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Follicle-Stimulating Hormone Exacerbates Cardiovascular Disease in the Presence of Low or Castrate Testosterone Levels.


ABSTRACT: Low testosterone (T), common in aging men, associates with cardiovascular disease. We investigated whether follicle-stimulating hormone (FSH), which is affected by T, modulates the cardiovascular effects associated with low T or castration. FSHβ-/-:low-density lipoprotein receptor (LDLR)-/- mice, untreated or castrated (orchiectomy, gonadotropin-releasing hormone agonist or antagonist), demonstrated significantly less atherogenesis compared with similarly treated LDLR-/- mice, but not following FSH delivery. Smaller plaque burden in LDLR-/- mice receiving gonadotropin-releasing hormone antagonists vs agonists were nullified in FSHβ-/-:LDLR-/- mice. Atherosclerotic and necrotic plaque size and macrophage infiltration correlated with serum FSH/T. In patients with prostate cancer, FSH/T following androgen-deprivation therapy initiation predicted cardiovascular events. FSH facilitates cardiovascular disease when T is low or eliminated.

SUBMITTER: Duivenvoorden WCM 

PROVIDER: S-EPMC10978407 | biostudies-literature | 2024 Mar

REPOSITORIES: biostudies-literature

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Follicle-Stimulating Hormone Exacerbates Cardiovascular Disease in the Presence of Low or Castrate Testosterone Levels.

Duivenvoorden Wilhelmina C M WCM   Margel David D   Subramony Gayathri Vishal V   Duceppe Emmanuelle E   Yousef Sadiya S   Naeim Magda M   Khajehei Mohammad M   Hopmans Sarah S   Popovic Snezana S   Ber Yaara Y   Heels-Ansdell Diane D   Devereaux Philip J PJ   Pinthus Jehonathan H JH  

JACC. Basic to translational science 20231220 3


Low testosterone (T), common in aging men, associates with cardiovascular disease. We investigated whether follicle-stimulating hormone (FSH), which is affected by T, modulates the cardiovascular effects associated with low T or castration. FSHβ<sup>-/-</sup>:low-density lipoprotein receptor (LDLR)<sup>-/-</sup> mice, untreated or castrated (orchiectomy, gonadotropin-releasing hormone agonist or antagonist), demonstrated significantly less atherogenesis compared with similarly treated LDLR<sup>-  ...[more]

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