Scholars in HeAlth Research Program, American University of Beirut, Beirut, Lebanon.
Clemenceau Medical Center, Beirut, Lebanon.
Endocrine. 2018 Jan;59(1):39-49. doi: 10.1007/s12020-017-1440-0. Epub 2017 Oct 13.
In adults, growth hormone deficiency (GHD) has been associated with low bone mineral density (BMD), an effect counteracted by growth hormone (GH) replacement. Whether GH is beneficial in adults with age-related bone loss and without hypopituitarism is unclear.
We conducted a systematic literature search using Medline, Embase and the Cochrane Register of Controlled Trials. We extracted and analyzed data according to the bone outcome included [bone mineral content (BMC), BMD, and bone biomarker, fracture risk]. We performed a meta-analysis when possible.
We included eight studies. Seven randomized 272 post-menopausal women, 61-69 years, to GH or control, for 6-24 months, and the eighth was an extension trial. Except for one study, all women received concurrent osteoporosis therapies. There was no significant effect of GH, as compared to control, on BMD at the lumbar spine (Weighted mean difference WMD = -0.01 [-0.04, 0.02]), total hip (WMD = 0 [-0.05, 0.06]) or femoral neck (WMD = 0 [-0.03, 0.04]). Similarly, no effect was seen on BMC. GH significantly increased the bone formation marker procollagen type-I carboxy-terminal propeptide (PICP) (WMD = 14.03 [2.68, 25.38]). GH resulted in a trend for increase in osteocalcin and in bone resorption markers. Patients who received GH had a significant decrease in fracture risk as compared to control (RR = 0.63 [0.46, 0.87]). Reported adverse events were not major, mostly related to fluid retention.
GH may not improve bone density in women with age-related bone loss but may decrease fracture risk. Larger studies of longer duration are needed to further explore these findings in both genders, and to investigate the effect of GH on bone quality.
在成年人中,生长激素缺乏症(GHD)与骨密度降低有关,而生长激素(GH)替代可以抵消这种影响。在没有垂体功能减退症的情况下,GH 是否对与年龄相关的骨丢失的成年人有益尚不清楚。
我们使用 Medline、Embase 和 Cochrane 对照试验登记处进行了系统的文献检索。我们根据所包括的骨结局[骨矿物质含量(BMC)、BMD 和骨生物标志物、骨折风险]提取和分析数据。当可能时,我们进行了荟萃分析。
我们纳入了八项研究。其中七项研究将 272 名绝经后 61-69 岁的女性随机分配至 GH 组或对照组,接受治疗 6-24 个月,第八项研究是一项扩展试验。除了一项研究外,所有女性都同时接受了骨质疏松症治疗。与对照组相比,GH 对腰椎(WMD=-0.01[-0.04, 0.02])、全髋(WMD=0[-0.05, 0.06])或股骨颈(WMD=0[-0.03, 0.04])的 BMD 无显著影响。同样,对 BMC 也没有影响。GH 显著增加了骨形成标志物Ⅰ型前胶原羧基端前肽(PICP)(WMD=14.03[2.68, 25.38])。GH 导致骨钙素和骨吸收标志物增加的趋势。与对照组相比,接受 GH 治疗的患者骨折风险显著降低(RR=0.63[0.46, 0.87])。报告的不良事件并不严重,主要与液体潴留有关。
GH 可能不会改善与年龄相关的骨丢失女性的骨密度,但可能降低骨折风险。需要进行更大规模、更长时间的研究,以进一步探索两性中的这些发现,并研究 GH 对骨质量的影响。