比较评估 G6PD 缺乏的供体和健康供体制备的红细胞浓缩物(RCC)在 RCC 储存期间的氧化和生化参数。

Samira Moshkelgosha, Mohammad Reza Deyhim, Ramazan Ali Khavari-Nejad, Mahdieh Meschi
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引用次数: 0

摘要

简介葡萄糖-6-磷酸脱氢酶(G6PD)缺乏症是红细胞(RBC)中最常见的遗传性酶紊乱。鉴于 G6PD 酶在红细胞中作为抗氧化剂的重要性,我们试图研究 G6PD 酶缺乏症供体与健康供体制备的红细胞浓缩物(RCC)中的氧化损伤:这项横断面研究的对象是 20 名男性供体。材料方法:这项横断面研究以 20 名男性供体为对象,其中 10 人患有 G6PD 缺乏症(作为病例),其他人酶活性正常(作为对照)。在 RCC 储存的第 0 天、第 7 天、第 14 天、第 21 天、第 28 天和第 35 天,对两组供体制备的 RCC 的生化指标和氧化损伤指标进行检测;数据比较采用 SPSS 统计软件进行分析:结果显示,与对照组(PC)相比,G6PD 缺乏供体的乳酸浓度在 RCC 储存第 7 天至第 35 天显著增加:我们的研究表明,与健康供体相比,G6PD缺陷供体的氧化变化明显增加,这可能会导致RCC储存病变和输血并发症的增加。鉴于 G6PD 酶缺乏症在大流行地区的高发病率,似乎应将酶筛查纳入献血者筛查计划。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparative evaluation of oxidative and biochemical parameters of red cell concentrates (RCCs) prepared from G6PD deficient donors and healthy donors during RCC storage.

Introduction: Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common inherited enzyme disorder in red blood cell (RBC). Due to the importance of G6PD enzyme as an antioxidant in RBC, we tried to investigate the oxidative damage in red cell concentrates (RCCs) prepared from donors with G6PD enzyme deficiency in comparison with healthy donors.

Material method: This cross-sectional study was conducted on 20 male donors. Ten of the donors had G6PD deficiency (as a case) and the others had normal enzyme activity (as a control). Biochemical and oxidative damage parameters were examined in RCCs prepared from two groups on days 0, 7, 14, 21, 28 and 35 of RCCs storage; data comparison was analyzed by SPSS statistical software.

Results: According to the result, lactate concentration increased significantly from the 7th day to the 35th day of RCC storage in G6PD-deficient donors compared to the control (P < 0.05). In addition, malondialdehyde (MDA) concentration in G6PD-deficient RCC showed a significant increase compared to the control in all days of storage (P < 0.05). Among the hematological parameters, mean corpuscular volume (MCV) and mean cell hemoglobin (MCH) increased significantly in all days of RCC storage in G6PD-deficient donors compared to the control (P < 0.05).

Conclusion: Our study showed that oxidative changes in G6PD-deficient donors were significantly increased compared to the healthy donors, which probably leads to RCC storage lesion and an increase in blood transfusion complications. Due to the high prevalence of G6PD enzyme deficiency in pandemic areas, it seems that enzyme screening should be included in donor screening programs.

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