College of Science for Women, University of Babylon, Babylon, Iraq.
Arch Razi Inst. 2022 Feb 28;77(1):187-198. doi: 10.22092/ARI.2021.356536.1863. eCollection 2022 Feb.
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).
由于一种称为β-地中海贫血的先天性疾病导致的β-球蛋白链减少或完全缺失,是威胁生命的疾病之一。患有β-地中海贫血的患者需要反复输血才能生存。β-地中海贫血患者的反复输血可能会因铁过载、抗氧化酶改变和其他必需微量元素水平改变而导致氧化应激和组织损伤。本研究旨在探讨β-地中海贫血患者氧化应激与血清微量元素水平和抗氧化酶状态的相关性。共从β-地中海贫血患者(n=100;男 50 例,女 50 例)和健康个体(n=30;男 15 例,女 15 例)中获得 130 份血清样本。两组的血液参数均通过全血细胞计数进行测量,包括血红蛋白 Hb、红细胞压积、红细胞计数、平均红细胞体积比、平均红细胞血红蛋白比、平均红细胞血红蛋白浓度、红细胞分布宽度、白细胞和血小板计数。除了红细胞和血小板计数明显增加外,所有这些血液参数在地中海贫血患者中均明显下降。男性和女性患者的铁含量最高均值分别为 233.768 和 219.150 µgm/dL,而对照组的铁含量显著降低(男性和女性分别为 113.40 和 103.33 µgm/dL)。结果表明,与对照组相比(男性和女性分别为 53.866 和 43.60 mg/dL),患者组男性和女性的尿酸水平均显著降低(男性和女性分别为 41.042 和 40.582 mg/L)。用高效液相色谱技术检测尿囊素浓度,结果显示,患者的最高值分别为男性和女性 62.822 和 25.480 mg/L,而对照组分别为男性和女性 2.342 和 1.481 mg/L。与对照组相比(男性和女性分别为 208.623 和 190.413 U/ml),患者组超氧化物歧化酶浓度降低(男性和女性分别为 129.635 和 111.848 U/ml)。