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Plasma omega-3 PUFA and white matter mediated executive decline in older adults

Introduction: Cross-sectional studies have identified long chain omega-3 polyunsaturated fatty acids (eicosapentaenoic acid 20:5n-3 and docosahexaenoic acid 22:6n-3 (O3PUFA) in association with fewer white matter lesions and better executive function in older adults. We hypothesized that O3PUFA are...

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Autores principales: Bowman, Gene L., Dodge, Hiroko H., Mattek, Nora, Barbey, Aron K., Silbert, Lisa C., Shinto, Lynne, Howieson, Diane B., Kaye, Jeffrey A., Quinn, Joseph F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3863786/
https://www.ncbi.nlm.nih.gov/pubmed/24379780
http://dx.doi.org/10.3389/fnagi.2013.00092
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author Bowman, Gene L.
Dodge, Hiroko H.
Mattek, Nora
Barbey, Aron K.
Silbert, Lisa C.
Shinto, Lynne
Howieson, Diane B.
Kaye, Jeffrey A.
Quinn, Joseph F.
author_facet Bowman, Gene L.
Dodge, Hiroko H.
Mattek, Nora
Barbey, Aron K.
Silbert, Lisa C.
Shinto, Lynne
Howieson, Diane B.
Kaye, Jeffrey A.
Quinn, Joseph F.
author_sort Bowman, Gene L.
collection PubMed
description Introduction: Cross-sectional studies have identified long chain omega-3 polyunsaturated fatty acids (eicosapentaenoic acid 20:5n-3 and docosahexaenoic acid 22:6n-3 (O3PUFA) in association with fewer white matter lesions and better executive function in older adults. We hypothesized that O3PUFA are associated with less executive decline over time and that total white matter hyperintensity volume (WMH) mediates this association. Methods: Eighty-six non-demented older adults were followed over 4 years after measurement of plasma O3PUFA with annual evaluations of cognitive function. A subset of these participants also had brain MRI of total WMH available to conduct a formal mediation analysis of a putative relationship between O3PUFA and cognitive function. Results: Mean age at baseline was 86, 62% were female and 11% carried the APOE4 allele. Each 100 μg/ml increase in plasma O3PUFA associated with 4 s less change in executive decline per year of aging (p = 0.02, fully adjusted model). O3PUFA was not associated with verbal memory or global cognitive changes. The significance of the association between O3PUFA and better executive function was lost once WMH was added to the regression model. Conclusion: Executive decline with age appears to be a cognitive domain particularly sensitive to plasma O3PUFA in longitudinal examination. O3PUFA may modulate executive functioning by mechanisms underlying the development of WMH, a biologically plausible hypothesis that warrants further investigation.
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spelling pubmed-38637862013-12-30 Plasma omega-3 PUFA and white matter mediated executive decline in older adults Bowman, Gene L. Dodge, Hiroko H. Mattek, Nora Barbey, Aron K. Silbert, Lisa C. Shinto, Lynne Howieson, Diane B. Kaye, Jeffrey A. Quinn, Joseph F. Front Aging Neurosci Neuroscience Introduction: Cross-sectional studies have identified long chain omega-3 polyunsaturated fatty acids (eicosapentaenoic acid 20:5n-3 and docosahexaenoic acid 22:6n-3 (O3PUFA) in association with fewer white matter lesions and better executive function in older adults. We hypothesized that O3PUFA are associated with less executive decline over time and that total white matter hyperintensity volume (WMH) mediates this association. Methods: Eighty-six non-demented older adults were followed over 4 years after measurement of plasma O3PUFA with annual evaluations of cognitive function. A subset of these participants also had brain MRI of total WMH available to conduct a formal mediation analysis of a putative relationship between O3PUFA and cognitive function. Results: Mean age at baseline was 86, 62% were female and 11% carried the APOE4 allele. Each 100 μg/ml increase in plasma O3PUFA associated with 4 s less change in executive decline per year of aging (p = 0.02, fully adjusted model). O3PUFA was not associated with verbal memory or global cognitive changes. The significance of the association between O3PUFA and better executive function was lost once WMH was added to the regression model. Conclusion: Executive decline with age appears to be a cognitive domain particularly sensitive to plasma O3PUFA in longitudinal examination. O3PUFA may modulate executive functioning by mechanisms underlying the development of WMH, a biologically plausible hypothesis that warrants further investigation. Frontiers Media S.A. 2013-12-16 /pmc/articles/PMC3863786/ /pubmed/24379780 http://dx.doi.org/10.3389/fnagi.2013.00092 Text en Copyright © 2013 Bowman, Dodge, Mattek, Barbey, Silbert, Shinto, Howieson, Kaye and Quinn. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Bowman, Gene L.
Dodge, Hiroko H.
Mattek, Nora
Barbey, Aron K.
Silbert, Lisa C.
Shinto, Lynne
Howieson, Diane B.
Kaye, Jeffrey A.
Quinn, Joseph F.
Plasma omega-3 PUFA and white matter mediated executive decline in older adults
title Plasma omega-3 PUFA and white matter mediated executive decline in older adults
title_full Plasma omega-3 PUFA and white matter mediated executive decline in older adults
title_fullStr Plasma omega-3 PUFA and white matter mediated executive decline in older adults
title_full_unstemmed Plasma omega-3 PUFA and white matter mediated executive decline in older adults
title_short Plasma omega-3 PUFA and white matter mediated executive decline in older adults
title_sort plasma omega-3 pufa and white matter mediated executive decline in older adults
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3863786/
https://www.ncbi.nlm.nih.gov/pubmed/24379780
http://dx.doi.org/10.3389/fnagi.2013.00092
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