葡萄糖-6-磷酸脱氢酶缺乏症及其与尼日利亚拉各斯州行政区划疟疾的关系

Oladayo M. Babalola, Adetunji A. Alli, M. Ashiru
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摘要

背景:葡萄糖-6-磷酸脱氢酶(G6PD)缺乏症是红细胞最常见的遗传性酶疾病之一。据信,目前全球约有5亿人受到影响。这种缺乏可能导致多种血液学疾病,包括急性溶血性贫血、新生儿黄疸和核黄疸。目的:本研究旨在确定拉各斯州五个行政区G6PD缺乏症的患病率。疟疾与G6PD缺乏之间的关系也被调查。材料和方法:本研究共招募了105名参与者,其中63名(60%)男性和42名(40%)女性,来自五个地区。采集静脉血2 ml,分成3份进行G6PD酶测定、血液学参数测定和疟疾诊断。使用定量分光光度法测定G6PD酶水平,而使用显微镜和快速诊断测试试剂盒检查疟疾寄生虫。结果:G6PD缺乏症的总体患病率为21%。男性(22.2%)和女性(19%)之间的患病率无显著差异,而男性G6PD活性略高(10.15±0.50比8.61±0.31 U/g Hb) (P < 0.05)。虽然5个采样点的患病率有轻微差异,但G6PD活性水平的单因素方差分析显示各组间无显著差异(P = 0.05)。此外,本研究结果显示疟疾与G6PD缺乏之间没有相关性(χ2 = 1.432, P = 0.231)。结论:本研究发现尼日利亚亚人群中G6PD缺乏症的患病率相对较高,表明G6PD缺乏症在该环境中很常见。这强调了对该国该地理区域出现急性溶血性贫血发作的患者进行定量G6PD检测作为实验室调查的一部分的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Glucose-6-phosphate dehydrogenase deficiency and its association with malaria in the administrative divisions of Lagos State, Nigeria
Background: Glucose-6-phosphate dehydrogenase (G6PD) deficiency is one of red blood cells' most common inherited enzyme disorders. It is currently believed to affect approximately 500 million individuals worldwide. The deficiency could result in several hematological conditions, including acute hemolytic anemia, neonatal jaundice, and kernicterus. Aim: This study aimed to determine the prevalence of G6PD deficiency in the five administrative divisions of Lagos State. The association between malaria and G6PD deficiency was also investigated. Materials and Methods: A total of 105 participants, comprising 63 (60%) males and 42 (40%) females, were recruited from five locations for this study. Two milliliters of venous blood were collected and divided into three portions for G6PD enzyme assay, hematological parameter, and malaria diagnosis. G6PD enzyme level was determined using a quantitative spectrophotometric assay, whereas the malaria parasite was examined using microscopy and rapid diagnostic test kits. Results: An overall prevalence of G6PD deficiency was 21%. There was no significant difference in prevalence between males (22.2%) and females (19%), whereas a marginally higher G6PD activity in males (10.15 ± 0.50 vs. 8.61 ± 0.31 U/g Hb) (P < 0.05) was recorded. Although there were slight differences in prevalence obtained in the five sampling locations, however, the one-way analysis of variance of the G6PD activity levels showed no significant difference between any pairs (P = 0.05). Furthermore, the results obtained from this study showed no association between malaria and G6PD deficiency (χ2 = 1.432, P = 0.231). Conclusions: The study found a relatively high prevalence of G6PD deficiency in the Nigerian subpopulation, indicating that G6PD deficiency is common in this environment. This emphasizes the need for a quantitative G6PD assay as part of laboratory investigations for those presenting with an episode of acute hemolytic anemia in this geographical region of the country.
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