Literature DB >> 21919067

γ/IgG ratio: role in distinguishing monoclonal spikes from fibrinogen.

Maria Teresa Lee1, Patrizio Caturegli, Richard L Humphrey, Richard E Thompson, Barbara Detrick.   

Abstract

Serum protein electrophoresis (SPEP) is a standard screening method for detecting monoclonal gammopathies. Presence of fibrinogen, however, can mimic a true monoclonal spike and interfere with accurate monoclonal protein identification. We describe a novel approach for distinguishing fibrinogen spikes from true monoclonal spikes. We classified 600 individual patient samples into four groups: group 1, 58 samples with a fibrinogen spike; group 2, 127 samples with a spike due to a monoclonal gammopathy; group 3, 181 samples with previously established monoclonal gammopathies but resolved posttreatment; and group 4, 234 control samples without monoclonal gammopathies. The value of using a γ region fraction/IgG ratio in distinguishing fibrinogen from true monoclonal spikes was assessed. The γ/IgG ratio in the fibrinogen group is significantly (P<0.0001) higher than this ratio in the other three groups. A γ/IgG ratio cut-off value of 1.13 discriminates true monoclonal gammopathies from fibrinogen. Moreover, exclusion of elevated IgA or IgM cases improves the ratio's predictive power. The probability cut-off is 0.756, corresponding to a γ/IgG ratio of 1 (93% sensitivity, 91% specificity). Using the γ/IgG ratio improves the screening power of SPEP and offers a simple and reliable diagnostic tool for distinguishing fibrinogen spikes from true monoclonal spikes.
© 2011 Wiley-Liss, Inc.

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Year:  2011        PMID: 21919067      PMCID: PMC6647624          DOI: 10.1002/jcla.20480

Source DB:  PubMed          Journal:  J Clin Lab Anal        ISSN: 0887-8013            Impact factor:   2.352


  9 in total

1.  The incidence and significance of pseudoparaproteins in a community hospital.

Authors:  S L Strobel
Journal:  Ann Clin Lab Sci       Date:  2000-07       Impact factor: 1.256

2.  Serum protein electrophoresis: reptilase treatment is superior to ethanol precipitation for specific removal of fibrinogen from heparinized plasma samples.

Authors:  Youssef Ibrahim; Martin Volkmann; Racha Hassoun; Walter Fiehn; Heidi Rossmann
Journal:  Clin Chem       Date:  2004-06       Impact factor: 8.327

3.  Ethanol precipitation is not reliable for selectively removing nonmonoclonal peaks seen in the fibrinogen region on capillary zone electrophoresis of serum proteins.

Authors:  Koenraad Gijbels; Godelieve Mariën; Xavier Bossuyt
Journal:  Clin Chem       Date:  2004-10       Impact factor: 8.327

4.  Can lithium-heparin plasma be used for protein electrophoresis and paraprotein identification?

Authors:  Andrew S Davison; Simon M Darn; Ravinder Sodi
Journal:  Ann Clin Biochem       Date:  2006-01       Impact factor: 2.057

Review 5.  Understanding and interpreting serum protein electrophoresis.

Authors:  Theodore X O'Connell; Timothy J Horita; Barsam Kasravi
Journal:  Am Fam Physician       Date:  2005-01-01       Impact factor: 3.292

6.  Protamine sulphate used in combination with thrombin to remove fibrinogen prior to electrophoresis of heparinised plasma.

Authors:  E Wright; M Briscoe; P McGing; S Maguire
Journal:  Br J Biomed Sci       Date:  1997-06       Impact factor: 3.829

7.  Identification of a spurious band on serum protein electrophoresis induced by ethanol treatment.

Authors:  Yusheng Zhu; Ronald J Elin
Journal:  Clin Chim Acta       Date:  2005-12-06       Impact factor: 3.786

8.  [The use of reptilase for electrophoresis of heparinized plasma (author's transl)].

Authors:  D Heimann; V Wolf; H Keller
Journal:  J Clin Chem Clin Biochem       Date:  1979-06

9.  Convenient and effective method for removing fibrinogen from serum specimens before protein electrophoresis.

Authors:  Ling L Qiu; Stanley S Levinson; Kristen L Keeling; Ronald J Elin
Journal:  Clin Chem       Date:  2003-06       Impact factor: 8.327

  9 in total

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