Growth hormone impaired secretion and antipituitary antibodies in patients with coeliac disease and poor catch-up growth after a long gluten-free diet period: a causal association?

被引:31
作者
Iughetti, Lorenzo
De Bellis, Annamaria
Predieri, Barbara
Bizzarro, Antonio
De Simone, Michele
Balli, Fiorella
Bellastella, Antonio
Bernasconi, Sergio
机构
[1] Univ Modena, Dept Pediat, I-41100 Modena, Italy
[2] Univ Naples 2, Dept Clin & Expt Med & Surg, Chair Endocrinol, I-80131 Naples, Italy
[3] Univ Naples 2, Dept Clin & Expt Med & Surg, Chair Immunol & Allergol, I-80131 Naples, Italy
[4] Univ Aquila, Dept Pediat, I-67100 Laquila, Italy
[5] Univ Parma, Dept Pediat, I-43100 Parma, Italy
关键词
antipituitary antibodies; Coeliac disease; gluten-free diet; catch-up growth; idiopathic growth hormone deficiency;
D O I
10.1007/s00431-006-0182-4
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Introduction Coeliac disease (CD) is usually associated with impaired growth in children. A gluten-free diet (GFD) induces a catch-up growth with the recovery of height in about 2 years. Aim and discussion The lack of the height improvement has been related to growth hormone (GH) secretion impairment. CD is an autoimmune disease often associated with other endocrine and non-endocrine autoimmune disease. The aim of this study was to evaluate antipituitary autoantibodies (APA) and antihypothalamus autoantibodies in CD children with poor clinical response to a GFD and growth hormone deficiency (GHD). We diagnosed CD on the basis of specific antibodies and endoscopic biopsies in 130 patients aged 1-15 years. Seven CD children, without catch-up growth after at least 12-months GFD, were tested for GH secretion and, in five out of seven patients, the diagnosis of GHD was made in the absence of metabolic and systemic diseases. Results APA and antihypothalamus antibodies were detected by the indirect immunofluorescence method in the seven CD children without catch-up growth factor and in 25 CD children without growth impairment matched for sex and age, and in 58 healthy children as control groups. APA resulted positive at high titres in four out of five CD-GHD patients and were also positive at low titres (< 1:8) in three of only CD children and in two out of 58 controls. Hypothalamic-pituitary magnetic resonance imaging (MRI) was normal in all patients except in one with cystic pineal. APA have been previously detected not only in adults with GHD, but also in idiopathic GHD children, suggesting the occurrence of an autoimmune hypophysitis in these patients. Conclusion In our study, the presence of APA in CD children without catch-up growth after GFD seems to be able to identify an autoimmune form of hypophysitis involving the somatotrophs cells.
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页码:897 / 903
页数:7
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