Literature DB >> 24986923

A genome-wide association study identifies susceptibility loci of silica-related pneumoconiosis in Han Chinese.

Minjie Chu1, Xiaoming Ji2, Weihong Chen3, Ruyang Zhang1, Chongqi Sun1, Ting Wang2, Chen Luo2, Jianhang Gong1, Meng Zhu1, Jingjing Fan2, Zhiguo Hou2, Juncheng Dai4, Guangfu Jin4, Tangchun Wu3, Feng Chen1, Zhibin Hu5, Chunhui Ni2, Hongbing Shen6.   

Abstract

Pneumoconiosis is the most serious occupational disease in China and its leading cause is occupational silica exposure. Pneumoconiosis takes several years to develop depending on the exposure level of silica. However, individual variation in the susceptibility to pneumoconiosis has been observed among the subjects with similar exposure. We conducted a genome-wide screening with 710,999 single nucleotide polymorphisms (SNPs) in a cohort of 400 coal workers (202 cases and 198 exposed controls) for pneumoconiosis susceptible loci. Seven promising variants were evaluated in an independent cohort of 568 coal workers (323 cases and 245 exposed controls), followed by a second replication on 463 iron ore workers (167 cases and 296 exposed controls). By pooling all of the genome-wide association studies and replication stages together, we found a genome-wide significant (P < 5.0 × 10(-8)) association for rs73329476 (P = 1.74 × 10(-8), OR = 2.17, 95% CI = 1.66-2.85) and two additional replicated associations for rs4320486 (P < 0.05) and rs117626015 (P < 0.05) with combined P-values of 4.29 × 10(-6) and 5.05 × 10(-6), respectively. In addition, the risk allele T of rs73329476 was significantly associated with lower mRNA expression levels of carboxypeptidase M (CPM) in total cellular RNA from whole blood of 156 healthy individuals (P = 0.0252). The identified pneumoconiosis susceptibility loci may provide new insights into the pathogenesis of pneumoconiosis, and may also have some clinical utility for risk prediction for pneumoconiosis and high-risk population screening for workers with occupational silica exposure.
© The Author 2014. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com.

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Year:  2014        PMID: 24986923     DOI: 10.1093/hmg/ddu333

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN: 0964-6906            Impact factor:   6.150


  4 in total

1.  Functional variant of the carboxypeptidase M (CPM) gene may affect silica-related pneumoconiosis susceptibility by its expression: a multistage case-control study.

Authors:  Minjie Chu; Shuangshuang Wu; Wei Wang; Yuhui Yu; Mingjiong Zhang; Lingli Sang; Tian Tian; Yihua Lu; Weiwei Yuan; Qiqing Huang; Min Yi; Yuexia Gao; Jing Xiao; Yulong Lian; Xun Zhuang; Zuo-Feng Zhang; Jianqing Wu
Journal:  Occup Environ Med       Date:  2019-01-23       Impact factor: 4.402

2.  The single nucleotide polymorphism rs1814521 in long non-coding RNA ADGRG3 associates with the susceptibility to silicosis: a multi-stage study.

Authors:  Wei Wang; Xiaofeng Chen; Chunping Li; Rui Zhao; Jinlong Zhang; Hong Qin; Miaomiao Wang; Yao Su; Minzhu Tang; Lei Han; Na Sun
Journal:  Environ Health Prev Med       Date:  2022       Impact factor: 4.395

3.  Associations of MMP1, MMP2 and MMP3 Genes Polymorphism with Coal Workers' Pneumoconiosis in Chinese Han Population.

Authors:  Xiaoming Ji; Lijuan Wang; Baiqun Wu; Ruhui Han; Lei Han; Ting Wang; Jingjin Yang; Chunhui Ni
Journal:  Int J Environ Res Public Health       Date:  2015-10-30       Impact factor: 3.390

4.  Polymorphisms in Long Noncoding RNA H19 Contribute to the Protective Effects of Coal Workers' Pneumoconiosis in a Chinese Population.

Authors:  Qiuyun Wu; Weiwen Yan; Ruhui Han; Jingjin Yang; Jiali Yuan; Xiaoming Ji; Yi Liu; Chunhui Ni
Journal:  Int J Environ Res Public Health       Date:  2016-09-12       Impact factor: 3.390

  4 in total

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