THYROID-FUNCTION TESTS AND CHARACTERIZATION OF THYROXINE-BINDING GLOBULIN IN THE CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME TYPE-I

被引:21
作者
MACCHIA, PE
HARRISON, HH
SCHERBERG, NH
SUNTHORNTHEPVARAKUL, T
JAEKEN, J
REFETOFF, S
机构
[1] UNIV CHICAGO, DEPT MED, CHICAGO, IL 60637 USA
[2] UNIV CHICAGO, DEPT PEDIAT, CHICAGO, IL 60637 USA
[3] UNIV CHICAGO, ENDOCRINE LAB, CHICAGO, IL 60637 USA
[4] UNIV CHICAGO, JOSEPH P KENNEDY JR MENTAL RETARDAT RES CTR, CHICAGO, IL 60637 USA
[5] GENETRIX INC, SCOTTSDALE, AZ 85251 USA
[6] UNIV LEUVEN, DEPT PEDIAT, LOUVAIN, BELGIUM
关键词
D O I
10.1210/jc.80.12.3744
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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 T-4 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 T-4, T-3, and rT(3). Serum total T-4, T-3, and rT(3) were below the normal range in seven, five, and seven patients, respectively. The free T-4 index was also below normal in four patients, but the free T-4 concentration, measured by equilibrium dialysis at low dilution, and serum TSH were in the midnormal range. The serum total T-4 and rT(3) 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 T-3/T-4 and lower rT(3)/T-4 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.
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页码:3744 / 3749
页数:6
相关论文
共 36 条
[1]   RELATIONSHIP OF OLIGOSACCHARIDE MODIFICATION TO THE CAUSE OF SERUM THYROXINE-BINDING GLOBULIN EXCESS [J].
AIN, KB ;
REFETOFF, S .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1988, 66 (05) :1037-1043
[2]   REDUCED CLEARANCE RATE OF THYROXINE-BINDING GLOBULIN (TBG) WITH INCREASED SIALYLATION - A MECHANISM FOR ESTROGEN-INDUCED ELEVATION OF SERUM TBG CONCENTRATION [J].
AIN, KB ;
MORI, Y ;
REFETOFF, S .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1987, 65 (04) :689-696
[3]   RECENT ACHIEVEMENTS IN STUDIES ON THYROID HORMONE-BINDING PROTEINS [J].
BARTALENA, L .
ENDOCRINE REVIEWS, 1990, 11 (01) :47-64
[4]  
BLENNOW G, 1991, ACTA PAEDIATR SC S, V375, P14
[5]   CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME - NORMAL GLYCOSYLATION IN THE FETUS [J].
CLAYTON, P ;
WINCHESTER, B ;
DITOMASO, E ;
YOUNG, E ;
KEIR, G ;
RODECK, C .
LANCET, 1993, 341 (8850) :956-956
[6]  
CONRADI N, 1991, ACTA PAEDIATR SC S, V375, P50
[7]  
DIROCCO M, 1993, RIV ITAL PED, V19, P179
[8]  
EEGOLOFSSON KE, 1991, ACTA PAEDIATR SC S, V375, P63
[9]  
GARTNER R, 1981, J CLIN ENDOCR METAB, V52, P657
[10]  
HARRISON HH, 1992, CLIN CHEM, V38, P1390