评估β-地中海贫血患者血清中的 5'-核苷酸酶水平和一些生化指标

Sameer M. Al-Gorany, Mohammed Rajeh Altutnchi
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引用次数: 0

摘要

催化 5'-核苷酸水解为核糖核苷和磷酸的水解酶之一是 5'核苷酸酶,它存在于多个器官中。氧化应激表现为谷胱甘肽(GSH)等抗氧化剂的耗竭和脂质过氧化产物(如 MDA)浓度的增加。这项研究共有 54 名受试者,包括年龄和性别匹配的地中海贫血症患者(27 人)和健康志愿者(27 人)。使用不同的方法和设备测量了血液学(血红蛋白和 PCV%)、5'-核苷酸酶、铁蛋白、GSH 和 MDA。与对照组相比,β-地中海贫血患者的 5'-核苷酸酶、铁蛋白和 MDA 水平明显升高(p<0.001)。与此相反,β-地中海贫血患者的 Hb、PCV% 和 GSH 水平明显下降(p<0.001)。Hb 和 5'- NT 酶之间以及 PCV%和 5'- NT 酶之间分别存在负相关(r = -0.146,-0.245,p<0.05)。而血红蛋白与 PCV% 呈高度显著相关(r = 0.956,p<0.05)。此外,5'-NT 酶与 GSH、MDA 和铁蛋白分别呈正相关(r = 0.584、0.442、0.735,p<0.05)。本研究结果表明,β 地中海贫血症患者 5'-核苷酸酶、铁蛋白和 GSH 的有效性水平升高,而 MDA 的有效性水平降低。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of the level of 5'-nucleotidase and some biochemical parameters in the sera of beta-thalassemia patients
One of the hydrolytic enzymes that catalyzes the hydrolysis of 5' -nucleotides into ribonucleosides and phosphate is the 5'nucleotidase, which is found in several organs. Oxidative stress shows depletion of antioxidants, such as glutathione (GSH), and the increased concentration of product of lipid peroxidation, such as MDA. The study comprised a total of 54 subjects including patients with beta thalassemia (n=27) and healthy volunteers (n=27) matched by age and gender. Hematology (Hb and % PCV), 5'-nucleotidase, Ferritin, GSH and MDA were measured using different methods and devices. The 5'nucleotidase, Ferritin, and MDA levels were significantly increased (p<0.001) in beta-thalassemia patients compared to the controls. As opposed to that, the Hb, % PCV and GSH levels were significantly decreased (p<0.001) in patients with beta-thalassemia. There was a negative significant correlation (r = -0.146, -0.245, p<0.05) between Hb and 5'- NT enzyme and PCV% with 5'- NT enzyme, respectively. While Hb had a high significant correlation (r = 0.956, p<0.05) with PCV%. In addition, 5'- NT enzyme had a positive significant correlation with GSH, MDA and Ferritin (r = 0.584, 0.442, 0.735, p<0.05), respectively. The present findings indicated an increase in the level of effectiveness of the 5'nucleotidase enzyme, ferritin and GSH in β thalassemia patients while decreasing in MDA.
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