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Adipocyte Turnover: Relevance to Human Adipose Tissue Morphology
OBJECTIVE: Adipose tissue may contain few large adipocytes (hypertrophy) or many small adipocytes (hyperplasia). We investigated factors of putative importance for adipose tissue morphology. RESEARCH DESIGN AND METHODS: Subcutaneous adipocyte size and total fat mass were compared in 764 subjects wit...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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American Diabetes Association
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2797910/ https://www.ncbi.nlm.nih.gov/pubmed/19846802 http://dx.doi.org/10.2337/db09-0942 |
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author | Arner, Erik Westermark, Pål O. Spalding, Kirsty L. Britton, Tom Rydén, Mikael Frisén, Jonas Bernard, Samuel Arner, Peter |
author_facet | Arner, Erik Westermark, Pål O. Spalding, Kirsty L. Britton, Tom Rydén, Mikael Frisén, Jonas Bernard, Samuel Arner, Peter |
author_sort | Arner, Erik |
collection | PubMed |
description | OBJECTIVE: Adipose tissue may contain few large adipocytes (hypertrophy) or many small adipocytes (hyperplasia). We investigated factors of putative importance for adipose tissue morphology. RESEARCH DESIGN AND METHODS: Subcutaneous adipocyte size and total fat mass were compared in 764 subjects with BMI 18–60 kg/m(2). A morphology value was defined as the difference between the measured adipocyte volume and the expected volume given by a curved-line fit for a given body fat mass and was related to insulin values. In 35 subjects, in vivo adipocyte turnover was measured by exploiting incorporation of atmospheric (14)C into DNA. RESULTS: Occurrence of hyperplasia (negative morphology value) or hypertrophy (positive morphology value) was independent of sex and body weight but correlated with fasting plasma insulin levels and insulin sensitivity, independent of adipocyte volume (β-coefficient = 0.3, P < 0.0001). Total adipocyte number and morphology were negatively related (r = −0.66); i.e., the total adipocyte number was greatest in pronounced hyperplasia and smallest in pronounced hypertrophy. The absolute number of new adipocytes generated each year was 70% lower (P < 0.001) in hypertrophy than in hyperplasia, and individual values for adipocyte generation and morphology were strongly related (r = 0.7, P < 0.001). The relative death rate (∼10% per year) or mean age of adipocytes (∼10 years) was not correlated with morphology. CONCLUSIONS: Adipose tissue morphology correlates with insulin measures and is linked to the total adipocyte number independently of sex and body fat level. Low generation rates of adipocytes associate with adipose tissue hypertrophy, whereas high generation rates associate with adipose hyperplasia. |
format | Text |
id | pubmed-2797910 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | American Diabetes Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-27979102011-01-01 Adipocyte Turnover: Relevance to Human Adipose Tissue Morphology Arner, Erik Westermark, Pål O. Spalding, Kirsty L. Britton, Tom Rydén, Mikael Frisén, Jonas Bernard, Samuel Arner, Peter Diabetes Original Article OBJECTIVE: Adipose tissue may contain few large adipocytes (hypertrophy) or many small adipocytes (hyperplasia). We investigated factors of putative importance for adipose tissue morphology. RESEARCH DESIGN AND METHODS: Subcutaneous adipocyte size and total fat mass were compared in 764 subjects with BMI 18–60 kg/m(2). A morphology value was defined as the difference between the measured adipocyte volume and the expected volume given by a curved-line fit for a given body fat mass and was related to insulin values. In 35 subjects, in vivo adipocyte turnover was measured by exploiting incorporation of atmospheric (14)C into DNA. RESULTS: Occurrence of hyperplasia (negative morphology value) or hypertrophy (positive morphology value) was independent of sex and body weight but correlated with fasting plasma insulin levels and insulin sensitivity, independent of adipocyte volume (β-coefficient = 0.3, P < 0.0001). Total adipocyte number and morphology were negatively related (r = −0.66); i.e., the total adipocyte number was greatest in pronounced hyperplasia and smallest in pronounced hypertrophy. The absolute number of new adipocytes generated each year was 70% lower (P < 0.001) in hypertrophy than in hyperplasia, and individual values for adipocyte generation and morphology were strongly related (r = 0.7, P < 0.001). The relative death rate (∼10% per year) or mean age of adipocytes (∼10 years) was not correlated with morphology. CONCLUSIONS: Adipose tissue morphology correlates with insulin measures and is linked to the total adipocyte number independently of sex and body fat level. Low generation rates of adipocytes associate with adipose tissue hypertrophy, whereas high generation rates associate with adipose hyperplasia. American Diabetes Association 2010-01 2009-10-19 /pmc/articles/PMC2797910/ /pubmed/19846802 http://dx.doi.org/10.2337/db09-0942 Text en © 2010 by the American Diabetes Association. Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. See http://creativecommons.org/licenses/by-nc-nd/3.0/ for details. |
spellingShingle | Original Article Arner, Erik Westermark, Pål O. Spalding, Kirsty L. Britton, Tom Rydén, Mikael Frisén, Jonas Bernard, Samuel Arner, Peter Adipocyte Turnover: Relevance to Human Adipose Tissue Morphology |
title | Adipocyte Turnover: Relevance to Human Adipose Tissue Morphology |
title_full | Adipocyte Turnover: Relevance to Human Adipose Tissue Morphology |
title_fullStr | Adipocyte Turnover: Relevance to Human Adipose Tissue Morphology |
title_full_unstemmed | Adipocyte Turnover: Relevance to Human Adipose Tissue Morphology |
title_short | Adipocyte Turnover: Relevance to Human Adipose Tissue Morphology |
title_sort | adipocyte turnover: relevance to human adipose tissue morphology |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2797910/ https://www.ncbi.nlm.nih.gov/pubmed/19846802 http://dx.doi.org/10.2337/db09-0942 |
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