Startseite Comparison of Freelite™ and N Latex serum free light chain assays in subjects with end stage kidney disease on haemodialysis
Artikel
Lizenziert
Nicht lizenziert Erfordert eine Authentifizierung

Comparison of Freelite™ and N Latex serum free light chain assays in subjects with end stage kidney disease on haemodialysis

  • Alice Kennard , Carmel Hawley , Jill Tate , Sandra Klingberg , Carel Pretorius , Colin Hutchison und Peter Mollee EMAIL logo
Veröffentlicht/Copyright: 18. Dezember 2015
Veröffentlichen auch Sie bei De Gruyter Brill

Abstract

Background: Quantification of serum free light chains (FLC) is important in the diagnosis of plasma cell diseases where an abnormal kappa:lambda ratio infers a population of monoclonal plasma cells. The Freelite™ and N Latex assays have been validated in populations without kidney disease but there is a paucity of data relating to the use of these assays in end stage kidney disease (ESKD). The aim of the study was to compare FLC assay performance in ESKD patients on haemodialysis.

Methods: Cross-sectional multi-centre study comparing the performance of the two assays on 112 haemodialysis patients without known paraproteinaemia. We quantified FLC pre- and post-dialysis using both the N Latex and the Freelite assays.

Results: FLC levels were elevated by both assays. Lambda FLC levels were considerably higher by the N Latex assay. Using the proposed renal reference range for Freelite (0.37–3.1) all but one patient had normal kappa:lambda FLC ratios. In contrast, there were no abnormal FLC ratios pre-dialysis using the N Latex assay. This was due to lambda FLC reading significantly higher by the N Latex assay. Kappa and lambda FLC levels decreased with dialysis but remained elevated above the normal range. The excess of lambda FLC by N Latex persisted post-dialysis but was somewhat attenuated. Dialysis adequacy and dialysis modality predicted clearance of kappa and lambda FLC by both assays.

Conclusions: The N Latex assay reported significantly higher pre-dialysis lambda FLC concentrations compared with the Freelite assays. Clinicians should be aware of the need for a separate renal reference range for interpreting FLC ratio using the Freelite assay but not for the N Latex assay in ESKD patients.


Corresponding author: Dr. Peter Mollee, Department of Haematology, Pathology Queensland, Princess Alexandra Hospital, Ipswich Road, Woolloongabba, Brisbane, Qld 4102, Australia, Phone: +61 7 3176 5080, Fax: +61 7 3176 5480

Acknowledgments

We thank Siemens Healthcare Diagnostics for providing N Latex free light chain reagents.

Author contributions: All the authors have accepted responsibility for the entire content of this submitted manuscript and approved submission.

Research funding: None declared.

Employment or leadership: JT is a member of the editorial board of CCLM.

Honorarium: None declared.

Competing interests: The funding organisation(s) played no role in the study design; in the collection, analysis, and interpretation of data; in the writing of the report; or in the decision to submit the report for publication.

References

1. Bradwell, AR, editor. Serum free light chain analysis, 5th ed. Birmingham: The Binding Site Ltd, 2008:167–73.Suche in Google Scholar

2. Abraham RS, Katzmann JA, Clark RJ, Bradwell AR, Kyle RA, Gertz MA. Quantitative analysis of serum free light chains. A new marker for the diagnostic evaluation of primary systemic amyloidosis. Am J Clin Pathol 2003;119:274–8.10.1309/LYWM47K2L8XYFFB3Suche in Google Scholar

3. Drayson M, Tang LX, Drew R, Mead GP, Carr-Smith H, Bradwell AR. Serum free light-chain measurements for identifying and monitoring patients with nonsecretory multiple myeloma. Blood 2001;97:2900–2.10.1182/blood.V97.9.2900Suche in Google Scholar PubMed

4. Dispenzieri A, Kyle R, Merlini G, Miguel JS, Ludwig H, Hajek R, et al. International Myeloma Working Group. International Myeloma Working Group guidelines for serum-free light chain analysis in multiple myeloma and related disorders. Leukemia 2009;23:215–24.10.1038/leu.2008.307Suche in Google Scholar PubMed

5. Hoedemakers RM, Pruijt JF, Hol S, Teunissen E, Martens H, Stam P, et al. Clinical comparison of new monoclonal antibody-based nephelometric assays for free light chain kappa and lambda to polyclonal antibody-based assays and immunofixation electrophoresis. Clin Chem Lab Med 2011:50:489–95.10.1515/cclm.2011.793Suche in Google Scholar PubMed

6. Hutchison CA, Plant T, Drayson M, Cockwell P, Kountouri M, Basnayake K, et al. Serum free light chain measurement aids the diagnosis of myeloma in patients with severe renal failure. BMC Nephrol 2008;9:11.10.1186/1471-2369-9-11Suche in Google Scholar PubMed PubMed Central

7. Hutchison CA, Harding S, Hewins P, Mead GP, Townsend J, Bradwell AR, et al. Quantitative assessment of serum and urinary polyclonal free light chains in patients with chronic kidney disease. Clin J Am Soc Nephrol 2008;3:1684–90.10.2215/CJN.02290508Suche in Google Scholar PubMed PubMed Central

8. Jacobs JF, Hoedemakers RM, Teunissen E, Te Velthuis H. N Latex FLC serum free light-chain assays in patients with renal impairment. Clin Chem Lab Med 2014;52:853–9.10.1515/cclm-2013-0864Suche in Google Scholar PubMed

