Department of Endocrinology, Dongyang People's Hospital, Dongyang, China;, Email:
Department of Endocrinology, Dongyang People's Hospital, Dongyang, China.
Pharmazie. 2021 Sep 1;76(9):428-430. doi: 10.1691/ph.2021.1559.
To explore an unusual cause of the decrease of T3/T4 through a new mutation of TBG gene in a family, so as to avoid habitual thinking and reduce subsequent over treatment. TSH, free total T4, T3 and free T4, T3 were determined by automatic chemiluminescence immunoassay. The TBG mutation was identified by direct DNA sequencing. A frameshift mutation of p. l372ffs * 32 was found in the TBG gene (c.1114delc) of the patient by direct DNA sequencing, and the proband of the family was heterozygous. In vitro expression showed that the affinity of TBG for T4 decreased. Further examination of the family members showed that T3 and T4 were decreased, while FT3, FT4 and TSH were normal. If the patients with low TT4 and TT3 but normal TSH are found, the serum TBG level and related genes should be detected to determine whether it is TBG deficiency and avoid wrong treatment.
为了通过 TBG 基因的新突变探索 T3/T4 降低的一个不常见原因,从而避免习惯性思维并减少后续过度治疗。采用全自动化学发光免疫分析法检测 TSH、游离总 T4、T3 和游离 T4、T3。通过直接 DNA 测序鉴定 TBG 突变。直接 DNA 测序发现患者的 TBG 基因(c.1114delc)出现 p.l372ffs*32 移码突变(c.1114delc),先证者为杂合子。体外表达表明 TBG 与 T4 的亲和力降低。对家庭成员的进一步检查显示 T3 和 T4 降低,而 FT3、FT4 和 TSH 正常。如果发现 TT4 和 TT3 低但 TSH 正常的患者,应检测血清 TBG 水平和相关基因,以确定是否存在 TBG 缺乏并避免错误治疗。