Associations between COVID-19 and Glucose-6-Phosphate Dehydrogenase Activity in Brazil

Author:

de Almeida Rodrigues Maria Gabriela12,Monteiro Wuelton Marcelo12,de Melo Gisely Cardoso12,Dias Ádila Liliane Barros12,Sartim Marco Aurélio34,Xavier Mariana Simão5,Netto Rebeca Linhares Abreu12,Almeida Fernando Fonseca12,Baía-da-Silva Djane Clarys12346,Brito-Sousa José Diego12,de Lacerda Marcus Vinicius Guimarães126,de Souza Sampaio Vanderson278

Affiliation:

1. Universidade do Estado do Amazonas, Manaus, Brazil;

2. Department of Education and Research, Fundação de Medicina Tropical Dr. Heitor Vieira Dourado, Manaus, Brazil;

3. Department of Postgraduate, Research and Innovation, Universidade Nilton Lins, Manaus, Brazil;

4. Institute of Biological Sciences, Universidade Federal do Amazonas, Manaus, Brazil;

5. Clinical Research Laboratory for Acute Febrile Illnesses, Instituto Nacional de Infectologia Carlos Chagas, Rio de Janeiro, Brazil;

6. Instituto Leônidas e Maria Deane/Fiocruz Amazônia, Instituto de Pesquisas Clínicas Carlos Borborema, Manaus, Brazil;

7. Fundação de Vigilância em Saúde do Amazonas, Manaus, Brazil;

8. Instituto Todos pela Saúde, São Paulo, Brazil

Abstract

ABSTRACT. Glucose-6 phosphate dehydrogenase deficiency (G6PDd) was suggested as a risk factor for severe disease in patients with COVID-19. We evaluated clinical outcomes and glucose-6 phosphate dehydrogenase (G6PD) activity during and after illness in patients with COVID-19. This prospective cohort study included adult participants (≥ 18 years old) who had clinical and/or radiological COVID-19 findings or positive reverse transcription–polymerase chain reaction results. Epidemiological and clinical data were extracted from electronic medical records. Glucose-6 phosphate dehydrogenase activity was measured using SD Biosensor STANDARD G6PD® equipment on admission and 1 year after discharge. Samples were genotyped for the three most common single nucleotide polymorphisms for G6PDd in the Brazilian Amazon. Seven hundred fifty-three patients were included, of whom 123 (16.3%) were G6PD deficient. There was no difference between groups regarding the risks of hospitalization (P = 0.740) or invasive mechanical ventilation (P = 0.31), but the risk of death was greater in patients with normal G6PD levels (P = 0.022). Only 29 of 116 participants (25%) carried the African G6PDd genotype. Of 30 participants tested as G6PD deficient during disease, only 11 (36.7%) results agreed 1 year after discharge. In conclusion, this study does not demonstrate an association of G6PDd with severity of COVID-19. Limitations of the test for detecting enzyme levels during COVID-19 illness were demonstrated by genotyping and retesting after the disease period. Care must be taken when screening for G6PDd in patients with acute COVID-19.

Publisher

American Society of Tropical Medicine and Hygiene

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