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Clinical Chemistry 39: 2115-2120, 1993;
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Clinical Chemistry, Vol 39, 2115-2120, Copyright © 1993 by American Association for Clinical Chemistry

Carbohydrate-deficient transferrin quantified by HPLC to determine heavy consumption of alcohol

JO Jeppsson, H Kristensson and C Fimiani
Department of Clinical Chemistry, University Hospital, Malmo, Sweden.

We developed a new fully automated ion-exchange chromatographic method for quantitating carbohydrate-deficient transferrin (CDT) on a Mono Q column. Quantitation relies on the selective absorbance of the iron- transferrin complex at 460 nm. Transferrin isoforms deficient in sialic acid, with pIs 5.7 and 5.9, can easily be separated and quantitated as a percentage of the total transferrin. This method has been applied to samples from teetotalers, occasional drinkers, patients with recent heavy alcohol consumption, and patients during detoxification. The sensitivity of the method was 55% in patients reporting 40-70 g daily ethanol consumption and nearly 100% in heavily intoxicated patients (70- 500 g daily consumption). The half-life of the dominating pI 5.7 isoform in this group was 9.5 (+/- 1) days during detoxification. A CDT value > 0.8% is a highly specific marker for alcohol abuse and is greatly superior to other currently available biological markers.


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A. Helander, J. P.M. Wielders, R. te Stroet, and J. P. Bergstrom
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F. J. Legros, V. Nuyens, E. Minet, P. Emonts, K. Z. Boudjeltia, A. Courbe, J.-L. Ruelle, J. Colicis, F. de L'Escaille, and J.-P. Henry
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U. Turpeinen, T. Methuen, H. Alfthan, K. Laitinen, M. Salaspuro, and U.-H. Stenman
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A. Helander, M. Fors, and B. Zakrisson
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A. Helander, G. Eriksson, H. Stibler, and J.-O. Jeppsson
Interference of Transferrin Isoform Types with Carbohydrate-deficient Transferrin Quantification in the Identification of Alcohol Abuse
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B. Wuyts, J. R. Delanghe, I. Kasvosve, A. Wauters, H. Neels, and J. Janssens
Determination of Carbohydrate-deficient Transferrin Using Capillary Zone Electrophoresis
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T. Arndt
Carbohydrate-deficient Transferrin as a Marker of Chronic Alcohol Abuse: A Critical Review of Preanalysis, Analysis, and Interpretation
Clin. Chem., January 1, 2001; 47(1): 13 - 27.
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L. Dibbelt
Does Trisialo-Transferrin Provide Valuable Information for the Laboratory Diagnosis of Chronically Increased Alcohol Consumption by Determination of Carbohydrate-deficient Transferrin?
Clin. Chem., August 1, 2000; 46(8): 1203 - 1205.
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R. Hackler, T. Arndt, A. Helwig-Rolig, J. Kropf, A. Steinmetz, and J. R. Schaefer
Investigation by Isoelectric Focusing of the Initial Carbohydrate-deficient Transferrin (CDT) and non-CDT Transferrin Isoform Fractionation Step Involved in Determination of CDT by the ChronAlcoI.D. Assay
Clin. Chem., April 1, 2000; 46(4): 483 - 492.
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A. Helander
Absolute or Relative Measurement of Carbohydrate-deficient Transferrin in Serum? Experiences with Three Immunological Assays
Clin. Chem., January 1, 1999; 45(1): 131 - 135.
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J. B. Whitfield, L. M. Fletcher, T. L. Murphy, L. W. Powell, J. Halliday, A. C. Heath, and N. G. Martin
Smoking, obesity, and hypertension alter the dose–response curve and test sensitivity of carbohydrate-deficient transferrin as a marker of alcohol intake
Clin. Chem., December 1, 1998; 44(12): 2480 - 2489.
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K. Viitala, K. Lahdesmaki, and O. Niemela
Comparison of the Axis %CDT TIA and the CDTect method as laboratory tests of alcohol abuse
Clin. Chem., June 1, 1998; 44(6): 1209 - 1215.
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T. Arndt, R. Hackler, T. O. Kleine, and A. M. Gressner
Validation by isoelectric focusing of the anion-exchange isotransferrin fractionation step involved in determination of carbohydrate-deficient transferrin by the CDTect assay
Clin. Chem., January 1, 1998; 44(1): 27 - 34.
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P. Bean, K. Liegmann, T. Lovli, C. Westby, and E. Sundrehagen
Semiautomated procedures for evaluation of carbohydrate-deficient transferrin in the diagnosis of alcohol abuse
Clin. Chem., June 1, 1997; 43(6): 983 - 989.
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F. Renner and R.-D. Kanitz
Quantification of carbohydrate-deficient transferrin by ion-exchange chromatography with an enzymatically prepared calibrator
Clin. Chem., March 1, 1997; 43(3): 485 - 490.
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