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英国生物银行中的基因-饮食相互作用分析确定了可改变鱼油补充剂与痴呆症发病率之间关联的基因位点。

Gene-Diet Interaction Analysis in UK Biobank Identified Genetic Loci That Modify the Association Between Fish Oil Supplementation and the Incidence of Dementia.

作者信息

Lu Yueqi, Xu Huifang, Sun Yitang, Ihejirika Susan Adanna, Chiang Charleston Wk, Darst Burcu F, Song Suhang, Shen Ye, Ye Kaixiong

机构信息

Department of Genetics, Franklin College of Arts and Sciences, University of Georgia, Athens, Georgia, United States.

Institute of Bioinformatics, University of Georgia, Athens, Georgia, United States.

出版信息

Curr Dev Nutr. 2025 Aug 5;9(9):107524. doi: 10.1016/j.cdnut.2025.107524. eCollection 2025 Sep.

Abstract

BACKGROUND

Dementia is a common disease influenced by both genetic and environmental factors. ε4 is well-known to increase risk of dementia, and it has been shown to attenuate the protective association of fish oil supplements (FOS) and the incidence of dementia.

OBJECTIVES

To identify additional genetic factors with modifying effects, we performed a genome-wide scan.

METHODS

We performed genome-wide association studies (GWAS) of incident all-cause dementia, Alzheimer's disease, and vascular dementia in 357,631 participants from UK Biobank and the FOS subgroups. Single-nucleotide polymorphisms (SNPs) suggestively associated with dementia ( < 1 × 10) were then evaluated for their interactions with fish oil status in Cox regression models. Furthermore, we conducted gene set enrichment analysis to identify the relevant cell types for these interaction signals.

RESULTS

Time-to-event GWAS identified 6, 5, and 2 genome-wide significant loci ( < 5 × 10) for the incidence of all-cause dementia, Alzheimer's disease, and vascular dementia, respectively. Most of them overlapped with previously known GWAS loci for Alzheimer's disease and related dementia. A total of 178 suggestive GWAS loci ( < 1 × 10) were passed onto interaction analysis, and 43 of them were found to significantly modify the association between FOS and dementia incidence ( < 2.8 × 10 with Bonferroni correction). One locus overlapped with a known Alzheimer's disease GWAS locus (/) and 2 with GWAS loci for circulating ω-3 fatty acids ( and ). Candidate interacting genes exhibited cell-type-specific expression in the nervous system.

CONCLUSIONS

In total, 43 genetic loci modify the association between FOS and dementia. These findings indicate a need for genome-informed personalized nutrition of FOS for the purpose of dementia prevention.

摘要

背景

痴呆症是一种受遗传和环境因素共同影响的常见疾病。众所周知,ε4会增加患痴呆症的风险,并且已表明它会削弱鱼油补充剂(FOS)与痴呆症发病率之间的保护关联。

目的

为了确定具有修饰作用的其他遗传因素,我们进行了全基因组扫描。

方法

我们对来自英国生物银行和FOS亚组的357,631名参与者进行了全因痴呆症、阿尔茨海默病和血管性痴呆症的全基因组关联研究(GWAS)。然后在Cox回归模型中评估与痴呆症有暗示性关联(<1×10)的单核苷酸多态性(SNP)与鱼油状态的相互作用。此外,我们进行了基因集富集分析,以确定这些相互作用信号的相关细胞类型。

结果

事件发生时间GWAS分别确定了6个、5个和2个全基因组显著位点(<5×10)与全因痴呆症、阿尔茨海默病和血管性痴呆症的发病率相关。其中大多数与先前已知的阿尔茨海默病和相关痴呆症的GWAS位点重叠。共有178个暗示性GWAS位点(<1×10)进入相互作用分析,其中43个被发现显著修饰了FOS与痴呆症发病率之间的关联(经Bonferroni校正后<2.8×10)。一个位点与已知的阿尔茨海默病GWAS位点(/)重叠,2个与循环ω-3脂肪酸的GWAS位点(和)重叠。候选相互作用基因在神经系统中表现出细胞类型特异性表达。

结论

总共有43个遗传位点修饰了FOS与痴呆症之间的关联。这些发现表明,为了预防痴呆症,需要基于基因组信息的FOS个性化营养。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18a8/12423404/9e4a80586409/gr1.jpg

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