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Growth hormone deficiency and coeliac disease: an unusual association?
Mauro Bozzola1, Diletta Giovenale, Elena Bozzola
1Pediatric Department, University of Pavia, Pavia, Italy. m.bozzola@smatteo.pv.iy
Insights
Growth hormone deficiency (GHD) occurs in some children with coeliac disease (CD). Evaluating GH secretion is crucial for coeliac patients with poor growth on a gluten-free diet, with GH therapy beneficial alongside dietary changes.
Area of Science:
- Pediatric Endocrinology
- Gastroenterology
- Genetics
Background:
- Short stature is a common concern in pediatric endocrinology.
- Coeliac disease (CD) is an autoimmune disorder triggered by gluten ingestion.
- The relationship between CD and growth hormone deficiency (GHD) requires further investigation.
Purpose of the Study:
- To determine the prevalence of GHD in children diagnosed with short stature.
- To investigate the incidence of coeliac disease in this cohort.
- To assess the impact of gluten-free diet and growth hormone therapy on growth in children with both conditions.
Main Methods:
- A cohort of 1066 children with short stature underwent evaluation.
- Screening for CD included antiendomysial antibodies (EMA) and intestinal biopsy.
- Patients diagnosed with CD were monitored for growth response to a gluten-free diet and, in some cases, growth hormone (GH) therapy.
Main Results:
- Of 1066 children, 19.7% had GHD. Twelve children (1.12%) were diagnosed with CD.
- Nine of the 12 CD children showed improved growth on a gluten-free diet.
- Three CD children did not experience catch-up growth, with two diagnosed with isolated GHD and one with multiple GHD, benefiting from GH therapy.
Conclusions:
- Growth hormone secretion should be assessed in coeliac patients who do not achieve catch-up growth on a gluten-free diet.
- Growth hormone replacement therapy should be initiated in children with coeliac disease and GHD while adhering to a gluten-free diet.
- Congenital GHD may be associated with CD, as suggested by MRI findings.
Objective:
To assess the occurrence of growth hormone deficiency (GHD) in patients with coeliac disease (CD).
Study Design:
A total of 1066 children diagnosed elsewhere with short stature were referred to our centre for second-line evaluation in a 6-year period. All patients were screened for CD by antiendomysial antibodies (EMA) and those with positive sera underwent intestinal biopsy.
Results:
Among the 1066 short children, 210 (19.7%) had GHD and 12 (1.12%; chronological age from 3.6 to 12.3 years, bone age from 1.5 to 10.5 years, SDS height from -3.05 to -0.48), having positive EMA, showed histologically confirmed CD. Nine of these latter 12 CD children had a beneficial effect on growth rate after the first year of gluten-free diet, while the remaining three showed no catch-up growth. A careful endocrinological investigation in these three CD boys showed an isolated GHD in two cases and a multiple GHD in one case. The congenital origin of GHD is supported by the congenital abnormalities documented by magnetic resonance imaging. GH therapy associated with gluten-free diet led to an increased growth rate.
Conclusion:
GH secretion should be evaluated in coeliac patients showing no catch-up growth after a period on a gluten-free diet in spite of reversion to seronegativity for EMA. In the case of GHD and CD, replacement GH therapy should be started during a gluten-free diet.
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