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Immunology - Otolaryngology


Polymorphisms in RYBP and AOAH Genes Are Associated with Chronic Rhinosinusitis in a Chinese Population: A Replication Study
Published: Tuesday, June 19, 2012
Author: Yuan Zhang et al.

by Yuan Zhang, Leandra Mfuna Endam, Abdelali Filali-Mouhim, Liping Zhao, Martin Desrosiers, Demin Han, Luo Zhang

Background

The development of CRS is believed to be the result of combined interactions between the genetic background of the affected subject and environmental factors.

Objectives

To replicate and extend our recent findings from genetic association studies in chronic rhinosinusitis (CRS) performed in a Canadian Caucasian population in a Chinese population.

Methods

In a case-control replication study, DNA samples were obtained from CRS with (n?=?306; CRSwNP) and without (n?=?332; CRSsNP) nasal polyps, and controls (n?=?315) in a Chinese population. A total of forty-nine single nucleotide polymorphisms (SNPs) selected from previous identified SNPs associated with CRS in Canadian population, and SNPs from the CHB HapMap dataset were individually genotyped.

Results

We identified two SNPs respectively in RYBP (rs4532099, p?=?2.15Eā€“06, OR?=?2.59) and AOAH (rs4504543, p?=?0.0001152, OR?=?0.58) significantly associated with whole CRS cohort. Subgroup analysis for the presence of nasal polyps (CRSwNP and CRSsNP) displayed significant association in CRSwNP cohorts regarding to one SNP in RYBP (P?=?3.24Eā€“006, OR?=?2.76). Evidence of association in the CRSsNP groups in terms of 2 SNPs (AOAH_rs4504543 and RYBP_rs4532099) was detected as well. Stratifying analysis by gender demonstrated that none of the selected SNPs were associated with CRSwNP as well as CRSsNP. Meanwhile 3 SNPs (IL1A_rs17561, P?=?0.005778; IL1A_rs1800587, P?=?0.009561; IRAK4_rs4251513, P?=?0.03837) were associated with serum total IgE level.

Conclusions

These genes are biologically plausible, with roles in regulation of transcription (RYBP) and inflammatory response (AOAH). The present data suggests the potential common genetic basis in the development of CRS in Chinese and Caucasian population.

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