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Alzheimer's disease (AD) causes a huge socioeconomic burden.
Prevention of blood vessels such as Sala-Vila A published an article in Am J Clin Nutr magazine.
To determine this, self-reported dietary intake of DHA was evaluated and tested in APOE-ε4 carriers (n=122, non-carriers; n=157, 1 allele; n=61, 2 alleles In a population rich in genes, look for neuropsychological tests (contextual memory and executive function), magnetic resonance markers of cerebral small vessel disease (WMHs and CMBs), and early AD-related neurodegeneration (cortical thickness in AD vulnerable areas) Correlation.
Among 340 subjects in the Alzheimer's disease (Alzheimer's disease and family) study, APOE-ε4 carriers (n=122, non-carriers; n=157, 1 allele) were assessed by FFQ ; N=61, 2 alleles) self-reported DHA intake.
A D A scatter plot of the relationship between self-reported DHA dietary intake and normalized residues of cortical thickness.
A D D A scatter plot of the relationship between self-reported DHA dietary intake and normalized residues of cortical thickness.
Three aspects of the results of this study are worth highlighting.
In summary, in middle-aged cognitively normal individuals with increased genetic risk of sporadic AD, self-reported dietary DHA was found to be associated with several beneficial cerebrovascular pathologies or neuroimaging phenotypes associated with AD-related neurodegeneration.
In middle-aged cognitively normal individuals with increased genetic risk of sporadic AD, self-reported dietary DHA was found to be associated with several beneficial cerebrovascular pathologies or neuroimaging phenotypes associated with AD-related neurodegeneration.
oup.
oup.
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