2002
DOI: 10.1093/gerona/57.1.m12
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Growth Hormone and Sex Steroid Effects on Bone Metabolism and Bone Mineral Density in Healthy Aged Women and Men

Abstract: Background. Aging is associated with concomitant declines in activity of the growth hormone (GH) and gonadal steroid axes, and in bone mineral density (BMD), in both sexes. Long-term estrogen replacement slows bone loss and prevents fractures in postmenopausal women, whereas the effects of supplementation of GH or testosterone on bone metabolism and BMD in aged individuals remains uncertain.

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Cited by 78 publications
(36 citation statements)
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“…In this group, the pre-existing sex hormone supplement may affected the observed GH effects on bone. One data suggest that short-term administration of hormone replacement therapy (HRT) exerts beneficial effects on bone metabolism and BMD in postmenopausal women, which are not significantly altered by the coadministration of GH; although in andropausal men, testosterone (T) administration to achieve physiologic levels did not result in significant effects on bone metabolism or BMD, whereas GH + T increased one marker of bone formation and decreased one marker of bone resorption [32]. Recent studies shows that oral estrogen reduces hepatic production of IGF-1, while testosterone increases it [33,34].…”
Section: Discussionmentioning
confidence: 99%
“…In this group, the pre-existing sex hormone supplement may affected the observed GH effects on bone. One data suggest that short-term administration of hormone replacement therapy (HRT) exerts beneficial effects on bone metabolism and BMD in postmenopausal women, which are not significantly altered by the coadministration of GH; although in andropausal men, testosterone (T) administration to achieve physiologic levels did not result in significant effects on bone metabolism or BMD, whereas GH + T increased one marker of bone formation and decreased one marker of bone resorption [32]. Recent studies shows that oral estrogen reduces hepatic production of IGF-1, while testosterone increases it [33,34].…”
Section: Discussionmentioning
confidence: 99%
“…Bone is a dynamic tissue that is constantly reshaped by osteoblasts, which build bone, and osteoclasts, which resorb bone. In mammals, reductions in bone density can result from restricted movement and a lack of mechanical stress on bones (disuse osteoporosis- Blouin et al 2007;Resnick 1988), prolonged spaceflight (a special case of disuse osteoporosis- LeBlanc et al 2000;Milstead et al 2004), changes in diet or mineral uptake (Demigne et al 2006;Gennari 2001;RodriguezMartinez and Garcia-Cohen 2002), reductions in baseline concentrations of gonadal steroids and growth hormone (Christmas et al 2002), or changes in life-history stage (Bonnick 2006;Genarri 2001).…”
mentioning
confidence: 99%
“…Although little research has been conducted on bone densities of free-living rodents, a large body of clinical evidence suggests that these changes likely have some influence on BMD. In male human subjects, for instance, the interaction of growth hormone and testosterone promotes bone growth, whereas estrogen replacement and growth hormone supplementation have been shown to slow bone loss in menopausal women (Christmas et al 2002). However, growth hormone does not appear to be affected by photoperiod in other tested mammalian species (Bartke et al 1980;Borer et al 1982;Kendall et al 2003;Klemcke et al 1983).…”
mentioning
confidence: 99%
“…(25), em protocolo randomizado, duplo-cego e placebo controlado que envolveu 57 mulheres e 74 homens, 68-88 anos, estudaram os efeitos da reposição de rhGH (0,09mg/kg/semana no início, com redução para 0,08mg/kg/semana) associado ou não a esteróides sexuais, versus placebo por 24 20 e 79 anos (cerca de 30 por década), que o declínio do eixo somatotrófico com o envelhecimento tem um grande impacto na absorção mineral (33). No entanto, embora os protocolos de reposição de GH mostrem elevação dos níveis dos marcadores de formação e de reabsorção óssea, a maior parte dos estudos não demostra efeitos benéficos desta reposição na massa óssea dos idosos (27,34). Existem ainda evidên-cias de que a combinação de rhGH com pamidronato prejudicou o efeito deste agente anti-reabsortivo na densidade óssea (35), e que GH associado à calcitonina mostrou efeito deletério no osso cortical de mulheres menopausadas (36).…”
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