Dept. of Food & Nutrition, Hoseo University, Institute of Basic Science, Obesity/Diabetes Center, Asan, Republic of Korea.
Dept. of Food & Nutrition, Hoseo University, Institute of Basic Science, Obesity/Diabetes Center, Asan, Republic of Korea.
Nutr Res. 2020 Oct;82:88-98. doi: 10.1016/j.nutres.2020.08.011. Epub 2020 Aug 26.
Non-alcoholic fatty liver(NAFLD) is prevalent in Asians despite the low obesity rate. We hypothesized that the haplotype of genetic variants in the 22q13 loci has a strong association with non-alcoholic fatty liver disease (NAFLD) that can be identified by genome-wide association study and that lifestyles may interact with the haplotype. We tested the hypothesis in middle-aged and elderly adults in a large city hospital-based cohort from the KoGES study. Men and women diagnosed with fatty liver, but who respectively consumed over 40 and 30 g ethanol per day were excluded. The haplotype of the selected SNPs from the 22q13 loci that influences NAFLD risk was generated. Among the 27374 participants, 1486 (5.4%) were diagnosed with NAFLD. LARGE_rs240072, RBFOX2_rs11089778, TRIOBP_rs12628603, PNPLA3_rs738409, and PARVB_rs2073080 in the 22q13 loci were included in the haplotype. Participants with the minor haplotype had 1.8, 2.3, and 1.8 times higher in the risk for NAFLD and serum AST and ALT activities, respectively, than those with the major haplotype. BMI, waist circumferences, serum glucose concentrations, and blood pressure interacted with the haplotype for NAFLD risk. We also found that a high carbohydrate intake and a dietary pattern characterized by high noodle and meat consumption significantly interacted with the minor haplotype to increase the risk of NAFLD. We hypothesized that the high incidence of NAFLD among Koreans, despite a relatively low incidence of obesity, might be due to genetic factors and perhaps their interactions with dietary patterns. The hypothesis was accepted since this study confirmed that participants with the minor allele of the haplotype in the 22q13 loci had a higher NAFLD risk that was exacerbated by high intakes of carbohydrates and a dietary pattern characterized by high noodle and meat consumption.
非酒精性脂肪性肝病(NAFLD)在亚洲人群中很普遍,尽管肥胖率较低。我们假设 22q13 基因座的遗传变异单体型与非酒精性脂肪性肝病(NAFLD)有很强的关联,可以通过全基因组关联研究来识别,并且生活方式可能与单体型相互作用。我们在 KoGES 研究的一个大城市医院队列中对中年和老年人进行了假设检验。排除了被诊断为脂肪肝但分别每天摄入超过 40 和 30 克乙醇的男性和女性。从 22q13 基因座中选择影响 NAFLD 风险的 SNP 的单体型。在 27374 名参与者中,有 1486 人(5.4%)被诊断为 NAFLD。22q13 基因座中的 LARGE_rs240072、RBFOX2_rs11089778、TRIOBP_rs12628603、PNPLA3_rs738409 和 PARVB_rs2073080 被纳入单体型。与主要单体型相比,单体型较小的参与者患 NAFLD 以及血清 AST 和 ALT 活性的风险分别增加 1.8、2.3 和 1.8 倍。BMI、腰围、血清葡萄糖浓度和血压与单体型对 NAFLD 风险的相互作用。我们还发现,高碳水化合物摄入和以高面条和肉类消费为特征的饮食模式与单体型显著相互作用,增加了患 NAFLD 的风险。我们假设,尽管肥胖率相对较低,但韩国人 NAFLD 的高发率可能是由于遗传因素,以及这些因素可能与饮食模式相互作用。该假设被接受,因为本研究证实,22q13 基因座单体型的次要等位基因携带者患 NAFLD 的风险更高,而高碳水化合物摄入和以高面条和肉类消费为特征的饮食模式会加剧这种风险。