Found small decreases in BMD at the hip in premenopausal women. After achieving peak bone mass in young adulthood, bone mineral density (BMD) remains relatively constant in both genders until middle life, although Slemenda et al.
Women undergo two phases of involutional bone loss whereas men undergo one. Any comprehensive model of pathogenesis should explain the differences and similarities of bone loss in aging women and men. These considerations have militated against Albright's unitary hypothesis that a relative or absolute deficiency in sex steroids causes all, or almost all, involutional bone loss. Moreover, aging men also lose bone despite clinically evident hypogonadism occurring only infrequently. However, factors in addition to E deficiency have been implicated as causes of bone loss in aging women, including secondary hyperparathyroidism, impaired osteoblast function, possibly due to changes in local cytokines or systemic growth factors, and, at least in some elderly persons, nutritional deficiency of vitamin D. Called attention to estrogen (E) deficiency as the cause of postmenopausal osteoporosis, and this mechanism has been strongly supported by subsequent studies showing that E administration prevented bone loss induced by oophorectomy in perimenopausal women, and that bone cells were targets of E action. For the most part, this unitary model is well supported by observational and experimental data and provides plausible explanations to traditional objections to a unitary hypothesis. In both genders, E deficiency increases bone resorption and may also impair a compensatory increase in bone formation. Because elderly men have low circulating levels of both bioavailable E and bioavailable testosterone (T) and because recent data suggest that E is at least as important as T in determining bone mass in aging men, E deficiency may also contribute substantially to the continuous bone loss of aging men. This phase is mediated mainly by loss of E action on extraskeletal calcium homeostasis which results in net calcium wasting and increases in the level of dietary calcium intake required to maintain bone balance. The ensuing slow phase continues throughout life in women, involves proportionate losses of cancellous and cortical bone, and is associated with progressive secondary hyperparathyroidism. The accelerated phase in women is most apparent during the first decade after menopause, involves disproportionate loss of cancellous bone, and is mediated mainly by loss of the direct restraining effects of E on bone cell function. We propose here a new unitary model for the pathophysiology of involutional osteoporosis that identifies estrogen (E) deficiency as the cause of both the early, accelerated and the late, slow phases of bone loss in postmenopausal women and as a contributing cause of the continuous phase of bone loss in aging men.
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