Abstract

BackgroundGallstones are abnormal masses caused by impaired metabolism of cholesterol, bilirubin, or bile salts in the gallbladder or biliary tract. ATP-binding cassette subfamily G member 8 (ABCG8) is a protein that regulates cholesterol efflux from the liver. Genome-wide association studies (GWAS) and meta-analyses of GWAS revealed the ABCG8 rs11887534 variant as the most common genetic determinant of gallstones in humans. These findings have not been extensively replicated in Taiwanese. Therefore, we appraised the relationship between gallstones and rs11887534 in a relatively large Taiwanese sample.MethodsWe retrieved data collected through questionnaires, physical and biochemical tests from the Taiwan Biobank Bank (TWB). The study participants comprised 7388 men and 13,880 women who voluntarily enrolled in the Taiwan Biobank project between 2008 and 2019. Gallstones were self-reported.ResultsThe overall sample size was 21,268 comprising 938 gallstone patients and 20,330 non-gallstone individuals. Among the participants, 20,640 had the GG and 628 had the GC + CC genotype. At p-value < 0.05, the baseline genotypes and gallstone status between men and women were not significantly different. The risk of gallstones was higher in participants having the GC + CC compared to the GG genotype: odds ratio (OR); 95% confidence interval (CI) = 1.698; 1.240–2.325), but was lower in men compared to women (OR = 0.763; 95% CI = 0.638–0.913). Compared to men with the rs11887534 GG genotype, women with the GG and GC + CC genotypes had a higher risk of gallstone (OR; 95% CI = 1.304; 1.087–1.565 for GG and 2.291; 1.514–3.467 for GC + CC). The positive association between GC + CC and gallstones was retained after we restricted the analysis to the female participants (OR; 95% CI = 1.789 = 1.208–2.648). Hormone use was associated with an elevated risk of gallstones (OR; 95% CI = 1.359; 1.107–1.668). Relative to GG and no hormone use, we found a significantly high risk among hormone users with the GC + CC genotype (OR; 95% CI = 3.596; 1.495–8.650).ConclusionsThe rs11887534 GC + CC genotype was independently associated with a higher risk of gallstones. This risk was much higher among women, especially those who used hormones for various gynecological purposes.

Highlights

  • IntroductionGallstones are characterized by abnormal (solid, pebble-like) masses composed of excessive cholesterol, bilirubin, or bile salts in the gallbladder [1]

  • Gallstones are characterized by abnormal masses composed of excessive cholesterol, bilirubin, or bile salts in the gallbladder [1]

  • The ATP-binding cassette subfamily G member 8 (ABCG8) rs11887534 SNP was used in this study because it met the quality control criteria stated above

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Summary

Introduction

Gallstones are characterized by abnormal (solid, pebble-like) masses composed of excessive cholesterol, bilirubin, or bile salts in the gallbladder [1]. In Taiwan, the prevalence of gallstones was 4.3% in 1989 [3] and 10.7% in 1995 [4] implying a 6.4% difference within this time interval Huang and his team conducted a nationwide study between 1997 and 2005 and reported a rise in the rate of hospitalization for severe gallstone disease [5]. Gallstones are abnormal masses caused by impaired metabolism of cholesterol, bilirubin, or bile salts in the gallbladder or biliary tract. Genome-wide association studies (GWAS) and meta-analyses of GWAS revealed the ABCG8 rs11887534 variant as the most common genetic determinant of gallstones in humans. These findings have not been extensively replicated in Taiwanese. We appraised the relationship between gallstones and rs11887534 in a relatively large Taiwanese sample

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