Klein A H, Foley T P, Larsen P R, Agustin A V, Hopwood N J
J Pediatr. 1976 Oct;89(4):545-9. doi: 10.1016/s0022-3476(76)80383-6.
In the cord blood of seven infants with congenital hypothyroidism detected in our newborn screening programs, thyroxine values ranged from 2.5 to 6.7 mug/dl and thyrotropin, from 105 to 975 muU/ml; triiodothyronine values were normal. On follow-up, T3 levels increased to normal in five infants, there was a significant negative correlation between the T3 value and the severity of thyroprevia as reflected in the TSH levels and the number of clinical features present. This increase in T3 may explain in part why the diagnosis of this disease is difficult during the first few months of life and why early treatment is effective. This observation provides further rationale for the widespread institution of newborn screening programs for congenital hypothyroidism.
在我们新生儿筛查项目中检测出的7例先天性甲状腺功能减退症婴儿的脐血中,甲状腺素值为2.5至6.7微克/分升,促甲状腺素为105至975微单位/毫升;三碘甲状腺原氨酸值正常。随访时,5例婴儿的T3水平升至正常,T3值与甲状腺功能减退严重程度之间存在显著负相关,甲状腺功能减退严重程度通过促甲状腺激素水平和存在的临床特征数量反映。T3的这种升高可能部分解释了为什么在生命的最初几个月难以诊断这种疾病以及为什么早期治疗有效。这一观察结果为广泛开展先天性甲状腺功能减退症新生儿筛查项目提供了进一步的理论依据。