Rothenbuhler Anya, Ormières Baptiste, Kalifa Gabriel, Bougnères Pierre
AP-HP, Department of Pediatric Endocrinology, Bicêtre Hospital, Paris Sud University, 94275 Le Kremlin Bicêtre, France.
Biomathematics Team, InsermU986, Pincus Building, Bicêtre Hospital, Paris Sud University, 94275 Le Kremlin Bicêtre, France.
Growth Horm IGF Res. 2015 Apr;25(2):96-102. doi: 10.1016/j.ghir.2015.01.002. Epub 2015 Jan 26.
The growth-promoting effect of starting recombinant human growth hormone (rhGH) at the time of near-ending growth has not been studied in sexually mature boys who will have idiopathic short stature (ISS) as adults because it is believed that such an advanced stage of puberty would preclude favorable results.
Fifteen boys aged 15.5 ± 1 years terminating puberty were growing at a rate < 2 cm/6 months towards a predicted adult height (PAH) <-2.5 SDS.
Participants received 0.50 ± 0.06 mg/kg · wk of rhGH according to a target-to-treat protocol. When growth became less than 0.5 cm in 3 months or when height has reached 169 cm, rhGH was ceased. Testosterone, growth velocity (GV), height, serum IGF-1, bone age (BA) at hand-wrist and knee score were measured at onset; IGF-1 and height were monitored every 3 months. A formula for PAH was developed. Height increment (HI, adult height-starting height) and height gain (HG, adult height-PAH) were calculated.
Following rhGH administration for 11.1 ± 4.8 months, GV-SDS increased from -2.5 ± 1.7 to 3.5 ± 4.3 (P = 2 × 10(-4)), HI = 8.5 ± 3.7 cm, HG = 6.8 ± 4.8 cm and adult height was -1.8 ± 0.9 SDS, compared to a PAH of -2.9 ± 0.6 SDS (P = 4 × 10(-4)). Knee score (P = 2 × 10(-3)), GV at rhGH onset (P = 8 × 10(-3)) and rhGH dose (P = 8 × 10(-3)) were identified as predictors of HI and HG, but BA was not.
Our study suggests that 1) a short period of rhGH administration can increase true adult height significantly in boys with ISS at time of near-ending growth; and 2) knee score rather than BA should be used to identify rhGH responders. These preliminary observations await confirmation by larger randomized trials.
对于成年后将患有特发性矮小症(ISS)的性成熟男孩,在生长接近尾声时开始使用重组人生长激素(rhGH)的促生长效果尚未进行研究,因为人们认为青春期的这种晚期阶段可能无法产生良好的效果。
1)探讨在患有ISS的男孩生长接近尾声时开始使用rhGH的效果。2)寻找对rhGH反应的预测指标。
15名年龄为15.5±1岁、青春期即将结束的男孩,其生长速度<2厘米/6个月,预测成年身高(PAH)<-2.5 SDS。
参与者按照目标治疗方案接受0.50±0.06毫克/千克·周的rhGH治疗。当3个月内生长小于0.5厘米或身高达到169厘米时,停止使用rhGH。在开始治疗时测量睾酮、生长速度(GV)、身高、血清胰岛素样生长因子-1(IGF-1)、手腕骨龄(BA)和膝关节评分;每3个月监测一次IGF-1和身高。制定了PAH的计算公式。计算身高增量(HI,成年身高-起始身高)和身高增长值(HG,成年身高-PAH)。
在使用rhGH治疗11.1±4.8个月后,GV-SDS从-2.5±1.7增加到3.5±4.3(P = 2×10⁻⁴),HI = 8.5±3.7厘米,HG = 6.8±4.8厘米,成年身高为-1.8±0.9 SDS,而PAH为-2.9±0.6 SDS(P = 4×10⁻⁴)。膝关节评分(P = 2×10⁻³)、rhGH开始使用时的GV(P = 8×10⁻³)和rhGH剂量(P = 8×10⁻³)被确定为HI和HG的预测指标,但BA不是。
我们的研究表明:1)在生长接近尾声的患有ISS的男孩中,短期使用rhGH可显著增加其真正的成年身高;2)应使用膝关节评分而非BA来识别rhGH反应者。这些初步观察结果有待更大规模的随机试验予以证实。