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GWAS Study

Identification of IGF1, SLC4A4, WWOX, and SFMBT1 as hypertension susceptibility genes in Han Chinese with a genome-wide gene-based association study.

Yang HC, Liang YJ, Chen JW et al.

22479346 PubMed ID
GWAS Study Type
6118 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

YH
Yang HC
LY
Liang YJ
CJ
Chen JW
CK
Chiang KM
CC
Chung CM
HH
Ho HY
TC
Ting CT
LT
Lin TH
SS
Sheu SH
TW
Tsai WC
CJ
Chen JH
LH
Leu HB
YW
Yin WH
CT
Chiu TY
CC
Chern CL
LS
Lin SJ
TB
Tomlinson B
GY
Guo Y
SP
Sham PC
CS
Cherny SS
LT
Lam TH
TG
Thomas GN
PW
Pan WH
Chapter II

Abstract

Summary of the research findings

Hypertension is a complex disorder with high prevalence rates all over the world. We conducted the first genome-wide gene-based association scan for hypertension in a Han Chinese population. By analyzing genome-wide single-nucleotide-polymorphism data of 400 matched pairs of young-onset hypertensive patients and normotensive controls genotyped with the Illumina HumanHap550-Duo BeadChip, 100 susceptibility genes for hypertension were identified and also validated with permutation tests. Seventeen of the 100 genes exhibited differential allelic and expression distributions between patient and control groups. These genes provided a good molecular signature for classifying hypertensive patients and normotensive controls. Among the 17 genes, IGF1, SLC4A4, WWOX, and SFMBT1 were not only identified by our gene-based association scan and gene expression analysis but were also replicated by a gene-based association analysis of the Hong Kong Hypertension Study. Moreover, cis-acting expression quantitative trait loci associated with the differentially expressed genes were found and linked to hypertension. IGF1, which encodes insulin-like growth factor 1, is associated with cardiovascular disorders, metabolic syndrome, decreased body weight/size, and changes of insulin levels in mice. SLC4A4, which encodes the electrogenic sodium bicarbonate cotransporter 1, is associated with decreased body weight/size and abnormal ion homeostasis in mice. WWOX, which encodes the WW domain-containing protein, is related to hypoglycemia and hyperphosphatemia. SFMBT1, which encodes the scm-like with four MBT domains protein 1, is a novel hypertension gene. GRB14, TMEM56 and KIAA1797 exhibited highly significant differential allelic and expressed distributions between hypertensive patients and normotensive controls. GRB14 was also found relevant to blood pressure in a previous genetic association study in East Asian populations. TMEM56 and KIAA1797 may be specific to Taiwanese populations, because they were not validated by the two replication studies. Identification of these genes enriches the collection of hypertension susceptibility genes, thereby shedding light on the etiology of hypertension in Han Chinese populations.

400 Han Chinese ancestry cases, 400 Han Chinese ancestry controls

Chapter III

Study Statistics

Key metrics and study information

6118
Total Participants
GWAS
Study Type
Yes
Replicated
315 Han Chinese ancestry individuals, 1,999 European ancestry cases, 3,004 European ancestry controls
Replication Participants
East Asian, European
Ancestry
China, U.K.
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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