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Visceral fat does not contribute to metabolic disease in lipodystrophy

OBJECTIVES: Lipodystrophies are characterized by regional or generalized loss of adipose tissue and severe metabolic complications. The role of visceral adipose tissue (VAT) in the development of metabolic derangements in lipodystrophy is unknown. The study aim was to investigate VAT contribution to...

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Autores principales: Malandrino, N., Reynolds, J. C., Brychta, R. J., Chen, K. Y., Auh, S., Gharib, A. M., Startzell, M., Cochran, E. K., Brown, R. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6381384/
https://www.ncbi.nlm.nih.gov/pubmed/30847226
http://dx.doi.org/10.1002/osp4.319
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author Malandrino, N.
Reynolds, J. C.
Brychta, R. J.
Chen, K. Y.
Auh, S.
Gharib, A. M.
Startzell, M.
Cochran, E. K.
Brown, R. J.
author_facet Malandrino, N.
Reynolds, J. C.
Brychta, R. J.
Chen, K. Y.
Auh, S.
Gharib, A. M.
Startzell, M.
Cochran, E. K.
Brown, R. J.
author_sort Malandrino, N.
collection PubMed
description OBJECTIVES: Lipodystrophies are characterized by regional or generalized loss of adipose tissue and severe metabolic complications. The role of visceral adipose tissue (VAT) in the development of metabolic derangements in lipodystrophy is unknown. The study aim was to investigate VAT contribution to metabolic disease in lipodystrophy versus healthy controls. METHODS: Analysis of correlations between VAT volume and biomarkers of metabolic disease in 93 patients and 93 age/sex‐matched healthy controls. RESULTS: Patients with generalized lipodystrophy (n = 43) had lower VAT compared with matched controls, while those with partial lipodystrophy (n = 50) had higher VAT versus controls. Both groups with lipodystrophy had lower leg fat mass versus controls (p < 0.05 for all; unpaired t‐test). In both generalized and partial lipodystrophy, there was no correlation between VAT and glucose, triglycerides or high‐density lipoprotein cholesterol (p > 0.05 for all; Spearman correlation). In controls matched to patients with generalized or partial lipodystrophy, VAT correlated with glucose (R = 0.42 and 0.36), triglycerides (R = 0.36 and 0.60) and high‐density lipoprotein cholesterol (R = −0.34 and −0.64) (p < 0.05 for all; Spearman correlation). CONCLUSIONS: In contrast to healthy controls, metabolic derangements in lipodystrophy did not correlate with VAT volume. These data suggest that, in lipodystrophy, impaired peripheral subcutaneous fat deposition may exert a larger effect than VAT accumulation on the development of metabolic complications. Interventions aimed at increasing functional subcutaneous adipose tissue may provide metabolic benefit.
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spelling pubmed-63813842019-03-07 Visceral fat does not contribute to metabolic disease in lipodystrophy Malandrino, N. Reynolds, J. C. Brychta, R. J. Chen, K. Y. Auh, S. Gharib, A. M. Startzell, M. Cochran, E. K. Brown, R. J. Obes Sci Pract Original Articles OBJECTIVES: Lipodystrophies are characterized by regional or generalized loss of adipose tissue and severe metabolic complications. The role of visceral adipose tissue (VAT) in the development of metabolic derangements in lipodystrophy is unknown. The study aim was to investigate VAT contribution to metabolic disease in lipodystrophy versus healthy controls. METHODS: Analysis of correlations between VAT volume and biomarkers of metabolic disease in 93 patients and 93 age/sex‐matched healthy controls. RESULTS: Patients with generalized lipodystrophy (n = 43) had lower VAT compared with matched controls, while those with partial lipodystrophy (n = 50) had higher VAT versus controls. Both groups with lipodystrophy had lower leg fat mass versus controls (p < 0.05 for all; unpaired t‐test). In both generalized and partial lipodystrophy, there was no correlation between VAT and glucose, triglycerides or high‐density lipoprotein cholesterol (p > 0.05 for all; Spearman correlation). In controls matched to patients with generalized or partial lipodystrophy, VAT correlated with glucose (R = 0.42 and 0.36), triglycerides (R = 0.36 and 0.60) and high‐density lipoprotein cholesterol (R = −0.34 and −0.64) (p < 0.05 for all; Spearman correlation). CONCLUSIONS: In contrast to healthy controls, metabolic derangements in lipodystrophy did not correlate with VAT volume. These data suggest that, in lipodystrophy, impaired peripheral subcutaneous fat deposition may exert a larger effect than VAT accumulation on the development of metabolic complications. Interventions aimed at increasing functional subcutaneous adipose tissue may provide metabolic benefit. John Wiley and Sons Inc. 2019-01-24 /pmc/articles/PMC6381384/ /pubmed/30847226 http://dx.doi.org/10.1002/osp4.319 Text en Published 2018. This article is a U.S. Government work and is in the public domain in the USA. Obesity Science & Practice published by John Wiley & Sons, World Obesity and The Obesity Society. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Articles
Malandrino, N.
Reynolds, J. C.
Brychta, R. J.
Chen, K. Y.
Auh, S.
Gharib, A. M.
Startzell, M.
Cochran, E. K.
Brown, R. J.
Visceral fat does not contribute to metabolic disease in lipodystrophy
title Visceral fat does not contribute to metabolic disease in lipodystrophy
title_full Visceral fat does not contribute to metabolic disease in lipodystrophy
title_fullStr Visceral fat does not contribute to metabolic disease in lipodystrophy
title_full_unstemmed Visceral fat does not contribute to metabolic disease in lipodystrophy
title_short Visceral fat does not contribute to metabolic disease in lipodystrophy
title_sort visceral fat does not contribute to metabolic disease in lipodystrophy
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6381384/
https://www.ncbi.nlm.nih.gov/pubmed/30847226
http://dx.doi.org/10.1002/osp4.319
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