Callan F P, Duffy M J, Duffy G J, Farrell R J, McKenna T J
Acta Endocrinol (Copenh). 1983 Apr;102(4):527-30. doi: 10.1530/acta.0.1020527.
The co-existence of thyroxine binding globulin (TBG) deficiency and euthyroid goitre in the same family raised the possibility that the disorders might be related. However, although both disorders co-existed in some members of the family, other members had either but not both conditions. These observations exclude the possibility that goitre development was solely due to alterations in thyroid activity brought about by TBG deficiency. It is possible, however, that the defect in protein binding might have enhanced goitre development in predisposed individuals as the two largest goitres occurred in TBG deficient subjects. Of the conventional parameters used to assess thyroid hormone levels in TBG deficient subjects, only the free triiodothyronine index consistently reflected the euthyroid status of these patients as established by clinical examination and TSH levels.
甲状腺素结合球蛋白(TBG)缺乏症与甲状腺功能正常的甲状腺肿在同一家族中并存,这增加了这两种疾病可能相关的可能性。然而,尽管这两种疾病在该家族的一些成员中同时存在,但其他成员仅患其中一种疾病,而非两种都患。这些观察结果排除了甲状腺肿的发生仅仅是由于TBG缺乏导致甲状腺活动改变的可能性。不过,蛋白质结合缺陷可能会使易患个体的甲状腺肿病情加重,因为两个最大的甲状腺肿出现在TBG缺乏的患者身上。在用于评估TBG缺乏患者甲状腺激素水平的传统参数中,只有游离三碘甲状腺原氨酸指数始终如一地反映了这些患者经临床检查和促甲状腺激素水平确定的甲状腺功能正常状态。