The relationship between neonatal factors and involving with glucose-6-phosphate dehydrogenase deficiency (G6PD) and patients\' outcome in Fars Province

S. Daliri, K. Asadollahi, Mir Hadi Musavi, Arezou Karimi, Gholamreza Khademi, M. Azizi, G. Abangah
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引用次数: 1

Abstract

Introduction: Glucose-6-phosphate dehydrogenase deficiency (G6PD) or fauvism is the most common enzyme deficiency in human, so that 400 million people are living with this disease worldwide. This study aimed to investigate the role of some neonatal factors among newborns suffering from G6PD deficiency and neonatal outcomes associated with this disease. Materials and methods: In this study, two methods including case-control and retrospective cohort regarding some neonatal factors associated with G6PD deficiency were used. These methods were performed on 142 children with this kind of deficiency and 142 healthy infants in the city of Marvdasht during 2013- 2014. The analysis of data was based on chi-square tests, t-test, logistic regression, descriptive statistics and estimation of odds ratios or relative risks via SPSS16 software. Results: Totally 284 newborns including 132 (46.6%)/ 152 (53.4%) boys/girls and mean weight on birth of 3163 ± 471 (gr) were analyzed. Comparison of case and control samples did not show any significant differences between sex and involving with G6PD deficiency but the chance of having a baby with this defect in pregnancy intervals between 6 to 8 years was increased (95% CI: 1- 4.4, OR: 2). Relative risk of jaundice in infected and healthy infants was estimated as 3.73, which demonstrated a statistically significant association (95% CI: 1.33- 10.4). The frequency of low birth weight, birth order and type of delivery was associated with the disease, but their differences were insignificant compared to the healthy group. Conclusion: The results of this study showed that the number of hospitalization is increased due to jaundice in infants with G6PD. There is also an insignificant relation between low birth weight, rank of birth and type of delivery. Thus, it is recommended that other consequences of this deficiency need to be revealed by screening other populations with more samples.
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法尔斯省新生儿因素与葡萄糖-6-磷酸脱氢酶缺乏症(G6PD)发病及预后的关系
葡萄糖-6-磷酸脱氢酶缺乏症(Glucose-6-phosphate dehydrogenase deficiency, G6PD)是人类最常见的酶缺乏症,全世界有4亿人患有此病。本研究旨在探讨一些新生儿因素在G6PD缺乏症新生儿中的作用以及与该疾病相关的新生儿结局。材料与方法:本研究采用病例对照和回顾性队列两种方法对新生儿G6PD缺乏症的相关因素进行研究。这些方法于2013- 2014年在Marvdasht市对142名这种缺乏症儿童和142名健康婴儿进行了研究。数据分析采用卡方检验、t检验、logistic回归、描述性统计,并通过SPSS16软件估计比值比或相对风险。结果:共284例新生儿,其中男/女132例(46.6%)/ 152例(53.4%),平均出生体重3163±471 (gr)。病例和对照样本的比较没有显示出性别和G6PD缺乏症之间的任何显著差异,但在怀孕间隔6至8年之间生育有这种缺陷的婴儿的机会增加(95% CI: 1- 4.4, OR: 2)。感染和健康婴儿黄疸的相对风险估计为3.73,这显示了统计学上显著的关联(95% CI: 1.33- 10.4)。低出生体重的频率、出生顺序和分娩类型与疾病有关,但与健康组相比差异不显著。结论:本研究结果显示,G6PD患儿因黄疸而住院的人数增加。低出生体重、出生等级和分娩方式之间的关系也不显著。因此,建议通过对其他人群进行更多的样本筛选来揭示这种缺乏的其他后果。
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