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Impact of sickle cell trait on morbidity and mortality from SARS-CoV-2 infection

Authors :
Maureen O Achebe
Hae Soo Park
David M. Dorfman
Gerda Menard
Revital Freedman
Katherine Jolley
Kavita Mistry
Lauren E. Merz
Donna Neuberg
Source :
Blood Advances
Publication Year :
2021
Publisher :
American Society of Hematology, 2021.

Abstract

The COVID-19 pandemic has highlighted racial health disparities within the United States. Although social determinants of health are the most likely drivers of this disparity, it is possible that genetic traits enriched in the black population like sickle cell trait (SCT) could worsen the morbidity and mortality of infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Patients admitted for SARS-CoV-2 infection who identified as black or African American were included in the study (n = 166). Blood remnants were tested for SCT, and clinical data were abstracted from the chart. There was no difference in mortality between those with SCT and those without. There was no difference in respiratory complications between groups, but those without SCT had a much higher burden of chronic lung disease (P = .004). Those with SCT had higher creatinine on admission (P = .004), but no difference in in-hospital renal complications (P = .532). Notably, 12% of the cohort had SCT, which is higher than the expected 7.31% (P = .025). Our study did not show any evidence of increased end organ damage, morbidity, or mortality from SARS-CoV-2 infection among patients with SCT but did show differences in admission creatinine and preexisting lung disease.<br />Key Points • There is no impact of SCT on respiratory, renal, or circulatory complications or mortality in patients with SARS-CoV-2 infection. • The prevalence of SCT in the hospitalized cohort was significantly higher than the prevalence in the community (12% vs 7.31%).

Details

ISSN :
24739537 and 24739529
Volume :
5
Database :
OpenAIRE
Journal :
Blood Advances
Accession number :
edsair.doi.dedup.....cca7167b4ddb81a9ef7545fec157a5b2
Full Text :
https://doi.org/10.1182/bloodadvances.2021004977