Evidence map›Paper›PMID 36649279›Full record

ArticlePloS one2023

Ancestral origins are associated with SARS-CoV-2 susceptibility and protection in a Florida patient population.

Yiran Shen, Bhuwan Khatri, Santosh Rananaware, Danmeng Li, David A Ostrov, Piyush K Jain, Christopher J Lessard, Cuong Q Nguyen

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.8field-weighted citation impact, top 32% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. Human coronavirus OC43-elicited CD4Nature communications · 2024
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Yiran ShenDepartment of Infectious Diseases and Immunology, College of Veterinary Medicine, University of Florida, Gainesville, Florida, United States of America.ORCID 0000-0002-4220-6862
Bhuwan KhatriGenes and Human Disease Research Program, Oklahoma Medical Research Foundation, Oklahoma City, Oklahoma, United States of America.ORCID 0000-0001-5456-2963
Santosh RananawareDepartment of Chemical Engineering, University of Florida, Gainesville, Florida, United States of America.ORCID 0000-0001-8789-5799
Danmeng LiDepartment of Pathology, Immunology & Laboratory Medicine, University of Florida, Gainesville, Florida, United States of America.ORCID 0000-0002-6905-554X
David A OstrovDepartment of Pathology, Immunology & Laboratory Medicine, University of Florida, Gainesville, Florida, United States of America.
Piyush K JainDepartment of Chemical Engineering, University of Florida, Gainesville, Florida, United States of America.ORCID 0000-0001-7153-442X
Christopher J LessardGenes and Human Disease Research Program, Oklahoma Medical Research Foundation, Oklahoma City, Oklahoma, United States of America.ORCID 0000-0003-2440-3843
Cuong Q NguyenDepartment of Infectious Diseases and Immunology, College of Veterinary Medicine, University of Florida, Gainesville, Florida, United States of America.ORCID 0000-0001-5633-4075
University of Florida · USOklahoma Medical Research Foundation · US

Funding

Mapping the T cell receptor/antigen complex and identifying the genetic-based treatment in Sjogren’s syndromeR01DE028544 · NIDCR · UNIVERSITY OF FLORIDA · PI NGUYEN, CUONG Q · 2019 to 2023
$2.6M
NIDCR NIH HHS R01 DE028544
6 · The paper itself

Abstract

COVID-19 is caused by severe acute respiratory syndrome-coronavirus-2 (SARS-CoV-2). The severity of COVID-19 is highly variable and related to known (e.g., age, obesity, immune deficiency) and unknown risk factors. The widespread clinical symptoms encompass a large group of asymptomatic COVID-19 patients, raising a crucial question regarding genetic susceptibility, e.g., whether individual differences in immunity play a role in patient symptomatology and how much human leukocyte antigen (HLA) contributes to this. To reveal genetic determinants of susceptibility to COVID-19 severity in the population and further explore potential immune-related factors, we performed a genome-wide association study on 284 confirmed COVID-19 patients (cases) and 95 healthy individuals (controls). We compared cases and controls of European (EUR) ancestry and African American (AFR) ancestry separately. We identified two loci on chromosomes 5q32 and 11p12, which reach the significance threshold of suggestive association (p<1x10-5 threshold adjusted for multiple trait testing) and are associated with the COVID-19 susceptibility in the European ancestry (index rs17448496: odds ratio[OR]  = 0.173; 95% confidence interval[CI], 0.08-0.36 for G allele; p = 5.15× 10-5 and index rs768632395: OR  =  0.166; 95% CI, 0.07-0.35 for A allele; p =  4.25×10-6, respectively), which were associated with two genes, PPP2R2B at 5q32, and LRRC4C at 11p12, respectively. To explore the linkage between HLA and COVID-19 severity, we applied fine-mapping analysis to dissect the HLA association with mild and severe cases. Using In-silico binding predictions to map the binding of risk/protective HLA to the viral structural proteins, we found the differential presentation of viral peptides in both ancestries. Lastly, extrapolation of the identified HLA from the cohort to the worldwide population revealed notable correlations. The study uncovers possible differences in susceptibility to COVID-19 in different ancestral origins in the genetic background, which may provide new insights into the pathogenesis and clinical treatment of the disease.

Indexed as

COVID-19Genetic Predisposition to DiseaseBlack or African AmericanFloridaGenome-Wide Association StudyHistocompatibility Antigens Class IHLA AntigensHumansSARS-CoV-2WhiteHistocompatibility Antigens Class IHLA Antigens

Identifiers

PMID36649279
PMCPMC9844918
OpenAlexW4316927770

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.