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Thyroid function tests and characterization of thyroxine-binding globulin in the carbohydrate-deficient glycoprotein syndrome type I.
Macchia, P E; Harrison, H H; Scherberg, N H; Sunthornthepfvarakul, T; Jaeken, J; Refetoff, S.
Afiliação
  • Macchia PE; Department of Medicine, University of Chicago, Illinois 60637, USA.
J Clin Endocrinol Metab ; 80(12): 3744-9, 1995 Dec.
Article em En | MEDLINE | ID: mdl-8530628
ABSTRACT
Carbohydrate-deficient glycoprotein (CDG) syndrome is a newly recognized hereditary disorder that presents with psychomotor retardation, cerebellar ataxia, peripheral sensorimotor neuropathy, and, variably, skeletal abnormalities, lipodystrophy, and retinitis pigmentosa. These abnormalities appear to be produced by a defect that causes reduced carbohydrate content in glycoproteins. We studied seven patients with CDG type I belonging to five unrelated families. The concentration of serum TBG, a glycoprotein of hepatic origin, was measured by RIA and T4 saturation and was found to be below the normal range in three of the seven patients and normal in four of them. More than half of the total serum TBG had reduced sialic acid content and localized on isoelectric focusing (IEF) as two prominent bands cathodal to the three major bands of normal TBG. The latter two bands are responsible for the characteristic IEF pattern or CDG syndrome. TBG in patients with CDG had immunoreactivity indistinguishable from that of normal TBG and had normal affinity for T4, T3, and rT3. Serum total T4, T3, and rT3 were below the normal range in seven, five, and seven patients, respectively. The free T4 index was also below normal in four patients, but the free T4 concentration, measured by equilibrium dialysis at low dilution, and serum TSH were in the midnormal range. The serum total T4 and rT3 levels were disproportionately reduced relative to the serum TBG concentration and compared to the concentrations of these iodothyronines in matched subjects with inherited partial TBG deficiency. Chronic illness cannot explain these changes, because, contrary to patients with nonthyroidal illness, those with CDG had significantly higher serum total T3/T4 and lower rT3/T4 ratios. It is concluded that IEF of TBG is a rapid and simple method for the diagnosis of CDG type I and that the abnormal pattern can be detected as early as 5 days postpartum. Patients with CDG are chemically euthyroid, and it is postulated that the reduction in serum iodothyronine concentrations beyond that explained on the basis of low TBG levels may be due to the interference with binding to TBG by an unidentified substance.
Assuntos
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Base de dados: MEDLINE Assunto principal: Glândula Tireoide / Proteínas de Ligação a Tiroxina / Defeitos Congênitos da Glicosilação Limite: Adolescent / Adult / Child / Child, preschool / Humans Idioma: En Ano de publicação: 1995 Tipo de documento: Article
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Base de dados: MEDLINE Assunto principal: Glândula Tireoide / Proteínas de Ligação a Tiroxina / Defeitos Congênitos da Glicosilação Limite: Adolescent / Adult / Child / Child, preschool / Humans Idioma: En Ano de publicação: 1995 Tipo de documento: Article