Home Analytical performance of the serum free light chain assay
Article
Licensed
Unlicensed Requires Authentication

Analytical performance of the serum free light chain assay

  • Pierre-Yves Briand , Olivier Decaux , Hélène Caillon , Bernard Grosbois , André Le Treut and Lucienne Guenet
Published/Copyright: November 25, 2009

Abstract

Background: The Freelite™ system for nephelometric or turbidimetric measurement of serum free light chains (FLCs) has been available since 2001. It has been valuable for the management of patients with oligosecretory myeloma, light chain myeloma and AL amyloidosis. However, there are several limitations of the method. The goal of this study was to evaluate the analytical performance of the FLC assay.

Methods: Titrated controls and clinical serum specimens were used to determine precision and post-dilution recovery.

Results: As reported elsewhere, we found that the assay had several limitations, including poor post-dilution linearity and overestimation by nephelometry.

Conclusions: These data demonstrate that the results of the FLC assay must be interpreted jointly by the clinician and the biologist, taking into account the individual patient's clinical and biological characteristics.

Clin Chem Lab Med 2010;48:73–9.


Corresponding author: Pierre-Yves Briand, Laboratoire de Biochimie Générale et Enzymologie, 2 rue Henri Le Guilloux, 35033 Rennes Cedex 9, France

Received: 2009-4-4
Accepted: 2009-9-8
Published Online: 2009-11-25
Published in Print: 2010-01-01

©2010 by Walter de Gruyter Berlin New York

Articles in the same Issue

  1. Editorials
  2. Rapid diagnosis of swine-origin influenza A (H1N1) virus (S-OIV): useful or hype?
  3. Application of traceability concepts to analytical quality control may reconcile total error with uncertainty of measurement
  4. Reviews
  5. Pandemic influenza A (H1N1) 2009: the experience of the first six months
  6. The role of anti-core antibody response in the detection of occult hepatitis B virus infection
  7. Opinion Papers
  8. Managing quality vs. measuring uncertainty in the medical laboratory
  9. Collective opinion paper on findings of the 2009 convocation of experts on quality control
  10. General Clinical Chemistry and Laboratory Medicine
  11. Diagnostic performance of rapid influenza antigen assays in patients infected with the new influenza A (H1N1) virus
  12. Achieving continuous improvement in laboratory organization through performance measurements: a seven-year experience
  13. Evaluation of errors in a clinical laboratory: a one-year experience
  14. Validation and Outcome Studies
  15. Analytical validation of serum bone alkaline phosphatase (BAP OSTASE) on Liaison
  16. Analytical performance of the serum free light chain assay
  17. A study on the stability of urinary free catecholamines and free methyl-derivatives at different pH, temperature and time of storage
  18. Plasma nitrite/nitrate concentrations in patients with schizophrenia
  19. Inverse relationship between serum high density lipoprotein and negative syndrome in antipsychotic-naive schizophrenia
  20. Reference Values and Biological Variations
  21. Biological variation of free plasma amino acids in healthy individuals
  22. Differences in serum potassium concentrations between Chinese, Indians and Malays
  23. Determination of median levels of the free β subunit of human chorionic gonadotropin in women from mainland China using a new time-resolved fluoroimmunoassay
  24. Age- and gender-specific reference ranges for serum insulin-like growth factor I (IGF-I) and IGF-binding protein-3 concentrations on the Immulite 2500: results of the Study of Health in Pomerania (SHIP)
  25. Cardiovascular Diseases
  26. Improvement of the cardiac marker N-terminal-pro brain natriuretic peptide through adjustment for renal function: a stratified multicenter trial
  27. Plasma homocysteine, apolipoprotein E status and vascular disease in elderly patients with mental illness
  28. Letters to the Editor
  29. Serum total and free sialic acid in patients with chronic liver disease
  30. Measurement of nitrotyrosine in plasma by immunoassays is fraught with danger: commercial availability is no guarantee of analytical reliability
  31. Problems with the determination of nitrotyrosine in human plasma are not solved in a satisfactory way and conclusions from clinical trials need to be carefully revised
Downloaded on 6.9.2025 from https://www.degruyterbrill.com/document/doi/10.1515/CCLM.2010.012/pdf
Scroll to top button