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低智商而非注意力缺陷多动障碍与甲状腺激素受体β基因突变R316H所致的甲状腺激素抵抗有关。

Low intelligence but not attention deficit hyperactivity disorder is associated with resistance to thyroid hormone caused by mutation R316H in the thyroid hormone receptor beta gene.

作者信息

Weiss R E, Stein M A, Duck S C, Chyna B, Phillips W, O'Brien T, Gutermuth L, Refetoff S

机构信息

Department of Medicine, University of Chicago, Illinois 60637.

出版信息

J Clin Endocrinol Metab. 1994 Jun;78(6):1525-8. doi: 10.1210/jcem.78.6.8200958.

Abstract

Resistance to thyroid hormone (RTH) is a syndrome of reduced responsiveness of tissues to thyroid hormone. The clinical manifestations are variable and 46-50% of children with RTH have attention deficit hyperactivity disorder (ADD). We present a new family with RTH (F120) found to have a mutation R316H in the thyroid hormone receptor beta (TR beta) gene identical for that reported in an unrelated family. Assignment of the mutant allele and haplotyping based on CA repeat polymorphism were done on 16 family members. Semistructured diagnostic interviews and psychometric testing were used to determine the psychiatric diagnosis of 12 family members by examiners blinded to the genotype. Three subjects were identified to have the R316H allele as well as mildly elevated free T4 index (168 +/- 12; normal range 77-135) and nonsuppressed TSH (4.1 +/- 1.7 mU/L). Only 2 of the subjects with RTH were found to have ADD, while one family member homozygous for the wild type TR beta and normal thyroid function tests also had ADD. Unaffected family members had higher full scale intelligence quotients (IQ) (93 +/- 7) than any of the 3 family members with RTH (77 +/- 5, p = 0.006). These data do not support the genetic linkage of ADD and RTH, but do suggest that RTH is associated with lower IQ scores that may confer a high likelihood of exhibiting ADD symptoms.

摘要

甲状腺激素抵抗(RTH)是一种组织对甲状腺激素反应性降低的综合征。其临床表现多样,46%至50%的RTH患儿患有注意力缺陷多动障碍(ADD)。我们报告了一个新的RTH家系(F120),发现其甲状腺激素受体β(TRβ)基因存在R316H突变,这与一个无关家系报道的相同。对16名家庭成员进行了基于CA重复多态性的突变等位基因分型和单倍型分析。由对基因型不知情的检查人员通过半结构化诊断访谈和心理测量测试来确定12名家庭成员的精神疾病诊断。三名受试者被鉴定携带R316H等位基因,同时游离T4指数轻度升高(168±12;正常范围77 - 135)且促甲状腺激素(TSH)未被抑制(4.1±1.7 mU/L)。仅2名RTH受试者被发现患有ADD,而一名野生型TRβ纯合且甲状腺功能测试正常的家庭成员也患有ADD。未受影响的家庭成员全量表智商(IQ)(93±7)高于3名患有RTH的家庭成员中的任何一人(77±5,p = 0.006)。这些数据不支持ADD与RTH的遗传连锁,但确实表明RTH与较低的IQ分数相关,这可能使出现ADD症状的可能性增加。

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