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Metabolic dysfunction-related liver disease as a risk factor for cancer
OBJECTIVE: The aim of this study was to investigate the association between obesity, diabetes and metabolic related liver dysfunction and the incidence of cancer. DESIGN: This study was conducted with health record data available from the National Health Service in Tayside and Fife. Genetics of Diab...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8961105/ https://www.ncbi.nlm.nih.gov/pubmed/35338048 http://dx.doi.org/10.1136/bmjgast-2021-000817 |
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author | Taylor, Alasdair Siddiqui, Moneeza K Ambery, Philip Armisen, Javier Challis, Benjamin G Haefliger, Carolina Pearson, Ewan R Doney, Alex S F Dillon, John F Palmer, Colin N A |
author_facet | Taylor, Alasdair Siddiqui, Moneeza K Ambery, Philip Armisen, Javier Challis, Benjamin G Haefliger, Carolina Pearson, Ewan R Doney, Alex S F Dillon, John F Palmer, Colin N A |
author_sort | Taylor, Alasdair |
collection | PubMed |
description | OBJECTIVE: The aim of this study was to investigate the association between obesity, diabetes and metabolic related liver dysfunction and the incidence of cancer. DESIGN: This study was conducted with health record data available from the National Health Service in Tayside and Fife. Genetics of Diabetes Audit and Research Tayside, Scotland (GoDARTS), Scottish Health Research Register (SHARE) and Tayside and Fife diabetics, three Scottish cohorts of 13 695, 62 438 and 16 312 patients, respectively, were analysed in this study. Participants in GoDARTS were a volunteer sample, with half having type 2 diabetes mellitus(T2DM). SHARE was a volunteer sample. Tayside and Fife diabetics was a population-level cohort. Metabolic dysfunction-related liver disease (MDLD) was defined using alanine transaminase measurements, and individuals with alternative causes of liver disease (alcohol abuse, viruses, etc) were excluded from the analysis. RESULTS: MDLD associated with increased cancer incidence with a HR of 1.31 in a Cox proportional hazards model adjusted for sex, type 2 diabetes, body mass index(BMI), and smoking status (95% CI 1.27 to 1.35, p<0.0001). This was replicated in two further cohorts, and similar associations with cancer incidence were found for Fatty Liver Index (FLI), Fibrosis-4 Index (FIB-4) and non-alcoholic steatohepatitis (NASH). Homozygous carriers of the common non-alcoholic fatty liver disease (NAFLD) risk-variant PNPLA3 rs738409 had increased risk of cancer. (HR=1.27 (1.02 to 1.58), p=3.1×10(−)(2)). BMI was not independently associated with cancer incidence when MDLD was included as a covariate. CONCLUSION: MDLD, FLI, FIB-4 and NASH associated with increased risk of cancer incidence and death. NAFLD may be a major component of the relationship between obesity and cancer incidence. |
format | Online Article Text |
id | pubmed-8961105 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-89611052022-04-11 Metabolic dysfunction-related liver disease as a risk factor for cancer Taylor, Alasdair Siddiqui, Moneeza K Ambery, Philip Armisen, Javier Challis, Benjamin G Haefliger, Carolina Pearson, Ewan R Doney, Alex S F Dillon, John F Palmer, Colin N A BMJ Open Gastroenterol Cancer OBJECTIVE: The aim of this study was to investigate the association between obesity, diabetes and metabolic related liver dysfunction and the incidence of cancer. DESIGN: This study was conducted with health record data available from the National Health Service in Tayside and Fife. Genetics of Diabetes Audit and Research Tayside, Scotland (GoDARTS), Scottish Health Research Register (SHARE) and Tayside and Fife diabetics, three Scottish cohorts of 13 695, 62 438 and 16 312 patients, respectively, were analysed in this study. Participants in GoDARTS were a volunteer sample, with half having type 2 diabetes mellitus(T2DM). SHARE was a volunteer sample. Tayside and Fife diabetics was a population-level cohort. Metabolic dysfunction-related liver disease (MDLD) was defined using alanine transaminase measurements, and individuals with alternative causes of liver disease (alcohol abuse, viruses, etc) were excluded from the analysis. RESULTS: MDLD associated with increased cancer incidence with a HR of 1.31 in a Cox proportional hazards model adjusted for sex, type 2 diabetes, body mass index(BMI), and smoking status (95% CI 1.27 to 1.35, p<0.0001). This was replicated in two further cohorts, and similar associations with cancer incidence were found for Fatty Liver Index (FLI), Fibrosis-4 Index (FIB-4) and non-alcoholic steatohepatitis (NASH). Homozygous carriers of the common non-alcoholic fatty liver disease (NAFLD) risk-variant PNPLA3 rs738409 had increased risk of cancer. (HR=1.27 (1.02 to 1.58), p=3.1×10(−)(2)). BMI was not independently associated with cancer incidence when MDLD was included as a covariate. CONCLUSION: MDLD, FLI, FIB-4 and NASH associated with increased risk of cancer incidence and death. NAFLD may be a major component of the relationship between obesity and cancer incidence. BMJ Publishing Group 2022-03-25 /pmc/articles/PMC8961105/ /pubmed/35338048 http://dx.doi.org/10.1136/bmjgast-2021-000817 Text en © Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | Cancer Taylor, Alasdair Siddiqui, Moneeza K Ambery, Philip Armisen, Javier Challis, Benjamin G Haefliger, Carolina Pearson, Ewan R Doney, Alex S F Dillon, John F Palmer, Colin N A Metabolic dysfunction-related liver disease as a risk factor for cancer |
title | Metabolic dysfunction-related liver disease as a risk factor for cancer |
title_full | Metabolic dysfunction-related liver disease as a risk factor for cancer |
title_fullStr | Metabolic dysfunction-related liver disease as a risk factor for cancer |
title_full_unstemmed | Metabolic dysfunction-related liver disease as a risk factor for cancer |
title_short | Metabolic dysfunction-related liver disease as a risk factor for cancer |
title_sort | metabolic dysfunction-related liver disease as a risk factor for cancer |
topic | Cancer |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8961105/ https://www.ncbi.nlm.nih.gov/pubmed/35338048 http://dx.doi.org/10.1136/bmjgast-2021-000817 |
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