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胰岛素样生长因子结合蛋白-3在疑似生长激素缺乏症矮小儿童评估与治疗中的临床应用

Clinical utility of insulin-like growth factor binding protein-3 in the evaluation and treatment of short children with suspected growth hormone deficiency.

作者信息

Hasegawa Y, Hasegawa T, Aso T, Kotoh S, Nose O, Ohyama Y, Araki K, Tanaka T, Saisyo S, Yokoya S

机构信息

Division of Endocrinology and Metabolism, Tokyo Metropolitan Kiyose Children's Hospital, Japan.

出版信息

Eur J Endocrinol. 1994 Jul;131(1):27-32. doi: 10.1530/eje.0.1310027.

Abstract

We have shown previously that serum insulin-like growth factor binding protein-3 (IGFBP-3) levels have good predictive value for complete, but not partial, growth hormone deficiency (GHD). In this study, we compare IGFBP-3 levels in short children previously divided into groups on the basis of their post-stimulation GH levels. Complete GHD (N = 59) included those children with peak post-stimulation GH < 5 micrograms/l. The partial GHD group (N = 49) had post-stimulation GH peaks of > 5 micrograms/l but < 10 micrograms/l. The normal children with short stature (N = 103) had post-stimulation GH peaks > 10 micrograms/l. Partial GHD and normal children with short stature also were divided into either low IGF-I or normal IGF-I subgroups. The clinical sensitivity of IGFBP-3 for complete GHD was 92%, whereas its sensitivity for partial GHD was 39%. For partial GHD, among those with low IGF-I (N = 19) 68% were also low for IGFBP-3, while 80% of those with normal IGF-I (N = 30) were also normal for IGFBP-3. The clinical specificity of IGFBP-3 for normal children with short stature was 69%. For these groups, among those with low IGF-I (N = 22) 73% also were low for IGFBP-3, while 80% of those with normal IGF-I (N = 81) also were normal for IGFBP-3. In addition, we tested whether IGFBP-3 can predict the response to GH treatment in prepubertal children by comparing pretreatment IGFBP-3 with the height gain achieved by 1 year of GH treatment.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

我们之前已经表明,血清胰岛素样生长因子结合蛋白-3(IGFBP-3)水平对完全性生长激素缺乏症(GHD)具有良好的预测价值,但对部分性生长激素缺乏症则不然。在本研究中,我们比较了先前根据刺激后生长激素(GH)水平分组的矮小儿童的IGFBP-3水平。完全性GHD组(N = 59)包括那些刺激后GH峰值<5微克/升的儿童。部分性GHD组(N = 49)刺激后GH峰值>5微克/升但<10微克/升。身材矮小的正常儿童(N = 103)刺激后GH峰值>10微克/升。部分性GHD组和身材矮小的正常儿童也被分为IGF-I低水平或正常IGF-I亚组。IGFBP-3对完全性GHD的临床敏感性为92%,而对部分性GHD的敏感性为39%。对于部分性GHD,在IGF-I低水平的儿童中(N = 19),68%的IGFBP-3水平也低,而在IGF-I正常的儿童中(N = 30),80%的IGFBP-3水平也正常。IGFBP-3对身材矮小的正常儿童的临床特异性为69%。对于这些组,在IGF-I低水平的儿童中(N = 22),73%的IGFBP-3水平也低,而在IGF-I正常的儿童中(N = 81),80%的IGFBP-3水平也正常。此外,我们通过比较治疗前IGFBP-3与1年GH治疗后的身高增长,来测试IGFBP-3是否能预测青春期前儿童对GH治疗的反应。(摘要截选至250字)

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