División Endocrinología, Hospital de Niños "Ricardo Gutiérrez", Centro de Investigaciones Endocrinológicas, CEDIE-CONICET, Gallo 1330, 1425 Buenos Aires, Argentina.
Endocrine. 2010 Dec;38(3):377-85. doi: 10.1007/s12020-010-9391-8. Epub 2010 Oct 23.
We describe the clinical, biochemical, and molecular findings of a cohort of Argentinean patients with congenital hypothyroidism (CH) and goiter studied to characterize iodide organification and thyroglobulin (TG) defects. 20 CH patients (16 unrelated) were grouped according to serum TG levels and a perchlorate discharge test (PDT) in: group 1 (G1): nine patients with high TG and PDT > 10% who were studied for tiroperoxidase (TPO), dual oxidase 2 (DUOX2), and dual oxidase A2 (DUOXA2) defects and group 2 (G2): 11 patients with low TG and PDT < 10% studied for TG defects. Goiter characteristics, outcome, and TT₄ and TT₃ levels without treatment were compared between groups. 6/9 G1 patients harbored mutations in TPO gene and 3/9 in DUOX2 gene. In G2, mutations of TG gene were found in 3/11 homozygous, 5/11 compound heterozygous, and 3/11 heterozygous patients. Goiter was only evidenced by thyroid scan in the neonatal period in both groups; was moderately enlarged in patients diagnosed during infancy. In the late detected patients, goiter was big and nodular in G1 while diffuse and moderate in G2. Early detected patients grew and developed normally while those diagnosed late were severely mentally retarded in G1 and only mildly retarded in G2. Thyroid hormone levels of G1 were significantly lower than those of G2 P < 0.01. Molecular approach to characterize defects in organification and TG defects was optimized by TG measurements and PDT. Clinical and biochemical differences based on molecular findings will allow further investigations on genotype-phenotype relationships.
我们描述了一组阿根廷先天性甲状腺功能减退症(CH)伴甲状腺肿患者的临床、生化和分子发现,旨在研究碘有机化和甲状腺球蛋白(TG)缺陷。20 名 CH 患者(16 名无亲缘关系)根据血清 TG 水平和高氯酸盐排出试验(PDT)分组:第 1 组(G1):9 名高 TG 和 PDT > 10%的患者,研究甲状腺过氧化物酶(TPO)、双氧化酶 2(DUOX2)和双氧化酶 A2(DUOXA2)缺陷;第 2 组(G2):11 名低 TG 和 PDT < 10%的患者,研究 TG 缺陷。比较两组间甲状腺肿特征、结局及 TT₄和 TT₃水平未经治疗。G1 组 6/9 名患者存在 TPO 基因突变,3/9 名患者存在 DUOX2 基因突变。G2 组 3/11 名纯合子、5/11 名复合杂合子和 3/11 名杂合子患者存在 TG 基因突变。两组新生儿期仅通过甲状腺扫描发现甲状腺肿;婴儿期确诊的患者甲状腺肿大。晚期发现的患者,G1 组甲状腺肿大且呈结节状,G2 组甲状腺肿弥漫且中度肿大。早期发现的患者生长发育正常,而晚期发现的患者,G1 组严重智力发育迟缓,G2 组仅轻度智力发育迟缓。G1 组甲状腺激素水平明显低于 G2 组,P < 0.01。通过 TG 测量和 PDT 优化了有机化和 TG 缺陷的分子特征方法。基于分子发现的临床和生化差异将允许进一步研究基因型-表型关系。