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Copeptin relates to a fatty liver and measures of obesity in a South African population with mixed ethnicities
PURPOSE: Elevated copeptin, a vasopressin marker, is linked to metabolic disease, and obese rats with low-vasopressin concentration had a decreased risk of liver steatosis. We here investigated the association between copeptin and nonalcoholic fatty liver disease (NAFLD) and possible differences in...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6656785/ https://www.ncbi.nlm.nih.gov/pubmed/31230225 http://dx.doi.org/10.1007/s12020-019-01977-y |
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author | Enhörning, Sofia Malan, Léone |
author_facet | Enhörning, Sofia Malan, Léone |
author_sort | Enhörning, Sofia |
collection | PubMed |
description | PURPOSE: Elevated copeptin, a vasopressin marker, is linked to metabolic disease, and obese rats with low-vasopressin concentration had a decreased risk of liver steatosis. We here investigated the association between copeptin and nonalcoholic fatty liver disease (NAFLD) and possible differences in copeptin concentration between ethnicities. METHODS: In this cross-sectional study of 361 South Africans (n = 172 African black, 189 = Caucasian) with a mean age of 45 years and 45% men, plasma copeptin was measured and associated with NAFLD according to a validated fatty liver index accounting for measures of BMI, waist, triglycerides, and gamma-glutamyltransferase. RESULTS: There was no significant difference in copeptin concentrations between ethnicities after age and gender adjustment (p = 0.24). Increasing copeptin tertile levels were significantly associated with obesity, overweight, and abdominal obesity, respectively, after multivariate adjustment for age, gender, ethnicity, and high HOMA-IR (p = 0.02 for all). Individuals in the second and third copeptin tertile had an increased odds (95% CI) of NAFLD of 1.77 (1.04–3.02) and 2.97 (1.74–5.06), respectively, compared to the bottom tertile (p < 0.001). The association between increasing copeptin tertile and NAFLD remained significant after adjustment for age, gender, ethnicity, high HOMA-IR, self-reported current alcohol intake, and statin treatment (p = 0.01). CONCLUSIONS: Elevated plasma copeptin is independently associated with NAFLD in a population with mixed ethnicities, pointing at the pharmacologically modifiable vasopressin system as a new mechanism behind NAFLD. |
format | Online Article Text |
id | pubmed-6656785 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-66567852019-08-09 Copeptin relates to a fatty liver and measures of obesity in a South African population with mixed ethnicities Enhörning, Sofia Malan, Léone Endocrine Original Article PURPOSE: Elevated copeptin, a vasopressin marker, is linked to metabolic disease, and obese rats with low-vasopressin concentration had a decreased risk of liver steatosis. We here investigated the association between copeptin and nonalcoholic fatty liver disease (NAFLD) and possible differences in copeptin concentration between ethnicities. METHODS: In this cross-sectional study of 361 South Africans (n = 172 African black, 189 = Caucasian) with a mean age of 45 years and 45% men, plasma copeptin was measured and associated with NAFLD according to a validated fatty liver index accounting for measures of BMI, waist, triglycerides, and gamma-glutamyltransferase. RESULTS: There was no significant difference in copeptin concentrations between ethnicities after age and gender adjustment (p = 0.24). Increasing copeptin tertile levels were significantly associated with obesity, overweight, and abdominal obesity, respectively, after multivariate adjustment for age, gender, ethnicity, and high HOMA-IR (p = 0.02 for all). Individuals in the second and third copeptin tertile had an increased odds (95% CI) of NAFLD of 1.77 (1.04–3.02) and 2.97 (1.74–5.06), respectively, compared to the bottom tertile (p < 0.001). The association between increasing copeptin tertile and NAFLD remained significant after adjustment for age, gender, ethnicity, high HOMA-IR, self-reported current alcohol intake, and statin treatment (p = 0.01). CONCLUSIONS: Elevated plasma copeptin is independently associated with NAFLD in a population with mixed ethnicities, pointing at the pharmacologically modifiable vasopressin system as a new mechanism behind NAFLD. Springer US 2019-06-22 2019 /pmc/articles/PMC6656785/ /pubmed/31230225 http://dx.doi.org/10.1007/s12020-019-01977-y Text en © The Author(s) 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Article Enhörning, Sofia Malan, Léone Copeptin relates to a fatty liver and measures of obesity in a South African population with mixed ethnicities |
title | Copeptin relates to a fatty liver and measures of obesity in a South African population with mixed ethnicities |
title_full | Copeptin relates to a fatty liver and measures of obesity in a South African population with mixed ethnicities |
title_fullStr | Copeptin relates to a fatty liver and measures of obesity in a South African population with mixed ethnicities |
title_full_unstemmed | Copeptin relates to a fatty liver and measures of obesity in a South African population with mixed ethnicities |
title_short | Copeptin relates to a fatty liver and measures of obesity in a South African population with mixed ethnicities |
title_sort | copeptin relates to a fatty liver and measures of obesity in a south african population with mixed ethnicities |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6656785/ https://www.ncbi.nlm.nih.gov/pubmed/31230225 http://dx.doi.org/10.1007/s12020-019-01977-y |
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