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Effect of virgin coconut oil supplementation on cognition of individuals with mild-to-moderate alzheimer's disease in Sri Lanka (VCO-AD study): A randomized placebo-controlled trial

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dc.contributor.author Fernando, M.G.
dc.contributor.author Silva, R.
dc.contributor.author Fernando, W.M.A.D.B.
dc.contributor.author de Silva, H.A.
dc.contributor.author Wickremasinghe, A.R.
dc.contributor.author Dissanayake, A.S.
dc.contributor.author Sohrabi, H.R.
dc.contributor.author Martins, R.N.
dc.contributor.author Williams, S.S.
dc.date.accessioned 2023-11-22T07:05:13Z
dc.date.available 2023-11-22T07:05:13Z
dc.date.issued 2023
dc.identifier.citation Journal of Alzheimer's Disease.2023;96(3):1195-1206. (Online ahead of print) en_US
dc.identifier.issn 1387-2877 (Print)
dc.identifier.issn 1875-8908 (Electronic)
dc.identifier.uri http://repository.kln.ac.lk/handle/123456789/27054
dc.description Indexed in MEDLINE en_US
dc.description.abstract BACKGROUND: Virgin coconut oil (VCO) is a potential therapeutic approach to improve cognition in Alzheimer’s disease (AD) due to its properties as a ketogenic agent and antioxidative characteristics. OBJECTIVE: This study aimed to investigate the effect of VCO on cognition in people with AD and to determine the impact of apolipoprotein E (APOE) ɛ4 genotype on cognitive outcomes. METHODS: Participants of this double-blind placebo-controlled trial (SLCTR/2015/018, 15.09.2015) were 120 Sri Lankan individuals with mild-to-moderate AD (MMSE = 15-25), aged > 65 years, and they were randomly allocated to treatment or control groups. The treatment group was given 30 mL/day of VCO orally and the control group, received similar amount of canola oil, for 24 weeks. The Mini-Mental Sate Examination (MMSE) and Clock drawing test were performed to assess cognition at baseline and at the end of the intervention. Blood samples were collected and analyzed for lipid profile and glycated hemoglobin (HbA1 C) levels.∥ RESULTS: There were no significant difference in cognitive scores, lipid profile, and HbA1 C levels between VCO and control groups post-intervention. The MMSE scores, however, improved among APOE ɛ4 carriers who had VCO, compared to non-carriers (2.37, p = 0.021). APOE ɛ4 status did not influence the cognitive scores in the control group. The attrition rate was 30%.∥ CONCLUSION: Overall, VCO did not improve cognition in individuals with mild-to-moderate AD following a 24-week intervention, compared to canola oil. However, it improved the MMSE scores in APOE ɛ4 carriers. Besides, VCO did not compromise lipid profile and HbA1 C levels and is thus safe to consume. en_US
dc.language.iso en en_US
dc.publisher IOS Press en_US
dc.subject Alzheimer’s disease en_US
dc.subject APOE ɛ4 en_US
dc.subject Cognition en_US
dc.subject HbA1 C en_US
dc.subject Lipid profile en_US
dc.subject Virgin coconut oil en_US
dc.title Effect of virgin coconut oil supplementation on cognition of individuals with mild-to-moderate alzheimer's disease in Sri Lanka (VCO-AD study): A randomized placebo-controlled trial en_US
dc.type Article en_US


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