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Differential Effects of ABCG5/G8 Gene Region Variants on Lipid Profile, Blood Pressure Status, and Gallstone Disease History in Taiwan

  • Ming Sheng Teng
  • , Kuan Hung Yeh
  • , Lung An Hsu
  • , Hsin Hua Chou
  • , Leay Kiaw Er
  • , Semon Wu
  • , Yu Lin Ko*
  • *Corresponding author for this work
  • Buddhist Tzu Chi Medical Foundation
  • Tzu Chi University
  • Chinese Culture University

Research output: Contribution to journalJournal Article peer-review

13 Scopus citations

Abstract

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.

Original languageEnglish
Article number754
JournalGenes
Volume14
Issue number3
DOIs
StatePublished - 20 03 2023

Bibliographical note

Publisher Copyright:
© 2023 by the authors.

Keywords

  • ABCG5
  • ABCG8
  • differential effect
  • gallstone disease
  • genetic variants
  • lipid profile
  • Gallstones/genetics
  • Cardiovascular Diseases
  • Humans
  • Blood Pressure/genetics
  • Cholesterol
  • ATP Binding Cassette Transporter, Subfamily G, Member 8/genetics
  • ATP Binding Cassette Transporter, Subfamily G, Member 5/genetics
  • Lipoproteins/genetics
  • Taiwan

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