Department of Biology, Science and Research Branch, Islamic Azad University, Tehran, Iran.
Blood Transfusion Research Center, High Institute for Research and Education in Transfusion Medicine, Tehran, Iran.
Transfus Clin Biol. 2024 Nov;31(4):201-208. doi: 10.1016/j.tracli.2024.08.003. Epub 2024 Aug 13.
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.
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.
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).
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.
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缺乏症。由于 G6PD 酶作为 RBC 中抗氧化剂的重要性,我们试图研究与健康供体相比,从 G6PD 酶缺乏供体中制备的浓缩红细胞(RCC)中的氧化损伤。
这是一项横断面研究,共纳入 20 名男性供体。其中 10 名供体存在 G6PD 缺乏症(病例组),其余 10 名供体酶活性正常(对照组)。在 RCC 储存的第 0、7、14、21、28 和 35 天,检测两组 RCC 中制备的 RBC 的生化和氧化损伤参数;采用 SPSS 统计软件进行数据分析。
结果显示,与对照组相比,G6PD 缺乏供体的 RCC 储存第 7 天至第 35 天,乳酸浓度明显升高(P<0.05)。此外,G6PD 缺乏的 RCC 中丙二醛(MDA)浓度在所有储存日与对照组相比均显著升高(P<0.05)。在血液学参数中,与对照组相比,G6PD 缺乏供体的 RCC 在所有储存日的平均红细胞体积(MCV)和平均红细胞血红蛋白(MCH)均明显升高(P<0.05)。
与健康供体相比,G6PD 缺乏供体的氧化变化明显增加,这可能导致 RCC 储存损伤和输血并发症增加。由于 G6PD 酶缺乏在大流行地区的高患病率,似乎应该将酶筛查纳入供体筛查计划。