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Diagnosis of Idiopathic GHD in Children Based on Response to rhGH Treatment: The Importance of GH Provocative Tests and IGF-1

机译:根据对rhGH治疗的反应诊断儿童特发性GHD:GH激发试验和IGF-1的重要性

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摘要

>Purpose: Serum IGF-1 (Insulin like growth factor 1) and Growth Hormone (GH) provocative tests are reasonable tools for screening and diagnosis of idiopathic GH Deficiency (IGHD). However, the average cut-off points applied on these tests have a lower level of evidence and produce large amounts of false results. The aim of this study is to evaluate the sensitivity, specificity, and accuracy of IGF-1 and GH stimulation tests as diagnostic tools for IGHD, using clinical response to recombinant human GH (rhGH) treatment as diagnostic standard [increase of at least 0.3 in height standard deviation (H-SD) in 1 year].>Methods: We performed a prospective study with 115 children and adolescents presenting short stature (SS), without secondary SS etiologies such as organic lesions, genetic syndromes, thyroid disorders. They were separated into Group 1 [patients with familial SS or constitutional delay of growth and puberty (CDGP), not treated with rhGH], Group 2 (patients with suspicion of IGHD with clinical response to rhGH treatment), and Group 3 (patients with suspicion of IGHD without growth response to rhGH treatment). Then, they were assessed for diagnostic performance of IGF-1, Insulin Tolerance Test (ITT) and clonidine test (CT) alone and combined at different cut-off points.>Results: Based on the ROC curve, the best cut-off points found for IGF-1, ITT, and CT when they were used isolated were −0.492 SDS (sensitivity: 50%; specificity: 53.8%; accuracy: 46.5%), 4.515 μg/L (sensitivity: 75.5%; specificity: 45.5%; accuracy: 52.7%), and 4.095 μg/L (sensitivity: 54.5%; specificity: 52.6%; accuracy: 56.9%), respectively. When we had combined IGF-1 with−2SD as cut-off alongside ITT or CT, we found 7 μg/L as the best cut-off point. In this situation, ITT had sensitivity, specificity and accuracy of 93.9, 81.8, and 90.1%, while CT had 93.2, 68.4, and 85.7%, respectively.>Conclusion: Our data suggest that diagnosis of IGHD should be established based on a combination of clinical expertise, auxologic, radiologic, and laboratorial data, using IGF-1 at the −2SD threshold combined, with ITT or CT at the cut-off point of 7 μg/L. Additional studies, similar to ours, are imperative to establish cut-off points based on therapeutic response to rhGH in IGHD, which would be directly related to a better treatment outcome.
机译:>目的:血清IGF-1(胰岛素样生长因子1)和生长激素(GH)激发试验是筛查和诊断特发性GH缺乏症(IGHD)的合理工具。但是,应用于这些测试的平均截止点的证据水平较低,并且会产生大量错误的结果。这项研究的目的是使用对重组人GH(rhGH)治疗的临床反应作为诊断标准,评估IGF-1和GH刺激试验作为IGHD诊断工具的敏感性,特异性和准确性[在试验中至少增加0.3。身高标准差(H-SD)在1年内]。>方法:我们对115名表现为矮身材(SS)的儿童和青少年进行了前瞻性研究,没有继发性SS病因,例如器质性病变,遗传综合征,甲状腺疾病。他们分为第1组[家族性SS或体质发育和青春期延迟(CDGP)的患者,未接受rhGH治疗],第2组(怀疑IGHD对rhGH治疗有临床反应的患者)和第3组(怀疑IGHD对rhGH治疗无生长反应)。然后,分别对它们进行IGF-1,胰岛素耐受性测试(ITT)和可乐定测试(CT)的诊断性能评估,并在不同的临界点进行组合。>结果:基于ROC曲线,当分离使用IGF-1,ITT和CT时,发现的最佳截止点为−0.492 SDS(灵敏度:50%;特异性:53.8%;准确度:46.5%),4.515μg/ L(灵敏度:75.5) %;特异性:45.5%;准确度:52.7%)和4.095μg/ L(灵敏度:54.5%;特异性:52.6%;准确度:56.9%)。当我们将IGF-1和-2SD作为截止值与ITT或CT结合使用时,我们发现7μg/ L是最佳截止点。在这种情况下,ITT的敏感性,特异性和准确性分别为93.9、81.8和90.1%,而CT分别为93.2、68.4和85.7%。>结论:我们的数据表明,IGHD的诊断应根据临床专业知识,生理,放射学和实验室数据的组合,使用在-2SD阈值处结合的IGF-1和在7μg/ L的临界点处结合ITT或CT来建立。类似于我们的研究,必须根据IGHD对rhGH的治疗反应来确定临界点,这将直接与更好的治疗结果相关。

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