Skip to main content

Lund University Publications

LUND UNIVERSITY LIBRARIES

Chronic rhinosinusitis patients show accumulation of genetic variants in PARS2

Henmyr, Viktor LU ; Lind-Halldén, Christina ; Halldén, Christer LU ; Säll, Torbjörn LU ; Carlberg, Daniel ; Bachert, Claus and Cardell, Lars Olaf LU (2016) In PLoS ONE 11(6).
Abstract

Genetic studies of chronic rhinosinusitis (CRS) have identified a total of 53 CRS-associated SNPs that were subsequently evaluated for their reproducibility in a recent study. The rs2873551 SNP in linkage disequilibrium with PARS2 showed the strongest association signal. The present study aims to comprehensively screen for rare variants in PARS2 and evaluate for accumulation of such variants in CRS-patients. Sanger sequencing and long-range PCR were used to screen for rare variants in the putative promoter region and coding sequence of 310 CRS-patients and a total of 21 variants were detected. The mutation spectrum was then compared with data from European populations of the 1000Genomes project (EUR) and the Exome Aggregation Consortium... (More)

Genetic studies of chronic rhinosinusitis (CRS) have identified a total of 53 CRS-associated SNPs that were subsequently evaluated for their reproducibility in a recent study. The rs2873551 SNP in linkage disequilibrium with PARS2 showed the strongest association signal. The present study aims to comprehensively screen for rare variants in PARS2 and evaluate for accumulation of such variants in CRS-patients. Sanger sequencing and long-range PCR were used to screen for rare variants in the putative promoter region and coding sequence of 310 CRS-patients and a total of 21 variants were detected. The mutation spectrum was then compared with data from European populations of the 1000Genomes project (EUR) and the Exome Aggregation Consortium (ExAC). The CRS population showed a significant surplus of low-frequency variants compared with ExAC data. Haplotype analysis of the region showed a significant excess of rare haplotypes in the CRS population compared to the EUR population. Two missense mutations were also genotyped in the 310 CRS patients and 372 CRS-negative controls, but no associations with the disease were found. This is the first re-sequencing study in CRS research and also the first study to show an association of rare variants with the disease.

(Less)
Please use this url to cite or link to this publication:
author
; ; ; ; ; and
organization
publishing date
type
Contribution to journal
publication status
published
subject
in
PLoS ONE
volume
11
issue
6
article number
e0158202
publisher
Public Library of Science (PLoS)
external identifiers
  • scopus:84977080493
  • pmid:27348859
  • wos:000378801200050
ISSN
1932-6203
DOI
10.1371/journal.pone.0158202
language
English
LU publication?
yes
id
37e443f0-31e8-4677-aa7f-7828f4f3679f
date added to LUP
2017-01-27 08:06:00
date last changed
2025-01-12 20:20:22
@article{37e443f0-31e8-4677-aa7f-7828f4f3679f,
  abstract     = {{<p>Genetic studies of chronic rhinosinusitis (CRS) have identified a total of 53 CRS-associated SNPs that were subsequently evaluated for their reproducibility in a recent study. The rs2873551 SNP in linkage disequilibrium with PARS2 showed the strongest association signal. The present study aims to comprehensively screen for rare variants in PARS2 and evaluate for accumulation of such variants in CRS-patients. Sanger sequencing and long-range PCR were used to screen for rare variants in the putative promoter region and coding sequence of 310 CRS-patients and a total of 21 variants were detected. The mutation spectrum was then compared with data from European populations of the 1000Genomes project (EUR) and the Exome Aggregation Consortium (ExAC). The CRS population showed a significant surplus of low-frequency variants compared with ExAC data. Haplotype analysis of the region showed a significant excess of rare haplotypes in the CRS population compared to the EUR population. Two missense mutations were also genotyped in the 310 CRS patients and 372 CRS-negative controls, but no associations with the disease were found. This is the first re-sequencing study in CRS research and also the first study to show an association of rare variants with the disease.</p>}},
  author       = {{Henmyr, Viktor and Lind-Halldén, Christina and Halldén, Christer and Säll, Torbjörn and Carlberg, Daniel and Bachert, Claus and Cardell, Lars Olaf}},
  issn         = {{1932-6203}},
  language     = {{eng}},
  month        = {{06}},
  number       = {{6}},
  publisher    = {{Public Library of Science (PLoS)}},
  series       = {{PLoS ONE}},
  title        = {{Chronic rhinosinusitis patients show accumulation of genetic variants in PARS2}},
  url          = {{http://dx.doi.org/10.1371/journal.pone.0158202}},
  doi          = {{10.1371/journal.pone.0158202}},
  volume       = {{11}},
  year         = {{2016}},
}