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Impact of thyroid disorders on the incidence of non‐alcoholic fatty liver disease in Germany
BACKGROUND: Studies investigating a potential association between hypothyroidism and non‐alcoholic fatty liver disease (NAFLD) showed conflicting results and large‐scale population‐based data from Germany on this topic are currently missing. OBJECTIVE: It was the aim of this analysis to investigate...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8435260/ https://www.ncbi.nlm.nih.gov/pubmed/34288580 http://dx.doi.org/10.1002/ueg2.12124 |
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author | Labenz, Christian Kostev, Karel Armandi, Angelo Galle, Peter R. Schattenberg, Jörn M. |
author_facet | Labenz, Christian Kostev, Karel Armandi, Angelo Galle, Peter R. Schattenberg, Jörn M. |
author_sort | Labenz, Christian |
collection | PubMed |
description | BACKGROUND: Studies investigating a potential association between hypothyroidism and non‐alcoholic fatty liver disease (NAFLD) showed conflicting results and large‐scale population‐based data from Germany on this topic are currently missing. OBJECTIVE: It was the aim of this analysis to investigate the impact of thyroid gland disorders on the prevalence of NAFLD in Germany. METHODS: In this case‐control study, using the German disease Analyzer database (IQVIA), NAFLD patients were matched to patients without NAFLD by age, sex, index year, treating physician, diabetes mellitus type II, and obesity. The main outcome of the study was an association between thyroid gland disorders (hypothyroidism, hyperthyroidism and autoimmune thyroiditis) and incident NAFLD and was evaluated using logistic regression analyses. RESULTS: 57,483 patients with NAFLD were matched to 57,483 patients without liver disease. Mean age of the cohort was 60.3 years (±14.1) and 52.3% were men. In regression analyses, hypothyroidism (OR 1.17, 95% CI 1.10 ‐ 1.24, p < 0.001) as well as autoimmune thyroiditis (OR 1.53, 95% CI 1.35–1.73, p < 0.001) were associated with a higher risk of NAFLD. In contrast, hyperthyroidism was associated with a lower risk of NAFLD (OR 0.85, 95% CI 0.77–0.94, p < 0.001). The effect of hypothyroidism on the prevalence of NAFLD remained significant across men (OR 1.31, 95% CI 1.15–1.48) as well as women (OR 1.12, 95% CI 1.05–1.21). CONCLUSION: Hypothyroidism seems to be a risk factor for incident NAFLD. |
format | Online Article Text |
id | pubmed-8435260 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-84352602021-09-15 Impact of thyroid disorders on the incidence of non‐alcoholic fatty liver disease in Germany Labenz, Christian Kostev, Karel Armandi, Angelo Galle, Peter R. Schattenberg, Jörn M. United European Gastroenterol J Hepatobiliary BACKGROUND: Studies investigating a potential association between hypothyroidism and non‐alcoholic fatty liver disease (NAFLD) showed conflicting results and large‐scale population‐based data from Germany on this topic are currently missing. OBJECTIVE: It was the aim of this analysis to investigate the impact of thyroid gland disorders on the prevalence of NAFLD in Germany. METHODS: In this case‐control study, using the German disease Analyzer database (IQVIA), NAFLD patients were matched to patients without NAFLD by age, sex, index year, treating physician, diabetes mellitus type II, and obesity. The main outcome of the study was an association between thyroid gland disorders (hypothyroidism, hyperthyroidism and autoimmune thyroiditis) and incident NAFLD and was evaluated using logistic regression analyses. RESULTS: 57,483 patients with NAFLD were matched to 57,483 patients without liver disease. Mean age of the cohort was 60.3 years (±14.1) and 52.3% were men. In regression analyses, hypothyroidism (OR 1.17, 95% CI 1.10 ‐ 1.24, p < 0.001) as well as autoimmune thyroiditis (OR 1.53, 95% CI 1.35–1.73, p < 0.001) were associated with a higher risk of NAFLD. In contrast, hyperthyroidism was associated with a lower risk of NAFLD (OR 0.85, 95% CI 0.77–0.94, p < 0.001). The effect of hypothyroidism on the prevalence of NAFLD remained significant across men (OR 1.31, 95% CI 1.15–1.48) as well as women (OR 1.12, 95% CI 1.05–1.21). CONCLUSION: Hypothyroidism seems to be a risk factor for incident NAFLD. John Wiley and Sons Inc. 2021-07-20 /pmc/articles/PMC8435260/ /pubmed/34288580 http://dx.doi.org/10.1002/ueg2.12124 Text en © 2021 The Authors. United European Gastroenterology Journal published by Wiley Periodicals LLC. on behalf of United European Gastroenterology. 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 | Hepatobiliary Labenz, Christian Kostev, Karel Armandi, Angelo Galle, Peter R. Schattenberg, Jörn M. Impact of thyroid disorders on the incidence of non‐alcoholic fatty liver disease in Germany |
title | Impact of thyroid disorders on the incidence of non‐alcoholic fatty liver disease in Germany |
title_full | Impact of thyroid disorders on the incidence of non‐alcoholic fatty liver disease in Germany |
title_fullStr | Impact of thyroid disorders on the incidence of non‐alcoholic fatty liver disease in Germany |
title_full_unstemmed | Impact of thyroid disorders on the incidence of non‐alcoholic fatty liver disease in Germany |
title_short | Impact of thyroid disorders on the incidence of non‐alcoholic fatty liver disease in Germany |
title_sort | impact of thyroid disorders on the incidence of non‐alcoholic fatty liver disease in germany |
topic | Hepatobiliary |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8435260/ https://www.ncbi.nlm.nih.gov/pubmed/34288580 http://dx.doi.org/10.1002/ueg2.12124 |
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