Literature DB >> 24326763

Study of parents of β-thalassemia major children to determine cutoff values of hematological parameters for diagnosis of β-thalassemia trait and assessment of anemia in them.

Dipal Bhukhanvala1, Vijeta Seliya, Avani Shah, Snehalata Gupte.   

Abstract

BACKGROUND: Because of the overlapping MCV, MCH and HbA 2 values in BTT and non-BTT subjects our laboratory determined own cutoffs. AIMS: To establish cutoff values by investigating the parents of thalassemia major children and to assess the degree of anemia in BTT subjects.
MATERIALS AND METHODS: Study includes 179 parents of thalassemia major children (BTT cases) and 287 non-BTT controls. Samples were analyzed on an electronic hematology analyzer. The samples having MCV ≤ 76 fl and MCH ≤ 27 pg were quantified for HbA 2 by cellulose acetate electrophoresis and grey zone samples were confirmed on HPLC. Statistical Analysis Mean ± SD, sensitivity, specificity, PPV, NPV and accuracy were calculated. The histograms were plotted for MCV, MCH and HbA 2 .
RESULTS: Cases having MCV ≤ 76 fl and MCH ≤ 27 pg if considered as suspected cases of BTT then we could have missed five known BTT samples. Sensitivity increased to 100% in all three diagnostic parameters when the cutoff values were raised and specificity for MCV and MCH was decreased. But specificity was 100% with raised cutoff for HbA 2 . Hb and HCT mean values were significantly reduced in BTT cases compared to controls (P < 0.001). In 100% females and 84.9% males having BTT, mild to moderate anemia was observed.
CONCLUSION: In our setup, the cutoff values are MCV (≤78.0 fl), MCH (≤28 pg) and HbA 2 (>3.8%) for BTT diagnosis and there is a mild to moderate anemia in BTT cases.

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Year:  2013        PMID: 24326763

Source DB:  PubMed          Journal:  Indian J Med Sci        ISSN: 0019-5359


  3 in total

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2.  Mean reticolocyte hemoglobin content index plays a key role to identify children who are carriers of β-thalassemia.

Authors:  Paolo Vicinanza; Mariella Vicinanza; Vincenzo Cosimato; Daniela Terracciano; Sergio Cancellario; Angelo Massari; Paolo Danise; Carmine Selleri; Bianca Serio
Journal:  Transl Med UniSa       Date:  2018-03-31

3.  Mean reticolocyte hemoglobin content index plays a key role to identify children who are carriers of β-thalassemia.

Authors:  Paolo Vicinanza; Mariella Vicinanza; Vincenzo Cosimato; Daniela Terracciano; Sergio Cancellario; Angelo Massari; Paolo Danise; Carmine Selleri; Bianca Serio
Journal:  Transl Med UniSa       Date:  2018-03-31
  3 in total

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