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Gallstone disease in Swedish twins: risk is associated with ABCG8 D19H genotype

.  Katsika D, Magnusson P, Krawczyk M, Grünhage F, Lichtenstein P, Einarsson C, Lammert F, Marschall H‐U (Karolinska University Hospital Huddinge, Karolinska Institutet, Stockholm, Sweden; Karolinska Institutet, Stockholm, Sweden; and Saarland University Hospital, Homburg, Germany). Gallstone diseas...

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Published in:Journal of internal medicine 2010-09, Vol.268 (3), p.279-285
Main Authors: Katsika, D., Magnusson, P., Krawczyk, M., Grünhage, F., Lichtenstein, P., Einarsson, C., Lammert, F., Marschall, H.‐U.
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Language:English
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Summary:.  Katsika D, Magnusson P, Krawczyk M, Grünhage F, Lichtenstein P, Einarsson C, Lammert F, Marschall H‐U (Karolinska University Hospital Huddinge, Karolinska Institutet, Stockholm, Sweden; Karolinska Institutet, Stockholm, Sweden; and Saarland University Hospital, Homburg, Germany). Gallstone disease in Swedish twins: risk is associated with ABCG8 D19H genotype. J Intern Med 2010; 268: 279–285. Objective.  Recently, variants of the hepatocanalicular cholesterol hemitransporters ABCG5/8 were linked to gallstone disease; ABCG8 D19H in Caucasians and ABCG5 Q604E in Chinese. We investigated these polymorphisms in Swedish twins by merging the Swedish Twin Registry with the Hospital Discharge and Causes of Death Registries for gallstone disease‐related diagnoses. Design.  All monozygotic (MZ) twins with gallstone disease alive in the Stockholm area were invited to participate. Gallstone disease was defined by entry in all above mentioned registries, questionnaire or abdominal ultrasound. Subjects.  ABCG5 Q604E and ABCG8 D19H genotyping was performed in 24 unique MZ and eight dizygotic (DZ) twins from concordant pairs. Screening of the TwinGene database for gallstone disease resulted in an additional 20 concordant MZ and 54 twins from concordant DZ pairs. We included 109 concordantly stone‐free MZ and 126 stone‐free independent DZ twins as controls. Results.  Amongst the 341 twins, 20.8% carried at least one D19H allele as compared to 9.4% of stone‐free controls. The association analysis showed that D19H positivity significantly increased the risk of gallstone disease [odds ratio (OR), 2.54; 95% confidence interval (CI), 1.33–4.82; P = 0.004]. We also found a trend for a positive association between gallstone disease and the Q604E variant (OR, 1.47; 95% CI, 1.00–2.16; P = 0.052). Conclusion.  Twins carrying a heterozygous or homozygous ABCG8 D19H genotype have a significantly increased risk of gallstone disease. Our study confirms the ABCG8 D19H genotype as a major risk factor for gallstone disease.
ISSN:0954-6820
1365-2796
1365-2796
DOI:10.1111/j.1365-2796.2010.02249.x