Haden S T, Glowacki J, Hurwitz S, Rosen C, LeBoff M S
Endocrine-Hypertension Division, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, 221 Longwood Avenue, Boston, Massachusetts 02115, USA.
Calcif Tissue Int. 2000 Jun;66(6):414-8. doi: 10.1007/s002230010084.
Data from animal and in vitro studies suggest that the growth-promoting effects of the adrenal androgen dehydroepiandrosterone sulfate (DHEAS) may be mediated by stimulation of insulin-like growth factor-I (IGF-I) and/or inhibition of interleukin 6 (IL-6), a cytokine mediator of bone resorption. This study tests the hypotheses that there are effects of age on serum DHEAS, IGF-I, and IL-6 levels, and that levels of IGF-I and IL-6 are related to DHEAS levels. The study included 102 women: 27 premenopausal and 75 postmenopausal, including 35 postmenopausal women with osteoporosis, as defined by bone mineral density scores by dual X-ray energy absorptiometry. DHEAS levels decreased significantly with age (r = -0.52, P < 0.0001) and IGF-I levels decreased significantly with age (r = -0.49, P < 0.0001). IL-6 levels increased significantly with age (r = 0.36, P = 0.008). IGF-I was positively correlated to DHEAS levels (r = 0.43, P < 0. 0001, n = 102) and IL-6 levels were negatively correlated to DHEAS levels (r = -0.32, P = 0.021, n = 54). Levels of DHEAS and IGF-I were correlated with T scores of the spine and some hip sites. In a multiple variable model to predict DHEAS, age was an important predictor (P < 0.001), but osteoporosis status, IGF-I, and IL-6 were not. The median DHEAS level was lower in the postmenopausal osteoporotic women (67 microg/dl, n = 35) than in the nonosteoporotic postmenopausal women (106.3 microg/dl, n = 40, P = 0. 03), but this was not significant after correction for age. Age accounted for 32% of the variance in DHEAS levels. In summary, DHEAS levels decreased with age and had a positive association with IGF-I levels and a negative association with IL-6 levels. DHEA deficiency may contribute to age-related bone loss through anabolic (IGF-I) and anti-osteolytic (IL-6) mechanisms.
来自动物和体外研究的数据表明,肾上腺雄激素硫酸脱氢表雄酮(DHEAS)的促生长作用可能是通过刺激胰岛素样生长因子-I(IGF-I)和/或抑制白细胞介素6(IL-6)来介导的,IL-6是骨吸收的一种细胞因子介质。本研究检验了以下假设:年龄对血清DHEAS、IGF-I和IL-6水平有影响,且IGF-I和IL-6水平与DHEAS水平相关。该研究纳入了102名女性:27名绝经前女性和75名绝经后女性,其中包括35名经双能X线骨密度仪测定骨密度评分确诊为骨质疏松的绝经后女性。DHEAS水平随年龄显著下降(r = -0.52,P < 0.0001),IGF-I水平也随年龄显著下降(r = -0.49,P < 0.0001)。IL-6水平随年龄显著升高(r = 0.36,P = 0.008)。IGF-I与DHEAS水平呈正相关(r = 0.43,P < 0.0001,n = 102),IL-6水平与DHEAS水平呈负相关(r = -0.32,P = 0.021,n = 54)。DHEAS和IGF-I水平与脊柱和一些髋部部位的T值相关。在一个预测DHEAS的多变量模型中,年龄是一个重要的预测因素(P < 0.001),但骨质疏松状态、IGF-I和IL-6不是。绝经后骨质疏松女性的DHEAS水平中位数(67μg/dl,n = 35)低于非骨质疏松绝经后女性(106.3μg/dl, n = 40,P = 0.03),但在校正年龄后差异无统计学意义。年龄占DHEAS水平变异的32%。总之,DHEAS水平随年龄下降,与IGF-I水平呈正相关,与IL-6水平呈负相关。DHEA缺乏可能通过合成代谢(IGF-I)和抗骨溶解(IL-6)机制导致与年龄相关的骨质流失。