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Liver fat accumulation is associated with reduced hepatic insulin extraction and beta cell dysfunction in healthy older individuals

BACKGROUND: There is a well-established association between type 2 diabetes and non-alcoholic fatty liver disease (NAFLD) secondary to excess accumulation of intrahepatic lipid (IHL), but the mechanistic basis for this association is unclear. Emerging evidence suggests that in addition to being asso...

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Autores principales: Finucane, Francis M, Sharp, Stephen J, Hatunic, Mensud, Sleigh, Alison, De Lucia Rolfe, Ema, Aihie Sayer, Avan, Cooper, Cyrus, Griffin, Simon J, Wareham, Nicholas J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3974597/
https://www.ncbi.nlm.nih.gov/pubmed/24669786
http://dx.doi.org/10.1186/1758-5996-6-43
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author Finucane, Francis M
Sharp, Stephen J
Hatunic, Mensud
Sleigh, Alison
De Lucia Rolfe, Ema
Aihie Sayer, Avan
Cooper, Cyrus
Griffin, Simon J
Wareham, Nicholas J
author_facet Finucane, Francis M
Sharp, Stephen J
Hatunic, Mensud
Sleigh, Alison
De Lucia Rolfe, Ema
Aihie Sayer, Avan
Cooper, Cyrus
Griffin, Simon J
Wareham, Nicholas J
author_sort Finucane, Francis M
collection PubMed
description BACKGROUND: There is a well-established association between type 2 diabetes and non-alcoholic fatty liver disease (NAFLD) secondary to excess accumulation of intrahepatic lipid (IHL), but the mechanistic basis for this association is unclear. Emerging evidence suggests that in addition to being associated with insulin resistance, NAFLD may be associated with relative beta-cell dysfunction. We sought to determine the influence of liver fat on hepatic insulin extraction and indices of beta-cell function in a cohort of apparently healthy older white adults. METHODS: We performed a cross-sectional analysis of 70 healthy participants in the Hertfordshire Physical Activity Trial (39 males, age 71.3 ± 2.4 years) who underwent oral glucose tolerance testing with glucose, insulin and C-Peptide levels measured every 30 minutes over two hours. The areas under the concentration curve for glucose, insulin and C-Peptide were used to quantify hepatic insulin extraction (HIE), the insulinogenic index (IGI), the C-Peptide increment (CGI), the Disposition Index (DI) and Adaptation Index (AI). Visceral fat was quantified with magnetic resonance (MR) imaging and IHL with MR spectroscopy. Insulin sensitivity was measured with the Oral Glucose Insulin Sensitivity (OGIS) model. RESULTS: 29 of 70 participants (41%) exceeded our arbitrary threshold for NAFLD, i.e. IHL >5.5%. Compared to those with normal IHL, those with NAFLD had higher weight, BMI, waist and MR visceral fat, with lower insulin sensitivity and hepatic insulin extraction. Alcohol consumption, age, HbA1c and alanine aminotransferase (ALT) levels were similar in both groups. Insulin and C-Peptide excursions after oral glucose loading were higher in the NAFLD group, but the CGI and AI were significantly lower, indicating a relative defect in beta-cell function that is only apparent when C-Peptide is measured and when dynamic changes in glucose levels and also insulin sensitivity are taken into account. There was no difference in IGI or DI between the groups. CONCLUSIONS: Although increased IHL was associated with greater insulin secretion, modelled parameters suggested relative beta-cell dysfunction with NAFLD in apparently healthy older adults, which may be obscured by reduced hepatic insulin extraction. Further studies quantifying pancreatic fat content directly and its influence on beta cell function are warranted. TRIAL REGISTRATION: ISRCTN60986572
