Journal of Pure and Applied Microbiology (Dec 2018)

Biochemical and Hematological Study with the Appreciation of some Immunological Parameters in Thalassemia Patients at Kerbala Province

  • Rusul Malik Al-Dedah,
  • Wafaa S. Al-wazni,
  • Mohammed Talat abbas,
  • Hussein H. Al-Ghanimi,
  • Fatema Abduallah

DOI
https://doi.org/10.22207/JPAM.12.4.33
Journal volume & issue
Vol. 12, no. 4
pp. 1965 – 1973

Abstract

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Thalassemia is a genetic disorder occurs as a result of the imbalance in the construction of haemoglobin chains cause haemolytic anaemia. This study was aimed to evaluate the serum level of immunological parameters (Transforming growth factor beta1, Interleukin-23) and hematological parameters in patients with alpha and beta thalassemia at Kerbala province. And was conducted at Kerbala Children’s Hospital / Thalassemia Department / Kerbala Governorate during the period from November 2017 to May 2018. Seventy patients involved 48 beta thalassemia patients and 22 alpha thalassemia patients with age ranged 10-20 years old and ten matched healthy controls were enrolled in the study. Result exposed non-significant increase (p>0.05) in IL-23 and TGF-β in thalassemia patients compared with control group. In β-thalassemia patients the results of the current study indicated that non-significant positive correlation between IL-23 with WBC, there was non-significant positive correlation between TGF-β1 with WBC and PLT. As for β-thalassemia patients the present study showed non-significant positive correlation between IL-23 with Hb and WBC, and there was non-significant positive correlation between TGF-β1 with WBC. The study showed changes in the immunological parameters in patients with thalassemia of both types, as the serum level of both IL-23 and TGF-β1 were raised in addition to changes in hematological and Biochemical parameters.

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