Publication Date:
2015-06-27
Description:
Nature Genetics 47, 793 (2015). doi:10.1038/ng.3322 Authors: Zhao Ye, Zhiqiang Li, Yongfei Wang, Ying Mao, Ming Shen, Qilin Zhang, Shiqi Li, Liangfu Zhou, Xuefei Shou, Jianhua Chen, Zhijian Song, Zengyi Ma, Zhaoyun Zhang, Yiming Li, Hongying Ye, Chuanxin Huang, Tao Wang, Wenqiang He, Yichao Zhang, Rong Xie, Nidan Qiao, Huijia Qiu, Shan Huang, Meng Wang, Jiawei Shen, Zujia Wen, Wenjin Li, Ke Liu, Juan Zhou, Lin Wang, Jue Ji, Yin Wang, Hong Chen, Haixia Cheng, Zhifeng Shi, Yuqian Zhu, Daoying Geng, Zhenwei Yao, Weijun Tang, Bin Lu, Li Pan, Yi Zhang, Weimin Bao, Jinsong Wu, Kang Zheng, Yongyong Shi & Yao Zhao Pituitary adenoma is one of the most common intracranial neoplasms, and its genetic basis remains largely unknown. To identify genetic susceptibility loci for sporadic pituitary adenoma, we performed a three-stage genome-wide association study (GWAS) in the Han Chinese population. We first analyzed genome-wide SNP data in 771 pituitary adenoma cases and 2,788 controls and then carried forward the promising variants for replication in another 2 independent sets (2,542 cases and 3,620 controls in total). We identified three new susceptibility loci below the genome-wide significance threshold (P 〈 5 × 10−8) in the combined analyses: 10p12.31 (rs2359536, Pmeta = 2.25 × 10−10 and rs10828088, Pmeta = 6.27 × 10−10), 10q21.1 (rs10763170, Pmeta = 6.88 × 10−10) and 13q12.13 (rs17083838, Pmeta = 1.89 × 10−8). This study is the first GWAS to our knowledge on sporadic pituitary adenoma, and our results provide insight into the genetic basis of this disease.
Print ISSN:
1061-4036
Electronic ISSN:
1546-1718
Topics:
Biology
,
Medicine
Permalink