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Inhibition of serum protein binding of thyroxine in a hypothyroid patient with familial dysalbuminemic hyperthyroxinemia

โœ Scribed by Bhartur N. Premachandra; Jacobo Wortsman; Irvin K. Williams


Publisher
Elsevier Science
Year
1996
Tongue
English
Weight
448 KB
Volume
29
Category
Article
ISSN
0009-9120

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โœฆ Synopsis


ObJecUve: To investigate unusual free thyroxine (FT4) responses to T 4 replacement doses in a hypothyroid patient with familial dysalbuminemic hyperthyroxinemia (FDH). Methods: In this FDH hypothyroid patient, serum FT4 concentration by equilibrium dialysis and T4, triiodothyronine (Ta), and thyroid stimulating hormone (TSH) determinations were supplemented by thyroxine binding globulin (TBG) and thyroxine binding prealbumin (TBPA) measurements. Results: Initial thyroid function tests were compatible with hypothyroidism and FDH (T 4 = 78 nmol/L, T 3 = 1.08 nmol/L, FT 4 = 11.6 pmol/L, TSH = 45 mU/L). When she was initially treated with T4 (0.112--0.088 mg/day) there was an increase in FT4 concentration to hyperthyroid levels accompanied by TSH inhibition (FT 4 = 31-51 pmol/L, TSH = <0.03 mU/L); the patient also complained of intolerance and nervousness, and T4 treatment was discontinued. Concentrations of thyroxine binding globulin (TBG) and thyroxine binding prealbumin (TBPA) were normal. When T4 therapy was later resumed at a dosage of 0.075 mg/day, there was a marked increase in percent dialyzable T4. The elevation in percent dialyzable T4 during T4 replacement in a patient with FDH is unusual in view of the very large T4 binding capacity of FDH albumin. Tl~e presence of an inhibitor that reduced T, binding by both TBG and FDH albumin probably explains the elevation in percent dialyzable T4 during T4 treatment.


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