# Metabolomic signatures reveal an association between healthy dietary patterns and brain aging

**Authors:** Lingyuan Hu, Zhuotong Wang, Aomiao Chen, Geningyue Wang, Xinran Xie, Qiuyu He, Yu Wang, Huali Shi, Zongji Zheng, Yijie Jia

PMC · DOI: 10.1016/j.jnha.2026.100806 · The Journal of Nutrition, Health & Aging · 2026-02-19

## TL;DR

This study finds that healthy diets like AHEI-2010 and DASH are linked to slower brain aging, with metabolomic signatures explaining part of this relationship.

## Contribution

The study identifies metabolomic signatures that mediate the link between healthy diets and reduced brain aging.

## Key findings

- Higher AHEI-2010 and DASH scores are associated with reduced brain age gap (BAG).
- Metabolomic signatures explain 30.43% and 35.47% of the associations between dietary patterns and BAG.
- DASH diets are particularly beneficial for reducing BAG in obese individuals.

## Abstract

The optimal dietary pattern of brain age and related diseases remains unclear, and the relationship between dietary metabolomic signature and these conditions is still poorly understood.

This cohort study included 13,691 participants from the UK Biobank (53.67% female, mean age 54.9 ± 7.5 years), we investigated the relationship between five healthy dietary patterns and brain age gap (BAG). Metabolomic signatures were constructed using a LASSO model, and multivariable linear regression was applied to examine the relationship between metabolomic signatures and brain age.

Higher AHEI-2010 and DASH scores were associated with reduced BAG. Specifically, higher DASH scores reduced BAG in obese populations. Metabolomic signatures accounted for 30.43% and 35.47% of the associations between dietary patterns and BAG, respectively, and were themselves significantly correlated with BAG.

AHEI-2010/DASH diets and plasma metabolites are associated with brain aging, offering a metabolomic basis for personalized dietary interventions.

## Full-text entities

- **Genes:** ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, APP (amyloid beta precursor protein) [NCBI Gene 351] {aka AAA, ABETA, ABPP, AD1, APPI, CTFgamma}, MAPT (microtubule associated protein tau) [NCBI Gene 4137] {aka DDPAC, FTD1, FTDP-17, MAPTL, MSTD, MTBT1}
- **Diseases:** cardiovascular disease (MESH:D002318), Hypertension (MESH:D006973), brain degeneration (MESH:D001927), epilepsy (MESH:D004827), chronic (MESH:D002908), cognitive decline (MESH:D003072), HND (MESH:D006250), multiple sclerosis (MESH:D009103), dementia (MESH:D003704), hippocampal pathological damage (MESH:D005598), schizophrenia (MESH:D012559), neuroinflammation (MESH:D000090862), diabetes (MESH:D003920), AD (MESH:D000544), BAG (MESH:C562538), Parkinson's disease (MESH:D010300), Dietary Inflammatory (MESH:D007249), Neurodegenerative Delay (MESH:D019636), metabolic dysfunction (MESH:D008659), neurological disorders (MESH:D009461), MIND (MESH:D017086), stroke (MESH:D020521), obese (MESH:D009765), mood disorders (MESH:D019964)
- **Chemicals:** fatty acids (MESH:D005227), sodium (MESH:D012964), PUFA (MESH:D005231), olive oil (MESH:D000069463), -chain (n-3) fats (-), glucose (MESH:D005947), alcohol (MESH:D000438), lipid (MESH:D008055), polyphenols (MESH:D059808), ketone (MESH:D007659), triglycerides (MESH:D014280), Choline (MESH:D002794), cholesterol (MESH:D002784), trans fatty acids (MESH:D044242), Omega-6 fatty acids (MESH:D043371), phospholipids (MESH:D010743)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12934320/full.md

## References

47 references — full list in the complete paper: https://tomesphere.com/paper/PMC12934320/full.md

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Source: https://tomesphere.com/paper/PMC12934320