Dietary sugar intake, genetic susceptibility, and risk of dementia: A prospective cohort study.

IF 7.8 Q2 BUSINESS
Yu An, Limin Cao, Gang Zheng, Yashu Liu, Honghao Yang, Liangkai Chen, Yuhong Zhao, Xiaopeng Zhang, Yang Xia
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引用次数: 0

Abstract

Background: Sugar intake has been identified as a risk factor for incident dementia; however, the role of genetic susceptibility in such association remains unclear.

Methods: This cohort study involved 158,408 participants from the UK Biobank to explore the effect of genetic susceptibility on the association between dietary sugar intake and dementia risk. Data on sugar intake were evaluated using repeated web-based 24-hour dietary recalls. Polygenic risk scores (PRS) for sugar metabolism (Triglyceride Glucose, TyG), gut microbiota, and disease susceptibility (Alzheimer's disease) were generated based on genome-wide association studies.

Results: Over a median follow-up period of 9.94 years, 1,219 dementia cases (0.7%) were documented. There were significant positive dose-response relationships between sugar intake and dementia risk (non-free sugar: HR, 95% CI, Quartile 4 vs. Quartile 1 = 1.26, 1.04-1.52; free sugar: 1.43, 1.20-1.70). Genetic susceptibility, including TyG-PRS, gut microbiota, and disease susceptibility, showed a combined effect on the association between sugar intake and dementia risk. Notably, significant interactions were observed between sugar intake, PRS for Ruminococcaceae UCG-014 and dementia, as well as between free sugar, PRS for Oscillospira and dementia. Participants with lower PRS of Ruminococcaceae UCG-014, or higher PRS of Oscillospira, posed a higher risk of dementia due to sugar intake.

Conclusion: Both free and non-free sugar intake are independent risk factors for dementia incidence. The role of genetic susceptibility among such association cannot be ignored. These results underscore the importance of personalized nutritional interventions targeting both dietary habits and genetic risk profiles in dementia prevention strategies.

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膳食糖摄入量、遗传易感性和痴呆风险:一项前瞻性队列研究。
背景:糖摄入已被确定为偶发性痴呆的危险因素;然而,遗传易感性在这种关联中的作用仍不清楚。方法:本队列研究涉及来自英国生物银行的158,408名参与者,以探索遗传易感性对饮食糖摄入量与痴呆风险之间关系的影响。通过重复的基于网络的24小时饮食回顾来评估糖摄入量的数据。基于全基因组关联研究,生成糖代谢(甘油三酯葡萄糖,TyG),肠道微生物群和疾病易感性(阿尔茨海默病)的多基因风险评分(PRS)。结果:在9.94年的中位随访期间,记录了1219例痴呆病例(0.7%)。糖摄入量与痴呆风险之间存在显著的正剂量反应关系(非游离糖:HR, 95% CI,四分位数4 vs四分位数1 = 1.26,1.04-1.52;游离糖:1.43,1.20-1.70)。遗传易感性,包括TyG-PRS、肠道微生物群和疾病易感性,显示出糖摄入量与痴呆风险之间的关联的综合影响。值得注意的是,糖摄入量、Ruminococcaceae UCG-014的PRS与痴呆之间,以及游离糖、Oscillospira的PRS与痴呆之间存在显著的相互作用。Ruminococcaceae UCG-014 PRS较低或Oscillospira PRS较高的参与者由于摄入糖而导致痴呆的风险更高。结论:游离糖和非游离糖摄入都是痴呆发病的独立危险因素。遗传易感性在此类关联中的作用不容忽视。这些结果强调了针对饮食习惯和遗传风险特征的个性化营养干预在痴呆症预防策略中的重要性。
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来源期刊
The Journal of Prevention of Alzheimer's Disease
The Journal of Prevention of Alzheimer's Disease Medicine-Psychiatry and Mental Health
CiteScore
9.20
自引率
0.00%
发文量
0
期刊介绍: The JPAD Journal of Prevention of Alzheimer’Disease will publish reviews, original research articles and short reports to improve our knowledge in the field of Alzheimer prevention including: neurosciences, biomarkers, imaging, epidemiology, public health, physical cognitive exercise, nutrition, risk and protective factors, drug development, trials design, and heath economic outcomes.JPAD will publish also the meeting abstracts from Clinical Trial on Alzheimer Disease (CTAD) and will be distributed both in paper and online version worldwide.We hope that JPAD with your contribution will play a role in the development of Alzheimer prevention.
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