Sex hormones drive changes in lipoprotein metabolism
Summary: Women have a reduced cardiovascular disease (CVD) risk compared with men, which could be partially driven by sex hormones influencing lipid levels post puberty. The interrelationship between sex hormones and lipids was explored in pre-pubertal children, young post-pubertal cis-men/women, an...
Guardado en:
Autores principales: | , , , , , , , |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Elsevier
2021
|
Materias: | |
Acceso en línea: | https://doaj.org/article/ba63a83455f646859af1394b4918fb68 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
id |
oai:doaj.org-article:ba63a83455f646859af1394b4918fb68 |
---|---|
record_format |
dspace |
spelling |
oai:doaj.org-article:ba63a83455f646859af1394b4918fb682021-11-20T05:08:57ZSex hormones drive changes in lipoprotein metabolism2589-004210.1016/j.isci.2021.103257https://doaj.org/article/ba63a83455f646859af1394b4918fb682021-11-01T00:00:00Zhttp://www.sciencedirect.com/science/article/pii/S2589004221012268https://doaj.org/toc/2589-0042Summary: Women have a reduced cardiovascular disease (CVD) risk compared with men, which could be partially driven by sex hormones influencing lipid levels post puberty. The interrelationship between sex hormones and lipids was explored in pre-pubertal children, young post-pubertal cis-men/women, and transgender individuals on cross-sex-hormone treatment (trans-men/women) using serum metabolomics assessing 149 lipids. High-density lipoproteins (HDL, typically atheroprotective) were significantly increased and very-low- and low-density lipoproteins (typically atherogenic) were significantly decreased in post-pubertal cis-women compared with cis-men. These differences were not observed pre-puberty and were induced appropriately by cross-sex-hormone treatment in transgender individuals, supporting that sex hormones regulate lipid metabolism in vivo. Only atheroprotective apolipoprotein (Apo)A1 expressing lipoproteins (HDL) were differentially expressed between all hormonally unique comparisons. Thus, estradiol drives a typically atheroprotective lipid profile through upregulation of HDL/ApoA1, which could contribute to the sexual dimorphism observed in CVD risk post puberty. Together, this could inform sex-specific therapeutic strategies for CVD management.George A. RobinsonJunjie PengHannah PeckhamAnna RadziszewskaGary ButlerInes Pineda-TorraElizabeth C. JuryCoziana CiurtinElsevierarticleBiological sciencesBiochemistryMetabolomicsScienceQENiScience, Vol 24, Iss 11, Pp 103257- (2021) |
institution |
DOAJ |
collection |
DOAJ |
language |
EN |
topic |
Biological sciences Biochemistry Metabolomics Science Q |
spellingShingle |
Biological sciences Biochemistry Metabolomics Science Q George A. Robinson Junjie Peng Hannah Peckham Anna Radziszewska Gary Butler Ines Pineda-Torra Elizabeth C. Jury Coziana Ciurtin Sex hormones drive changes in lipoprotein metabolism |
description |
Summary: Women have a reduced cardiovascular disease (CVD) risk compared with men, which could be partially driven by sex hormones influencing lipid levels post puberty. The interrelationship between sex hormones and lipids was explored in pre-pubertal children, young post-pubertal cis-men/women, and transgender individuals on cross-sex-hormone treatment (trans-men/women) using serum metabolomics assessing 149 lipids. High-density lipoproteins (HDL, typically atheroprotective) were significantly increased and very-low- and low-density lipoproteins (typically atherogenic) were significantly decreased in post-pubertal cis-women compared with cis-men. These differences were not observed pre-puberty and were induced appropriately by cross-sex-hormone treatment in transgender individuals, supporting that sex hormones regulate lipid metabolism in vivo. Only atheroprotective apolipoprotein (Apo)A1 expressing lipoproteins (HDL) were differentially expressed between all hormonally unique comparisons. Thus, estradiol drives a typically atheroprotective lipid profile through upregulation of HDL/ApoA1, which could contribute to the sexual dimorphism observed in CVD risk post puberty. Together, this could inform sex-specific therapeutic strategies for CVD management. |
format |
article |
author |
George A. Robinson Junjie Peng Hannah Peckham Anna Radziszewska Gary Butler Ines Pineda-Torra Elizabeth C. Jury Coziana Ciurtin |
author_facet |
George A. Robinson Junjie Peng Hannah Peckham Anna Radziszewska Gary Butler Ines Pineda-Torra Elizabeth C. Jury Coziana Ciurtin |
author_sort |
George A. Robinson |
title |
Sex hormones drive changes in lipoprotein metabolism |
title_short |
Sex hormones drive changes in lipoprotein metabolism |
title_full |
Sex hormones drive changes in lipoprotein metabolism |
title_fullStr |
Sex hormones drive changes in lipoprotein metabolism |
title_full_unstemmed |
Sex hormones drive changes in lipoprotein metabolism |
title_sort |
sex hormones drive changes in lipoprotein metabolism |
publisher |
Elsevier |
publishDate |
2021 |
url |
https://doaj.org/article/ba63a83455f646859af1394b4918fb68 |
work_keys_str_mv |
AT georgearobinson sexhormonesdrivechangesinlipoproteinmetabolism AT junjiepeng sexhormonesdrivechangesinlipoproteinmetabolism AT hannahpeckham sexhormonesdrivechangesinlipoproteinmetabolism AT annaradziszewska sexhormonesdrivechangesinlipoproteinmetabolism AT garybutler sexhormonesdrivechangesinlipoproteinmetabolism AT inespinedatorra sexhormonesdrivechangesinlipoproteinmetabolism AT elizabethcjury sexhormonesdrivechangesinlipoproteinmetabolism AT cozianaciurtin sexhormonesdrivechangesinlipoproteinmetabolism |
_version_ |
1718419562711482368 |