Literature DB >> 25357094

Evaluating eosin-5-maleimide binding as a diagnostic test for hereditary spherocytosis in newborn infants.

R D Christensen1, A M Agarwal2, R H Nussenzveig3, N Heikal2, M A Liew3, H M Yaish4.   

Abstract

OBJECTIVE: Neonates with undiagnosed hereditary spherocytosis (HS) are at risk for developing hazardous hyperbilirubinemia and anemia. Making an early diagnosis of HS in a neonate can prompt anticipatory guidance to prevent these adverse outcomes. A recent comparison study showed that a relatively new diagnostic test for HS, eosin-5-maleimide (EMA)-flow cytometry, performs better than other available tests in confirming HS. However, reports have not specifically examined the performance of this test among neonates. STUDY
DESIGN: We compared EMA-flow cytometry from blood samples of healthy control neonates vs samples from neonates suspected of having HS on the basis of severe Coombs-negative jaundice and spherocytes on blood film. The diagnosis of HS was later either confirmed or excluded based on clinical findings and next generation sequencing (NGS) after which we correlated the EMA-flow results with the diagnosis. RESULT: EMA-flow was performed on the blood of 31 neonates; 20 healthy term newborns and 11 who were suspected of having HS. Eight of the 11 were later confirmed positive for HS and one was confirmed positive for hereditary elliptocytosis (HE). All nine had persistently abnormal erythroid morphology, reticulocytosis and anemia, and eight of the nine had relevant mutations discovered using NGS. The other was confirmed positive for HS on the basis that a parent had HS, and the neonate's spherocytosis, reticulocytosis and anemia persisted. The 20 healthy controls and the 2 in whom HS was initially suspected but later excluded all had EMA-flow results in the range reported in healthy children and adults. In contrast, all nine in whom HS or HE was confirmed had abnormal EMA-flow results consistent with previous reports in older children and adults with HS.
CONCLUSION: Although our sample size is small, our findings are consistent with the literature in older children and adults suggesting that EMA-flow cytometric testing performs well in supporting the diagnosis of HS/HE during the early neonatal period.

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Year:  2014        PMID: 25357094     DOI: 10.1038/jp.2014.202

Source DB:  PubMed          Journal:  J Perinatol        ISSN: 0743-8346            Impact factor:   2.521


  32 in total

1.  A de novo band 3 mutation in hereditary spherocytosis.

Authors:  Hannah H Bogardus; Yelena D Maksimova; Bernard G Forget; Patrick G Gallagher
Journal:  Pediatr Blood Cancer       Date:  2011-12-13       Impact factor: 3.167

2.  A new ankyrin mutation (ANK1 EXON E9X) causing severe hereditary spherocytosis in the neonatal period.

Authors:  Florian Gundel; Stefan Eber; Axel Heep
Journal:  Ann Hematol       Date:  2010-05-30       Impact factor: 3.673

3.  Incidence of hereditary spherocytosis in a population of jaundiced neonates.

Authors:  Véronique Saada; Thérèse Cynober; Yves Brossard; Pierre Olivier Schischmanoff; Alfred Sender; Henri Cohen; Jean Delaunay; Gil Tchernia
Journal:  Pediatr Hematol Oncol       Date:  2006 Jul-Aug       Impact factor: 1.969

4.  Usefulness of the eosin-5'-maleimide cytometric method as a first-line screening test for the diagnosis of hereditary spherocytosis: comparison with ektacytometry and protein electrophoresis.

Authors:  François Girodon; Loïc Garçon; Emilie Bergoin; Marie Largier; Jean Delaunay; Madeleine Fénéant-Thibault; Marc Maynadié; Gérard Couillaud; Sophie Moreira; Thérèse Cynober
Journal:  Br J Haematol       Date:  2007-12-19       Impact factor: 6.998

5.  Delay in the measurement of eosin-5′-maleimide (EMA) binding does not affect the test result for the diagnosis of hereditary spherocytosis.

Authors:  Olga Ciepiela; Iwona Kotuła; Elżbieta Górska; Anna Stelmaszczyk-Emmel; Katarzyna Popko; Anna Szmydki-Baran; Anna Adamowicz-Salach; Urszula Demkow
Journal:  Clin Chem Lab Med       Date:  2013-04       Impact factor: 3.694

6.  Neonatal hemolytic jaundice: morphologic features of erythrocytes that will help you diagnose the underlying condition.

