Familial Euthyroid Thyroxine Excess: An Appropriate Response to Abnormal Thyroxine Binding Associated with Albumin

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Abstract
Responses of the pituitary-thyroid axis and T4 [thyroxine] binding to plasma proteins were studied in 3 kindreds with familial euthyroid T4 excess, an autosomal dominant condition in which affected subjects have high concentrations of plasma T4 with a high free T4 index, but normal free T4 by equilibrium dialysis. Treatment of affected subjects with exogenous T4 or T3 led to gradual suppression of TSH secretion when the free level of T4 or T3 [triiodothyronine] increased above normal. When total T4 was reduced toward normal by KI treatment or previous subtotal thyroidectomy, the findings suggested mild hormone deficiency. In affected subjects from all 3 families, equilibrium dialysis showed increased [125I]T4 binding, with evidence of abnormal high capacity binding when an excess of unlabeled T4 was added. T3 binding showed no major abnormality. Serum concentrations of T4-binding globulin, prealbumin and albumin were normal, but gel electrophoresis and immunoprecipitation of binding proteins indicated that 25-30% of tracer [125I]T4 was albumin bound (normal, 10-12%). Abnormal binding, studied by an adsorption separation system in the presence of T4 excess, was inhibited by increments of barbitone. T4 excess is an appropriate response to abnormal T4 binding so as to maintain normal free T4. The excess bound T4 is associated with a normal quantity of albumin. The basis for increased T4-albumin binding remains to be determined.