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Subcutaneous Adipose Cell Size and Distribution: Relationship to Insulin Resistance and Body Fat
Metabolic heterogeneity among obese individuals may be attributable to differences in adipose cell size. We sought to clarify this by quantifying adipose cell-size distribution, body fat, and insulin-mediated glucose uptake in overweight/moderately-obese individuals. 148 healthy nondiabetic subjects...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2013
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4344365/ https://www.ncbi.nlm.nih.gov/pubmed/23666871 http://dx.doi.org/10.1002/oby.20209 |
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author | McLaughlin, T Lamendola, C Coghlan, N Liu, TC Lerner, K Sherman, A Cushman, SW |
author_facet | McLaughlin, T Lamendola, C Coghlan, N Liu, TC Lerner, K Sherman, A Cushman, SW |
author_sort | McLaughlin, T |
collection | PubMed |
description | Metabolic heterogeneity among obese individuals may be attributable to differences in adipose cell size. We sought to clarify this by quantifying adipose cell-size distribution, body fat, and insulin-mediated glucose uptake in overweight/moderately-obese individuals. 148 healthy nondiabetic subjects with BMI 25–38 kg/m(2) underwent subcutaneous adipose tissue biopsies and quantification of insulin-mediated glucose uptake with steady-state plasma glucose concentrations (SSPG) during the modified insulin suppression test. Cell-size distributions were obtained with Beckman Coulter Multisizer. Primary endpoints included % small adipose cells and diameter of large adipose cells. Cell-size and metabolic parameters were compared by regression for the whole group; according to IR and IS subgroups; and by body fat quintile. Both large and small adipose cells were present in nearly equal proportions. Percent small cells was associated with SSPG (r=0.26, p=0.003). Compared to BMI-matched IS individuals, IR counterparts demonstrated fewer, but larger large adipose cells, and a greater proportion of small-to-large adipose cells. Diameter of the large adipose cells was associated with %body fat (r=0.26, p=0.014), female sex (r=0.21, p=0.036), and SSPG (r=0.20, p=0.012). In the highest vs lowest % body fat quintile, adipose cell size increased by only 7% whereas adipose cell number increased by 74%. Recruitment of adipose cells is required for expansion of body fat mass beyond BMI of 25 kg/m(2). Insulin resistance is associated with accumulation of small adipose cells and enlargement of large adipose cells. These data support the notion that impaired adipogenesis may underlie insulin resistance. |
format | Online Article Text |
id | pubmed-4344365 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
record_format | MEDLINE/PubMed |
spelling | pubmed-43443652015-02-27 Subcutaneous Adipose Cell Size and Distribution: Relationship to Insulin Resistance and Body Fat McLaughlin, T Lamendola, C Coghlan, N Liu, TC Lerner, K Sherman, A Cushman, SW Obesity (Silver Spring) Article Metabolic heterogeneity among obese individuals may be attributable to differences in adipose cell size. We sought to clarify this by quantifying adipose cell-size distribution, body fat, and insulin-mediated glucose uptake in overweight/moderately-obese individuals. 148 healthy nondiabetic subjects with BMI 25–38 kg/m(2) underwent subcutaneous adipose tissue biopsies and quantification of insulin-mediated glucose uptake with steady-state plasma glucose concentrations (SSPG) during the modified insulin suppression test. Cell-size distributions were obtained with Beckman Coulter Multisizer. Primary endpoints included % small adipose cells and diameter of large adipose cells. Cell-size and metabolic parameters were compared by regression for the whole group; according to IR and IS subgroups; and by body fat quintile. Both large and small adipose cells were present in nearly equal proportions. Percent small cells was associated with SSPG (r=0.26, p=0.003). Compared to BMI-matched IS individuals, IR counterparts demonstrated fewer, but larger large adipose cells, and a greater proportion of small-to-large adipose cells. Diameter of the large adipose cells was associated with %body fat (r=0.26, p=0.014), female sex (r=0.21, p=0.036), and SSPG (r=0.20, p=0.012). In the highest vs lowest % body fat quintile, adipose cell size increased by only 7% whereas adipose cell number increased by 74%. Recruitment of adipose cells is required for expansion of body fat mass beyond BMI of 25 kg/m(2). Insulin resistance is associated with accumulation of small adipose cells and enlargement of large adipose cells. These data support the notion that impaired adipogenesis may underlie insulin resistance. 2013-12-17 2014-03 /pmc/articles/PMC4344365/ /pubmed/23666871 http://dx.doi.org/10.1002/oby.20209 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article McLaughlin, T Lamendola, C Coghlan, N Liu, TC Lerner, K Sherman, A Cushman, SW Subcutaneous Adipose Cell Size and Distribution: Relationship to Insulin Resistance and Body Fat |
title | Subcutaneous Adipose Cell Size and Distribution: Relationship to Insulin Resistance and Body Fat |
title_full | Subcutaneous Adipose Cell Size and Distribution: Relationship to Insulin Resistance and Body Fat |
title_fullStr | Subcutaneous Adipose Cell Size and Distribution: Relationship to Insulin Resistance and Body Fat |
title_full_unstemmed | Subcutaneous Adipose Cell Size and Distribution: Relationship to Insulin Resistance and Body Fat |
title_short | Subcutaneous Adipose Cell Size and Distribution: Relationship to Insulin Resistance and Body Fat |
title_sort | subcutaneous adipose cell size and distribution: relationship to insulin resistance and body fat |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4344365/ https://www.ncbi.nlm.nih.gov/pubmed/23666871 http://dx.doi.org/10.1002/oby.20209 |
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