Abstract

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.

Highlights

  • Children whose stature is two height standard deviation (HSD) below the mean for age and sex [1] or who have a height deficit greater than one H-Standard Deviation (SD) relative to the family height should be referred for a complete short stature investigation [2]

  • The serum growth hormone (GH) levels in response to Insulin Tolerance Test (ITT) and to Clonidine Test (CT) were different between all groups

  • When we compared initial and final data of each group, we found a significant increase in H-SD, PH, and Predicted Height standard deviations (PH-SDS) only in Group 2 after follow-up

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Summary

Introduction

Children whose stature is two height standard deviation (HSD) below the mean for age and sex [1] or who have a height deficit greater than one H-SD relative to the family height should be referred for a complete short stature investigation [2]. After considering and excluding other short stature (SS) etiologies such as familial SS (FSS), constitutional delay of growth and puberty (CDGP) and secondary causes (organic lesions, thyroid disorders), the investigation for Growth Hormone Deficiency (GHD) should be conducted [3]. Hussein et al [4], evaluating 637 children and adolescents with SS, found FSS in 42% of them, CDGP in 16%, GHD in 12% and idiopathic SS (ISS), aside CDGP and FSS, in 2% [4]. Increases in predicted height and changes in growth rate are useful to analyze clinical response [12]

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