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Salah Noori, R, Abdul-RedhaIsmaiel, M. (1400). Relationship between Oxidative Stress and the Blood Iron Concentration and Antioxidant Status in Major ß-thalassemia in Iraq. سامانه مدیریت نشریات علمی, 77(1), 187-198. doi: 10.22092/ari.2021.356536.1863
R Salah Noori; M Abdul-RedhaIsmaiel. "Relationship between Oxidative Stress and the Blood Iron Concentration and Antioxidant Status in Major ß-thalassemia in Iraq". سامانه مدیریت نشریات علمی, 77, 1, 1400, 187-198. doi: 10.22092/ari.2021.356536.1863
Salah Noori, R, Abdul-RedhaIsmaiel, M. (1400). 'Relationship between Oxidative Stress and the Blood Iron Concentration and Antioxidant Status in Major ß-thalassemia in Iraq', سامانه مدیریت نشریات علمی, 77(1), pp. 187-198. doi: 10.22092/ari.2021.356536.1863
Salah Noori, R, Abdul-RedhaIsmaiel, M. Relationship between Oxidative Stress and the Blood Iron Concentration and Antioxidant Status in Major ß-thalassemia in Iraq. سامانه مدیریت نشریات علمی, 1400; 77(1): 187-198. doi: 10.22092/ari.2021.356536.1863

Relationship between Oxidative Stress and the Blood Iron Concentration and Antioxidant Status in Major ß-thalassemia in Iraq

Archives of Razi Institute
مقاله 26، دوره 77، شماره 1، فروردین و اردیبهشت 2022، صفحه 187-198    اصل مقاله (765.06 K)
نوع مقاله: Original Articles
شناسه دیجیتال (DOI): 10.22092/ari.2021.356536.1863
نویسندگان
R Salah Noori* ؛ M Abdul-RedhaIsmaiel
College of Science for Women, University of Babylon, Babylon, Iraq
چکیده
Reduction or total lack of beta-globin chains caused by a congenital disease called ß-thalassemia major is one of the lives threatening diseases. Patients who suffer from ß-thalassemia need a repeated blood transfusion for survival. The repeated blood transfusion in ß-thalassemia patients may cause oxidative stress and tissue injury due to iron overload, altered antioxidant enzymes, and other essential trace element levels. The current study aimed to investigate the correlation of oxidative stress with serum trace element levels and antioxidant enzyme status in ß-thalassemia major patients. A total of 130 serum samples were obtained from ß-thalassemia major patients (n=100; 50 males and 50 females) and healthy individuals (n=30; 15 males and 15 females). Hematological parameters were measured on both groups by a comprehensive blood test that included the amount of hemoglobin Hb, packed cells volume, number of red blood cells, mean corpuscular volume ratio, mean corpuscular hemoglobin ratio, mean corpuscular hemoglobin concentration, red cell distribution width, white blood cells, and platelets counts. All of these blood parameters showed a clear decrease in thalassemia patients, except for red blood cells and platelets counts, which demonstrated a significant increase. The highest significant mean for iron in males and females were 233.768 and 219.150 µgm\dL in patients, respectively, while the mean level of iron significantly reduced in the control group (113.40 and 103.33 µgm\dL in males and females, respectively). The results indicated a significant decrease in uric acid in males and females in the patient group (41.042 and 40.582 mg\L in males and females, respectively), compared to the control group (53.866 and 43.60 mg\L in males and females, respectively). Allantoin concentration was detected by high-performance liquid chromatography technique, the results of which showed that the highest values in patients were 62.822 and 25.480 mg\L in males and females, respectively, compared to the control group 2.342 and 1.481 mg\L in males and females, respectively. Superoxide dismutase concentration decreased in patients (129.635 and 111.848 U\mL in males and females, respectively), compared to the control group (208.623 and 190.413 U\ml in males and females, respectively).
کلیدواژه‌ها
Antioxidant؛ Beta-thalassemia؛ Superoxide dismutase؛ Trace elements؛ Uric acidAllantoin
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مراجع
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