Authors:  Robert D Christensen; Hassan M Yaish; Richard S Lemons
Journal:  Neonatology       Date:  2014-02-08       Impact factor: 4.035

7.  Clinico-hematological profile of hereditary spherocytosis: experience from a tertiary care center in North India.

Authors:  Rakhee Kar; Seema Rao; Upendra M Srinivas; Pravas Mishra; Hara P Pati
Journal:  Hematology       Date:  2009-06       Impact factor: 2.269

8.  Ankyrin-linked hereditary spherocytosis in an African-American kindred.

Authors:  Jose Sangerman; Yelena Maksimova; E Jennifer Edelman; Jon S Morrow; Bernard G Forget; Patrick G Gallagher
Journal:  Am J Hematol       Date:  2008-10       Impact factor: 10.047

9.  Rapid flow cytometric test using eosin-5-maleimide for diagnosis of red blood cell membrane disorders.

Authors:  Kalaya Tachavanich; Voravarn S Tanphaichitr; Wiyakan Utto; Vip Viprakasit
Journal:  Southeast Asian J Trop Med Public Health       Date:  2009-05       Impact factor: 0.267

10.  Hereditary spherocytosis diagnosed with the eosin-5'-maleimide binding test.

Authors:  Toru Watanabe; Hiroyuki Ono; Iwao Tajima; Hidetoshi Ishigaki; Akio Hakamata; Masami Shirai; Akira Endoh; Teruaki Hongo
Journal:  Pediatr Int       Date:  2014-06       Impact factor: 1.524

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  7 in total

Review 1.  A pediatrician's practical guide to diagnosing and treating hereditary spherocytosis in neonates.

Authors:  Robert D Christensen; Hassan M Yaish; Patrick G Gallagher
Journal:  Pediatrics       Date:  2015-06       Impact factor: 7.124

2.  Rapid Identification of Biallelic SPTB Mutation in a Neonate with Severe Congenital Hemolytic Anemia and Liver Failure.

Authors:  Christopher M Richmond; Sally Campbell; Hee W Foo; Sebastian Lunke; Zornitza Stark; Amanda Moody; Elizabeth Bannister; Anthea Greenway; Natasha Brown
Journal:  Mol Syndromol       Date:  2020-02-01

3.  Conjugate of Doxorubicin to Albumin-Binding Peptide Outperforms Aldoxorubicin.

Authors:  Parisa Yousefpour; Lucie Ahn; Joel Tewksbury; Soumen Saha; Simone A Costa; Joseph J Bellucci; Xinghai Li; Ashutosh Chilkoti
Journal:  Small       Date:  2019-02-13       Impact factor: 13.281

4.  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
Journal:  EJHaem       Date:  2021-09-09

Review 5.  Old and new insights into the diagnosis of hereditary spherocytosis.

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

6.  Mean corpuscular volume of control red blood cells determines the interpretation of eosin-5'-maleimide (EMA) test result in infants aged less than 6 months.

Authors:  Olga Ciepiela; Anna Adamowicz-Salach; Weronika Bystrzycka; Jan Łukasik; Iwona Kotuła
Journal:  Ann Hematol       Date:  2015-04-25       Impact factor: 3.673

7.  A novel 33-Gene targeted resequencing panel provides accurate, clinical-grade diagnosis and improves patient management for rare inherited anaemias.

Authors:  Noémi B A Roy; Edward A Wilson; Shirley Henderson; Katherine Wray; Christian Babbs; Steven Okoli; Wale Atoyebi; Avery Mixon; Mary R Cahill; Peter Carey; Jonathan Cullis; Julie Curtin; Helene Dreau; David J P Ferguson; Brenda Gibson; Georgina Hall; Joanne Mason; Mary Morgan; Melanie Proven; Amrana Qureshi; Joaquin Sanchez Garcia; Nongnuch Sirachainan; Juliana Teo; Ulf Tedgård; Doug Higgs; David Roberts; Irene Roberts; Anna Schuh
Journal:  Br J Haematol       Date:  2016-07-19       Impact factor: 6.998

  7 in total

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