Literature DB >> 34079632

Diagnostic accuracy of reticulocyte parameters on the sysmex XN 1000 for discriminating iron deficiency anaemia and thalassaemia in Saudi Arabia.

Qanita Sedick1, Ghaleb Elyamany1, Huda Hawsawi1, Sultan Alotaibi2, Fahad Alabbas3, Mohammed Almohammadi4, Hassan A Alahmari3, Hassan Aljasem2, Arnel G Ferrer1, Ahmed S Alzahrani1, May AlMoshary5, Omar Alsuhaibani1.   

Abstract

INTRODUCTION: Iron deficient erythropoiesis and Thalassaemia are both associated with microcytic erythropoiesis albeit from different pathological mechanisms. Given the high prevalence of Hemoglobinopathies in the Mediterranean region, discriminating these two conditions is important. Several algorithms using conventional red cell indices have been developed to facilitate diagnosis, however, their diagnostic accuracy is low. The new generation haematology analyzers enabled the use of more innovative parameters such as reticulocyte parameters. We aimed to evaluate the diagnostic performance of the reticulocyte parameters on the Sysmex XN 1000 to distinguish between IDA and Thalassemia in our population.
METHODS: We performed a retrospective analysis of blood samples sent to our laboratory for haemoglobin electrophoresis screening. We categorized our cohort into Thalassemia and Iron Deficient patients based on known diagnostic criteria. We analyzed the reticulocyte parameters using receiver operator curve analysis (ROC) and determined the cut off value for each parameter.
RESULTS: Reticulocyte parameters most accurate for discriminating IDA from Thalassemia patients was: RET, RET-HE and IRF. The RET-HE had the best statistical significance for IDA patients with AUC = 0.69 for cut off 22.25. The RET-HE for dual positive patients was more accurate with AUC = 0.78 for cut off 21.25. The IRF had the best statistical significance for Alpha Thalassemia with AUC = 0.66 for cut off value 18.
CONCLUSION: An IRF cut off below 15.5 and RET-HE cut off below 22.25 was the most accurate variable in predicting IDA with a sensitivity of 59.4% and 68.3%. AJBR
Copyright © 2021.

Entities:  

Keywords:  Reticulocyte haemoglobin concentration; iron deficiency anaemia; sysmex XN 1000; thalassaemia

Year:  2021        PMID: 34079632      PMCID: PMC8165718     

Source DB:  PubMed          Journal:  Am J Blood Res        ISSN: 2160-1992


  25 in total

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Journal:  Rev Assoc Med Bras (1992)       Date:  2003 Apr-Jun       Impact factor: 1.209

2.  Additional erythrocytic and reticulocytic parameters helpful for diagnosis of hereditary spherocytosis: results of a multicentre study.

Authors:  François Mullier; Elodie Lainey; Odile Fenneteau; Lydie Da Costa; Françoise Schillinger; Nicolas Bailly; Yvan Cornet; Christian Chatelain; Jean-Michel Dogne; Bernard Chatelain
Journal:  Ann Hematol       Date:  2010-12-22       Impact factor: 3.673

3.  Reticulocyte hemoglobin equivalent in a thalassemia-prevalent area.

Authors:  Praguywan Kadegasem; Duantida Songdej; Surapong Lertthammakiat; Ampaiwan Chuansumrit; Karan Paisooksantivatana; Lalita Mahaklan; Pakawan Wongwerawattanakoon; Noppawan Tangbubpha; Nongnuch Sirachainan
Journal:  Pediatr Int       Date:  2019-03-10       Impact factor: 1.524

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Authors:  W C Mentzer
Journal:  Lancet       Date:  1973-04-21       Impact factor: 79.321

5.  Reticulocyte Hemoglobin Equivalent (Ret-He) Combined with Red Blood Cell Distribution Width Has a Differentially Diagnostic Value for Thalassemias.

Authors:  Yu Lian; Jun Shi; Neng Nie; Zhendong Huang; Yingqi Shao; Jing Zhang; Jinbo Huang; Xingxin Li; Meili Ge; Peng Jin; Min Wang; Yizhou Zheng
Journal:  Hemoglobin       Date:  2019-09-03       Impact factor: 0.849

Review 6.  The inherited diseases of hemoglobin are an emerging global health burden.

Authors:  David J Weatherall
Journal:  Blood       Date:  2010-03-16       Impact factor: 22.113

7.  Gene regulation in hematopoiesis: new lessons from thalassemia.

Authors:  Douglas R Higgs
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2004

8.  Twenty-year outcome analysis of genetic screening programs for Tay-Sachs and beta-thalassemia disease carriers in high schools.

Authors:  J J Mitchell; A Capua; C Clow; C R Scriver
Journal:  Am J Hum Genet       Date:  1996-10       Impact factor: 11.025

9.  Efficacy of advanced discriminating algorithms for screening on iron-deficiency anemia and β-thalassemia trait: a multicenter evaluation.

Authors:  Margreet Schoorl; Marianne Schoorl; Jo Linssen; Miriam Martinez Villanueva; José A Velasco NoGuera; Pedro Hernandez Martinez; Piet C M Bartels
Journal:  Am J Clin Pathol       Date:  2012-08       Impact factor: 2.493

10.  Reticulocyte hemoglobin equivalent (Ret He) and assessment of iron-deficient states.

Authors:  C Brugnara; B Schiller; J Moran
Journal:  Clin Lab Haematol       Date:  2006-10
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