key: cord-0959111-nbcjv47q
authors: Jamerson, Brenda; Haryadi, Tirtadharyana; Bohannon, Arline
title: Glucose 6 Phosphate Dehydrogenase Deficiency: An Actionable Risk Factor for Patients with COVID-19?
date: 2020-06-07
journal: Arch Med Res
DOI: 10.1016/j.arcmed.2020.06.006
sha: c8640fd95998e72acf7325c488f28d7bbf6f2572
doc_id: 959111
cord_uid: nbcjv47q

Glucose-6-phosphate dehydrogenase (G6PD) deficiency is a common X-linked mutation that is more prevalent in African, Asian, Latin American and Mediterranean populations. Although most individuals are asymptomatic, exposure to certain food, drugs, or infections can trigger acute hemolytic anemia. Given the potential for coronavirus to trigger oxidative stress, unrecognized G6PD deficiency in the presence of the COVID-19 viral infection may cause hemolytic crisis and worse outcome in affected individuals. Further, since certain drugs that may be used to treat COVID-19 infection may cause hemolytic crisis in individuals with G6PD deficiency, it may be warranted to recommend adding G6PD deficiency to the list of screening elements in a COVID-19 workup for those patients where there is a high suspicion for this genetic mutation.

COVID-19 presents as mild to moderate disease in the majority of patients, but as severe acute respiratory syndrome in hospitalized patients who progress to a severe form. Risk factors identified for susceptibility to worse outcomes for COVID-19 include comorbidities such as hypertension, diabetes, cardiovascular disease, chronic lung disease, and older age (1).

Several factors are associated with more severe disease and fatal outcomes in COVID-19 patients. In a cross sectional analysis examining laboratory parameters of COVID-19 cases associated with mortality, a significant elevation of d-dimer, a biomarker of fibrin formation and degradation, was present in those patients who did not survive. Other biomarkers that are present in those with more severe disease are an increase in inflammatory biomarkers of IL6, increase in liver transaminases, lower platelets and increase ferritin (2) . Venous thromboembolism has been reported in those who die from the disease (1). This presentation has overlapping features of individuals with glucose 6 phosphate dehydrogenase (G6PD) deficiency who experience hemolytic crisis after being exposed to oxidative agents or viral infections and therefore raises the specter that G6PD deficiency is a predisposing factor that could lead to a more severe COVID-19 illness.

Arch Med Res E20_855 2 G6PD deficiency is a common X linked disorder affecting approximately 350-400 million people worldwide (3). G6PD is found in all cells of the body and catalyzes the initial step in the pentose phosphate pathway (4, 5) . This pathway functions to protect red blood cells against oxidative stress through the production of nicotinamide adenine dinucleotide phosphate which is generated by G6PD to supply glutathione.4 G6PD deficiency is categorized as class I-IV corresponding to G6PD enzyme activity. The majority of persons are defined class II-III (associated with 10-60% enzyme activity) with fewer persons having a more severe class I form (associated with less than 10% G6PD activity).

5 Classical events which trigger red cell hemolysis are the ingestion of fava beans, certain drugs and infection (4) . Hydroxychloroquine, a drug that is under investigation to treat COVID-19, has been reported to trigger hemolytic crisis in patients with G6PD deficiency (6,7). Therefore, when an unexpected drop in hemoglobin occurs in a patient with COVID-19, it may also alert the clinician to the need to further evaluate for the possibility of G6PD deficiency.

The G6PD genetic mutation has a higher prevalence across African, Asian, Latin America, and Mediterranean countries (3). The prevalence of G6PD deficiency commonly maps to populations where historically malaria was prevalent and is likely to have been a protective adaptation since cells deficient in G6PD inhibit the growth of specific types of malaria (4). In the United States, estimated prevalence of G6PD deficiency based on estimates from the military population is 12% in African American males, 4% in African American females, 4% in Asian males, 2% in Hispanic males and 0.3% in nonhispanic Caucasian males (8) .

Arch Med Res E20_855 3 A recent report indicates G6PD deficiency may also result in a susceptibility to coronavirus infection.

A study examining G6PD deficient incubated cells found that these cells exhibited significantly higher coronavirus viral gene expression and viral particle production (9) . Further, older individuals with G6PD deficiency are more at risk of a preexisting state of having red blood cells with lower amounts of G6PD, lower glutathione and a higher red blood cell turnover (10) . This may predispose older aged patients with G6PD deficiency to have a lower threshold for hemolytic crisis following exposure to certain triggering event such as coronavirus.

Taken together, there are multiple pathways where unrecognized G6PD deficiency could be associated with severe COVID-19 infection and worse outcomes: a) Unrecognized G6PD deficiency in the presence of the viral infection itself may cause hemolytic crisis and worse outcome. b) Unrecognized G6PD deficiency is a risk factor for complications -not associated with hemolytic crisis but associated with venous thrombosis and cascade of CV complications. c) Administration of hydroxycholorquine for treatment of COVID 19 in patients with unrecognized G6PD deficiency could lead to worse outcomes associated with hemolytic crisis.

Based on this evidence, it may be warranted to recommend adding G6PD deficiency to the list of screening elements in a COVID-19 workup for those patients where there is a high suspicion for this genetic mutation.

Does comorbidity increase the risk of patients with COVID-19: evidence from meta-analysis

Clinical course and risk factors for mortality of adult inpatients with COVID-19 in Wuhan, China: a retrospective cohort study

The global prevalence of glucose-6-phosphate dehydrogenase deficiency: a systematic review and meta-analysis

Favism and glucose-6-phosphate dehydrogenase deficiency

Diagnosis and management of G6PD deficiency

COVID 19 infection and treatment with

Acute hemolysis by hydroxycloroquine was observed

G6PD-deficient patient with severe COVD-19 related lung injury

Prevalence of glucose-6-phosphate dehydrogenase deficiency in US Army personnel

Glucose-6-phosphate dehydrogenase deficiency enhances human coronavirus 229E infection

Enhanced suicidal erythrocyte death contributing to anemia in the elderly