Determination of carbohydrate-deficient transferrin in human serum using the Bio-Rad %CDT by HPLC test

被引:38
作者
Helander, Anders
Bergstrom, Jonas P.
机构
[1] Karolinska Univ Hosp, Alcohol Lab, SE-17176 Stockholm, Sweden
[2] Karolinska Inst, Dept Clin Neurosci, Stockholm, Sweden
关键词
alcohol biomarker; carbohydrate-deficient transferrin; CDT; HPLC; serum; PERFORMANCE LIQUID-CHROMATOGRAPHY; ALCOHOL-ABUSE; CAPILLARY-ELECTROPHORESIS; CONSUMPTION; MARKER; QUANTIFICATION; IDENTIFICATION; IMMUNOASSAY;
D O I
10.1016/j.cca.2006.03.010
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background: Carbohydrate-deficient transferrin (CDT) in serum is a biomarker used to identify individuals with sustained, heavy alcohol consumption. This study evaluated the performance of a new commercial method for CDT, the Bio-Rad %CDT by HPLC test, that measures relative amounts of separate transferrin glycoforms in proportion to total transferrin. Method: The samples used were two human serum pools (low/high disialotransferrin), 150 clinical sera with low to highly elevated disialotransferrin values, and 18 genetic transferrin variants. Glycoforms are separated on a gradient HPLC system, followed by specific measurement of the iron-transferrin complex at 460 nm. Comparison was made with an HPLC candidate reference method on an Agilent 1100 LC system. Results: The Bio-Rad %CDT by HPLC test allowed for reproducible separation and quantification of the transferrin glycoforms within similar to 6 min. Genetic variants were readily identified. For the low and high serum pool, the total CV was 8.5% and 4.3%, respectively. The relative amounts of disialotransferrin, the main CDT glycoform, were in good agreement with the results of the HPLC candidate reference method (r(2)=0.998, p < 0.0001). Conclusions: The present results demonstrated that the Bio-Rad %CDT by HPLC test is appropriate for confirmatory and routine %CDT testing in human serum, with the added advantage over previously published HPLC methods of an improved serum sample pretreatment and a shorter total analysis time. (c) 2006 Elsevier B.V All rights reserved.
引用
收藏
页码:187 / 190
页数:4
相关论文
共 24 条
[1]  
[Anonymous], 1998, LAKARTIDNINGEN
[2]   Asia lotransferrin - An alternative to carbohydrate-deficient transferrin? [J].
Arndt, T .
CLINICAL CHEMISTRY, 2003, 49 (06) :1022-1023
[3]  
Arndt T, 2001, CLIN CHEM, V47, P13
[4]   The carbohydrate-deficient transferrin test in hospital practice [J].
Batey, RG ;
Madsen, G .
DRUG AND ALCOHOL REVIEW, 1998, 17 (01) :105-109
[5]  
Bean P, 1997, CLIN CHEM, V43, P983
[6]  
Helander A, 2003, J NEURAL TRANSM-SUPP, P15
[7]   Comparison of HPLC and capillary electrophoresis for confirmatory testing of the alcohol misuse marker carbohydrate-deficient transferrin [J].
Helander, A ;
Wielders, JPM ;
te Stroet, R ;
Bergström, JP .
CLINICAL CHEMISTRY, 2005, 51 (08) :1528-1531
[8]   Improved HPLC method for carbohydrate-deficient transferrin in serum [J].
Helander, A ;
Husa, A ;
Jeppsson, JO .
CLINICAL CHEMISTRY, 2003, 49 (11) :1881-1890
[9]   Study of axis-shield new %CDT immunoassay for quantification of carbohydrate-deficient transferrin (CDT) in serum [J].
Helander, A ;
Fors, M ;
Zakrisson, B .
ALCOHOL AND ALCOHOLISM, 2001, 36 (05) :406-412
[10]  
Helander A, 2001, CLIN CHEM, V47, P1225