Rodrigues Martineli A M, Braga M, De Lacerda L, Raskin S, Graf H
Department of Internal Medicine, Clinical Hospital of the Federal University of Paraná, Curitiba, Brazil.
Thyroid. 1998 Apr;8(4):299-304. doi: 10.1089/thy.1998.8.299.
The pituitary-specific transcription factor Pit-1/GHF-1 is responsible for pituitary development and expression of somatotrophs and lactotrophs as well as hormonal regulation of the prolactin (PRL) and thyrotropin (TSH) beta genes by thyrotropin-releasing hormone (TRH) and cyclic adenosine monophosphate (cAMP). Pit-1 gene mutations result in complete growth hormone (GH) and PRL deficiencies and variable degrees of TSH deficiency, producing the clinical syndrome of combined pituitary hormone deficiency (CPHD). Several cases of mutations in the Pit-1 gene have been reported; the most common one is a sporadic mutation altering an arginine (R) to a tryptophan (W) in codon 271, in one allele of the Pit-1 gene. We describe a case of a 38-year-old woman, born to consanguineous parents, presenting with growth failure and hypothyroidism. Growth failure was noted from early infancy, whereas hypothyroidism was only apparent from adolescence. She had almost undetectable GH and PRL levels and an inappropriate low TSH for very low triiodothyronine (T3) and thyroxine (T4) levels, while the remaining pituitary evaluation was normal. The pituitary gland was hypoplastic by magnetic resonance imaging. A point mutation in exon 6, monoallelic, causing a C to T substitution that changes amino acid 271 from Arg (R) to Trp (W) was identified. Children with Pit 1 mutations and delayed onset of hypothyroidism may be initially diagnosed as isolated GH deficiency.
垂体特异性转录因子Pit-1/GHF-1负责垂体发育以及生长激素细胞和催乳激素细胞的表达,还负责促甲状腺激素释放激素(TRH)和环磷酸腺苷(cAMP)对催乳素(PRL)和促甲状腺激素(TSH)β基因的激素调节。Pit-1基因突变会导致完全性生长激素(GH)和PRL缺乏以及不同程度的TSH缺乏,从而产生联合垂体激素缺乏症(CPHD)的临床综合征。已有多例Pit-1基因突变的病例报道;最常见的一种是在Pit-1基因的一个等位基因中,第271密码子处的一个散发性突变,将精氨酸(R)改变为色氨酸(W)。我们描述了一例38岁女性病例,其父母为近亲结婚,该女性表现出生长发育迟缓及甲状腺功能减退。生长发育迟缓自婴儿早期即被注意到,而甲状腺功能减退直到青春期才明显表现出来。她的GH和PRL水平几乎检测不到,且在极低的三碘甲状腺原氨酸(T3)和甲状腺素(T4)水平下,TSH水平却不适当的低,而其余垂体评估均正常。磁共振成像显示垂体发育不全。在外显子6中发现了一个单等位基因突变,导致C到T的替换,使第271位氨基酸从精氨酸(R)变为色氨酸(W)。患有Pit-1基因突变且甲状腺功能减退发病较晚的儿童最初可能被诊断为单纯性生长激素缺乏症。