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GWAS Study

Genome-wide association study identifies two risk loci for tuberculosis in Han Chinese.

Zheng R, Li Z, He F et al.

30287856 PubMed ID
GWAS Study Type
8039 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

ZR
Zheng R
LZ
Li Z
HF
He F
LH
Liu H
CJ
Chen J
CJ
Chen J
XX
Xie X
ZJ
Zhou J
CH
Chen H
WX
Wu X
WJ
Wu J
CB
Chen B
LY
Liu Y
CH
Cui H
FL
Fan L
SW
Sha W
LY
Liu Y
WJ
Wang J
HX
Huang X
ZL
Zhang L
XF
Xu F
WJ
Wang J
FY
Feng Y
QL
Qin L
YH
Yang H
LZ
Liu Z
CZ
Cui Z
LF
Liu F
CX
Chen X
GS
Gao S
SS
Sun S
SY
Shi Y
GB
Ge B
Chapter II

Abstract

Summary of the research findings

Tuberculosis (TB) is an infectious disease caused by Mycobacterium tuberculosis (Mtb), and remains a leading public health problem. Previous studies have identified host genetic factors that contribute to Mtb infection outcomes. However, much of the heritability in TB remains unaccounted for and additional susceptibility loci most likely exist. We perform a multistage genome-wide association study on 2949 pulmonary TB patients and 5090 healthy controls (833 cases and 1220 controls were genome-wide genotyped) from Han Chinese population. We discover two risk loci: 14q24.3 (rs12437118, Pcombined = 1.72 × 10-11, OR = 1.277, ESRRB) and 20p13 (rs6114027, Pcombined = 2.37 × 10-11, OR = 1.339, TGM6). Moreover, we determine that the rs6114027 risk allele is related to decreased TGM6 transcripts in PBMCs from pulmonary TB patients and severer pulmonary TB disease. Furthermore, we find that tgm6-deficient mice are more susceptible to Mtb infection. Our results provide new insights into the genetic etiology of TB.

833 Han Chinese ancestry cases, 1,220 Han Chinese ancestry controls

Chapter III

Study Statistics

Key metrics and study information

8039
Total Participants
GWAS
Study Type
Yes
Replicated
2,116 Han Chinese ancestry cases, 3,870 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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