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Non-alcoholic fatty liver disease and mortality among US adults: prospective cohort study

Objective To evaluate the association between non-alcoholic fatty liver disease and all cause and cause specific mortality in a representative sample of the US general population. Design Prospective cohort study. Setting US Third National Health and Nutrition Examination Survey (NHANES III: 1988-94)...

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Autores principales: Lazo, Mariana, Hernaez, Ruben, Bonekamp, Susanne, Kamel, Ihab R, Brancati, Frederick L, Guallar, Eliseo, Clark, Jeanne M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group Ltd. 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3220620/
https://www.ncbi.nlm.nih.gov/pubmed/22102439
http://dx.doi.org/10.1136/bmj.d6891
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author Lazo, Mariana
Hernaez, Ruben
Bonekamp, Susanne
Kamel, Ihab R
Brancati, Frederick L
Guallar, Eliseo
Clark, Jeanne M
author_facet Lazo, Mariana
Hernaez, Ruben
Bonekamp, Susanne
Kamel, Ihab R
Brancati, Frederick L
Guallar, Eliseo
Clark, Jeanne M
author_sort Lazo, Mariana
collection PubMed
description Objective To evaluate the association between non-alcoholic fatty liver disease and all cause and cause specific mortality in a representative sample of the US general population. Design Prospective cohort study. Setting US Third National Health and Nutrition Examination Survey (NHANES III: 1988-94) with follow-up of mortality to 2006. Participants 11 371 adults aged 20-74 participating in the Third National Health and Nutrition Examination Survey, with assessment of hepatic steatosis. Main outcome measure Mortality from all causes, cardiovascular disease, cancer, and liver disease (up to 18 years of follow-up). Results The prevalence of non-alcoholic fatty liver disease with and without increased levels of liver enzymes in the population was 3.1% and 16.4%, respectively. Compared with participants without steatosis, those with non-alcoholic fatty liver disease but normal liver enzyme levels had multivariate adjusted hazard ratios for deaths from all causes of 0.92 (95% confidence interval 0.78 to 1.09), from cardiovascular disease of 0.86 (0.67 to 1.12), from cancer of 0.92 (0.67 to 1.27), and from liver disease of 0.64 (0.12 to 3.59). Compared with participants without steatosis, those with non-alcoholic fatty liver disease and increased liver enzyme levels had adjusted hazard ratios for deaths from all causes of 0.80 (0.52 to 1.22), from cardiovascular disease of 0.59 (0.29 to 1.20), from cancer of 0.53 (0.26 to 1.10), and from liver disease of 1.17 (0.15 to 8.93). Conclusions Non-alcoholic fatty liver disease was not associated with an increased risk of death from all causes, cardiovascular disease, cancer, or liver disease.
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spelling pubmed-32206202011-11-25 Non-alcoholic fatty liver disease and mortality among US adults: prospective cohort study Lazo, Mariana Hernaez, Ruben Bonekamp, Susanne Kamel, Ihab R Brancati, Frederick L Guallar, Eliseo Clark, Jeanne M BMJ Research Objective To evaluate the association between non-alcoholic fatty liver disease and all cause and cause specific mortality in a representative sample of the US general population. Design Prospective cohort study. Setting US Third National Health and Nutrition Examination Survey (NHANES III: 1988-94) with follow-up of mortality to 2006. Participants 11 371 adults aged 20-74 participating in the Third National Health and Nutrition Examination Survey, with assessment of hepatic steatosis. Main outcome measure Mortality from all causes, cardiovascular disease, cancer, and liver disease (up to 18 years of follow-up). Results The prevalence of non-alcoholic fatty liver disease with and without increased levels of liver enzymes in the population was 3.1% and 16.4%, respectively. Compared with participants without steatosis, those with non-alcoholic fatty liver disease but normal liver enzyme levels had multivariate adjusted hazard ratios for deaths from all causes of 0.92 (95% confidence interval 0.78 to 1.09), from cardiovascular disease of 0.86 (0.67 to 1.12), from cancer of 0.92 (0.67 to 1.27), and from liver disease of 0.64 (0.12 to 3.59). Compared with participants without steatosis, those with non-alcoholic fatty liver disease and increased liver enzyme levels had adjusted hazard ratios for deaths from all causes of 0.80 (0.52 to 1.22), from cardiovascular disease of 0.59 (0.29 to 1.20), from cancer of 0.53 (0.26 to 1.10), and from liver disease of 1.17 (0.15 to 8.93). Conclusions Non-alcoholic fatty liver disease was not associated with an increased risk of death from all causes, cardiovascular disease, cancer, or liver disease. BMJ Publishing Group Ltd. 2011-11-18 /pmc/articles/PMC3220620/ /pubmed/22102439 http://dx.doi.org/10.1136/bmj.d6891 Text en © Lazo et al 2011 This is an open-access article distributed under the terms of the Creative Commons Attribution Non-commercial License, which permits use, distribution, and reproduction in any medium, provided the original work is properly cited, the use is non commercial and is otherwise in compliance with the license. See: http://creativecommons.org/licenses/by-nc/2.0/ and http://creativecommons.org/licenses/by-nc/2.0/legalcode.
spellingShingle Research
Lazo, Mariana
Hernaez, Ruben
Bonekamp, Susanne
Kamel, Ihab R
Brancati, Frederick L
Guallar, Eliseo
Clark, Jeanne M
Non-alcoholic fatty liver disease and mortality among US adults: prospective cohort study
title Non-alcoholic fatty liver disease and mortality among US adults: prospective cohort study
title_full Non-alcoholic fatty liver disease and mortality among US adults: prospective cohort study
title_fullStr Non-alcoholic fatty liver disease and mortality among US adults: prospective cohort study
title_full_unstemmed Non-alcoholic fatty liver disease and mortality among US adults: prospective cohort study
title_short Non-alcoholic fatty liver disease and mortality among US adults: prospective cohort study
title_sort non-alcoholic fatty liver disease and mortality among us adults: prospective cohort study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3220620/
https://www.ncbi.nlm.nih.gov/pubmed/22102439
http://dx.doi.org/10.1136/bmj.d6891
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