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. 2022 Jul;3(7):e501-e512.
doi: 10.1016/s2666-7568(22)00120-9. Epub 2022 Jul 4.

Nutrition state of science and dementia prevention: recommendations of the Nutrition for Dementia Prevention Working Group

Affiliations

Nutrition state of science and dementia prevention: recommendations of the Nutrition for Dementia Prevention Working Group

Hussein N Yassine et al. Lancet Healthy Longev. 2022 Jul.

Abstract

Observational studies suggest that nutritional factors have a potential cognitive benefit. However, systematic reviews of randomised trials of dietary and nutritional supplements have reported largely null effects on cognitive outcomes and have highlighted study inconsistencies and other limitations. In this Personal View, the Nutrition for Dementia Prevention Working Group presents what we consider to be limitations in the existing nutrition clinical trials for dementia prevention. On the basis of this evidence, we propose recommendations for incorporating dietary patterns and the use of genetic, and nutrition assessment tools, biomarkers, and novel clinical trial designs to guide future trial developments. Nutrition-based research has unique challenges that could require testing both more personalised interventions in targeted risk subgroups, identified by nutritional and other biomarkers, and large-scale and pragmatic study designs for more generalisable public health interventions across diverse populations.

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Figures

Figure 1:
Figure 1:. Biological pathways mediating the relationship of the diet with cognition
The effect of the diet on cognition involves complex interactions that include behavioural, genetic, systemic, and brain factors. The diet can affect the brain directly or indirectly through chronic diseases (dementia risk factors). The blood-brain barrier has pleiotropic functions that include nutrient brain delivery, and a leaky blood-brain barrier in Alzheimer’s disease is associated with brain glucose hypometabolism.
Figure 2:
Figure 2:. Two contrasting study designs to nutrition-based interventions for dementia prevention
Two contrasting approaches to nutrition-based clinical trials are shown. The first column shows intensive and personalised interventions guided by biomarkers that capture brain functions. In the second column, interventions are tailored to a population level in groups at risk of dementia and uses pragmatic outcomes. Although certain trials will have to share elements from both approaches, clear study designs that match the intensity of the intervention with the outcome proposed promises to maximise the chances of finding effective therapies.

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