Key result
Male sex and postmenopausal status accelerate ESRD progression, highlighting sex steroid influence on renal decline.
Why the study?
Male sex is an independent risk factor for renal disease development and progression, but mechanisms by which sex steroids impact renal disease in humans are poorly understood.
Sex differences may warrant closer renal monitoring in hypertensive men; leaves open hormone mechanisms from animal models.
E pidemiological studies have shown that male sex is an independent risk factor for the development and progression of renal disease, and men progress to end stage renal disease (ESRD) faster than premenopausal women in such diseases as autoimmune glomerulonephritis, hypertensive glomerulosclerosis, and polycystic kidney disease.[1][2][3] Although the age-related decline in renal function is also faster in men, women become more susceptible to renal diseases after menopause.4 Insight from in vitro studies and animal models suggest that sex steroids play pivotal roles in modifying the progression to ESRD.Because there is a paucity of data in humans showing the mechanisms by which sex steroids impact renal disease, most of the studies discussed this review will be in animals, mainly rats.Furthermore, determining the roles of sex steroids in various diseases has been done using gonedectomized animals; however, although gonadectomy removes more than sex steroids and most studies only replace the sex steroid of interest, these are still the best studies in which to evaluate mechanisms responsible for sex differences in renal disease.Studies in postmenopausal women will also be kept to a minimum in this review because it is likely that sex steroids change action with aging, as suggested by the Women's Health Initiative study.
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Yanes et al. (2008) conducted a review in Renal disease. Sex steroids was evaluated. Male sex accelerates progression to end stage renal disease, while women become more susceptible after menopause, suggesting sex steroids play a pivotal role in modifying renal disease progression.
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