Indian Journal of Animal Research
SCOPUSWeb of Science
  • Year: 2024
  • Volume: 58
  • Issue: 8

Hemoglobin E prevalence among people residing in malaria areas

  • Author:
  • Murad A. Mubaraki1,*, Mohammed A. Haijan2, Majed Ahmed Adawi2, Taghreed A. Hafiz1, Rewaida Abdel-Gaber3, Saeed El-Ashram4, Mohamed A. Dkhil5,6
  • Total Page Count: 8
  • Page Number: 1423 to 1430

1Clinical Laboratory Sciences Department, College of Applied Medical Sciences, King Saud University, Riyadh, Saudi Arabia

2Clinical Laboratory and Blood Bank Department, King Fahd Central Hospital, Ministry of Health, Jazan, Saudi Arabia

3Department of Zoology, Faculty of Science, Cairo University, Giza, Egypt

4College of Life Science and Engineering, Foshan University, 18 Jiangwan Street, Foshan, 528231, Guangdong Province, China

5Department of Zoology and Entomology, Faculty of Science, Helwan University, Cairo, Egypt

6Applied Science Research Center, Applied Science Private University, Amman, Jordan

*Corresponding Author: Murad A. Mubaraki, Clinical Laboratory Sciences Department, College of Applied Medical Sciences, King Saud University, Riyadh, Saudi Arabia, Email: mmubaraki@ksu.edu.sa

Online published on 11 October, 2024.

Abstract

Malaria can infect erythrocytes and hence cause different pathogenesis episodes leading to death mostly in pregnant women and children under the age of 5 years. The selective pressure of these parasites leads to the production of new human genetic diseases. The most prevalent genetic alterations in the human genome are thalassemia and hemoglobinopathies (Hb E, Hb S), which are recognized throughout the world, including Saudi Arabia.

From May 2018 to August 2019, 13972 Saudi citizens from King Fahd Central Hospital and premarital facilities in the Saudi Arabian province of Jazan participated in this study. This study aims to compare the prevalence of Hb E and other hemoglobinopathies in positive versus negative cases of malaria. So, CBC, malaria test, Hb-electrophoresis, and molecular study were investigated.

For thalassemias and Hb disorders, 36% with abnormal Hb (47% of them) carried Hb S in their blood, 37% with α-thalassemia, 11% for β-thalassemia and 4% of Hb E. Significant variations in CBC parameters were observed in Hb E patients. There was significant decrease in MCV, MCH and MCHC and slightly increase in WBCs, RBCs, RDW and PLT as compared to controls.

Keywords

Consanguineous marriage, Hb A, Hb E, Hemoglobinopathies, Jazan, Malaria