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单独使用生长激素疗法或联合促性腺激素释放激素类似物疗法以改善先天性肾上腺皮质增生症患儿的身高缺陷。

Growth hormone therapy alone or in combination with gonadotropin-releasing hormone analog therapy to improve the height deficit in children with congenital adrenal hyperplasia.

作者信息

Quintos J B, Vogiatzi M G, Harbison M D, New M I

机构信息

Department of Pediatrics, Division of Pediatric Endocrinology, Weill Medical College of Cornell University-New York Presbyterian Hospital, New York City, New York 10021, USA.

出版信息

J Clin Endocrinol Metab. 2001 Apr;86(4):1511-7. doi: 10.1210/jcem.86.4.7412.

Abstract

Short stature in the adult patient with congenital adrenal hyperplasia (CAH) is commonly seen, even among patients in excellent adrenal control during childhood and puberty. In this study we examine the effect of GH therapy on height prediction in children with both CAH and compromised height prediction. Leuprolide acetate, a GnRH analog (GnRHa), was given to patients with evidence of early puberty. GH (n = 12) or the combination of GH and GnRHa (n = 8) was administered to 20 patients with CAH while they continued therapy with glucocorticoids. Each patient in the treatment group was matched according to age, sex, bone age, puberty, and type of CAH with another CAH patient treated only with glucocorticoid replacement. The match was made at the start of GH treatment. Of the 20 patients, 12 have completed 2 yr of therapy. After 1 yr of GH or combination GH and GnRHa therapy, the mean growth rate increased from 5 +/- 1.9 to 7.8 +/- 1.6 cm/yr vs. 5.4 +/- 1.7 to 5 +/- 2 cm/yr in the group not receiving GH (P < 0.0001). During the second year of treatment, the mean growth rate was 6 +/- 1.6 vs. 4.2 +/- 2.1 cm/yr in the group not receiving GH (P < 0.001). The height SD score for chronological age in the treatment group at the end of 1 and 2 yr of treatment improved significantly more than the nontreatment group (P < 0.01). A similar improvement in the height SD score for bone age was found in the treatment group after 1 (-1.4 +/- 0.9 vs. -1.7 +/- 0.9; P < 0.0001) and 2 yr of therapy (-0.67 +/- 0.68 vs. -1.7 +/- 1.2; P < 0.0004). The mean predicted adult height improved from 159 +/- 11 (baseline) to 170 +/- 7.5 cm (after 2 yr of therapy) closely approximating target height (173 +/- 8 cm). All patients continued the hydrocortisone treatment. In patients with CAH and compromised height prediction, treatment with GH or the combination of GH and GnRHa results in an improvement of growth rate and height prediction and a reduction in height deficit for bone age.

摘要

先天性肾上腺皮质增生症(CAH)成年患者身材矮小很常见,即便在儿童期和青春期肾上腺功能控制良好的患者中也是如此。在本研究中,我们探讨了生长激素(GH)治疗对CAH且身高预测受损患儿身高预测的影响。对有性早熟迹象的患者给予醋酸亮丙瑞林,一种促性腺激素释放激素类似物(GnRHa)。对20例CAH患者在继续接受糖皮质激素治疗的同时给予GH(n = 12)或GH与GnRHa联合治疗(n = 8)。治疗组的每例患者根据年龄、性别、骨龄、青春期状态和CAH类型,与另一名仅接受糖皮质激素替代治疗的CAH患者进行匹配。匹配在GH治疗开始时进行。20例患者中,12例已完成2年治疗。接受GH或GH与GnRHa联合治疗1年后,平均生长速率从5±1.9增加至7.8±1.6cm/年,而未接受GH治疗组从5.4±1.7增加至5±2cm/年(P < 0.0001)。在治疗的第二年,平均生长速率为6±1.6cm/年,未接受GH治疗组为�.2±2.1cm/年(P < 0.001)。治疗组在治疗1年和2年后,按实际年龄计算的身高标准差评分改善程度显著大于未治疗组(P < 0.01)。治疗组在治疗1年(-1.4±0.9对-1.7±0.9;P < 0.0001)和2年后(-0.67±0.68对-1.7±1.2;P < 0.0004),按骨龄计算的身高标准差评分也有类似改善。平均预测成年身高从159±11(基线)提高至170±7.5cm(治疗2年后),非常接近目标身高(173±8cm)。所有患者均继续接受氢化可的松治疗。对于CAH且身高预测受损的患者,GH或GH与GnRHa联合治疗可提高生长速率和身高预测,并减少骨龄对应的身高差距。

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