Abstract

BackgroundNumerous short-statured children are evaluated for growth hormone (GH) deficiency (GHD). In most patients, GH provocative tests are normal and are thus in retrospect unnecessary.MethodsA retrospective cohort study was conducted to identify predictors of growth hormone (GH) deficiency (GHD) in children seen for short stature, and to construct a very sensitive and fairly specific predictive tool to avoid unnecessary GH provocative tests. GHD was defined by the presence of 2 GH concentration peaks < 10 ng/ml. Certain GHD was defined as GHD and viewing pituitary stalk interruption syndrome on magnetic resonance imaging. Independent predictors were identified with uni- and multi-variate analyses and then combined in a decision rule that was validated in another population.ResultsThe initial study included 167 patients, 36 (22%) of whom had GHD, including 5 (3%) with certain GHD. Independent predictors of GHD were: growth rate < -1 DS (adjusted odds ratio: 3.2; 95% confidence interval [1.3–7.9]), IGF-I concentration < -2 DS (2.8 [1.1–7.3]) and BMI z-score ≥ 0 (2.8 [1.2–6.5]). A clinical decision rule suggesting that patients be tested only if they had a growth rate < -1 DS and a IGF-I concentration < -2 DS achieved 100% sensitivity [48–100] for certain GHD and 63% [47–79] for GHD, and a specificity of 68% [60–76]. Applying this rule to the validation population (n = 40, including 13 patients with certain GHD), the sensitivity for certain GHD was 92% [76–100] and the specificity 70% [53–88].ConclusionWe have derived and performed an internal validation of a highly sensitive decision rule that could safely help to avoid more than 2/3 of the unnecessary GH tests. External validation of this rule is needed before any application.

Highlights

  • Numerous short-statured children are evaluated for growth hormone (GH) deficiency (GHD)

  • The analysis included 167 children. Their mean age was 8.2 years and 49% were boys; 36 (22%) children diagnosed with Growth hormone deficiency (GHD), including 5 (3%) with certain GHD

  • A trend that did not reach statistical significance was seen between GHD and both a prepubertal Tanner stage (p = 0.09) and Insulin-like growth factor-I (IGF-I) < -2 Studies IGF-I (SD) (p = 0.09)

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Summary

Introduction

Numerous short-statured children are evaluated for growth hormone (GH) deficiency (GHD). GH provocative tests are normal and are in retrospect unnecessary. After ruling out other causes of short stature (intestinal malabsorption, chronic liver or kidney disease, hypothyroidism, etc), the possibility of growth hormone (GH) deficiency (GHD) is often considered. This deficiency is associated with excess mortality and substantial morbidity [1,2], and it can be treated. Many children are referred by their physicians to specialist departments to test for GHD. GHD cannot be considered certain unless there are one or more of the following confirmatory markers: familial GHD, other deficiency of the hypothalamic-pituitary axis, micropenis, neonatal hypoglycemia, abnormalities of the median line and pituitary stalk interruption syndrome (PSIS) on magnetic resonance imaging (MRI) [5]

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