Epigenetics may characterize asymptomatic COVID-19 infection.


Journal

Human genomics
ISSN: 1479-7364
Titre abrégé: Hum Genomics
Pays: England
ID NLM: 101202210

Informations de publication

Date de publication:
27 07 2022
Historique:
received: 04 01 2022
accepted: 01 07 2022
entrez: 27 7 2022
pubmed: 28 7 2022
medline: 30 7 2022
Statut: epublish

Résumé

RT-PCR is the foremost clinical test for diagnosis of COVID-19. Unfortunately, PCR-based testing has limitations and may not result in a positive test early in the course of infection before symptoms develop. Enveloped RNA viruses, such as coronaviruses, alter peripheral blood methylation and DNA methylation signatures may characterize asymptomatic versus symptomatic infection. We used Illumina's Infinium MethylationEPIC BeadChip array to profile peripheral blood samples from 164 patients who tested positive for SARS-CoV-2 by RT-PCR, of whom 8 had no symptoms. Epigenome-wide association analysis identified 10 methylation sites associated with infection and a quantile-quantile plot showed little inflation. These preliminary results suggest that differences in methylation patterns may distinguish asymptomatic from symptomatic infection.

Identifiants

pubmed: 35897116
doi: 10.1186/s40246-022-00401-3
pii: 10.1186/s40246-022-00401-3
pmc: PMC9327394
doi:

Types de publication

Letter Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

27

Subventions

Organisme : NHLBI NIH HHS
ID : F32 HL160123
Pays : United States
Organisme : NHLBI NIH HHS
ID : 1F32HL160123
Pays : United States
Organisme : NIH HHS
ID : CTSI TR001082
Pays : United States

Informations de copyright

© 2022. The Author(s).

Références

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Auteurs

Cosby G Arnold (CG)

Department of Emergency Medicine, University of California, Davis, Sacramento, USA. cgarnold@ucdavis.edu.

Iain Konigsberg (I)

Division of Biomedical Informatics and Personalized Medicine, University of Colorado - Anschutz Medical Campus, 13001 East 17th Place, Campus Box C290, Aurora, CO, 80045, USA.

Jason Y Adams (JY)

Division of Pulmonary, Critical Care and Sleep Medicine, University of California, Davis, 2835 J Street, Suite 400, Sacramento, CA, 95816, USA.

Sunita Sharma (S)

Division of Pulmonary Sciences and Critical Care Medicine, University of Colorado - Anschutz Medical Campus, 12700 East 19th Avenue, Aurora, CO, 9C0380045, USA.

Neil Aggarwal (N)

Division of Pulmonary Sciences and Critical Care Medicine, University of Colorado - Anschutz Medical Campus, 12700 East 19th Avenue, Aurora, CO, 9C0380045, USA.

Andrew Hopkinson (A)

Department of Emergency Medicine, University of Colorado - Anschutz Medical Campus, 12401 East 17th Avenue, 7th Floor, Aurora, CO, 80045, USA.

Alexis Vest (A)

Department of Emergency Medicine, University of Colorado - Anschutz Medical Campus, 12401 East 17th Avenue, 7th Floor, Aurora, CO, 80045, USA.

Monica Campbell (M)

Division of Biomedical Informatics and Personalized Medicine, University of Colorado - Anschutz Medical Campus, 13001 East 17th Place, Campus Box C290, Aurora, CO, 80045, USA.

Meher Boorgula (M)

Division of Biomedical Informatics and Personalized Medicine, University of Colorado - Anschutz Medical Campus, 13001 East 17th Place, Campus Box C290, Aurora, CO, 80045, USA.

Ivana Yang (I)

Division of Biomedical Informatics and Personalized Medicine, University of Colorado - Anschutz Medical Campus, 13001 East 17th Place, Campus Box C290, Aurora, CO, 80045, USA.

Christopher Gignoux (C)

Division of Biomedical Informatics and Personalized Medicine, University of Colorado - Anschutz Medical Campus, 13001 East 17th Place, Campus Box C290, Aurora, CO, 80045, USA.

Kathleen C Barnes (KC)

Division of Biomedical Informatics and Personalized Medicine, University of Colorado - Anschutz Medical Campus, 13001 East 17th Place, Campus Box C290, Aurora, CO, 80045, USA.

Andrew A Monte (AA)

Department of Emergency Medicine, University of Colorado - Anschutz Medical Campus, 12401 East 17th Avenue, 7th Floor, Aurora, CO, 80045, USA.

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Classifications MeSH