Commutability Assessment of Candidate Reference Materials for Pancreatic α-Amylase

Author:

Deprez Liesbet1,Toussaint Brigitte1,Zegers Ingrid1,Schimmel Heinz1,Grote-Koska Denis2,Klauke Rainer2,Gella F Javier3,Orth Matthias45,Lessinger Jean-Marc6,Trenti Tommaso7,Nilsson Göran8,Ceriotti Ferruccio9

Affiliation:

1. European Commission's Joint Research Centre (JRC), Geel, Belgium

2. Medizinische Hochschule Hannover, Institut für Klinische Chemie, Hannover, Germany

3. Biosystems S.A., Barcelona, Spain

4. Vinzenz von Paul Kliniken gGmbH, Institut für Laboratoriumsmedizin, Stuttgart, Germany

5. Ruprecht Karls Universität, Medizinische Fakultät Mannheim, Mannheim, Germany

6. Laboratory of Biochemistry and Molecular Biology, Hôpitaux Universitaires de Strasbourg, Strasbourg, France

7. Department of Laboratory Medicine and Pathology, Ospedale S. Agostino Estense, Modena, Italy

8. Retired, Uppsala, Sweden

9. Clinical Laboratory, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy

Abstract

Abstract BACKGROUND Measurement standardization of the catalytic concentration of α-amylase in serum is based on 3 pillars: the primary reference measurement procedure (PRMP), reference laboratories, and suitable certified reference materials (CRMs). Commutability is a prerequisite when using a CRM for calibration and trueness control of routine methods or for value transfer from the PRMP to end-user calibrators of routine methods through a calibration hierarchy. METHODS We performed a commutability study with 30 serum pools and 5 candidate reference materials (RMs) for pancreatic α-amylase using an automated version of the PRMP and 5 different routine methods. Four candidate RMs had an artificial matrix, each with a different composition, and 1 candidate RM was based on human serum. Data were analyzed according to a linear regression analysis with prediction interval as described in the Clinical and Laboratory Standards Institute guideline EP30-A and a difference in bias analysis as described in the recommendations of the IFCC Working Group on Commutability. RESULTS The commutability profile of the 4 candidate RMs with an artificial matrix was variable. Only 1 candidate RM, with human serum albumin in the matrix, showed a good profile like that of the candidate RM based on serum. The comparison of both commutability assessment approaches indicated some differences because of inconclusive results for the difference in bias approach, suggesting a large uncertainty on the commutability assessment. CONCLUSIONS A CRM for pancreatic amylase in an artificial matrix can be commutable for routine methods using the same substrate as the PRMP, but the matrix composition is crucial.

Publisher

Oxford University Press (OUP)

Subject

Biochemistry, medical,Clinical Biochemistry

Reference19 articles.

1. American College of Gastroenterology guideline: management of acute pancreatitis;Tenner;Am J Gastroenterol,2013

2. Role of amylase and lipase levels in diagnosis of blunt trauma abdomen;Singh;J Clin Diagn Res,2016

3. A category 1 EQA scheme for comparison of laboratory performance and method performance: an international pilot study in the framework of the Calibration 2000 project;Jansen;Clin Chim Acta,2014

4. Trueness verification and traceability assessment of results from commercial systems for measurement of six enzyme activities in serum;Jansen;Clin Chim Acta,2006

5. In vitro diagnostic medical devices—measurement of quantities in biological samples—metrological traceability of values assigned to calibrators and control materials;ISO 17511:2003,2003

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