Literature DB >> 30369737

HbE Level and Red Cell Parameters in Heterozygous HbE With and Without α0-Thalassemia Trait.

Sakorn Pornprasert1, Monthathip Tookjai2, Manoo Punyamung2, Panida Pongpunyayuen2.   

Abstract

We compared hemoglobin (Hb) E levels and red cell parameters between heterozygous HbE with and without α0-thalassemia trait and also determine their appropriated cut-off points for differentiating these two groups. High performance liquid chromatography analysis results and mean levels of red blood cell (RBC) parameters, including RBC count, total Hb, hematocrit, MCV, MCH and MCHC of heterozygous HbE with α0-thalassemia trait (n = 183) and without α0-thalassemia trait (n = 1437) were reviewed and compared. The α0-thalassemia status in these samples was detected by real-time PCR with SYBR Green1 and high resolution melting analysis. Mean levels of HbE, total Hb, MCV, MCH and MCHC of heterozygous HbE with α0-thalassemia trait were significantly lower than those of heterozygous HbE without α0-thalassemia trait (P < 0.001). In addition, HbE level at a cut-off value of < 24% was superior to MCV (< 80 fL) and MCH (< 27 pg) for differentiating the heterozygous HbE with and without α0-thalassemia trait with 100% sensitivity and 87.2% specificity. Despite certain limitations of this study like missing RDW and reticulocyte counts, and not testing for α+-thalassemia and Hb Constant Spring, we conclude that the HbE level at a cut-off point of < 24% is a useful marker for initial discrimination between heterozygous HbE with and without α0-thalassemia trait.

Entities:  

Keywords:  Coinheritance; HbE; High performance liquid chromatography; Screening; α0-Thalassemia

Year:  2018        PMID: 30369737      PMCID: PMC6186250          DOI: 10.1007/s12288-018-0947-8

Source DB:  PubMed          Journal:  Indian J Hematol Blood Transfus        ISSN: 0971-4502            Impact factor:   0.900


  15 in total

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2.  Evaluating five dedicated automatic devices for haemoglobinopathy diagnostics in multi-ethnic populations.

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3.  Effective screening for double heterozygosity of Hb E/alpha0-thalassemia.

Authors:  Kanokwan Sanchaisuriya; Sunisa Chirakul; Hataichanok Srivorakun; Goonnapa Fucharoen; Supan Fucharoen; Yossombat Changtrakul; Pattara Sanchaisuriya
Journal:  Ann Hematol       Date:  2008-06-25       Impact factor: 3.673

4.  The Hb E (HBB: c.79G>A), Mean Corpuscular Volume, Mean Corpuscular Hemoglobin Cutoff Points in Double Heterozygous Hb E/- -SEA α-Thalassemia-1 Carriers are Dependent on Hemoglobin Levels.

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Review 5.  Hemoglobinopathies in Southeast Asia.

Authors:  S Fucharoen; P Winichagoon
Journal:  Hemoglobin       Date:  1987       Impact factor: 0.849

6.  Silent thalassemias: genotypes and phenotypes.

Authors:  I Bianco; M P Cappabianca; E Foglietta; M Lerone; G Deidda; L Morlupi; P Grisanti; D Ponzini; S Rinaldi; B Graziani
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7.  HPLC in characterization of hemoglobin profile in thalassemia syndromes and hemoglobinopathies: a clinicohematological correlation.

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Journal:  Indian J Hematol Blood Transfus       Date:  2014-06-05       Impact factor: 0.900

Review 8.  Thalassemia in SouthEast Asia: problems and strategy for prevention and control.

Authors:  S Fucharoen; P Winichagoon
Journal:  Southeast Asian J Trop Med Public Health       Date:  1992-12       Impact factor: 0.267

9.  Detection of α-thalassemia-1 Southeast Asian and Thai type deletions and β-thalassemia 3.5-kb deletion by single-tube multiplex real-time PCR with SYBR Green1 and high-resolution melting analysis.

Authors:  Sakorn Pornprasert; Thanatcha Wiengkum; Sarinee Srithep; Isarapong Chainoi; Panthong Singboottra; Sanchai Wongwiwatthananukit
Journal:  Korean J Lab Med       Date:  2011-06-28

Review 10.  Haemoglobinopathies in southeast Asia.

Authors:  Suthat Fucharoen; Pranee Winichagoon
Journal:  Indian J Med Res       Date:  2011-10       Impact factor: 2.375

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