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Non-alcoholic fatty liver disease severity, central fat mass and adinopectin: a close relationship

AIM: Non-alcoholic fatty liver disease (NAFLD) is the most common chronic liver disease in the general population. Overweight is a common condition in patients with NAFLD, and body composition (BC) assessment is useful to evaluate nutritional status and the efficacy of nutritional strategies. A vali...

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Autores principales: ABENAVOLI, LUDOVICO, DI RENZO, LAURA, GUZZI, PIETRO HIRAM, PELLICANO, RINALDO, MILIC, NATASA, DE LORENZO, ANTONINO
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Iuliu Hatieganu University of Medicine and Pharmacy 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4689242/
https://www.ncbi.nlm.nih.gov/pubmed/26733747
http://dx.doi.org/10.15386/cjmed-595
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author ABENAVOLI, LUDOVICO
DI RENZO, LAURA
GUZZI, PIETRO HIRAM
PELLICANO, RINALDO
MILIC, NATASA
DE LORENZO, ANTONINO
author_facet ABENAVOLI, LUDOVICO
DI RENZO, LAURA
GUZZI, PIETRO HIRAM
PELLICANO, RINALDO
MILIC, NATASA
DE LORENZO, ANTONINO
author_sort ABENAVOLI, LUDOVICO
collection PubMed
description AIM: Non-alcoholic fatty liver disease (NAFLD) is the most common chronic liver disease in the general population. Overweight is a common condition in patients with NAFLD, and body composition (BC) assessment is useful to evaluate nutritional status and the efficacy of nutritional strategies. A valid tool for assessing BC is dual-energy X-ray absorptiometry (DXA). Adiponectin has been shown to be relevant to the pathogenesis of NAFLD. The aim of this observational study is to define the relationship between the severity of NAFLD, the central fat mass evaluated by DXA, and the circulating levels of adiponectin. METHODS: The study was carried out in 31 overweight patients. The degree of liver steatosis was evaluated by ultrasound (US) examination. Anthropometric parameters were measured according to standard methods. Fasting glucose and insulin level were used also to calculate insulin resistance (IR), according to the homeostasis model assessment-insulin resistance (HOMA-IR). The enzyme-linked immunosorbent assay technique was performed to dose fasting serum levels of adiponectin. RESULTS: NAFLD progression was significantly associated with increased central fat (p<0.05). Using DXA, we quantified the regional distribution of adipose tissue and found the expected association between central fat and the US severity of NAFLD. Serum levels of adiponectin, were inversely related to NAFLD progression (p<0.05). CONCLUSION: BC evaluated by anthropometry and DXA, may be used as indicator of NAFLD severity in overweight patients. The evaluation of BC in clinical practice, can improve the nutritional strategies and follow-up. In the clinical setting adiponectin may represent a potential marker for the staging of NAFLD.
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spelling pubmed-46892422016-01-05 Non-alcoholic fatty liver disease severity, central fat mass and adinopectin: a close relationship ABENAVOLI, LUDOVICO DI RENZO, LAURA GUZZI, PIETRO HIRAM PELLICANO, RINALDO MILIC, NATASA DE LORENZO, ANTONINO Clujul Med Original Research AIM: Non-alcoholic fatty liver disease (NAFLD) is the most common chronic liver disease in the general population. Overweight is a common condition in patients with NAFLD, and body composition (BC) assessment is useful to evaluate nutritional status and the efficacy of nutritional strategies. A valid tool for assessing BC is dual-energy X-ray absorptiometry (DXA). Adiponectin has been shown to be relevant to the pathogenesis of NAFLD. The aim of this observational study is to define the relationship between the severity of NAFLD, the central fat mass evaluated by DXA, and the circulating levels of adiponectin. METHODS: The study was carried out in 31 overweight patients. The degree of liver steatosis was evaluated by ultrasound (US) examination. Anthropometric parameters were measured according to standard methods. Fasting glucose and insulin level were used also to calculate insulin resistance (IR), according to the homeostasis model assessment-insulin resistance (HOMA-IR). The enzyme-linked immunosorbent assay technique was performed to dose fasting serum levels of adiponectin. RESULTS: NAFLD progression was significantly associated with increased central fat (p<0.05). Using DXA, we quantified the regional distribution of adipose tissue and found the expected association between central fat and the US severity of NAFLD. Serum levels of adiponectin, were inversely related to NAFLD progression (p<0.05). CONCLUSION: BC evaluated by anthropometry and DXA, may be used as indicator of NAFLD severity in overweight patients. The evaluation of BC in clinical practice, can improve the nutritional strategies and follow-up. In the clinical setting adiponectin may represent a potential marker for the staging of NAFLD. Iuliu Hatieganu University of Medicine and Pharmacy 2015 2015-11-15 /pmc/articles/PMC4689242/ /pubmed/26733747 http://dx.doi.org/10.15386/cjmed-595 Text en http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License
spellingShingle Original Research
ABENAVOLI, LUDOVICO
DI RENZO, LAURA
GUZZI, PIETRO HIRAM
PELLICANO, RINALDO
MILIC, NATASA
DE LORENZO, ANTONINO
Non-alcoholic fatty liver disease severity, central fat mass and adinopectin: a close relationship
title Non-alcoholic fatty liver disease severity, central fat mass and adinopectin: a close relationship
title_full Non-alcoholic fatty liver disease severity, central fat mass and adinopectin: a close relationship
title_fullStr Non-alcoholic fatty liver disease severity, central fat mass and adinopectin: a close relationship
title_full_unstemmed Non-alcoholic fatty liver disease severity, central fat mass and adinopectin: a close relationship
title_short Non-alcoholic fatty liver disease severity, central fat mass and adinopectin: a close relationship
title_sort non-alcoholic fatty liver disease severity, central fat mass and adinopectin: a close relationship
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4689242/
https://www.ncbi.nlm.nih.gov/pubmed/26733747
http://dx.doi.org/10.15386/cjmed-595
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