Clinical perspective on the impact of coronavirus (COVID-19) pandemic on individuals with glucose -6- phosphate dehydrogenase deficiency (G6PD)

Abdelrahim A Hunaiti
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Abstract

Trends Med, 2017 Volume 3: 1-2 Glucose-6-phosphate dehydrogenase (G6PD) is an enzyme that catalyzes the initial and the rate-limiting reaction step in the pentose phosphate pathway (HMP) which converts NADP into NADPH. NADPH is required for the generation of reduced glutathione an important antioxidant used to protects red blood cells from oxidative damage.Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common enzymopathy worldwide, affecting an estimated 400 million people and exists in concentrated regions in Africa, the Middle East, and Southeast Asia, and about one in 10 African-American males are affected in the United States [1-3]. G6PD-deficient patients may develop acute hemolytic anemia after exposure to oxidative stress because the HMP shunt is their only source of NADPH. Oxidative stress constitutes a failure of anti-oxidation defence systems to keep reactive oxygen and nitrogen species under control due to decrease of reduced glutathione synthesis in G6PD-deficient patients [4]. Hemolytic anemia may be life-threatening in some individuals due to three main triggers for hemolytic anemia in G6PD-deficient patients these are bacterial or viral infections, certain foods, and certain drugs [5]. These factors can increase the levels of reactive oxygen species, causing red blood cells to be destroyed faster than the body can replace them. Investigators found that G6PD-deficient cells were more susceptible to infection and death by human coronavirus, HCoV229E, a common pathogen for respiratory tract infection [6].In previous study we noticed a concurrent decrease in the concentration of reduced glutathione when the G6PD activity decreased [7]. Furthermore, we presented evidence that maintaining glutathione levels may help in easing the symptoms of certain diseases and supplementation of bilingual glutathione as a therapeutic strategy [8]. Since the onset of the COVID-19 pandemic and in light of the notion that some people become severely ill while others are asymptomatic, researchers started to believe that people who have a G6PD deficiency may be significantly affected by COVID-19 pandemic like the human coronavirus, HCoV229E and raised the question: Is there any scientific evidences to support a correlation/ association between G6PD deficiency and COVID-19 infection, susceptibility, severity or mortality [9]. Recent retrospective studies strongly suggesting that G6PD-deficient COVID-19 patients may suffer highest chloroquine induced toxicity a drug along with hydroxychloroquine are commonly prescribed widely used worldwide in the treatment of COVID-19 pandemic [10,11]. Moreover, a brief overview of the protective action of GSH against the exacerbated inflammation triggered by COVID-19 upon ACE/ACE2 imbalance was reported [12]. Additional evidence continued to suggest G6PD deficiency may not only play a role in COVID-19 susceptibility, but also severity of infection, therefore in order to answer this question, it would be Clinical perspective on the impact of coronavirus (COVID-19) pandemic on individuals with glucose -6phosphate dehydrogenase deficiency (G6PD)
新冠肺炎大流行对葡萄糖-6-磷酸脱氢酶缺乏症(G6PD)患者影响的临床观察
葡萄糖-6-磷酸脱氢酶(G6PD)是一种催化戊糖磷酸途径(HMP)中将NADP转化为NADPH的初始和限速反应步骤的酶。NADPH是生成还原性谷胱甘肽所必需的,还原性谷胱甘肽是一种重要的抗氧化剂,用于保护红细胞免受氧化损伤。葡萄糖-6-磷酸脱氢酶(Glucose-6-phosphate dehydrogenase, G6PD)缺乏症是世界范围内最常见的酶病,估计有4亿人受其影响,主要分布在非洲、中东和东南亚的集中地区,在美国约有十分之一的非洲裔美国男性受其影响[1-3]。g6pd缺陷患者暴露于氧化应激后可能发生急性溶血性贫血,因为HMP分流是其NADPH的唯一来源。氧化应激是指g6pd缺乏患者由于还原性谷胱甘肽合成减少而导致抗氧化防御系统无法控制活性氧和活性氮[4]。由于细菌或病毒感染、某些食物和某些药物是g6pd缺乏症患者溶血性贫血的三种主要诱因,在某些个体中,溶血性贫血可能危及生命[5]。这些因素会增加活性氧的水平,导致红细胞被破坏的速度比身体替换它们的速度要快。研究者发现g6pd缺陷细胞更容易被呼吸道感染常见病原体HCoV229E感染和死亡[6]。在之前的研究中,我们注意到G6PD活性降低时还原性谷胱甘肽浓度也随之降低[7]。此外,我们提出的证据表明,维持谷胱甘肽水平可能有助于缓解某些疾病的症状,并补充双语谷胱甘肽作为一种治疗策略[8]。自COVID-19大流行爆发以来,考虑到有些人病情严重,有些人无症状,研究者开始认为G6PD缺乏症患者可能会像人类冠状病毒HCoV229E一样受到COVID-19大流行的显著影响,并提出了一个问题:G6PD缺乏症与COVID-19感染、易感性、严重程度或死亡率之间是否存在相关/关联的科学证据[9]。最近的回顾性研究有力地表明,g6pd缺乏的COVID-19患者可能会遭受氯喹引起的最高毒性,该药物与羟氯喹一起被广泛用于治疗COVID-19大流行[10,11]。此外,有报道简要概述了谷胱甘肽对ACE/ACE2失衡引发的COVID-19加重炎症的保护作用[12]。越来越多的证据表明G6PD缺乏可能不仅与COVID-19易感性有关,而且与感染的严重程度有关,因此为了回答这个问题,从临床角度研究冠状病毒(COVID-19)大流行对葡萄糖-6磷酸脱氢酶缺乏症(G6PD)患者的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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