolic dysfunction-associated fatty liver disease with coronary artery calcification: a cross-sectional and longitudinal cohort study
Comparative associations of nonalcoholic fatty liver disease and metabolic dysfunction-associated fatty liver disease with coronary artery calcification: a cross-sectional and longitudinal cohort study
Background: in cross-sectional and retrospective cohort studies, we examined comparative associations between nonalcoholic fatty liver disease (NAFLD) and metabolic dysfunction–associated fatty liver disease (MAFLD) and risk of having or developing coronary artery calcification (CAC).

Methods: participants who had health examinations between 2010 and 2019 were analyzed. Liver ultrasonography and coronary artery computed tomography were used to diagnose fatty liver and CAC. Participants were divided into a MAFLD and no-MAFLD group and then NAFLD and no-NAFLD groups. Participants were further divided into no fatty liver disease (reference), NAFLD-only, MAFLD-only, and both NAFLD and MAFLD groups. Logistic regression modeling was performed. Cox proportional hazard model was used to examine the risk of incident CAC in participants without CAC at baseline and who had at least two CAC measurements.

Results: in cross-sectional analyses, 162 180 participants were included. Compared with either the no-NAFLD or no-MAFLD groups, the NAFLD and MAFLD groups were associated with a higher risk of prevalent CAC (NAFLD: adjusted odds ratio [OR], 1.34 [95% CI, 1.29–1.39]; MAFLD: adjusted OR, 1.44 [95% CI, 1.39–1.48]). Among the 4 groups, the MAFLD-only group had the strongest association with risk of prevalent CAC (adjusted OR, 1.60 [95% CI, 1.52–1.69]). Conversely, the NAFLD-only group was associated with a lower risk of prevalent CAC (adjusted OR, 0.76 [95% CI, 0.66–0.87]). In longitudinal analyses, 34 233 participants were included. Compared with either the no-NAFLD or no-MAFLD groups, the NAFLD and MAFLD groups were associated with a higher risk of incident CAC (NAFLD: adjusted hazard ratio, 1.68 [95% CI, 1.43–1.99]; MAFLD: adjusted hazard ratio, 1.82 [95% CI, 1.56–2.13]). Among these 4 groups, the MAFLD-only group had the strongest associations with risk of incident CAC (adjusted hazard ratio, 2.03,[95% CI, 1.62–2.55]). The NAFLD-only group was not independently associated with risk of incident CAC (adjusted hazard ratio, 0.88 [95% CI, 0.44–1.78])

Conclusions: both NAFLD and MAFLD are significantly associated with an increased prevalence and incidence of CAC. These associations tended to be stronger for MAFLD.
cardiovascular disease, coronary artery, lipoprotein, nonalcoholic fatty liver disease, prevalence
1079-5642
482-491
Sung, Ki-Chul
541a0adc-40e7-481f-9517-c7013ab479b7
Yoo, Tae Kyung
242b5816-bd74-41ad-bc8d-1b1ab11093cf
Lee, Mi Yeon
75f2aed3-3b9d-48c3-9c16-16389183862e
Byrne, Christopher D.
1370b997-cead-4229-83a7-53301ed2a43c
Zheng, Ming-Hua
92d70242-2502-4230-95cb-ab40010c3ad4
Targher, Giovanni
9f4b4a4f-28a8-4729-9aaa-f8d9f2f20f65
Sung, Ki-Chul
541a0adc-40e7-481f-9517-c7013ab479b7
Yoo, Tae Kyung
242b5816-bd74-41ad-bc8d-1b1ab11093cf
Lee, Mi Yeon
75f2aed3-3b9d-48c3-9c16-16389183862e
Byrne, Christopher D.
1370b997-cead-4229-83a7-53301ed2a43c
Zheng, Ming-Hua
92d70242-2502-4230-95cb-ab40010c3ad4
Targher, Giovanni
9f4b4a4f-28a8-4729-9aaa-f8d9f2f20f65

Sung, Ki-Chul, Yoo, Tae Kyung, Lee, Mi Yeon, Byrne, Christopher D., Zheng, Ming-Hua and Targher, Giovanni (2023) Comparative associations of nonalcoholic fatty liver disease and metabolic dysfunction-associated fatty liver disease with coronary artery calcification: a cross-sectional and longitudinal cohort study. Arteriosclerosis, Thrombosis, and Vascular Biology, 43 (3), 482-491. (doi:10.1161/ATVBAHA.122.318661).

