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接受生长激素治疗的特纳综合征青春期前女孩的骨矿物质密度

Bone mineral density of prepubertal age girls with Turner's syndrome while on growth hormone therapy.

作者信息

Lanes R, Gunczler P, Paoli M, Weisinger J R

机构信息

Unidad de Endocrinologia Pediatrica, Hospital de Clinicas Caracas, Venezuela.

出版信息

Horm Res. 1995;44(4):168-71. doi: 10.1159/000184619.

Abstract

Bone mineral densities and growth velocities of young girls with Turner's syndrome treated with recombinant human growth hormone at an age before the decreased levels of estrogens secondary to their ovarian failure could contribute to osteopenia were studied. Twelve patients with a mean chronological age of 8.9 +/- 0.9 years and a mean bone age of 6.9 +/- 0.8 years received growth hormone therapy for over 2 years (0.5 IU/kg/week s.c.) Mean growth velocities increased significantly from a baseline level of 3.5 +/- 0.4 cm/year to 6.4 +/- 0.3 and 5.7 +/- 0.4 cm/year at 12 and 24 months of therapy, while height SDS improved from -3.1 +/- 0.4 at baseline to -2.7 +/- 0.3 and -2.4 +/- 0.3 at 12 and 24 months, respectively. Total bone calcium as well as cortical bone mineral density of our density of our patients while on recombinant human growth hormone were similar to that of a control group of prepubertal healthy growth children paired for bone age and height; bone density of trabecular bone was however increased in our patients when compared to healthy controls (0.791 +/- 0.04 vs. 0.669 +/- 0.02 g/cm2; p < 0.025). We conclude from our study that the bone mineral status of young girls with Turner's syndrome on growth hormone therapy seems to be normal.

摘要

对患有特纳综合征的年轻女孩在因卵巢功能衰竭导致雌激素水平下降进而可能导致骨质减少之前的年龄阶段接受重组人生长激素治疗时的骨矿物质密度和生长速度进行了研究。12名平均实际年龄为8.9±0.9岁、平均骨龄为6.9±0.8岁的患者接受了超过2年的生长激素治疗(皮下注射,0.5 IU/kg/周)。治疗12个月和24个月时,平均生长速度从基线水平的3.5±0.4厘米/年显著增加至6.4±0.3厘米/年和5.7±0.4厘米/年,而身高标准差评分分别从基线时的-3.1±0.4改善至12个月时的-2.7±0.3和24个月时的-2.4±0.3。接受重组人生长激素治疗的患者的总骨钙以及皮质骨矿物质密度与按骨龄和身高配对的青春期前健康生长儿童对照组相似;然而,与健康对照组相比,我们的患者的小梁骨密度有所增加(0.791±0.04 vs. 0.669±0.02克/平方厘米;p<0.025)。我们从研究中得出结论,接受生长激素治疗的患有特纳综合征的年轻女孩的骨矿物质状况似乎正常。

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