001; Fig. 2, left column). Corresponding estimates multifactorially adjusted (for age, sex, physical activity, hormonal replacement

buy Venetoclax therapy, and alcohol consumption) were 2.84 (95% CI: 2.32-3.46; P for trend: <0.001; Fig. 2, right column). Stratifying on sex revealed a stronger association of BMI with symptomatic gallstone disease in women, compared to men (Fig. 2). Multifactorially adjusted HRs for individuals in the fifth versus the first BMI quintile were 3.36 (95% CI: 2.62-4.31) and 1.51 (95% CI: 1.09-2.11) in women and men, respectively (P for interaction between sex and BMI on risk of symptomatic gallstone disease = 0.01). BMI did not interact with age, physical activity, hormone replacement therapy, or alcohol consumption on risk of symptomatic gallstone disease (data not shown). The association Ceritinib of the combined allele score with BMI is shown in Fig. 3 (left column). An increasing number of BMI-increasing alleles was associated with a stepwise increase in mean BMI

of up to +5.2% (1.3 kg/m2) for 6 versus 0-1 alleles, +4.3% (1.1 kg/m2) in women and +6.1% (1.6 kg/m2) in men (all P for trend: <0.001). The individual variants (FTO [rs9939609], MC4R [rs17782313], and TMEM18 [rs6548238]) were associated with stepwise increases in BMI of up to +2.6% (all P < 0.001; Supporting Figure). We tested whether potential confounding factors were associated with BMI, symptomatic gallstone disease, and allele score (Fig. 4). Age, sex, physical activity, consumption of alcohol, fast food, and vegetables, and (in women) hormone replacement therapy and parity were all strongly associated with BMI and risk of symptomatic gallstone disease and thus constitute potential confounders for the observational BMI-gallstone association (Fig. 4, left and middle

columns). In contrast, allele score was not associated with any of these potential confounders (Fig. 4, right column). ABCG8 D19H (a known genetic risk factor for gallstone disease) was associated with symptomatic gallstone disease in our cohort (Fig. 4, middle column, bottom, DH+HH versus DD; OR, 2.1 [95% CI: 1.9-2.2]), but not with BMI or with the BMI-increasing allele score (P = 0.72 and 0.77).[11] 上海皓元 Assuming that increased BMI causes symptomatic gallstones, lifelong increased BMI levels resulting from genetic variation should confer a similar increase in risk of symptomatic gallstones as that observed for increased BMI in the general population. For example, the 5.2% increase in BMI for individuals with 6 versus 0-1 BMI-increasing alleles would theoretically predict an increased risk of symptomatic gallstones with an HR of 1.10 (95% CI: 1.08-1.11; Fig. 3, middle column). During a mean follow-up of 33.0 years (range, 0.0-34.4), the multifactorially adjusted HR for symptomatic gallstone disease was 1.43 (95% CI: 0.99-2.05) in individuals with 6 versus 0-1 BMI-increasing alleles (P for trend = 0.007; Fig. 3, right column). The corresponding HRs were 1.54 (95% CI: 1.00-2.35) in women and 1.19 (95% CI: 0.60-2.