Assistance Publique-Hôpitaux de Paris, Hôpital Robert Debré, Service d'Endocrinologie Pédiatrique, 75019 Paris, France.
J Clin Endocrinol Metab. 2013 Jul;98(7):2746-54. doi: 10.1210/jc.2012-4201. Epub 2013 Apr 26.
Recombinant human GH (rhGH) improves growth and body composition in glucocorticoid-treated children. Its effects on muscle strength are poorly evaluated.
Our objective was to evaluate rhGH effects on muscle strength in children receiving long-term glucocorticoid therapy; effects on height SD score (SDS) and body composition were assessed also.
A randomized, controlled, delayed-start study of rhGH for 12 months was started after randomization (baseline) or 6 months later (M6).
Patients included 30 children with various diagnoses.
rhGH was administered at 0.065 mg/kg/d for 6 months and then in the dosage maintaining serum IGF-I levels below +2 SDS for chronological age.
The primary criterion was the between-group difference in composite index of muscle strength (CIMS) change at M6. Secondary criteria included between-group differences in CIMS SDS(height), lean mass (LM), thigh muscle area (MA), and height SDS changes at M6; these parameters were also assessed in the overall population after 1 year of rhGH therapy.
At M6, rhGH therapy did not significantly affect changes in CIMS or CIMS SDS(height) (+17.6% vs +7.5% and +0.14 ± 0.38 vs +0.11 ± 0.62, respectively); the rhGH-treated group had significantly larger changes in height SDS (+0.2 [0.3] vs -0.2 [0.3]; P = 0.003), LM (+7.3% [+3.7%; +21.6%] vs 0% [-4.7%; +3.2%]; P = 0.002), and MA (+8.8% [+5%; +15.6%] vs. -0.6% [-6.3%; +7.7%]; P = 0.01) compared with the untreated group. After 1 year of rhGH, height SDS, LM, and MA increased significantly, CIMS increased by 24.7% (+5.8%; +34.2%), and CIMS SDS(height) remained within the normal range.
rhGH increased height, LM, and MA. However, muscle strength did not improve significantly.
重组人生长激素(rhGH)可改善糖皮质激素治疗儿童的生长和身体成分。但其对肌肉力量的影响评价不佳。
我们的目的是评估 rhGH 对长期接受糖皮质激素治疗的儿童肌肉力量的影响;还评估了 rhGH 对身高标准差评分(SDS)和身体成分的影响。
一项 rhGH 治疗 12 个月的随机、对照、延迟启动研究,在随机分组(基线)或 6 个月后(M6)开始。
纳入 30 名患有各种疾病的患儿。
rhGH 以 0.065mg/kg/d 的剂量治疗 6 个月,然后根据血清 IGF-I 水平维持在年龄别+2 SDS 以下的剂量继续治疗。
主要标准是 M6 时肌肉力量综合指数(CIMS)变化的组间差异。次要标准包括 M6 时 CIMS SDS(身高)、瘦体重(LM)、大腿肌肉面积(MA)和身高 SDS 变化的组间差异;这些参数在 rhGH 治疗 1 年后也在总体人群中进行了评估。
M6 时,rhGH 治疗并未显著影响 CIMS 或 CIMS SDS(身高)的变化(+17.6%比+7.5%和+0.14±0.38比+0.11±0.62);rhGH 治疗组的身高 SDS 变化显著更大(+0.2[0.3]比-0.2[0.3];P=0.003)、LM(+7.3%[+3.7%;+21.6%]比 0%[-4.7%;+3.2%];P=0.002)和 MA(+8.8%[+5%;+15.6%]比-0.6%[-6.3%;+7.7%];P=0.01)与未治疗组相比。rhGH 治疗 1 年后,身高 SDS、LM 和 MA 显著增加,CIMS 增加 24.7%(+5.8%;+34.2%),CIMS SDS(身高)仍在正常范围内。
rhGH 增加了身高、LM 和 MA。然而,肌肉力量并没有显著改善。