TY - JOUR
T1 - Genome-wide Association Study of Susceptibility to Respiratory Syncytial Virus Hospitalization in Young Children <5 Years of age
AU - Egeskov-Cavling, Amanda Marie
AU - Van Wijhe, Maarten
AU - Yakimov, Victor
AU - Johannesen, Caroline Klint
AU - Pollard, Andrew
AU - Trebbien, Ramona
AU - Bybjerg-Grauholm, Jonas
AU - Fischer, Thea Kølsen
AU - Nair, Harish
AU - Campbell, Harry
AU - Beutels, Philippe
AU - Bont, Louis
AU - Pollard, Andrew
AU - Openshaw, Peter
AU - Martinon-Torres, Federico
AU - Heikkinen, Terho
AU - Meijer, Adam
AU - Fischer, Thea
AU - Van Den Berge, Maarten
AU - Giaquinto, Carlo
AU - Abram, Michael
AU - Swanson, Kena
AU - Rizkalla, Bishoy
AU - Vernhes, Charlotte
AU - Gallichan, Scott
AU - Aerssens, Jeroen
AU - Kumar, Veena
AU - Molero, Eva
N1 - Publisher Copyright:
© 2023 The Author(s).
PY - 2024/8/15
Y1 - 2024/8/15
N2 - Background: Worldwide, respiratory syncytial virus (RSV) infections are among the most common causes of infant hospitalization. Host genetic factors influencing the risk and severity of RSV infection are not well known. Methods: We conducted a genome-wide association study (GWAS) to investigate single-nucleotide polymorphisms (SNPs) associated with severe RSV infections using a nested case-control design based on 2 Danish cohorts. We compared SNPs from 1786 children hospitalized with RSV to 45 060 controls without an RSV-coded hospitalization. We performed gene-based testing, tissue enrichment, gene-set enrichment, and a meta-analysis of the 2 cohorts. Finally, an analysis of potential associations between the severity of RSV infection and genetic markers was performed. Results: We did not detect any significant genome-wide associations between SNPs and RSV infection or the severity of RSV. We did find potential loci associated with RSV infections on chromosome 5 in 1 cohort but failed to replicate any signals in both cohorts. Conclusions: Despite being the largest GWAS of severe RSV infection, we did not detect any genome-wide significant loci. This may be an indication of a lack of power or an absence of signal. Future studies might include mild illness and need to be larger to detect any significant associations.
AB - Background: Worldwide, respiratory syncytial virus (RSV) infections are among the most common causes of infant hospitalization. Host genetic factors influencing the risk and severity of RSV infection are not well known. Methods: We conducted a genome-wide association study (GWAS) to investigate single-nucleotide polymorphisms (SNPs) associated with severe RSV infections using a nested case-control design based on 2 Danish cohorts. We compared SNPs from 1786 children hospitalized with RSV to 45 060 controls without an RSV-coded hospitalization. We performed gene-based testing, tissue enrichment, gene-set enrichment, and a meta-analysis of the 2 cohorts. Finally, an analysis of potential associations between the severity of RSV infection and genetic markers was performed. Results: We did not detect any significant genome-wide associations between SNPs and RSV infection or the severity of RSV. We did find potential loci associated with RSV infections on chromosome 5 in 1 cohort but failed to replicate any signals in both cohorts. Conclusions: Despite being the largest GWAS of severe RSV infection, we did not detect any genome-wide significant loci. This may be an indication of a lack of power or an absence of signal. Future studies might include mild illness and need to be larger to detect any significant associations.
KW - genetic association studies
KW - genome-wide association study
KW - respiratory syncytial virus
KW - RSV
UR - http://www.scopus.com/inward/record.url?scp=85195492191&partnerID=8YFLogxK
U2 - 10.1093/infdis/jiad370
DO - 10.1093/infdis/jiad370
M3 - Article
C2 - 37666001
AN - SCOPUS:85195492191
SN - 0022-1899
VL - 230
SP - e333-e341
JO - Journal of Infectious Diseases
JF - Journal of Infectious Diseases
IS - 2
ER -