葡萄糖-6-磷酸脱氢酶缺乏对镰状细胞性贫血患者血管闭塞危象发生频率的影响

IF 0.5 Q4 HEMATOLOGY
Hilary Igwilo, L. Salawu, Tewogbade Adeoye Adedeji
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引用次数: 5

摘要

背景与目的镰状细胞性贫血(SCA)和葡萄糖-6-磷酸脱氢酶(G6PD)缺乏症都是导致溶血的遗传性红细胞疾病。这两种情况的相互作用对临床和实验室表现的影响是稀疏的。因此,本研究通过比较G6PD缺乏的SCA患者与G6PD活性正常的SCA患者的疾病严重程度,将G6PD活性与SCA患者的疾病严重程度联系起来。这项横断面研究是在尼日利亚Ile-Ife奥巴费米·阿沃洛沃大学教学医院综合医院的血液学和输血科进行的。对67例SCA患者的G6PD活性、SCA疾病严重程度和血流变参数(包括网状红细胞计数、亨氏体估计、胆红素和天冬氨酸转氨酶)进行了评估。将G6PD缺乏症SCA患者与酶活性正常的SCA患者进行比较。结果G6PD缺乏症患病率为23.9%。g6pd缺陷SCA患者中男性4例(25.0%),女性12例(75.0%)。G6PD缺乏症在女性中明显更高(P = 0.047)。g6pd缺陷和g6pd非缺陷SCA患者的疾病严重程度评分无显著差异。然而,g6pd缺陷者每年报告的严重血管闭合性危象(VOC)发生率明显更高(P = 0.048)。G6PD缺乏症SCA患者血液学和生化指标与G6PD正常SCA患者相似,但G6PD缺乏症SCA患者网状细胞反应明显高于正常SCA患者(P = 0.001)。SCA患者在稳定状态下,G6PD活性降低导致的疾病严重程度与亨氏体形成之间没有相关性。结论G6PD缺乏对SCA患者稳定状态下复发性疼痛性血管闭合性危像有重要影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Impact of Glucose-6-Phosphate Dehydrogenase Deficiency on the Frequency of Vasoocclusive Crisis in Patients with Sickle Cell Anemia
Background and Objectives Sickle cell anemia (SCA) and glucose-6-phosphate dehydrogenase (G6PD) deficiency are both hereditary diseases of the red blood cells that cause hemolysis. The impact of the interaction of both conditions on the clinical and laboratory presentations of the affected persons is sparse. This study, therefore, correlated G6PD activity with disease severity in persons with SCA by comparing disease severity in G6PD-deficient SCA persons with those with normal G6PD activity. Methodology This cross-sectional study was conducted in the department of Haematology and Blood Transfusion of the Obafemi Awolowo University Teaching Hospitals Complex, Ile-Ife, Nigeria. G6PD activity, SCA disease severity, and hematological parameters including reticulocyte counts and Heinz body estimation, bilirubin, and aspartate transaminase were estimated in 67 SCA persons. The results were compared between SCA persons with G6PD deficiency and those with normal enzyme activity. Results The prevalence of G6PD deficiency was found to be 23.9%. The G6PD-deficient SCA patients included 4 (25.0%) males and 12 (75.0%) females. G6PD deficiency was significantly higher in females (P = .047). There was no significant difference in disease severity scores between G6PD-deficient and G6PD-nondeficient SCA patients. However, G6PD-deficient persons reported significantly higher episodes of severe vasoocclusive crisis (VOC) per annum (P = .048). The hematological and biochemical parameters were similar between G6PD-deficient and G6PD normal SCA persons except that the G6PD-deficient SCA persons have significantly higher reticulocyte response (P = .001). There was no correlation between disease severity resulting from reduced G6PD activity and Heinz body formation in SCA persons in the steady state. Conclusion G6PD deficiency significantly contributes to recurrent painful vasoocclusive crisis in SCA persons in the steady state.
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来源期刊
Plasmatology
Plasmatology HEMATOLOGY-
CiteScore
1.10
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