4.7 Review

Dehydroepiandrosterone on metabolism and the cardiovascular system in the postmenopausal period

Journal

JOURNAL OF MOLECULAR MEDICINE-JMM
Volume 98, Issue 1, Pages 39-57

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s00109-019-01842-5

Keywords

Dehydroepiandrosterone; Menopause; Adiposity; Insulin resistance; Metabolic syndrome; Cardiovascular disease

Funding

  1. Brazilian research agency: Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES) [001]
  2. Brazilian research agency: Fundacao de Amparo a Pesquisa do Estado de Sao Paulo [FAPESP-2012/14183-7]
  3. Brazilian research agency: Conselho Nacional de Desenvolvimento Cientifico e Tecnologico [CNPq-303543/2014-0]

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Dehydroepiandrosterone (DHEA), mostly present as its sulfated ester (DHEA-S), is an anabolic hormone that naturally declines with age. Furthermore, it is the most abundant androgen and estrogen precursor in humans. Low plasma levels of DHEA have been strongly associated with obesity, insulin resistance, dyslipidemia, and high blood pressure, increasing the risk of cardiovascular disease. In this respect, DHEA could be regarded as a promising agent against metabolic syndrome (MetS) in postmenopausal women, since several age-related metabolic diseases are reported during aging. There are plenty of experimental evidences showing beneficial effects after DHEA therapy on carbohydrate and lipid metabolism, as well as cardiovascular health. However, its potential as a therapeutic agent appears to attract controversy, due to the lack of effects on some symptoms related to MetS. In this review, we examine the available literature regarding the impact of DHEA therapy on adiposity, glucose metabolism, and the cardiovascular system in the postmenopausal period. Both clinical studies and in vitro and in vivo experimental models were selected, and where possible, the main cellular mechanisms involved in DHEA therapy were discussed.

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