Fatayerji D, Eastell R
Department of Human Metabolism and Clinical Biochemistry, Clinical Sciences Center, Northern General Hospital, Sheffield, United Kingdom.
J Bone Miner Res. 1999 Jul;14(7):1203-10. doi: 10.1359/jbmr.1999.14.7.1203.
Biochemical markers of bone turnover can be used to study the pathophysiology of osteoporosis. So far there have been few such studies in men. The aims of this study were to determine the effect of aging on bone turnover and to identify which hormones might regulate bone turnover in men. We studied 178 healthy Caucasian men, ages 20-79 years (30 per decade). The data for the effect of age on bone turnover was best fit by a quadratic function (nadirs at age 56, 57, 53, 39, and 58 years for intact propeptide of type I procollagen, osteocalcin, bone alkaline phosphatase, free deoxypyridinoline, and cross-linked N-telopeptides of type I collagen, respectively). For most markers, bone turnover tended to be highest in the third decade, lowest in the fifth and sixth decade, with a small increase in some markers in the eighth decade. Insulin-like growth factor-I (IGF-I), insulin-like growth factor binding protein-3, dehydroepiandrosterone sulfate, testosterone, estradiol, and free androgen index all decreased significantly with age (54, 17, 76, 26, 33, and 57%, respectively), while sex hormone binding globulin and parathyroid hormone increased significantly with age (62% and 43%). IGF-I and sex hormones were positively correlated with bone turnover, and this association was stronger in young men than older men. In conclusion, increased IGF-I and sex hormones may be associated with increased bone turnover in young men, with less influence on bone turnover in older men.
骨转换的生化标志物可用于研究骨质疏松症的病理生理学。到目前为止,针对男性的此类研究较少。本研究的目的是确定衰老对骨转换的影响,并确定哪些激素可能调节男性的骨转换。我们研究了178名年龄在20 - 79岁的健康白种男性(每十年30名)。年龄对骨转换影响的数据最适合用二次函数拟合(I型前胶原完整前肽、骨钙素、骨碱性磷酸酶、游离脱氧吡啶啉和I型胶原交联N端肽分别在56、57、53、39和58岁时出现最低点)。对于大多数标志物,骨转换在第三个十年往往最高,在第五和第六个十年最低,在第八个十年一些标志物略有增加。胰岛素样生长因子-I(IGF-I)、胰岛素样生长因子结合蛋白-3、硫酸脱氢表雄酮、睾酮、雌二醇和游离雄激素指数均随年龄显著下降(分别为54%、17%、76%、26%、33%和57%),而性激素结合球蛋白和甲状旁腺激素随年龄显著增加(分别为62%和43%)。IGF-I和性激素与骨转换呈正相关,且这种关联在年轻男性中比老年男性更强。总之,IGF-I和性激素增加可能与年轻男性骨转换增加有关,而对老年男性骨转换的影响较小。