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.

Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme
|August 14, 2026
PubMed

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.

Related Concept Videos

Insulin: Dosing Regimen and Adverse Effects01:16

Insulin: Dosing Regimen and Adverse Effects

Insulin-replacement therapy usually includes both long-acting insulin (basal) and short-acting insulin (to cater to postprandial needs). In a diverse group of type 1 diabetes patients, the average daily insulin dose is typically 0.5-0.7 units/kg body weight. However, obese patients and pubertal adolescents may need more due to insulin resistance.
The basal dose constitutes about 40%-50% of the total daily dose, with the rest as premeal insulin. The mealtime insulin dose should mirror...
Hypoglycemia and Glucagon01:15

Hypoglycemia and Glucagon

Without prolonged fasting, healthy individuals maintain blood glucose levels above 3.5 mM due to a well-adapted neuroendocrine counterregulatory system that effectively prevents acute hypoglycemia, a potentially life-threatening condition. The primary clinical scenarios for hypoglycemia encompass diabetes treatment, inappropriate production of endogenous insulin or insulin-like substances by tumors, and the use of glucose-lowering agents in non-diabetic individuals. Notably, hypoglycemia in the...
Hyperglycemia01:29

Hyperglycemia

Hyperglycemia is an abnormally high blood glucose level. It is diagnosed by fasting glucose ≥126 mg/dL, 2-hour oral glucose tolerance test (or OGTT) ≥200 mg/dL, random glucose ≥200 mg/dL with symptoms, or HbA1c ≥6.5%. However, HbA1c results may be unreliable in certain conditions, such as anemia or hemoglobinopathies, and the diagnosis should be confirmed unless classic symptoms are present. Postprandial hyperglycemia is typically considered significant when glucose levels exceed 180 mg/dL two...
Type II Diabetes Mellitus III: Clinical Manifestations and Diagnosis01:25

Type II Diabetes Mellitus III: Clinical Manifestations and Diagnosis

Type 2 diabetes mellitus develops gradually and is often asymptomatic in early stages.Clinical ManifestationsWhen symptoms appear, they include fatigue, blurred vision, pruritus, delayed wound healing, and recurrent infections, particularly candidal infections. Peripheral neuropathy may present as numbness or tingling in the extremities. Classic hyperglycemia symptoms—polyuria, polydipsia, and polyphagia—are less common. Most patients are overweight and frequently have associated hypertension...
Diabetes Mellitus: Type 2 and Gestational01:22

Diabetes Mellitus: Type 2 and Gestational

Type 2 diabetes, characterized by insulin resistance, arises when the insulin receptors on cells lose responsiveness to insulin, diminishing the cell's capacity to take up glucose, resulting in elevated blood glucose levels. To receive a diagnosis of Type 2 diabetes, a series of blood glucose tests are necessary to assess whether the blood glucose falls within normal parameters. If the result is out of the normal range, a patient may be diagnosed as prediabetic or diabetic, depending on the...
Glucagon-like Receptor Agonists01:24

Glucagon-like Receptor Agonists

Incretins include glucagon-like peptide-1 (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP), which stimulate insulin secretion post-meals. In type 2 diabetes, GIP's efficacy is reduced, making GLP-1 a viable drug target. GIP originates from preproGIP.
GLP-1, when administered in high doses intravenously, triggers insulin secretion, inhibits glucagon release, slows gastric emptying, reduces food intake, and restores normal insulin secretion. However, its rapid inactivation by the...