Tree nuts (for example brazil nuts, almonds, hazelnuts, walnuts, cashew nuts etc) contain a wide variety of nutrients including fatty acids, polyphenols and micronutrients. The beneficial health effects ascribed to the consumption of tree nuts include improvements to cardiovascular outcomes and regulation of glucose levels and inflammation. Emerging evidence suggests that specific components of nuts may also contribute to brain health and function. The aim of the present study is to assess the effects of four weeks' supplementation of nut components on cognition and subjective measures. Urinary metabolites and intestinal microbial communities will also be assessed allowing biomarkers of nut exposure to be highlighted.
To date, only two small human intervention trials have evaluated the effects of nuts as a sole intervention on cognition. One study reported a benefit verbal fluency and constructional praxis following daily consumption of 6 g brazil nuts for 6 months in older adults diagnosed with mild cognitive impairment. Eight weeks' consumption of 60 g/d walnuts in healthy young adults aged 18-25 years also resulted in improved inferential verbal reasoning scores compared to placebo. The development of various 'omics' technologies has enabled researchers to investigate the influence of nutrients or dietary change on metabolic pathways at multiple levels with a view to developing biological markers of dietary intake. Metabolomic approaches have been used successfully to study nut consumption; for example putative biomarkers of nut consumption have been revealed as metabolites associated with serotonin pathways. Furthermore, certain nut biomarkers identified using metabolomics appear to be negatively associated with health parameters which is suggested to be due to gut microbiota dysbiosis and provides an important link between nut consumption, the gut microflora and metabolic pathways. This study will assess the effects of four weeks' supplementation with nut components on cognition. Metabolomic and metagenomic approaches will be utilised to analyse urinary metabolites and intestinal microbial communities allowing biomarkers of nut exposure to be highlighted. Metabolic and gut microbiota responses will then be correlated with changes in cognition in order to identify inter-individual differences in response, and further understanding of the mechanisms underpinning cognitive benefits of nut consumption.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
OTHER
Masking
TRIPLE
Enrollment
81
nut components consumed daily for a period of 28 days
Placebo consumed daily for a period of 28 days
Northumbria University
Newcastle upon Tyne, Tyne & Wear, United Kingdom
Logical reasoning
Cognition - executive function
Time frame: At 28 days post dose, adjusted for baseline
Location learning
Cognition - spatial memory
Time frame: At 28 days post dose, adjusted for baseline
Choice reaction time
Cognition - attention
Time frame: At 28 days post dose, adjusted for baseline
Rapid Visual Information Processing
Cognition - working memory
Time frame: At 28 days post dose, adjusted for baseline
Numeric working memory
Cognition - working memory
Time frame: At 28 days post dose, adjusted for baseline
Stroop
Cognition - executive function
Time frame: At 28 days post dose, adjusted for baseline
Peg and Ball
Cognition - executive function
Time frame: At 28 days post dose, adjusted for baseline
Word recall
Cognition - episodic memory
Time frame: At 28 days post dose, adjusted for baseline
Word recognition
Cognition - episodic memory
Time frame: At 28 days post dose, adjusted for baseline
Picture recognition
Cognition - episodic memory
Time frame: At 28 days post dose, adjusted for baseline
Bond-Lader
Mood
Time frame: At 28 days post dose, adjusted for baseline
Profile of Mood States (POMS)
Mood
Time frame: At 28 days post dose, adjusted for baseline
Urinary metabolites (fingerprinting and profiling)
Liquid chromatography/mass spectrometry, combined with data mining using specific software to identify specific metabolites influenced by supplementation
Time frame: At 28 days post dose, adjusted for baseline
Intestinal microbial communities
Analysis of total DNA using standardised procedures targeting bacteria using the 16S rRNA gene.
Time frame: At 28 days post dose, adjusted for baseline
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