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Risk of cardiovascular disease and loss in life expectancy in NAFLD
BACKGROUND AND AIMS: Conflicting evidence exists on cardiovascular disease (CVD) risk in patients with NAFLD, and data are lacking on whether NAFLD increases mortality after a CVD event. Moreover, life expectancy in NAFLD has not been studied. We therefore examined CVD risk and life expectancy in pa...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9790251/ https://www.ncbi.nlm.nih.gov/pubmed/35403232 http://dx.doi.org/10.1002/hep.32519 |
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author | Shang, Ying Nasr, Patrik Widman, Linnea Hagström, Hannes |
author_facet | Shang, Ying Nasr, Patrik Widman, Linnea Hagström, Hannes |
author_sort | Shang, Ying |
collection | PubMed |
description | BACKGROUND AND AIMS: Conflicting evidence exists on cardiovascular disease (CVD) risk in patients with NAFLD, and data are lacking on whether NAFLD increases mortality after a CVD event. Moreover, life expectancy in NAFLD has not been studied. We therefore examined CVD risk and life expectancy in patients with NAFLD compared with the general population. APPROACH AND RESULTS: In this nationwide population‐based cohort, all patients with NAFLD diagnosis and without baseline CVD (ascertaining from the Swedish National Patient Register from 1987 to 2016, n = 10,023) were matched 10:1 on age, sex, and municipality to individuals from the general population (controls, n = 96,313). CVD diagnosis and mortality were derived from national registers. Multistate models and flexible parametric survival models were used to estimate adjusted hazard ratios (aHRs) for CVD risk and loss in life expectancy due to NAFLD. We identified 1037 (10.3%) CVD events in patients with NAFLD and 4041 (4.2%) in controls. CVD risk was 2.6‐fold higher in NAFLD compared with controls (aHR = 2.61, 95% CI = 2.36–2.88) and was strongest for nonfatal CVD (aHR = 3.71, 95% CI = 3.29–4.17). After a nonfatal CVD event, the risk for all‐cause mortality was similar between patients with NAFLD and controls (aHR = 0.89, 95% CI = 0.64–1.25). Life expectancy in patients with NAFLD was, on average, 2.8 years lower than controls, with the highest loss of life‐years when NAFLD was diagnosed in middle age (40–60 years). CONCLUSIONS: NAFLD was associated with a higher risk of nonfatal CVD but did not affect post‐CVD mortality risk. Patients diagnosed with NAFLD have a lower life expectancy than the general population. |
format | Online Article Text |
id | pubmed-9790251 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-97902512022-12-28 Risk of cardiovascular disease and loss in life expectancy in NAFLD Shang, Ying Nasr, Patrik Widman, Linnea Hagström, Hannes Hepatology Original Articles BACKGROUND AND AIMS: Conflicting evidence exists on cardiovascular disease (CVD) risk in patients with NAFLD, and data are lacking on whether NAFLD increases mortality after a CVD event. Moreover, life expectancy in NAFLD has not been studied. We therefore examined CVD risk and life expectancy in patients with NAFLD compared with the general population. APPROACH AND RESULTS: In this nationwide population‐based cohort, all patients with NAFLD diagnosis and without baseline CVD (ascertaining from the Swedish National Patient Register from 1987 to 2016, n = 10,023) were matched 10:1 on age, sex, and municipality to individuals from the general population (controls, n = 96,313). CVD diagnosis and mortality were derived from national registers. Multistate models and flexible parametric survival models were used to estimate adjusted hazard ratios (aHRs) for CVD risk and loss in life expectancy due to NAFLD. We identified 1037 (10.3%) CVD events in patients with NAFLD and 4041 (4.2%) in controls. CVD risk was 2.6‐fold higher in NAFLD compared with controls (aHR = 2.61, 95% CI = 2.36–2.88) and was strongest for nonfatal CVD (aHR = 3.71, 95% CI = 3.29–4.17). After a nonfatal CVD event, the risk for all‐cause mortality was similar between patients with NAFLD and controls (aHR = 0.89, 95% CI = 0.64–1.25). Life expectancy in patients with NAFLD was, on average, 2.8 years lower than controls, with the highest loss of life‐years when NAFLD was diagnosed in middle age (40–60 years). CONCLUSIONS: NAFLD was associated with a higher risk of nonfatal CVD but did not affect post‐CVD mortality risk. Patients diagnosed with NAFLD have a lower life expectancy than the general population. John Wiley and Sons Inc. 2022-04-23 2022-11 /pmc/articles/PMC9790251/ /pubmed/35403232 http://dx.doi.org/10.1002/hep.32519 Text en © 2022 The Authors. Hepatology published by Wiley Periodicals LLC on behalf of American Association for the Study of Liver Diseases. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Shang, Ying Nasr, Patrik Widman, Linnea Hagström, Hannes Risk of cardiovascular disease and loss in life expectancy in NAFLD |
title | Risk of cardiovascular disease and loss in life expectancy in NAFLD |
title_full | Risk of cardiovascular disease and loss in life expectancy in NAFLD |
title_fullStr | Risk of cardiovascular disease and loss in life expectancy in NAFLD |
title_full_unstemmed | Risk of cardiovascular disease and loss in life expectancy in NAFLD |
title_short | Risk of cardiovascular disease and loss in life expectancy in NAFLD |
title_sort | risk of cardiovascular disease and loss in life expectancy in nafld |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9790251/ https://www.ncbi.nlm.nih.gov/pubmed/35403232 http://dx.doi.org/10.1002/hep.32519 |
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