Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.jpsychires.2020.10.038
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dc.titleEffect of mindfulness intervention versus health education program on salivary Aβ-42 levels in community-dwelling older adults with mild cognitive impairment: A randomized controlled trial
dc.contributor.authorNg, Ted Kheng Siang
dc.contributor.authorSlowey, Paul D.
dc.contributor.authorBeltran, David
dc.contributor.authorHo, Roger C. M.
dc.contributor.authorCenter of Excellence in Behavioral Medicine, Nguyen Tat Thanh University, Faculty of Education, Huaibei Normal University, Vietnam, China.
dc.contributor.authorKua, Ee Heok
dc.contributor.authorMahendran, Rathi
dc.date.accessioned2022-10-11T08:09:31Z
dc.date.available2022-10-11T08:09:31Z
dc.date.issued2021-04-01
dc.identifier.citationNg, Ted Kheng Siang, Slowey, Paul D., Beltran, David, Ho, Roger C. M., Center of Excellence in Behavioral Medicine, Nguyen Tat Thanh University, Faculty of Education, Huaibei Normal University, Vietnam, China., Kua, Ee Heok, Mahendran, Rathi (2021-04-01). Effect of mindfulness intervention versus health education program on salivary Aβ-42 levels in community-dwelling older adults with mild cognitive impairment: A randomized controlled trial. Journal of Psychiatric Research 136 : 619-625. ScholarBank@NUS Repository. https://doi.org/10.1016/j.jpsychires.2020.10.038
dc.identifier.issn0022-3956
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/232237
dc.description.abstractBackground: Few randomized controlled trials have investigated the effects of mindfulness intervention on older adults diagnosed with mild cognitive impairment (MCI). Specifically, scarce literature exists on the potential benefits of mindfulness intervention on biomarkers representing AD hallmarks. Our previous studies showed the potential of Mindful Awareness Practice (MAP) in improving multiple biomarkers of gut microbiota, systemic inflammation, and synaptic functions. Extending these findings, in this study, we conducted analysis on bio-banked saliva samples, examining whether MAP improved salivary amyloid beta-42 (Aβ-42) levels in community-dwelling older adults diagnosed with MCI. We also explored the moderating role of education level, an indicator of cognitive reserve, on intervention effect. Methods: A total of 55 community-dwelling older adults diagnosed with MCI were randomized into either the treatment arm, MAP, or the active control arm, the health education program (HEP). Interventions were performed for a total of nine months. Field and laboratory investigators who were blinded to the treatment allocations collected saliva samples at baseline, 3-month, and 9-month follow-ups. Salivary Aβ-42 levels were quantified using a commercial assay. Linear-mixed models were used to examine the effect of MAP on salivary Aβ-42 levels. Results: Compared to the HEP arm, MAP participants had no significantly modified Aβ-42 levels throughout the 9-month intervention period, regardless of subgroup analyses stratified by either sex or MCI-subtypes (amnestic and non-amnestic). Exploring the moderating effect of education, participants in the HEP arm with higher education levels had significantly lower salivary Aβ-42 at 3-month time-point. Discussion: Taken together with our previous findings and other mindfulness interventional studies failing to find a significant effect on peripheral Aβ-42, we conclude the non-significant effects of mindfulness intervention on ameliorating peripheral Aβ-42 levels. Conversely, participants in the HEP arm with higher cognitive reserve had significantly improved salivary Aβ-42, highlighting the role of cognitive reserve in moderating treatment response in MCI. © 2020 The Authors
dc.publisherElsevier Ltd
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.sourceScopus OA2021
dc.typeArticle
dc.contributor.departmentDUKE-NUS MEDICAL SCHOOL
dc.contributor.departmentPSYCHOLOGICAL MEDICINE
dc.description.doi10.1016/j.jpsychires.2020.10.038
dc.description.sourcetitleJournal of Psychiatric Research
dc.description.volume136
dc.description.page619-625
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