TY - JOUR
T1 - Differential Effects of ABCG5/G8 Gene Region Variants on Lipid Profile, Blood Pressure Status, and Gallstone Disease History in Taiwan
AU - Teng, Ming Sheng
AU - Yeh, Kuan Hung
AU - Hsu, Lung An
AU - Chou, Hsin Hua
AU - Er, Leay Kiaw
AU - Wu, Semon
AU - Ko, Yu Lin
N1 - Publisher Copyright:
© 2023 by the authors.
PY - 2023/3/20
Y1 - 2023/3/20
N2 - ABCG5 and ABCG8 are two key adenosine triphosphate-binding cassette (ABC) proteins that regulate whole-body sterol trafficking. This study aimed to elucidate the association between
ABCG5/G8 gene region variants and lipid profile, cardiometabolic traits, and gallstone disease history in Taiwan. A total of 1494 Taiwan Biobank participants with whole-genome sequencing data and 117,679 participants with Axiom Genome-Wide CHB Array data were enrolled for analysis. Using genotype-phenotype and stepwise linear regression analyses, we found independent associations of four Asian-specific
ABCG5 variants, rs119480069, rs199984328, rs560839317, and rs748096191, with total, low-density lipoprotein (LDL), and non-high-density lipoprotein (HDL) cholesterol levels (all
p ≤ 0.0002). Four other variants, which were in nearly complete linkage disequilibrium, exhibited genome-wide significant associations with gallstone disease history, and the
ABCG8 rs11887534 variant showed a trend of superiority for gallstone disease history in a nested logistic regression model (
p = 0.074). Through regional association analysis of various other cardiometabolic traits, two variants of the
PLEKHH2, approximately 50 kb from the
ABCG5/G8 region, exhibited significant associations with blood pressure status (
p < 10
-6). In conclusion, differential effects of
ABCG5/G8 region variants were noted for lipid profile, blood pressure status, and gallstone disease history in Taiwan. These results indicate the crucial role of individualized assessment of
ABCG5/G8 variants for different cardiometabolic phenotypes.
AB - ABCG5 and ABCG8 are two key adenosine triphosphate-binding cassette (ABC) proteins that regulate whole-body sterol trafficking. This study aimed to elucidate the association between
ABCG5/G8 gene region variants and lipid profile, cardiometabolic traits, and gallstone disease history in Taiwan. A total of 1494 Taiwan Biobank participants with whole-genome sequencing data and 117,679 participants with Axiom Genome-Wide CHB Array data were enrolled for analysis. Using genotype-phenotype and stepwise linear regression analyses, we found independent associations of four Asian-specific
ABCG5 variants, rs119480069, rs199984328, rs560839317, and rs748096191, with total, low-density lipoprotein (LDL), and non-high-density lipoprotein (HDL) cholesterol levels (all
p ≤ 0.0002). Four other variants, which were in nearly complete linkage disequilibrium, exhibited genome-wide significant associations with gallstone disease history, and the
ABCG8 rs11887534 variant showed a trend of superiority for gallstone disease history in a nested logistic regression model (
p = 0.074). Through regional association analysis of various other cardiometabolic traits, two variants of the
PLEKHH2, approximately 50 kb from the
ABCG5/G8 region, exhibited significant associations with blood pressure status (
p < 10
-6). In conclusion, differential effects of
ABCG5/G8 region variants were noted for lipid profile, blood pressure status, and gallstone disease history in Taiwan. These results indicate the crucial role of individualized assessment of
ABCG5/G8 variants for different cardiometabolic phenotypes.
KW - ABCG5
KW - ABCG8
KW - differential effect
KW - gallstone disease
KW - genetic variants
KW - lipid profile
KW - Gallstones/genetics
KW - Cardiovascular Diseases
KW - Humans
KW - Blood Pressure/genetics
KW - Cholesterol
KW - ATP Binding Cassette Transporter, Subfamily G, Member 8/genetics
KW - ATP Binding Cassette Transporter, Subfamily G, Member 5/genetics
KW - Lipoproteins/genetics
KW - Taiwan
UR - https://www.scopus.com/pages/publications/85151111864
U2 - 10.3390/genes14030754
DO - 10.3390/genes14030754
M3 - 文章
C2 - 36981027
AN - SCOPUS:85151111864
SN - 2073-4425
VL - 14
JO - Genes
JF - Genes
IS - 3
M1 - 754
ER -