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Efficacy of Low Insulin-Like Growth Factor-1 Levels and a Single Insulin Tolerance Test in Diagnosing Growth Hormone
Chayanit Yuenyong1, Worapimon Lerdrassameethad1, Khomsak Srilanchakon1
1Chulalongkorn University, Division of Pediatric Endocrinology, Department of Pediatrics, Faculty of Medicine, Thailand, Bangkok.
Insights
Combining a low insulin-like growth factor-1 (IGF-1) level with a failed insulin tolerance test (ITT) may help identify children with a higher probability of growth hormone deficiency. However, current diagnostic standards still require two tests for confirmation.
Area of Science:
- Pediatric Endocrinology
- Diagnostic Accuracy
- Biochemical Markers
Background:
- Pediatric growth hormone deficiency diagnosis is complex due to pulsatile hormone secretion.
- The insulin tolerance test (ITT) is a key diagnostic tool, but current standards require multiple tests.
- Insulin-like growth factor-1 (IGF-1) alone has limited diagnostic value.
Purpose of the Study:
- To evaluate if combining low IGF-1 levels with a single failed ITT improves diagnostic efficiency for pediatric growth hormone deficiency.
- To assess the diagnostic performance of this combined criterion in children with short stature.
Main Methods:
- Retrospective cohort study of 214 children (aged 2-16 years) with short stature.
- Analyzed IGF-1 standard deviation scores (SDS) at various cutoffs combined with failed ITT results.
- Calculated diagnostic performance indices including sensitivity, specificity, and predictive values.
Main Results:
- An IGF-1 SDS of ≤-2.5 combined with a failed ITT showed 38.6% sensitivity and 92.6% specificity.
- This combination yielded a positive predictive value of 73.9% and a negative predictive value of 73.5%.
- Discordance was observed between ITT and clonidine tests in 37% of patients, highlighting potential reference standard limitations.
Conclusions:
- Combining a low IGF-1 SDS (≤-2.5) with a single failed ITT identifies a subgroup with higher growth hormone deficiency probability.
- The modest sensitivity and positive predictive values, along with reference standard circularity, suggest these findings are hypothesis-generating.
- Prospective, multicenter validation is needed before altering current diagnostic practices requiring two independent stimulation tests.
Abstract:
Pediatric growth hormone deficiency requires dynamic testing for accurate diagnosis because of the pulsatile secretion of growth hormone. The insulin tolerance test (ITT) is regarded as one of the most robust individual provocative tests for growth hormone deficiency, although the broader pediatric diagnostic standard requires a composite of auxological, clinical, and biochemical criteria together with an inadequate response to two independent stimulation tests, except in specific high-probability contexts; insulin-like growth factor-1 (IGF-1) alone has limited diagnostic accuracy. This study evaluated whether combining low IGF-1 levels with a single failed ITT could improve diagnostic efficiency for pediatric growth hormone deficiency. We conducted a retrospective cohort study of 214 children with short stature (aged 2-16 y) evaluated at King Chulalongkorn Memorial Hospital between August 2019 and January 2025. Growth hormone deficiency was confirmed in 63 patients using two growth hormone stimulation tests (peak growth hormone level: < 7 ng/mL). IGF-1 levels were expressed as standard deviation scores and analyzed at cutoff values of ≤ -1, -1.5, -2, and -2.5 in combination with failed ITT results. Diagnostic performance indices were calculated at each predefined cutoff/test combination, including sensitivity, specificity, positive predictive values, negative predictive values, area under the receiver operating characteristic curve, odds ratios, and accuracy. An IGF-1 standard deviation score of ≤ -2.5 combined with a single failed ITT showed a sensitivity of 38.6% and a specificity of 92.6%, with a positive predictive value and a negative predictive value of 73.9% and 73.5%, respectively (p<0.001). Because the reference standard for the growth hormone deficiency required failure of two stimulation tests, one of which was the ITT, we assessed this circularity directly: among 100 patients with both the ITT and clonidine results, findings were discordant in 37 (exact McNemar p=0.008), and IGF-1 standard deviation scores did not differ significantly across concordant and discordant subgroups (Kruskal-Wallis p=0.407). An IGF-1 standard deviation score cutoff of ≤ -2.5 combined with a single failed ITT identifies a subgroup of children at higher probability of growth hormone deficiency who may be prioritized for confirmatory evaluation. Given the modest sensitivity and positive predictive values of this criterion and the circularity inherent in a reference standard that itself incorporates the ITT, these findings should be regarded as hypothesis-generating rather than as a basis for changing current diagnostic practice, which continues to require two independent stimulation tests except in specific high-probability contexts; prospective, multicenter validation is required.
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