De Bellis Annamaria, Salerno Mariacarolina, Conte Marisa, Coronella Concetta, Tirelli Gilda, Battaglia Marina, Esposito Valentina, Ruocco Giuseppe, Bellastella Giuseppe, Bizzarro Antonio, Bellastella Antonio
Chair of Endocrinology, Second University of Naples, Via S. Pansini, 5, 80131 Naples, Italy.
J Clin Endocrinol Metab. 2006 Jul;91(7):2484-9. doi: 10.1210/jc.2006-0040. Epub 2006 Apr 18.
Antipituitary antibodies (APA) recognizing GH-secreting cells may indicate an autoimmune pituitary involvement in adults with idiopathic GH deficiency (IGHD).
We aimed 1) to investigate the presence of APA in prepubertal children with IGHD or idiopathic short stature (ISS), identifying the pituitary hormone-producing cells targeted by APA; and 2) to verify whether in patients with ISS the presence of APA could predict the development of GHD.
We performed a cross-sectional and partially longitudinal cohort study.
The study was performed at the Endocrinology Unit and Pediatric Unit of the Second University and University Federico II of Naples, respectively.
Twenty-six children with IGHD (group 1), 60 children with ISS (group 2), 33 children with GHD caused by lesions/abnormalities of the hypothalamus or pituitary (group 3), and 40 controls participated in the study. Nineteen children of group 2 were reevaluated after 2 yr.
IGF-I levels, GH secretion, and APA (by indirect immunofluorescence) were evaluated in all participants.
At study entry, APA recognizing GH-producing cells were detected in seven of 26 children in group 1 and in 14 of 60 in group 2. Two years later, all eight initially APA-positive and all 11 APA-negative of the 19 reevaluated patients persisted positive and negative, respectively. The reevaluation of GH secretion in these patients revealed the development of GHD in all but one of the APA-positive children but in none of the APA-negative ones.
IGHD in children can be frequently associated with APA targeting GH-secreting cells; thus, the detection of APA in children with ISS could identify those prone to develop GHD.
识别生长激素分泌细胞的抗垂体抗体(APA)可能提示特发性生长激素缺乏症(IGHD)成人患者存在自身免疫性垂体受累情况。
我们旨在1)研究IGHD或特发性身材矮小(ISS)青春期前儿童中APA的存在情况,确定APA靶向的垂体激素产生细胞;2)验证在ISS患者中,APA的存在是否可预测生长激素缺乏症(GHD)的发生。
我们进行了一项横断面和部分纵向队列研究。
该研究分别在那不勒斯第二大学和费德里科二世大学的内分泌科和儿科进行。
26名IGHD儿童(第1组)、60名ISS儿童(第2组)、33名由下丘脑或垂体病变/异常导致GHD的儿童(第3组)以及40名对照参与了研究。第2组的19名儿童在2年后进行了重新评估。
对所有参与者评估胰岛素样生长因子-I(IGF-I)水平、生长激素分泌和APA(通过间接免疫荧光法)。
研究开始时,第1组26名儿童中有7名检测到识别生长激素产生细胞的APA,第2组60名儿童中有14名检测到。两年后,重新评估的19名患者中,最初8名APA阳性和11名APA阴性的患者分别保持阳性和阴性。对这些患者生长激素分泌的重新评估显示,除1名APA阳性儿童外,其余所有APA阳性儿童均发生了GHD,而APA阴性儿童均未发生。
儿童IGHD常与靶向生长激素分泌细胞的APA相关;因此,在ISS儿童中检测APA可识别那些易发生GHD的儿童。