The action of ovarian hormones in cardiovascular disease

dc.contributor.authorMedina, Rodolfo
dc.contributor.authorAranda, Evelyn
dc.contributor.authorVerdugo, César
dc.contributor.authorKato, Sumie
dc.contributor.authorOwen, Gareth
dc.date.accessioned2013-12-18T20:37:02Z
dc.date.accessioned2016-05-23T21:08:15Z
dc.date.available2013-12-18T20:37:02Z
dc.date.available2016-05-23T21:08:15Z
dc.date.issued2003
dc.descriptionIndexación: Scieloes
dc.description.abstractThe incidence of cardiovascular disease (CAD) differs between men and women, in part because of differences in risk factors and hormones. This sexual dimorphism means a lower incidence in atherosclerotic diseases in premenopausal women, which subsequently rises in postmenopausal women to eventually equal that of men. These observations point towards estrogen and progesterone playing a lifetime protective role against CAD in women. As exogenous estrogen and estrogen plus progesterone preparations produce significant reductions in low-density lipoprotein (LDL) cholesterol levels and significant increases in high-density lipoprotein (HDL) cholesterol, this should in theory lower the risk of CAD. However, results from oral contraceptive (OC) use and combined estrogen and progesterone hormone replacement therapy (HRT) have suggested that hormone replacement regimes do not provide cardiovascular protection. In fact, depending on the preparation and the presence or absence of genetic risk factors, an increased risk of cardiovascular diseases such as venous thrombosis, myocardial infarction (MI) and stroke have been observed. Interestingly, in the majority of studies the increase in risk was highest in the first year, after which an increase in risk was not observed, and in some studies a lower risk of CAD was evident after four or five years of exogenous hormone administration. While the debate continues about the merits of HRT, and several good reviews exist on the statistics of CAD in relation to exogenous hormones, we have decided to review the literature to piece together the physiological actions of estrogen and progesterone preparations on the individual mechanistic components leading to CAD; namely, the altered endothelium and the haemostatic balance between coagulation and fibrinolysis. We present possible mechanisms for how HRT and OCs protect against MI in the absence of cardiovascular risk factors but increase the incidence of MI in their presence. We also speculate on the roles played by hormones on the short- and long-term risks of cardiovascular disease.en
dc.description.urihttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0716-97602003000300005&lng=es&nrm=iso
dc.identifier.citationBiological Research, vol. 36 n° 3-4, 2003.es
dc.identifier.issn0716-9760
dc.identifier.otherDOI: 10.4067/S0716-97602003000300005
dc.identifier.urihttp://repositorio.unab.cl/xmlui/handle/ria/2265
dc.language.isoenen
dc.publisherSociedad de Biología de Chilees
dc.subjectHormone replacement therapy (HRT)es
dc.subjectOral contraceptiveses
dc.subjectAtherosclerosis cardiovascular diseasees
dc.subjectEstrogenes
dc.subjectprogestinses
dc.subjectVenous thrombosises
dc.subjectMyocardial infarctiones
dc.titleThe action of ovarian hormones in cardiovascular diseaseen
dc.typeArtículoes
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