Classical pathway activity C3c, C4 and C1-inhibitor protein reference intervals determination in EDTA plasma

Author:

Lopez Benjamin1,Majerus Victoria2,Dubucquoi Sylvain1,Labalette Myriam1,Lefèvre Guillaume3,Launay David4,Rogeau Stéphanie1,Deleplancque Anne-Sophie2,Moitrot Emmanuelle2,Maanaoui Mehdi5,Joudinaud Romane2,Ledoult Emmanuel6,Bertier Nicolas2

Affiliation:

1. Department of Immunology, Lille University Hospital, Lille, France; Lille Inflammation Research International Center, University of Lille, Lille, France

2. Department of Immunology, Lille University Hospital, Lille, France

3. Department of Immunology, Lille University Hospital, Lille, France; Lille Inflammation Research International Center, University of Lille, Lille, France; Department of Internal Medicine and Clinical Immunology, Lille University Hospital, Lille, France

4. Lille Inflammation Research International Center, University of Lille, Lille, France; Department of Internal Medicine and Clinical Immunology, Lille University Hospital, Lille, France; National Reference Center for Angioedema (CREAK), Grenoble, France

5. Department of Immunology, Lille University Hospital, Lille, France; Department of Nephrology, Lille University Hospital, Lille, France

6. Department of Immunology, Lille University Hospital, Lille, France; Department of Internal Medicine and Clinical Immunology, Lille University Hospital, Lille, France

Abstract

Introduction: Reference intervals (RIs) for complement assays in EDTA plasma samples have not previously been published. The objectives of the present study were to validate and/or determine RIs for classical pathway (CP50) activity and C3c, C4 and C1 inhibitor protein (C1INH) assays and to assess the need for age-specific RIs in EDTA plasma. Materials and methods: We retrospectively evaluated a cohort of 387 patients attending our university hospital and known to be free of complement- modifying diseases. The need for age partitioning was assessed and RIs were calculated according to the CLSI protocol. Results: No need for age partitioning was evidenced for CP50 activity, C3c and C4 concentrations and RIs (90% CI) were calculated from the pooled data: 35.4 (33.1-37.2) to 76.3 (73.7-83.6) U/mL for CP50 activity, 0.80 (0.75-0.87) to 1.64 (1.59-1.72) g/L for C3c, and 0.12 (0.10-0.14) to 0.38 (0.36- 0.40) g/L for C4. Our results highlight a positive association between age and C1INH concentrations. We derived 3 age partitions (6 months to 30 years, 30-50 and > 50 years) and the related RIs: 0.20 (0.18-0.21) to 0.38 (0.36-0.40) g/L, 0.22 (0.20-0.24) to 0.39 (0.36-0.41) g/L and 0.25 (0.22-0.27) to 0.41 (0.40-0.43) g/L, respectively). Conclusions: The newly determined RIs for CP50 activity were higher than those provided by the manufacturer for EDTA plasma samples, whereas those for C3c and C4 RIs were similar to the values provided for serum samples. The C1INH concentration and activity were found to be associated with age and age-specific RIs are mandatory for this analyte.

Publisher

Croatian Society for Medical Biochemistry and Laboratory Medicine

Subject

Biochemistry (medical),Clinical Biochemistry

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