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Non-alcoholic fatty liver disease and risk of fatal and nonfatal cardiovascular events: an updated systematic review and meta-analysis

Non-alcoholic fatty liver disease and risk of fatal and nonfatal cardiovascular events: an updated systematic review and meta-analysis
Non-alcoholic fatty liver disease and risk of fatal and nonfatal cardiovascular events: an updated systematic review and meta-analysis

BACKGROUND: Studies have reported a significant association between non-alcoholic fatty liver disease (NAFLD) and increased incidence of cardiovascular disease (CVD). However, the magnitude of the risk and whether this risk changes with the severity of NAFLD remains uncertain. We performed a meta-analysis of observational studies to quantify the magnitude of the association between NAFLD and risk of incident CVD events. METHODS: We systematically searched PubMed, Scopus, and Web of Science from database inception to July 1, 2021, to identify eligible observational studies examining the risk of incident CVD events amongst adult (age ≥18 years) individuals with and without NAFLD and in which NAFLD was diagnosed by imaging, International Classification of Diseases codes, or liver biopsy. The primary outcomes were CVD death, non-fatal CVD events, or both. Data from selected studies were extracted, and meta-analysis was performed using random-effects models to obtain summary hazard ratios (HRs) with 95% CIs. The quality of the evidence was assessed with the Cochrane risk of bias tool. This study is registered on Open Science Framework, number osf.io/5z7gf. FINDINGS: We identified 36 longitudinal studies with aggregate data on 5 802 226 middle-aged individuals (mean age 53 years [SD 7]) and 99 668 incident cases of fatal and non-fatal CVD events over a median follow-up of 6·5 years (IQR 5·0-10·2). NAFLD was associated with a moderately increased risk of fatal or non-fatal CVD events (pooled random-effects HR 1·45, 95% CI 1·31-1·61; I2=86·18%). This risk markedly increased across the severity of NAFLD, especially the stage of fibrosis (pooled random-effects HR 2·50, 95% CI 1·68-3·72; I2=73·84%). All risks were independent of age, sex, adiposity measures, diabetes, and other common cardiometabolic risk factors. Sensitivity analyses did not modify these results. INTERPRETATION: NAFLD is associated with an increased long-term risk of fatal or non-fatal CVD events. CVD risk is further increased with more advanced liver disease, especially with higher fibrosis stage. These results provide evidence that NAFLD might be an independent risk factor for CVD morbidity and mortality.None.

2468-1253
903-913
Mantovani, Alessandro
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Csermely, Alessandro
d391aa96-f16a-4294-b704-fe7c36e00d1c
Petracca, Graziana
ef291430-9f90-4b36-b949-c1c676a27942
Beatrice, Giorgia
bb80880e-2ae5-4e6c-8ea0-142a97d3e6fd
Corey, Kathleen E.
8604f40c-fce9-40c3-acb8-f8fe9ebf99b7
Simon, Tracey G.
811c76cb-e258-4532-9c86-8cf76e8448d0
Byrne, Christopher
1370b997-cead-4229-83a7-53301ed2a43c
Targher, Giovanni
043e0811-b389-4922-974e-22e650212c5f
Mantovani, Alessandro
d91227b3-a445-4511-9f7d-7824839eb17d
Csermely, Alessandro
d391aa96-f16a-4294-b704-fe7c36e00d1c
Petracca, Graziana
ef291430-9f90-4b36-b949-c1c676a27942
Beatrice, Giorgia
bb80880e-2ae5-4e6c-8ea0-142a97d3e6fd
Corey, Kathleen E.
8604f40c-fce9-40c3-acb8-f8fe9ebf99b7
Simon, Tracey G.
811c76cb-e258-4532-9c86-8cf76e8448d0
Byrne, Christopher
1370b997-cead-4229-83a7-53301ed2a43c
Targher, Giovanni
043e0811-b389-4922-974e-22e650212c5f

Mantovani, Alessandro, Csermely, Alessandro, Petracca, Graziana, Beatrice, Giorgia, Corey, Kathleen E., Simon, Tracey G., Byrne, Christopher and Targher, Giovanni (2021) Non-alcoholic fatty liver disease and risk of fatal and nonfatal cardiovascular events: an updated systematic review and meta-analysis. The Lancet Gastroenterology & Hepatology, 6 (11), 903-913. (doi:10.1016/S2468-1253(21)00308-3).

Record type: Article

Abstract

BACKGROUND: Studies have reported a significant association between non-alcoholic fatty liver disease (NAFLD) and increased incidence of cardiovascular disease (CVD). However, the magnitude of the risk and whether this risk changes with the severity of NAFLD remains uncertain. We performed a meta-analysis of observational studies to quantify the magnitude of the association between NAFLD and risk of incident CVD events. METHODS: We systematically searched PubMed, Scopus, and Web of Science from database inception to July 1, 2021, to identify eligible observational studies examining the risk of incident CVD events amongst adult (age ≥18 years) individuals with and without NAFLD and in which NAFLD was diagnosed by imaging, International Classification of Diseases codes, or liver biopsy. The primary outcomes were CVD death, non-fatal CVD events, or both. Data from selected studies were extracted, and meta-analysis was performed using random-effects models to obtain summary hazard ratios (HRs) with 95% CIs. The quality of the evidence was assessed with the Cochrane risk of bias tool. This study is registered on Open Science Framework, number osf.io/5z7gf. FINDINGS: We identified 36 longitudinal studies with aggregate data on 5 802 226 middle-aged individuals (mean age 53 years [SD 7]) and 99 668 incident cases of fatal and non-fatal CVD events over a median follow-up of 6·5 years (IQR 5·0-10·2). NAFLD was associated with a moderately increased risk of fatal or non-fatal CVD events (pooled random-effects HR 1·45, 95% CI 1·31-1·61; I2=86·18%). This risk markedly increased across the severity of NAFLD, especially the stage of fibrosis (pooled random-effects HR 2·50, 95% CI 1·68-3·72; I2=73·84%). All risks were independent of age, sex, adiposity measures, diabetes, and other common cardiometabolic risk factors. Sensitivity analyses did not modify these results. INTERPRETATION: NAFLD is associated with an increased long-term risk of fatal or non-fatal CVD events. CVD risk is further increased with more advanced liver disease, especially with higher fibrosis stage. These results provide evidence that NAFLD might be an independent risk factor for CVD morbidity and mortality.None.

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Accepted/In Press date: 17 August 2021
Published date: 1 November 2021
Additional Information: Publisher Copyright: Copyright © 2021 Elsevier Ltd. All rights reserved.

Identifiers

Local EPrints ID: 450902
URI: http://eprints.soton.ac.uk/id/eprint/450902
ISSN: 2468-1253
PURE UUID: 0a394ec0-27bc-4c28-a422-1d61e97e23a7
ORCID for Christopher Byrne: ORCID iD orcid.org/0000-0001-6322-7753

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Date deposited: 19 Aug 2021 16:34
Last modified: 17 Mar 2024 02:49

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Contributors

Author: Alessandro Mantovani
Author: Alessandro Csermely
Author: Graziana Petracca
Author: Giorgia Beatrice
Author: Kathleen E. Corey
Author: Tracey G. Simon
Author: Giovanni Targher

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