Changes in abdominal subcutaneous adipose tissue phenotype following menopause is associated with increased visceral fat mass.

Bibliographic Details
Title: Changes in abdominal subcutaneous adipose tissue phenotype following menopause is associated with increased visceral fat mass.
Authors: Abildgaard, Julie, Ploug, Thorkil, Al-Saoudi, Elaf, Wagner, Thomas, Thomsen, Carsten, Ewertsen, Caroline, Bzorek, Michael, Pedersen, Bente Klarlund, Pedersen, Anette Tønnes, Lindegaard, Birgitte
Source: Scientific Reports; 7/20/2021, Vol. 11 Issue 1, p1-12, 12p
Subject Terms: ADIPOSE tissues, PHENOTYPES, MENOPAUSE, OBESITY, INSULIN resistance
Abstract: Menopause is associated with a redistribution of adipose tissue towards central adiposity, known to cause insulin resistance. In this cross-sectional study of 33 women between 45 and 60 years, we assessed adipose tissue inflammation and morphology in subcutaneous adipose tissue (SAT) and visceral adipose tissue (VAT) across menopause and related this to menopausal differences in adipose tissue distribution and insulin resistance. We collected paired SAT and VAT biopsies from all women and combined this with anthropometric measurements and estimated whole-body insulin sensitivity. We found that menopause was associated with changes in adipose tissue phenotype related to metabolic dysfunction. In SAT, postmenopausal women showed adipocyte hypertrophy, increased inflammation, hypoxia and fibrosis. The postmenopausal changes in SAT was associated with increased visceral fat accumulation. In VAT, menopause was associated with adipocyte hypertrophy, immune cell infiltration and fibrosis. The postmenopausal changes in VAT phenotype was associated with decreased insulin sensitivity. Based on these findings we suggest, that menopause is associated with changes in adipose tissue phenotype related to metabolic dysfunction in both SAT and VAT. Whereas increased SAT inflammation in the context of menopause is associated with VAT accumulation, VAT morphology is related to insulin resistance. [ABSTRACT FROM AUTHOR]
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  Data: Changes in abdominal subcutaneous adipose tissue phenotype following menopause is associated with increased visceral fat mass.
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  Data: Scientific Reports; 7/20/2021, Vol. 11 Issue 1, p1-12, 12p
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  Data: <searchLink fieldCode="DE" term="%22ADIPOSE+tissues%22">ADIPOSE tissues</searchLink><br /><searchLink fieldCode="DE" term="%22PHENOTYPES%22">PHENOTYPES</searchLink><br /><searchLink fieldCode="DE" term="%22MENOPAUSE%22">MENOPAUSE</searchLink><br /><searchLink fieldCode="DE" term="%22OBESITY%22">OBESITY</searchLink><br /><searchLink fieldCode="DE" term="%22INSULIN+resistance%22">INSULIN resistance</searchLink>
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  Data: Menopause is associated with a redistribution of adipose tissue towards central adiposity, known to cause insulin resistance. In this cross-sectional study of 33 women between 45 and 60 years, we assessed adipose tissue inflammation and morphology in subcutaneous adipose tissue (SAT) and visceral adipose tissue (VAT) across menopause and related this to menopausal differences in adipose tissue distribution and insulin resistance. We collected paired SAT and VAT biopsies from all women and combined this with anthropometric measurements and estimated whole-body insulin sensitivity. We found that menopause was associated with changes in adipose tissue phenotype related to metabolic dysfunction. In SAT, postmenopausal women showed adipocyte hypertrophy, increased inflammation, hypoxia and fibrosis. The postmenopausal changes in SAT was associated with increased visceral fat accumulation. In VAT, menopause was associated with adipocyte hypertrophy, immune cell infiltration and fibrosis. The postmenopausal changes in VAT phenotype was associated with decreased insulin sensitivity. Based on these findings we suggest, that menopause is associated with changes in adipose tissue phenotype related to metabolic dysfunction in both SAT and VAT. Whereas increased SAT inflammation in the context of menopause is associated with VAT accumulation, VAT morphology is related to insulin resistance. [ABSTRACT FROM AUTHOR]
– Name: Abstract
  Label:
  Group: Ab
  Data: <i>Copyright of Scientific Reports is the property of Springer Nature and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.)
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        Value: 10.1038/s41598-021-94189-2
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        Text: English
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              Text: 7/20/2021
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