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spelling pubmed-39745972014-04-04 Liver fat accumulation is associated with reduced hepatic insulin extraction and beta cell dysfunction in healthy older individuals Finucane, Francis M Sharp, Stephen J Hatunic, Mensud Sleigh, Alison De Lucia Rolfe, Ema Aihie Sayer, Avan Cooper, Cyrus Griffin, Simon J Wareham, Nicholas J Diabetol Metab Syndr Research BACKGROUND: There is a well-established association between type 2 diabetes and non-alcoholic fatty liver disease (NAFLD) secondary to excess accumulation of intrahepatic lipid (IHL), but the mechanistic basis for this association is unclear. Emerging evidence suggests that in addition to being associated with insulin resistance, NAFLD may be associated with relative beta-cell dysfunction. We sought to determine the influence of liver fat on hepatic insulin extraction and indices of beta-cell function in a cohort of apparently healthy older white adults. METHODS: We performed a cross-sectional analysis of 70 healthy participants in the Hertfordshire Physical Activity Trial (39 males, age 71.3 ± 2.4 years) who underwent oral glucose tolerance testing with glucose, insulin and C-Peptide levels measured every 30 minutes over two hours. The areas under the concentration curve for glucose, insulin and C-Peptide were used to quantify hepatic insulin extraction (HIE), the insulinogenic index (IGI), the C-Peptide increment (CGI), the Disposition Index (DI) and Adaptation Index (AI). Visceral fat was quantified with magnetic resonance (MR) imaging and IHL with MR spectroscopy. Insulin sensitivity was measured with the Oral Glucose Insulin Sensitivity (OGIS) model. RESULTS: 29 of 70 participants (41%) exceeded our arbitrary threshold for NAFLD, i.e. IHL >5.5%. Compared to those with normal IHL, those with NAFLD had higher weight, BMI, waist and MR visceral fat, with lower insulin sensitivity and hepatic insulin extraction. Alcohol consumption, age, HbA1c and alanine aminotransferase (ALT) levels were similar in both groups. Insulin and C-Peptide excursions after oral glucose loading were higher in the NAFLD group, but the CGI and AI were significantly lower, indicating a relative defect in beta-cell function that is only apparent when C-Peptide is measured and when dynamic changes in glucose levels and also insulin sensitivity are taken into account. There was no difference in IGI or DI between the groups. CONCLUSIONS: Although increased IHL was associated with greater insulin secretion, modelled parameters suggested relative beta-cell dysfunction with NAFLD in apparently healthy older adults, which may be obscured by reduced hepatic insulin extraction. Further studies quantifying pancreatic fat content directly and its influence on beta cell function are warranted. TRIAL REGISTRATION: ISRCTN60986572 BioMed Central 2014-03-26 /pmc/articles/PMC3974597/ /pubmed/24669786 http://dx.doi.org/10.1186/1758-5996-6-43 Text en Copyright © 2014 Finucane et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited.
spellingShingle Research
Finucane, Francis M
Sharp, Stephen J
Hatunic, Mensud
Sleigh, Alison
De Lucia Rolfe, Ema
Aihie Sayer, Avan
Cooper, Cyrus
Griffin, Simon J
Wareham, Nicholas J
Liver fat accumulation is associated with reduced hepatic insulin extraction and beta cell dysfunction in healthy older individuals
title Liver fat accumulation is associated with reduced hepatic insulin extraction and beta cell dysfunction in healthy older individuals
title_full Liver fat accumulation is associated with reduced hepatic insulin extraction and beta cell dysfunction in healthy older individuals
title_fullStr Liver fat accumulation is associated with reduced hepatic insulin extraction and beta cell dysfunction in healthy older individuals
title_full_unstemmed Liver fat accumulation is associated with reduced hepatic insulin extraction and beta cell dysfunction in healthy older individuals
title_short Liver fat accumulation is associated with reduced hepatic insulin extraction and beta cell dysfunction in healthy older individuals
title_sort liver fat accumulation is associated with reduced hepatic insulin extraction and beta cell dysfunction in healthy older individuals
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3974597/
https://www.ncbi.nlm.nih.gov/pubmed/24669786
http://dx.doi.org/10.1186/1758-5996-6-43
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