Iughetti Lorenzo, De Bellis Annamaria, Predieri Barbara, Bizzarro Antonio, De Simone Michele, Balli Fiorella, Bellastella Antonio, Bernasconi Sergio
Department of Pediatrics, University of Modena and Reggio Emilia, Via del Pozzo, 71, 41.100, Modena, Italy.
Eur J Pediatr. 2006 Dec;165(12):897-903. doi: 10.1007/s00431-006-0182-4. Epub 2006 Aug 3.
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.
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.
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.
乳糜泻(CD)通常与儿童生长发育受损有关。无麸质饮食(GFD)可促使身高在约2年内实现追赶性增长并恢复。目的与讨论:身高未改善与生长激素(GH)分泌受损有关。CD是一种自身免疫性疾病,常与其他内分泌和非内分泌自身免疫性疾病相关。本研究的目的是评估对GFD临床反应不佳且存在生长激素缺乏(GHD)的CD儿童中的抗垂体自身抗体(APA)和抗下丘脑自身抗体。我们根据特异性抗体和内镜活检对130名1至15岁的患者进行了CD诊断。7名CD儿童在接受至少12个月的GFD后未出现追赶性生长,对其进行了GH分泌检测,其中7名患者中有5名在无代谢和全身性疾病的情况下被诊断为GHD。
通过间接免疫荧光法在7名无追赶性生长的CD儿童、25名年龄和性别匹配且无生长障碍的CD儿童以及58名健康儿童(作为对照组)中检测到了APA和抗下丘脑抗体。5名CD - GHD患者中有4名APA呈高滴度阳性,仅CD儿童中有3名呈低滴度(<1:8)阳性,58名对照组中有2名呈低滴度阳性。除1名患有松果体囊肿的患者外,所有患者的下丘脑 - 垂体磁共振成像(MRI)均正常。此前不仅在患有GHD的成人中检测到了APA,在特发性GHD儿童中也检测到了,这表明这些患者发生了自身免疫性垂体炎。
在我们的研究中,GFD后无追赶性生长的CD儿童中存在APA似乎能够识别一种涉及生长激素细胞的自身免疫性垂体炎形式。