Serum substances that interfere with thyroid hormone assays in patients with chronic renal failure

被引:25
作者
Iitaka, M
Kawasaki, S
Sakurai, S
Hara, Y
Kuriyama, R
Yamanaka, K
Kitahama, S
Miura, S
Kawakami, Y
Katayama, S
机构
[1] Saitama Med Sch, Dept Internal Med 4, Moroyama, Saitama 35004, Japan
[2] Ohme Municipal Gen Hosp, Tokyo, Japan
关键词
D O I
10.1046/j.1365-2265.1998.00419.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE Serum thyroid hormone concentrations in patients with chronic renal failure are usually low, despite normal serum TSH levels. We investigated the effect on thyroid hormone assays of serum dialysable organic acids that are elevated in uraemic patients. PATIENTS Serum samples from 42 patients with chronic renal failure who were receiving haemodialysis and 37 sex- and age-matched healthy subjects were examined. DESIGN AND MEASUREMENTS Serum thyroid hormone concentrations were measured with an analogue radioimmunoassay (RIA), a labelled antibody assay, and an equilibrium dialysis/RIA method, Serum concentrations of organic acids were determined with high performance liquid chromatography. RESULTS Serum thyroid hormone levels determined by an analogue RIA and a labelled antibody assay in uraemic patients increased, and serum concentrations of organic acids decreased following haemodialysis, A significant association existed between serum free T3 (Ff3) levels determined by an analogue RIA and serum concentrations of indoxyl sulphate (IS) prior to dialysis, There was also a significant association between serum free T4 (FT4) levels determined by an analogue RIA and serum concentration of IS and hippuric acid (HA) prior to dialysis, There was a significant association between the changes of serum concentrations of indole acetic acid (IAA) and FT4 concentrations prior to and following haemodialysis when determined by an analogue RIA, Serum FT3 and FT4 levels significantly decreased after the addition of IS to serum from healthy subjects when determined by an analogue RIA but not by a labelled antibody assay. Serum FT4 levels, but not FT3 levels, decreased after addition of IAA when determined by an analogue RIA. Serum FT4 concentrations determined by an equilibrium dialysis/RIA were significantly higher than those determined by the other two methods. The addition of IS, IAA, and HA to serum samples from healthy subjects significantly increased FT4 concentrations when determined by an equilibrium dialysis/RIA method. CONCLUSIONS Increased serum levels of indoxyl sulphate, indole acetic acid and hippuric acid in sera of uraemic patients may interfere with thyroid hormone measurements when an analogue radioimmunoassay is used. In contrast, there was little interference with a labelled antibody assay. Dialysable organic acids may also interfere with thyroid hormone assays determined by an equilibrium dialysis/radioimmunoassay method.
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收藏
页码:739 / 746
页数:8
相关论文
共 30 条
[2]   DECREASED DRUG-BINDING IN UREMIA - EFFECT OF INDOXYL SULFATE AND OTHER ENDOGENOUS SUBSTANCES ON THE BINDING OF DRUGS AND DYES TO HUMAN-ALBUMIN [J].
BOWMER, CJ ;
LINDUP, WE .
BIOCHEMICAL PHARMACOLOGY, 1982, 31 (03) :319-323
[3]  
CHOPRA IJ, 1979, J CLIN ENDOCR METAB, V49, P63, DOI 10.1210/jcem-49-1-63
[4]   SERUM FREE-THYROXINE IN THYROIDAL AND NON-THYROIDAL ILLNESSES - A COMPARISON OF MEASUREMENTS BY RADIOIMMUNOASSAY, EQUILIBRIUM DIALYSIS, AND FREE-THYROXINE INDEX [J].
CHOPRA, IJ ;
VANHERLE, AJ ;
TECO, GNC ;
NGUYEN, AH .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1980, 51 (01) :135-143
[5]   Clinical review 86 - Euthyroid sick syndrome: Is it a misnomer? [J].
Chopra, IJ .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1997, 82 (02) :329-334
[6]   SERUM THYROID-HORMONE BINDING INHIBITOR IN NONTHYROIDAL ILLNESSES [J].
CHOPRA, IJ ;
HUANG, TS ;
BEREDO, A ;
SOLOMON, DH ;
TECO, GNC .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1986, 35 (02) :152-159
[7]  
CHOPRA IJ, 1979, ANN MED, V98, P946
[8]  
CHRISTOFIDES ND, 1992, CLIN CHEM, V38, P11
[9]   FREE-THYROXINE ESTIMATES IN NON-THYROIDAL ILLNESS - COMPARISON OF 8 METHODS [J].
KAPTEIN, EM ;
MACINTYRE, SS ;
WEINER, JM ;
SPENCER, CA ;
NICOLOFF, JT .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1981, 52 (06) :1073-1077
[10]  
LIEWENDAHL K, 1984, CLIN CHEM, V30, P760