Yamamoto Reina, Takeshita Yumie, Tsujiguchi Hiromasa, Kannon Takayuki, Sato Takehiro, Hosomichi Kazuyoshi, Suzuki Keita, Kita Yuki, Tanaka Takeo, Goto Hisanori, Nakano Yujiro, Yamashita Tatsuya, Kaneko Shuichi, Tajima Atsushi, Nakamura Hiroyuki, Takamura Toshinari
Department of Endocrinology and Metabolism, Kanazawa University Graduate School of Medical Sciences, Kanazawa, Japan.
Department of Environmental and Preventive Medicine, Kanazawa University Graduate School of Medical Sciences, Kanazawa, Japan.
Curr Dev Nutr. 2023 Mar 2;7(4):100051. doi: 10.1016/j.cdnut.2023.100051. eCollection 2023 Apr.
Recent genome-wide association studies have revealed that nonalcoholic fatty liver disease (NAFLD) is correlated with genetic polymorphisms. However, the effects of genetic variation on nutritional metabolism and NAFLD are complex and further studies are still needed.
This study aimed to assess the nutritional characteristics interacting with the correlation between genetic predisposition and NAFLD.
We assessed the 2013-2017 health examination data of 1191 adults aged ≥40 y living in Shika town, Ishikawa Prefecture, Japan. Adults with moderate or heavy alcohol consumption and hepatitis were excluded, and 464 participants who underwent genetic analyses were included in the study. Abdominal echography was performed to diagnose fatty liver condition, and dietary intake and nutritional balance were evaluated using the brief self-administered diet history questionnaire. NAFLD-related gene polymorphisms were identified using Japonica Array v2 (Toshiba).
Among the 31 single nucleotide polymorphisms, only the polymorphism T-455C in the apolipoprotein C3 () gene (rs2854116) was significantly associated with fatty liver condition. The condition was more common in participants with heterozygotes of the gene (rs2854116) than in those with the TT and CC genotypes. Significant interactions were observed between NAFLD and the intake of fat, vegetable fat, MUFAs, PUFAs, cholesterol, n-3 FAs, and n-6 FAs. Moreover, participants with NAFLD who presented with the TT genotype had a significantly higher fat intake than those without NAFLD.
The polymorphism T-455C in the gene (rs2854116) and fat intake are associated with the NAFLD risk in Japanese adults. Participants with a fatty liver who presented with the TT genotype of rs2854116 had a higher fat intake. Such nutrigenetic interaction can deepen our understanding of the NAFLD pathology. Moreover, in clinical settings, the correlation between genetic factors and nutrition intake should be considered in personalized nutritional interventions against NAFLD. 2023;xx:xx.The study was registered in the University Hospital Medical Information Network Clinical Trials Registry as UMIN 000024915.
最近的全基因组关联研究表明,非酒精性脂肪性肝病(NAFLD)与基因多态性相关。然而,基因变异对营养代谢和NAFLD的影响较为复杂,仍需进一步研究。
本研究旨在评估与遗传易感性和NAFLD之间相关性相互作用的营养特征。
我们评估了居住在日本石川县鹿贺町的1191名年龄≥40岁成年人2013 - 2017年的健康检查数据。排除中度或重度饮酒者和肝炎患者,464名接受基因分析的参与者被纳入研究。通过腹部超声检查诊断脂肪肝状况,并使用简短的自填式饮食史问卷评估饮食摄入和营养平衡。使用粳稻芯片v2(东芝)鉴定NAFLD相关基因多态性。
在31个单核苷酸多态性中,只有载脂蛋白C3()基因(rs2854116)中的T - 455C多态性与脂肪肝状况显著相关。该基因(rs2854116)杂合子参与者的脂肪肝状况比TT和CC基因型参与者更常见。在NAFLD与脂肪、植物脂肪、单不饱和脂肪酸、多不饱和脂肪酸、胆固醇、n - 3脂肪酸和n - 6脂肪酸的摄入量之间观察到显著的相互作用。此外,具有TT基因型的NAFLD参与者的脂肪摄入量显著高于无NAFLD者。
载脂蛋白C3基因(rs2854116)中的T - 455C多态性和脂肪摄入与日本成年人的NAFLD风险相关。具有rs2854116 TT基因型的脂肪肝参与者脂肪摄入量更高。这种营养基因相互作用可以加深我们对NAFLD病理的理解。此外,在临床环境中针对NAFLD的个性化营养干预中,应考虑遗传因素与营养摄入之间的相关性。2023;xx:xx。该研究已在大学医院医学信息网络临床试验注册中心注册,注册号为UMIN 000024915。