Omega-3 Fatty Acid Status Enhances the Prevention of Cognitive Decline by B Vitamins in Mild Cognitive Impairment
Abstract
A
randomized trial (VITACOG) in people with mild cognitive impairment
(MCI) found that B vitamin treatment to lower homocysteine slowed the
rate of cognitive and clinical decline. We have used data from this
trial to see whether baseline omega-3 fatty acid status interacts with
the effects of B vitamin treatment. 266 participants with MCI aged ≥70
years were randomized to B vitamins (folic acid, vitamins B6 and B12) or
placebo for 2 years. Baseline cognitive test performance, clinical
dementia rating (CDR) scale, and plasma concentrations of total
homocysteine, total docosahexaenoic and eicosapentaenoic acids (omega-3
fatty acids) were measured. Final scores for verbal delayed recall,
global cognition, and CDR sum-of-boxes were better in the B
vitamin-treated group according to increasing baseline concentrations of
omega-3 fatty acids, whereas scores in the placebo group were similar
across these concentrations. Among those with good omega-3 status, 33%
of those on B vitamin treatment had global CDR scores >0 compared
with 59% among those on placebo. For all three outcome measures, higher
concentrations of docosahexaenoic acid alone significantly enhanced the
cognitive effects of B vitamins, while eicosapentaenoic acid appeared
less effective. When omega-3 fatty acid concentrations are low, B
vitamin treatment has no effect on cognitive decline in MCI, but when
omega-3 levels are in the upper normal range, B vitamins interact to
slow cognitive decline. A clinical trial of B vitamins combined with
omega-3 fatty acids is needed to see whether it is possible to slow the
conversion from MCI to AD.
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