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Reversal of nonalcoholic fatty liver disease reduces the risk of cardiovascular disease among Korean
Nonalcoholic fatty liver disease (NAFLD) is considered an independent risk factor for the development of cardiovascular disease. However, the association between changes in NAFLD status and the risk of cardiovascular disease (CVD) remains uncertain. Starting January 1, 2013, participants were follow...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10627619/ https://www.ncbi.nlm.nih.gov/pubmed/37933021 http://dx.doi.org/10.1097/MD.0000000000035804 |
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author | Oh, Yun Hwan Jeong, Seogsong Park, Sun Jae Ahn, Joseph C Park, Sang Min |
author_facet | Oh, Yun Hwan Jeong, Seogsong Park, Sun Jae Ahn, Joseph C Park, Sang Min |
author_sort | Oh, Yun Hwan |
collection | PubMed |
description | Nonalcoholic fatty liver disease (NAFLD) is considered an independent risk factor for the development of cardiovascular disease. However, the association between changes in NAFLD status and the risk of cardiovascular disease (CVD) remains uncertain. Starting January 1, 2013, participants were followed until the occurrence of CVD event, death, or December 31, 2020. This was a population-based cohort study that included data from adults aged ≥ 20, who underwent 2 consecutive health screenings from 2009 to 2012. NAFLD was defined as a Fatty Liver Index ≥ 60 at each screening. The primary endpoint was a CVD event, which encompassed ischemic heart disease and cerebrovascular disease. The association between changes in NAFLD status and the risk of CVD was determined using multivariable Cox proportional hazards regression. This cohort comprised 4656,305 adults with a median age of 53 years. During 36,396,968 person-years of follow-up, 238,933 (5.1%) CVD events were observed. Compared to patients with no NAFLD at both screenings, patients who developed NAFLD at the second screening exhibited an increased risk of CVD (adjusted hazard ratio, 1.15; 95% confidence interval, 1.13–1.17). In contrast, individuals who recovered from NAFLD at the second screening demonstrated a reduced CVD risk compared to those with persistent NAFLD (adjusted hazard ratio, 0.91; 95% confidence interval, 0.90–0.92). The reversal of NAFLD is associated with a reduced risk of CVD. Therefore, focusing on NAFLD treatment could serve as a clinical target for lowering CVD risk. |
format | Online Article Text |
id | pubmed-10627619 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-106276192023-11-07 Reversal of nonalcoholic fatty liver disease reduces the risk of cardiovascular disease among Korean Oh, Yun Hwan Jeong, Seogsong Park, Sun Jae Ahn, Joseph C Park, Sang Min Medicine (Baltimore) 4500 Nonalcoholic fatty liver disease (NAFLD) is considered an independent risk factor for the development of cardiovascular disease. However, the association between changes in NAFLD status and the risk of cardiovascular disease (CVD) remains uncertain. Starting January 1, 2013, participants were followed until the occurrence of CVD event, death, or December 31, 2020. This was a population-based cohort study that included data from adults aged ≥ 20, who underwent 2 consecutive health screenings from 2009 to 2012. NAFLD was defined as a Fatty Liver Index ≥ 60 at each screening. The primary endpoint was a CVD event, which encompassed ischemic heart disease and cerebrovascular disease. The association between changes in NAFLD status and the risk of CVD was determined using multivariable Cox proportional hazards regression. This cohort comprised 4656,305 adults with a median age of 53 years. During 36,396,968 person-years of follow-up, 238,933 (5.1%) CVD events were observed. Compared to patients with no NAFLD at both screenings, patients who developed NAFLD at the second screening exhibited an increased risk of CVD (adjusted hazard ratio, 1.15; 95% confidence interval, 1.13–1.17). In contrast, individuals who recovered from NAFLD at the second screening demonstrated a reduced CVD risk compared to those with persistent NAFLD (adjusted hazard ratio, 0.91; 95% confidence interval, 0.90–0.92). The reversal of NAFLD is associated with a reduced risk of CVD. Therefore, focusing on NAFLD treatment could serve as a clinical target for lowering CVD risk. Lippincott Williams & Wilkins 2023-11-03 /pmc/articles/PMC10627619/ /pubmed/37933021 http://dx.doi.org/10.1097/MD.0000000000035804 Text en Copyright © 2023 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC) (https://creativecommons.org/licenses/by-nc/4.0/) , where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. |
spellingShingle | 4500 Oh, Yun Hwan Jeong, Seogsong Park, Sun Jae Ahn, Joseph C Park, Sang Min Reversal of nonalcoholic fatty liver disease reduces the risk of cardiovascular disease among Korean |
title | Reversal of nonalcoholic fatty liver disease reduces the risk of cardiovascular disease among Korean |
title_full | Reversal of nonalcoholic fatty liver disease reduces the risk of cardiovascular disease among Korean |
title_fullStr | Reversal of nonalcoholic fatty liver disease reduces the risk of cardiovascular disease among Korean |
title_full_unstemmed | Reversal of nonalcoholic fatty liver disease reduces the risk of cardiovascular disease among Korean |
title_short | Reversal of nonalcoholic fatty liver disease reduces the risk of cardiovascular disease among Korean |
title_sort | reversal of nonalcoholic fatty liver disease reduces the risk of cardiovascular disease among korean |
topic | 4500 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10627619/ https://www.ncbi.nlm.nih.gov/pubmed/37933021 http://dx.doi.org/10.1097/MD.0000000000035804 |
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