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GWAS Study

A genome-wide association study reveals that variants within the HLA region are associated with risk for nonobstructive azoospermia.

Zhao H, Xu J, Zhang H et al.

22541561 PubMed ID
GWAS Study Type
6802 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

ZH
Zhao H
XJ
Xu J
ZH
Zhang H
SJ
Sun J
SY
Sun Y
WZ
Wang Z
LJ
Liu J
DQ
Ding Q
LS
Lu S
SR
Shi R
YL
You L
QY
Qin Y
ZX
Zhao X
LX
Lin X
LX
Li X
FJ
Feng J
WL
Wang L
TJ
Trent JM
XC
Xu C
GY
Gao Y
ZB
Zhang B
GX
Gao X
HJ
Hu J
CH
Chen H
LG
Li G
ZJ
Zhao J
ZS
Zou S
JH
Jiang H
HC
Hao C
ZY
Zhao Y
MJ
Ma J
ZS
Zheng SL
CZ
Chen ZJ
Chapter II

Abstract

Summary of the research findings

A genome-wide association study of Han Chinese subjects was conducted to identify genetic susceptibility loci for nonobstructive azoospermia (NOA). In the discovery stage, 802 azoospermia cases and 1,863 controls were screened for genetic variants in the genome. Promising SNPs were subsequently confirmed in two independent sets of subjects: 818 azoospermia cases and 1,755 controls from northern China, and 606 azoospermia cases and 958 controls from central and southern China. We detected variants at human leukocyte antigen (HLA) regions that were independently associated with NOA (HLA-DRA, rs3129878, p(combine) = 3.70 × 10(-16), odds ratio [OR] = 1.37; C6orf10 and BTNL2, rs498422, p(combine) = 2.43 × 10(-12), OR = 1.42). These findings provide additional insight into the pathogenesis of NOA.

802 Han Chinese ancestry cases, 1,863 Han Chinese ancestry controls

Chapter III

Study Statistics

Key metrics and study information

6802
Total Participants
GWAS
Study Type
Yes
Replicated
1,424 Han Chinese ancestry cases, 2,713 Han Chinese ancestry controls
Replication Participants
East Asian
Ancestry
China
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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