Literature DB >> 23958391

A systematic review and meta-analysis of common mutations of SLC26A4 gene in Asian populations.

Wan Du1, Yufen Guo, Changlan Wang, Yanli Wang, Xiaowen Liu.   

Abstract

OBJECTIVES: The IVS7-2A>G (c.919-2A>G) and p.H723R (c.2168A>G) mutations of SLC26A4 gene are recognized as a risk factor for the non-syndromic hearing loss. To elucidate the variable results, a meta-analysis and systematic review was performed from all case-control studies by pooling data on them.
METHODS: The case-control studies were assessed with a modification of the Newcastle-Ottawa Scale (NOS). The strength of association between c.919-2A>G, c.2168A>G and hearing loss risk was measured by odds ratios (ORs) with 95% confidence intervals (CIs).
RESULTS: We included 14 case-control studies and 16 case series studies in present study. There was a higher prevalence of the c.919-2A>G mutation in the case group than that in the control group (12.4% vs 0.9%; OR = 13.05, 95% CI: 8.41-20.23, Z = 11.47, P<0.00001).
CONCLUSIONS: In conclusion, the results from this meta-analysis suggest that NSHL patients have an increased risk of the c.919-2A>G mutation of SLC26A4 gene in Asians, especially in Chinese.
Copyright © 2013 Elsevier Ireland Ltd. All rights reserved.

Entities:  

Keywords:  Meta-analysis; Non-syndromic hearing loss (NSHL); SLC26A4, IVS7-2A>G; p.H723R

Mesh:

Substances:

Year:  2013        PMID: 23958391     DOI: 10.1016/j.ijporl.2013.07.023

Source DB:  PubMed          Journal:  Int J Pediatr Otorhinolaryngol        ISSN: 0165-5876            Impact factor:   1.675


  7 in total

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  7 in total

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