Rapid haemoglobin A and S quantification using Tosoh HLC‐723G8 in variant mode for patients with sickle cell disease

Author:

Fadel Julien1ORCID,Noyelle Juliette1,Maingon Mathieu1,Homedan Chadi1,Dieu Xavier12,de la Barca Juan Manuel Chao12,Reynier Pascal12,Mallebranche Coralie3,Brasme Jean‐François3,Mirebeau‐Prunier Delphine12,Orvain Corentin4,Chabrun Floris12ORCID

Affiliation:

1. Laboratory of Biochemistry and Molecular Biology University Hospital of Angers Angers France

2. Mitolab, Mitovasc, Mixed Research Unit (UMR) Inserm U1083, CNRS 6015 University of Angers Angers France

3. Department of Paediatric Haematology, Oncology and Immunology University Hospital of Angers Angers France

4. Department of Clinical Haematology University Hospital of Angers Angers France

Abstract

AbstractThe management of life‐threatening complications in patients with sickle cell disease (SCD) requires an accurate and reproducible quantification of haemoglobin A (HbA) and S (HbS) with a short turnaround time and 24‐7 availability. We propose a novel method for quantifying HbA and HbS using the glycated haemoglobin (HbA1c) assay on a Tosoh HLC‐723G8 (G8) analyser in variant mode. HbA and HbS results obtained using our method highly correlated with results obtained using a reference method (r > 0.99 for 124 samples of patients with SCD or sickle cell trait). Our method met laboratory requirements for linearity (coefficient of variation [CV] and bias <5%), between‐run and within‐run reproducibility (CV <10%) and carryover (<0.5%) over the range of HbS and HbA values expected in a therapeutic context. Using the G8 analyser in variant mode is viable for monitoring HbA and HbS concentrations in dire situations. This method is easy to use, quick (1.6 min per sample), and automatable and produces highly reproducible results without significant bias. Finally, it does not require modifications to the analytical pipeline recommended by the supplier, enabling a 24‐7 availability without disrupting routine monitoring of HbA1c in the laboratory.

Publisher

Wiley

Subject

Clinical Biochemistry,Drug Discovery,Pharmacology,Molecular Biology,General Medicine,Biochemistry,Analytical Chemistry

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