Record type: Article

Abstract

Background: in cross-sectional and retrospective cohort studies, we examined comparative associations between nonalcoholic fatty liver disease (NAFLD) and metabolic dysfunction–associated fatty liver disease (MAFLD) and risk of having or developing coronary artery calcification (CAC).

Methods: participants who had health examinations between 2010 and 2019 were analyzed. Liver ultrasonography and coronary artery computed tomography were used to diagnose fatty liver and CAC. Participants were divided into a MAFLD and no-MAFLD group and then NAFLD and no-NAFLD groups. Participants were further divided into no fatty liver disease (reference), NAFLD-only, MAFLD-only, and both NAFLD and MAFLD groups. Logistic regression modeling was performed. Cox proportional hazard model was used to examine the risk of incident CAC in participants without CAC at baseline and who had at least two CAC measurements.

Results: in cross-sectional analyses, 162 180 participants were included. Compared with either the no-NAFLD or no-MAFLD groups, the NAFLD and MAFLD groups were associated with a higher risk of prevalent CAC (NAFLD: adjusted odds ratio [OR], 1.34 [95% CI, 1.29–1.39]; MAFLD: adjusted OR, 1.44 [95% CI, 1.39–1.48]). Among the 4 groups, the MAFLD-only group had the strongest association with risk of prevalent CAC (adjusted OR, 1.60 [95% CI, 1.52–1.69]). Conversely, the NAFLD-only group was associated with a lower risk of prevalent CAC (adjusted OR, 0.76 [95% CI, 0.66–0.87]). In longitudinal analyses, 34 233 participants were included. Compared with either the no-NAFLD or no-MAFLD groups, the NAFLD and MAFLD groups were associated with a higher risk of incident CAC (NAFLD: adjusted hazard ratio, 1.68 [95% CI, 1.43–1.99]; MAFLD: adjusted hazard ratio, 1.82 [95% CI, 1.56–2.13]). Among these 4 groups, the MAFLD-only group had the strongest associations with risk of incident CAC (adjusted hazard ratio, 2.03,[95% CI, 1.62–2.55]). The NAFLD-only group was not independently associated with risk of incident CAC (adjusted hazard ratio, 0.88 [95% CI, 0.44–1.78])

Conclusions: both NAFLD and MAFLD are significantly associated with an increased prevalence and incidence of CAC. These associations tended to be stronger for MAFLD.

Text
MAFLD_CAC_revisionsubmission_trackchange - Accepted Manuscript
Download (419kB)
Text
SUPPLEMENTAL MATERIAL_2 - Accepted Manuscript
Download (352kB)
Image
Figure1 - Accepted Manuscript
Available under License Creative Commons Attribution.
Download (4MB)
Image
Graphical abstract - Accepted Manuscript
Restricted to Repository staff only
Request a copy

More information

Accepted/In Press date: 18 January 2023
e-pub ahead of print date: 2 February 2023
Published date: 2 February 2023
Additional Information: Funding Information: G. Targher is supported in part by grants from the University School of Medicine of Verona, Verona, Italy. C.D. Byrne was supported in part by the Southampton National Institute for Health Research Biomedical Research Centre (NIHR203319), United Kingdom.
Keywords: cardiovascular disease, coronary artery, lipoprotein, nonalcoholic fatty liver disease, prevalence

Identifiers

Local EPrints ID: 474509
URI: http://eprints.soton.ac.uk/id/eprint/474509
ISSN: 1079-5642
PURE UUID: 7e72b045-ebee-4d2c-9c6c-c6e85b34a02e
ORCID for Christopher D. Byrne: ORCID iD orcid.org/0000-0001-6322-7753

Catalogue record

Date deposited: 23 Feb 2023 17:44
Last modified: 17 Mar 2024 07:39

Export record

Altmetrics

Contributors

Author: Ki-Chul Sung
Author: Tae Kyung Yoo
Author: Mi Yeon Lee
Author: Ming-Hua Zheng
Author: Giovanni Targher

Download statistics

Downloads from ePrints over the past year. Other digital versions may also be available to download e.g. from the publisher's website.

View more statistics

Atom RSS 1.0 RSS 2.0

Contact ePrints Soton: eprints@soton.ac.uk

ePrints Soton supports OAI 2.0 with a base URL of http://eprints.soton.ac.uk/cgi/oai2

This repository has been built using EPrints software, developed at the University of Southampton, but available to everyone to use.

We use cookies to ensure that we give you the best experience on our website. If you continue without changing your settings, we will assume that you are happy to receive cookies on the University of Southampton website.

×