Rota F, Savanelli M C, Tauchmanova L, Savastano S, Lombardi G, Colao A, Di Somma C
Department of Molecular and Clinical Endocrinology, Federico II University of Naples, 80131 Naples, Italy.
J Endocrinol Invest. 2008 Feb;31(2):94-102. doi: 10.1007/BF03345574.
GH deficiency (GHD) in adults is accompanied by reduced bone mass that may revert only after 2 yr of GH replacement. However, it is unclear whether the gender may modify bone responsiveness to GH replacement in adults. In this study we have evaluated whether bone mineral density (BMD) and turnover improve after GH replacement according to patients' gender. BMD at lumbar spine (LS) and femoral neck (FN), serum osteocalcin (OC), and urinary cross-linked N-telopeptides of type I collagen (Ntx) were assessed in 64 hypopituitaric patients (35 men, 30-50 yr) before and 2 yr after the beginning of GH replacement. Values of IGF-I and BMD at LS and at FN were expressed as Zscores. At study entry, IGF-I and BMD resulted similar among men and women with GHD. During GH replacement, IGF-I levels increased in both men and women without any difference in the percentage of IGF-I increase between the genders (p=0.47). In women receiving estrogen replacement, however, the percentage of IGF-I increase (p<0.05), and the Z IGF-I score (p<0.001) were significant lower than estrogen untreated women, although IGF-I levels were similar in the 2 groups (p=0.53). The GH dose adjusted for body weight required to restore normal age- and sex- matched IGF-I levels was lower in men than in women (p<0.001), and was higher in women receiving than in those not receiving estrogen replacement (p<0.05). In contrast, hypogonadal men treated with testosterone and eugonadal men received a similar GH dose (p=0.97). Also OC, Ntx levels, lumbar and femoral BMD improved (p<0.001) in all patients. Nevertheless, a greater increase in lumbar BMD increase was observed in men than in women (8.0+/-2.1 vs 2.6+/-0.4%; p<0.05). No significant difference was revealed in bone parameters in women treated or untreated with estrogen replacement and in men treated or not with testosterone replacement for concomitant hypogonadism. At the multiple correlation analysis, gender was a stronger predictor for the required GH dose than the age (p<0.001 and p=0.02, respectively). In conclusion, a 2-yr GH replacement normalizes IGF-I levels, increases bone mass and improves bone turnover both in men and in women with GHD without any difference between the 2 groups, provided that the dose of GH was modulated on the basis of IGF-I levels. Women receiving oral estrogens should receive a GH dose approximately doubled, as compared to men and women not receiving oral estrogens, to achieve similar effects on bone density and turnover. In particular, GH replacement dose, to be successful on bone mass and turnover, depends on gender in hypopituitary patients aged below 50 yr.
成人生长激素缺乏症(GHD)伴有骨量减少,这种情况可能只有在接受2年生长激素替代治疗后才会恢复。然而,尚不清楚性别是否会影响成人骨骼对生长激素替代治疗的反应。在本研究中,我们评估了根据患者性别,生长激素替代治疗后骨矿物质密度(BMD)和骨转换是否会改善。在64例垂体功能减退患者(35名男性,年龄30 - 50岁)开始生长激素替代治疗前及治疗2年后,评估其腰椎(LS)和股骨颈(FN)的骨密度、血清骨钙素(OC)以及尿I型胶原交联N端肽(Ntx)。LS和FN处的IGF - I值及骨密度以Z评分表示。在研究开始时,患有GHD的男性和女性的IGF - I和骨密度相似。在生长激素替代治疗期间,男性和女性的IGF - I水平均升高,两性之间IGF - I升高的百分比无差异(p = 0.47)。然而,在接受雌激素替代治疗的女性中,IGF - I升高的百分比(p < 0.05)和Z IGF - I评分(p < 0.001)显著低于未接受雌激素治疗的女性,尽管两组的IGF - I水平相似(p = 0.53)。恢复正常年龄和性别匹配的IGF - I水平所需的按体重调整的生长激素剂量,男性低于女性(p < 0.001),接受雌激素替代治疗的女性高于未接受雌激素替代治疗的女性(p < 0.05)。相比之下,接受睾酮治疗的性腺功能减退男性和性腺功能正常男性接受的生长激素剂量相似(p = 0.97)。所有患者的OC、Ntx水平、腰椎和股骨骨密度也有所改善(p < 0.001)。然而,观察到男性腰椎骨密度的增加幅度大于女性(8.0±2.1%对2.6±0.4%;p < 0.05)。在接受或未接受雌激素替代治疗的女性以及接受或未接受睾酮替代治疗以治疗伴发性腺功能减退的男性中,骨参数无显著差异。在多元相关分析中,性别比年龄更能强烈预测所需的生长激素剂量(分别为p < 0.001和p = 0.02)。总之,2年的生长激素替代治疗可使患有GHD的男性和女性的IGF - I水平正常化,增加骨量并改善骨转换,两组之间无任何差异,前提是根据IGF - I水平调整生长激素剂量。与未接受口服雌激素的男性和女性相比,接受口服雌激素的女性应接受约两倍的生长激素剂量,以对骨密度和骨转换产生类似效果。特别是,要在骨量和骨转换方面取得成功,生长激素替代剂量在50岁以下的垂体功能减退患者中取决于性别。