尼日利亚卡拉巴尔卡拉巴尔大学教学医院镰状细胞贫血患者谷胱甘肽和胆红素浓度作为氧化应激标志物的测定

E. E. Onukak, E. Akwiwu, J. Akpotuzor, A. Okafor, A. Onukak
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摘要

目的:本研究以谷胱甘肽和胆红素水平为指标,结合红细胞参数,探讨镰状细胞性贫血患者的氧化应激水平。研究设计:病例对照研究。学习地点和时间:2018年8月至2019年7月,尼日利亚卡拉巴大学教学医院。方法:45例SCA患者(女性27例,男性18例;年龄范围10-45岁)在尼日利亚卡拉巴尔大学教学医院就诊,以及相同数量的年龄和性别匹配的Hb AA对照受试者。血液样本采集和分析由原始研究文章Onukak等人;中国生物医学工程学报,2019,35 (2):1-6;文章no.IBRR。52192 2种标准方法。采用FY-Smart-1型全自动血液学分析仪对红细胞参数进行自动化分析。胆红素采用比色法测定,谷胱甘肽采用酶联免疫吸附法测定。结果:SCA患者的红细胞计数、血红蛋白浓度和红细胞压积值与对照组相比显著降低(p=0.001),而红细胞指数和红细胞分布宽度值则增加(p=0.001)。与对照组相比,SCA受试者的总胆红素、偶联胆红素和未偶联胆红素显著升高(p=0.001),而谷胱甘肽浓度值降低(p=0.001)。结论:SCA患者有明显的红细胞大小变化、淋巴细胞增多和血小板增多。在镰状细胞性贫血中发生的溶血事件导致谷胱甘肽耗竭。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Glutathione and Bilirubin Concentrations as Markers of Oxidative Stress Measured among Sickle Cell Anaemia Subjects Attending University of Calabar Teaching Hospital, Calabar Nigeria
Aims: This study aimed at examining the oxidative stress level of sickle cell anaemia subjects using glutathione and bilirubin levels as markers as well as the red cell parameters. Study Design: Case-control study. Place and Duration of Study: University of Calabar Teaching Hospital, Calabar-Nigeria, between August 2018 and July 2019. Methodology: Subjects comprised 45 SCA patients (27 females, 18 males; age range 10-45 years) attending clinic at University of Calabar Teaching Hospital Calabar, Nigeria and equal number of age and sex-matched control subjects with Hb AA. Blood samples were collected and analyzed by Original Research Article Onukak et al.; IBRR, 10(2): 1-6, 2019; Article no.IBRR.52192 2 standard methods. The red cell parameters were analysed by automation using FY-Smart-1 auto haematology analyzer. Bilirubin assay was performed using the colorimetric method, while glutathione was performed by enzyme-linked immunosorbent assay technique. Results: The red blood cell count, haemoglobin concentration, and haematocrit values of SCA subjects were significantly lower (p=0.001) compared to values from control subjects, while the red cell indices and red cell distribution width values were increased in SCA subjects (p=0.001). The Total bilirubin, conjugated bilirubin and unconjugated bilirubin were significantly increased (p=0.001) among SCA subjects, while the glutathione concentration values were reduced (p=0.001) when compared to values obtained from control subjects. Conclusion: SCA subjects have marked red cell size variation, lymphocytosis and thrombocytosis. The haemolytic events that occur in sickle cell anaemia results in glutathione depletion.
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