9. Tate J, Bazeley S, Klinberg S, Pretorius CJ, Hawley C, Mollee P. Comparison of the Freelite and N Latex srum free light chain (FLC) assays in chronic kidney disease [abstract]. Clin Biochem Rev 2012;33:S41.Suche in Google Scholar

10. Data from manufacturer’s dialyser data sheets. www.fmc-ag.com, www.nipro.com, www.baxter.com.Suche in Google Scholar

11. Jenner W, Klingberg S, Tate JR, Wilgen U, Ungerer JP, Pretorius CJ. Combined light chain immunofixation to detect monoclonal gammopathy: a comparison to standard electrophoresis in serum and urine. Clin Chem Lab Med 2014;52:981–7.10.1515/cclm-2014-0023Suche in Google Scholar PubMed

12. MedCalc for Windows v. 15.2.2 (2015). www.medcalc.org.Suche in Google Scholar

13. Lavatelli F, Brambilla F, Valentini V, Rognoni P, Casarini S, Di Silvestre D, et al. A novel approach for the purification and proteomic analysis of pathogenic immunoglobulin free light chains from serum. Biochim Biophys Acta 2011;1814:409–19.10.1016/j.bbapap.2010.12.012Suche in Google Scholar PubMed

14. Hutchison CA, Cockwell P, Reid S, Chandler K, Mead GP, Harrison J, et al. Efficient removal of immunoglobulin free light chains by hemodialysis for multiple myeloma: in vitro and in vivo studies. Clin J Am Soc Nephrol 2007;18:886–95.10.1182/blood.V108.11.5112.5112Suche in Google Scholar

15. Hutchison CA, Basnayake K, Cockwell P. Serum free light chain assessment in monoclonal gammopathy and kidney disease. Nat Rev Nephrol 2009;11:621–8.10.1038/nrneph.2009.151Suche in Google Scholar PubMed

16. Berlanga O, Carr-Smith H, Harding S. Response to Jacobs: N Latex FLC serum free light-chain assays in patients with renal impairment. Clin Chem Lab Med 2014;52:e243–5.10.1515/cclm-2014-0420Suche in Google Scholar PubMed


Supplemental Material:

The online version of this article (DOI: 10.1515/cclm-2015-0799) offers supplementary material, available to authorised users.


Received: 2015-8-19
Accepted: 2015-11-9
Published Online: 2015-12-18
Published in Print: 2016-6-1

©2016 by De Gruyter

Artikel in diesem Heft

  1. Frontmatter
  2. Editorial
  3. Protein electrophoresis and serum free light chains in the diagnosis and monitoring of plasma cell disorders: laboratory testing and current controversies
  4. Laboratory Testing as Recommended by the Guidelines and the International Myeloma Working Group
  5. Laboratory testing requirements for diagnosis and follow-up of multiple myeloma and related plasma cell dyscrasias
  6. Free light chain testing for the diagnosis, monitoring and prognostication of AL amyloidosis
  7. Laboratory testing in monoclonal gammopathy of renal significance (MGRS)
  8. The impact of renal function on the clinical performance of FLC measurement in AL amyloidosis
  9. Serum and Urine Protein Electrophoresis and Immunofixation Testing
  10. Challenges of measuring monoclonal proteins in serum
  11. Screening immunofixation should replace protein electrophoresis as the initial investigation of monoclonal gammopathy: Point
  12. Should routine laboratories stop doing screening serum protein electrophoresis and replace it with screening immune-fixation electrophoresis? No quick fixes: Counterpoint
  13. Moving towards harmonized reporting of serum and urine protein electrophoresis
  14. Multiple qualitative and quantitative methods for free light chain analysis are necessary as first line tests for AL amyloidosis
  15. Use of isoelectric focusing to discriminate transient oligoclonal bands from monoclonal protein in treated myeloma
  16. New patterns of relapse in multiple myeloma: a case of “light chain escape” in which FLC predicted relapse earlier than urine and serum immunofixation
  17. Serum Free Light Chain Methods and Controversies
  18. Analytical issues of serum free light chain assays and the relative performance of polyclonal and monoclonal based reagents
  19. Measurement of free light chains with assays based on monoclonal antibodies
  20. Measurement of free light chains – pros and cons of current methods
  21. Is accuracy of serum free light chain measurement achievable?
  22. Performance goals for immunoglobulins and serum free light chain measurements in plasma cell dyscrasias can be based on biological variation
  23. A patient with AL amyloidosis with negative free light chain results
  24. Strengths and weaknesses of methods for identifying monoclonal free light chains of Ig: examples from two cases with renal disease
  25. Comparison of Freelite™ and N Latex serum free light chain assays in subjects with end stage kidney disease on haemodialysis
  26. New Laboratory Assays and Challenges
  27. Quantification of β-region IgA monoclonal proteins – should we include immunochemical Hevylite® measurements? Point
  28. Quantification of β region IgA paraproteins – should we include immunochemical “heavy/light chain” measurements? Counterpoint
  29. Free light chains and heavy/light chains in monitoring POEMS patients
  30. Monitoring free light chains in serum using mass spectrometry
  31. Monoclonal antibody therapeutics as potential interferences on protein electrophoresis and immunofixation
  32. Monitoring multiple myeloma patients treated with daratumumab: teasing out monoclonal antibody interference
  33. Interference of daratumumab in monitoring multiple myeloma patients using serum immunofixation electrophoresis can be abrogated using the daratumumab IFE reflex assay (DIRA)
  34. Letter to the Editor
  35. Discrepancy between FLC assays: only a problem of quantification?
Heruntergeladen am 8.9.2025 von https://www.degruyterbrill.com/document/doi/10.1515/cclm-2015-0799/pdf
Button zum nach oben scrollen