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Clinical Chemistry and Laboratory Medicine (CCLM)

Published in Association with the European Federation of Clinical Chemistry and Laboratory Medicine (EFLM)

Editor-in-Chief: Plebani, Mario

Ed. by Gillery, Philippe / Greaves, Ronda / Lackner, Karl J. / Lippi, Giuseppe / Melichar, Bohuslav / Payne, Deborah A. / Schlattmann, Peter


IMPACT FACTOR 2018: 3.638

CiteScore 2018: 2.44

SCImago Journal Rank (SJR) 2018: 1.191
Source Normalized Impact per Paper (SNIP) 2018: 1.205

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1437-4331
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Volume 40, Issue 1

Issues

Approved IFCC Reference Method for the Measurement of HbA1c in Human Blood

Jan-Olof Jeppsson / Uwe Kobold / John Barr / Andreas Finke / Wieland Hoelzel / Tadao Hoshino / Kor Miedema / Andrea Mosca / Pierluigi Mauri / Rita Paroni / Linda Thienpont / Masao Umemoto / Cas Weykamp
Published Online: 2005-06-01 | DOI: https://doi.org/10.1515/CCLM.2002.016

Abstract

HbA1c is the stable glucose adduct to the N-terminal group of the β-chain of HbA0. The measurement of HbA1c in human blood is most important for the long-term control of the glycaemic state in diabetic patients. Because there was no internationally agreed reference method the IFCC Working Group on HbA1c Standardization developed a reference method which is here described. In a first step haemoglobin is cleaved into peptides by the enzyme endoproteinase Glu-C, and in a second step the glycated and non-glycated N-terminal hexapeptides of the β-chain obtained are separated and quantified by HPLC and electrospray ionisation mass spectrometry or in a two-dimensional approach using HPLC and capillary electrophoresis with UV-detection. Both principles give identical results. HbA1c is measured as ratio between the glycated and non-glycated hexapeptides. Calibrators consisting of mixtures of highly purified HbA1c and HbA0 are used. The analytical performance of the reference method has been evaluated by an international network of reference laboratories comprising laboratories from Europe, Japan and the USA. The intercomparison studies of the network showed excellent results with intra-laboratory CVs of 0.5 to 2% and inter-laboratory CVs of 1.4 to 2.3%. Possible interferences have been carefully investigated. Due to the higher specificity of the reference method the results are lower than those generated with most of the present commercial methods which currently are calibrated with unspecific designated comparison methods. The new reference method has been approved by the member societies of the International Federation of Clinical Chemistry and Laboratory Medicine and will be the basis for the future uniform standardization of HbA1c routine assays worldwide.

About the article

Published Online: 2005-06-01

Published in Print: 2002-01-29


Citation Information: Clinical Chemistry and Laboratory Medicine, Volume 40, Issue 1, Pages 78–89, ISSN (Print) 1434-6621, DOI: https://doi.org/10.1515/CCLM.2002.016.

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