Categorization of Glucose 6 Phosphate Dehydrogenase (G6PD) Deficiency on the Basis of Enzyme Activity and its Clinico Haematological Correlation

Babar Zaman, Hamid Saeed Malik, Muhammad Umar, Fauzia Khan, Manzar Bozdar, Afshan Bilal
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Abstract

Objective: To categorize glucose-6-phosphate dehydrogenase (G6PD) deficiency based on enzyme activity and its clinical haematological correlation. Methodology: This Cross-sectional study was conducted at the Department of Haematology, Armed Forces Institute of Pathology (AFIP), Rawalpindi, from February 2022 to August 2022. Sampling was done using the nonprobability consecutive sampling technique. Test analysis included a complete blood picture, RBC morphology and reticulocyte count, G6PD quantitative test, and serum bilirubin. Thus, to categorize G6PDD based on its enzyme and clinic-haematological correlation, study included patients of both gender with an age ranging from 0-76 years. Descriptive statistics were expressed as mean ± standard deviation (SD) and categorical data were presented as frequency and percentage. Results: Out of 120 study participants, 30 (25%) were females and 90 (75%) were males. The mean age of study participants was 10.83±12.75. G6PD PCR was detected among participants having G6PD deficiency level <1 U/g Hb and between 2-3 U/gm Hb. Hb levels below 8g/dL were found only in individuals with G6PD deficiency levels <1 U/gm Hb. Conclusion: GDPD deficiency can be diagnosed by blood analysis comprising of complete blood count and RBC morphology aided by clinical correlation. The signs and symptoms increase in severity with a decline in GDPD enzyme function along with blood haemoglobin levels.
葡萄糖6磷酸脱氢酶(G6PD)缺乏的酶活性分类及其临床血液学相关性
目的:根据葡萄糖-6-磷酸脱氢酶(G6PD)活性及其临床血液学相关性对G6PD缺乏症进行分类。方法:横断面研究于2022年2月至2022年8月在拉瓦尔品第武装部队病理研究所(AFIP)血液科进行。抽样采用非概率连续抽样技术。试验分析包括全血图、红细胞形态和网织红细胞计数、G6PD定量检测和血清胆红素。因此,为了根据G6PDD的酶和临床血液学相关性对其进行分类,研究纳入了年龄在0-76岁的男女患者。描述性统计数据以均数±标准差(SD)表示,分类数据以频率和百分比表示。结果:在120名研究参与者中,30名(25%)是女性,90名(75%)是男性。研究参与者的平均年龄为10.83±12.75岁。在G6PD缺乏水平<1 U/g Hb和2-3 U/gm Hb的参与者中检测到G6PD PCR。Hb水平低于8g/dL仅在G6PD缺乏症<1 U/gm Hb的个体中发现。结论:GDPD缺乏症可通过全血细胞计数和红细胞形态分析,结合临床相关性进行诊断。随着GDPD酶功能和血红蛋白水平的下降,症状和体征加重。
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