Brixen K, Kassem M, Eriksen E F, Nielsen H K, Flyvbjerg A, Mosekilde L
Department of Endocrinology and Metabolism, Aarhus University Hospital, Denmark.
J Pediatr Endocrinol. 1993 Jan-Mar;6(1):65-71. doi: 10.1515/jpem.1993.6.1.65.
Decreased osteoblastic activity seems to be of major importance in the pathogenesis of postmenopausal and senile osteoporosis and several lines of evidence suggest that GH may become useful in treatment of osteoporosis. GH stimulates osteoblastic proliferation and differentiation in vitro and increases production of Insulin-like Growth Factor-I and II (IGF-I and IGF-II) which both have profound stimulatory effects on osteoblasts and are important local regulators of bone remodeling. GH affects several other osteotropic hormones in vivo and increases bone turnover while the effect on bone mass is less pronounced and depends on the skeletal compartment. The few published clinical studies on the use of GH in treatment of osteoporosis have been inconclusive and well controlled studies of adequate size are greatly needed. Future research should focus on intermittent use of GH in combination with other hormones stimulating IGF production or antiresorptive agents.
成骨细胞活性降低似乎在绝经后骨质疏松症和老年性骨质疏松症的发病机制中起主要作用,并且有几条证据表明生长激素(GH)可能对骨质疏松症的治疗有用。GH在体外刺激成骨细胞的增殖和分化,并增加胰岛素样生长因子-I和II(IGF-I和IGF-II)的产生,这两种因子对成骨细胞都有深远的刺激作用,并且是骨重塑的重要局部调节因子。GH在体内影响其他几种促骨激素,并增加骨转换,而对骨量的影响不太明显,并且取决于骨骼部位。少数已发表的关于使用GH治疗骨质疏松症的临床研究尚无定论,因此非常需要进行足够规模的严格对照研究。未来的研究应集中在GH与其他刺激IGF产生的激素或抗吸收剂联合间歇使用上。