The GSDMB rs7216389 SNP is associated with chronic rhinosinusitis in a multi‐institutional cohort
AuthorZack, Dana E.
Stern, Debra A.
Willis, Amanda L.
Kim, Alexander S.
Mansfield, Corinne J.
Reed, Danielle R.
Brooks, Steven G.
Adappa, Nithin D.
Palmer, James N.
Cohen, Noam A.
Chiu, Alexander G.
Song, Brian H.
Le, Chris H.
Chang, Eugene H.
AffiliationDepartment of Otolaryngology, University of Arizona
Asthma and Airway Disease Research Center, University of Arizona
MetadataShow full item record
CitationZack, D. E., Stern, D. A., Willis, A. L., Kim, A. S., Mansfield, C. J., Reed, D. R., Brooks, S. G., Adappa, N. D., Palmer, J. N., Cohen, N. A., Chiu, A. G., Song, B. H., Le, C. H., & Chang, E. H. (2021). The GSDMB rs7216389 SNP is associated with chronic rhinosinusitis in a multi-institutional cohort. International Forum of Allergy and Rhinology.
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AbstractBackground: Chronic rhinosinusitis (CRS) is a multifactorial disease with a high co-occurrence with asthma. In this multicohort study, we tested whether single nucleotide polymorphisms (SNPs) associated with childhood asthma and rhinovirus (RV)-associated disease are related to an increased susceptibility to adult CRS in a multicohort retrospective case-control study. Methods: Participants at two tertiary academic rhinology centers, University of Arizona (UofA) and University of Pennsylvania (UPenn) were recruited. Cases were defined as those with physician diagnosed CRS (UofA, n = 149; UPenn, n = 250), and healthy controls were those without CRS (UofA, n = 66; UPenn, n = 275). Genomic DNA was screened for the GSDMB rs7216389 SNP and CDHR3 rs6967330 SNP. Gene dosage, or the number of combined risk alleles in a single subject was calculated. Meta-analysis of the association between GSDMB or CDHR3 genotypes and CRS was performed and additive gene dosage effect for each population calculated using p for trend. Results: A meta-analysis revealed a combined increased risk for CRS in subjects with the GSDMB rs7216389 SNP (odds ratio [OR] 1.40; 95% confidence interval [CI], 1.16–1.76; p = 0.004). Both the UofA (OR 1.73; 95% CI, 1.23–2.43; p = 0.002) and UPenn (OR 1.27; 95% CI, 1.02–1.58; p = 0.035) populations showed a significant positive association between the number of combined risk alleles of GSDMB rs7216389 SNP and CDHR3 rs6967330 SNP and risk for CRS. Conclusion: Carriers of the GSDMB rs7216389 SNP and CDHR3 rs6967330 SNP are at increased susceptibility for CRS. These data suggest that therapeutic approaches to target aberrant responses to RV infection may play a role in the treatment of unified airway disease. © 2021 ARS-AAOA, LLC
Note12 month embargo; first published: 02 June 2021
VersionFinal accepted manuscript