Literature DB >> 29573337

Flow cytometric osmotic fragility test and eosin-5'-maleimide dye-binding tests are better than conventional osmotic fragility tests for the diagnosis of hereditary spherocytosis.

R D Arora1, J Dass1, S Maydeo1, V Arya1, N Radhakrishnan2, A Sachdeva2, J Kotwal1, M Bhargava1.   

Abstract

INTRODUCTION: Hereditary spherocytosis (HS) is the most common inherited hemolytic anemia with heterogeneous clinico-laboratory manifestations. We evaluated the flow-cytometric tests: eosin-5'-maleimide (EMA) and flow-cytometric osmotic fragility test (FOFT) and the conventional osmotic fragility tests (OFT) for the diagnosis of hereditary spherocytosis (HS).
METHODS: One hundred two suspected HS patients underwent EMA, FOFT, incubated OFT (IOFT), and room temperature OFT (RT-OFT). In addition, 10 cases of immune hemolytic anemia (IHA) were included, and performance of the above 4 tests was evaluated. For EMA and FOFT, 5 normal controls were assessed together with the patients and cutoffs were calculated using receiver-operator-characteristics curve (ROC) analysis.
RESULTS: The best cutoff for %EMA decrease was 12.5%, and for FOFT, %residual red cells (%RRC) was 25.6%. The sensitivity and specificity of RT-OFT was 62.06% and 86.3%, respectively, while that of IOFT was 79.31% and 87.67%, respectively. Both flow cytometric tests performed better. Sensitivity and specificity of EMA was 86.2% and 93.9% respectively, and that of FOFT was 96.6% and 98.63%, respectively. The combination of the FOFT with IOFT or EMA dye-binding test yields a sensitivity of 100%, but with EMA, it had a higher specificity. Hb/MCHC was a predictor of the severity of the disease while %EMA decrease and %RRC did not correlate with severity of the disease.
CONCLUSION: Flow-cytometric osmotic fragility test is the best possible single test followed by EMA for diagnosis of HS. A combination of FOFT and EMA can correctly diagnose 100% patients. These tests are likely to replace conventional OFTs in future.
© 2018 John Wiley & Sons Ltd.

Entities:  

Keywords:  % eosin-5’-maleimide decrease; % residual red cells; Hereditary spherocytosis; eosin-5’-maleimide; flow cytometric; flow osmotic fragility tests

Mesh:

Substances:

Year:  2018        PMID: 29573337     DOI: 10.1111/ijlh.12794

Source DB:  PubMed          Journal:  Int J Lab Hematol        ISSN: 1751-5521            Impact factor:   2.877


  6 in total

Review 1.  Korean clinical practice guidelines for the diagnosis of hereditary hemolytic anemia.

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2.  Facilitating EMA binding test performance using fluorescent beads combined with next-generation sequencing.

Authors:  Andreas Glenthøj; Christian Brieghel; Amina Nardo-Marino; Richard van Wijk; Henrik Birgens; Jesper Petersen
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Journal:  Cancers (Basel)       Date:  2022-05-31       Impact factor: 6.575

Review 4.  Old and new insights into the diagnosis of hereditary spherocytosis.

Authors:  Olga Ciepiela
Journal:  Ann Transl Med       Date:  2018-09

5.  The effects of incubation media on the assessment of the shape of human erythrocytes by flow cytometry: a contribution to mathematical data interpretation to enable wider application of the method.

Authors:  Ivana Drvenica; Slavko Mojsilović; Ana Stančić; Dragana Marković; Marijana Kovačić; Irina Maslovarić; Ivana Rapajić; Dušan Vučetić; Vesna Ilić
Journal:  Eur Biophys J       Date:  2021-04-04       Impact factor: 1.733

6.  Clinical and genetic diagnosis of thirteen Japanese patients with hereditary spherocytosis.

Authors:  Keiko Shimojima Yamamoto; Taiju Utshigisawa; Hiromi Ogura; Takako Aoki; Takahiro Kawakami; Shoichi Ohga; Akira Ohara; Etsuro Ito; Toshiyuki Yamamoto; Hitoshi Kanno
Journal:  Hum Genome Var       Date:  2022-01-12
  6 in total

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