Kolousková S, Zemková D, Snajderová M, Lebl J
2. dĕtská klinika 2. LF UK a FN, Praha - Motol.
Cas Lek Cesk. 1995 Nov 1;134(21):689-91.
The growth of children with congenital adrenal hyperplasia (CAH) can be impaired by overproduction of endogenous androgens which after the initial growth acceleration lead to early ossification of the growth plates and a low adult height, and by excessive glucocorticoid treatment as the latter antagonize the effect of growth hormone and cause growth retardation. In order to identify the life period decisive for the adult height of patients with CAH the authors analyzed retrospectively their growth data.
In 35 children with 21-hydroxylase deficiency (24 girls, age 4.8 - 22.3 years and 11 boys, age 6.3 - 22.3 years) the height and bone maturation was evaluated at the age of 3, 7, 10 and 12 years and the adult height. In all girls and in 5/11 boys treatment of CAH was started at the age of 0.0 - 1.5 years (median 0.1) (early diagnosis), in 6/11 boys at the age of 4.5 - 7.0 years (median 5.2) (late diagnosis). In children with an early diagnosis growth retardation by the age of 3 years occurred (SDS of the girls' height' -1.4 +/- 0.2, n = 24, boys -0.7 +/- 0.4, n = 5). The height deficit in girls at the age of 3 predicted significantly the loss of adult height, as compared with the expected height in the family (r = 0.68, p = 0.02). By the age of 7 years the height deficit declined insignificantly (SDS of girls' height -1.0 +/- 0.2, n = 21), but bone maturation proceeded rapidly (3 years: SDS 0.1 +/- 0.4, n = 7, 7 years: SDS 1.4 +/- 0.5, n = 11). The adult height of girls (n = 12) is 147.0 - 162.5 cm (mean 156.7), i.e. -1.6 +/- 0.2 SDS, in early diagnosed boys (n = 4) 159 - 176.6 cm (mean 167.6), i.e. -1.7 +/- 0.5 SDS, in boys with a late diagnosis (n =4) 165.0 - 172.0 (mean 169.5), i.e. -1.5 +/- 0.3 SDS.
In treated children with CAH growth retardation occurs already from the age of 3 years, apparently due to excessive glucocorticoid doses. This retardation predicts a loss of adult height. Between the age of 3 and 7 years the growth prognosis deteriorates further due to accelerated bone maturation resulting from inadequate suppression of androgens. Optimal treatment during these periods in life can improve the prerequisites for attaining the predicted adult height.
先天性肾上腺皮质增生症(CAH)患儿的生长可能会受到内源性雄激素过度分泌的影响,在最初的生长加速后,内源性雄激素会导致生长板过早骨化,从而使成年身高降低;同时,过度的糖皮质激素治疗也会影响生长,因为后者会拮抗生长激素的作用并导致生长迟缓。为了确定对CAH患者成年身高起决定性作用的时期,作者回顾性分析了他们的生长数据。
对35例21 - 羟化酶缺乏症患儿(24例女孩,年龄4.8 - 22.3岁;11例男孩,年龄6.3 - 22.3岁)在3岁、7岁、10岁和12岁时评估身高和骨成熟度,并记录成年身高。所有女孩和11例男孩中的5例在0.0 - 1.5岁(中位数0.1)开始CAH治疗(早期诊断),11例男孩中的6例在4.5 - 7.0岁(中位数5.2)开始治疗(晚期诊断)。早期诊断的患儿在3岁时出现生长迟缓(女孩身高标准差SDS为 - 1.4 ± 0.2,n = 24;男孩为 - 0.7 ± 0.4,n = 5)。与家族预期身高相比,3岁时女孩的身高缺陷显著预测了成年身高的损失(r = 0.68,p = 0.02)。到7岁时,身高缺陷下降不明显(女孩身高SDS为 - 1.0 ± 0.2,n = 21),但骨成熟加速(3岁时SDS为0.1 ± 0.4,n = 7;7岁时SDS为1.4 ± 0.5,n = 11)。早期诊断的女孩(n = 12)成年身高为147.0 - 162.5 cm(平均156.7),即 - 1.6 ± 0.2 SDS;早期诊断的男孩(n = 4)成年身高为159 - 176.6 cm(平均167.6),即 - 1.7 ± 0.5 SDS;晚期诊断的男孩(n = 4)成年身高为165.0 - 172.0(平均169.5),即 - 1.5 ± 0.3 SDS。
在接受治疗的CAH患儿中,3岁起就出现生长迟缓,显然是由于糖皮质激素剂量过大。这种生长迟缓预示着成年身高的损失。在3至7岁之间,由于雄激素抑制不足导致骨成熟加速,生长预后进一步恶化。在生命中的这些时期进行最佳治疗可以改善达到预期成年身高的条件。