Circulating Omega-3 and Omega-6 Fatty Acids, Cognitive Decline, and Dementia in Older Adults

Author:

de Oliveira Otto Marcia C.1,Wu Jason H.Y.2,Thacker Evan L.3,Lai Heidi Tsz Mung45,Lemaitre Rozenn N.6,Padhye Nikhil7,Song Xiaoling8,King Irena B.9,Lopez Oscar10,Siscovick David S.11,Mozaffarian Dariush4

Affiliation:

1. Division of Epidemiology, Human Genetics and Environmental Science, The University of Texas Health Science Center at Houston School of Public Health, Houston, TX, USA

2. The George Institute for Global Health and the Faculty of Medicine, University of New South Wales, Sydney, Australia

3. Department of Public Health, Brigham Young University, Provo, UT, USA

4. Friedman School of Nutrition Science and Policy, Tufts University, Boston, MA, USA

5. Department of Primary Care and Public Health, Imperial College London, London, UK

6. Cardiovascular Health Research Unit, Department of Medicine, University of Washington, Seattle, WA, USA

7. Center for Nursing Research, The University of Texas Health Science Center, School of Nursing, Houston, TX, USA

8. Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA

9. Department of Internal Medicine, University of New Mexico, Albuquerque, NM, USA

10. Department of Neurology, University of Pittsburg School of Medicine, Pittsburg, PA, USA

11. New York Academy of Medicine, New York, NY, USA

Abstract

Background: Comprising nearly 35% of brain lipids, polyunsaturated fatty acids (PUFA) are essential for optimal brain function. However, the role of PUFA on cognitive health outcomes later in life is largely unknown. Objective: We investigated prospective associations of plasma phospholipid omega-3 (ALA [18 : 3], EPA [20 : 5], DPA [22 : 5], DHA [22 : 6]) and omega-6 (LA [18 : 2], AA [20 : 4]) PUFA with cognitive decline, risk of cognitive impairment and dementia among adults aged≥65 years in the Cardiovascular Health Study. Methods: Circulating fatty acid concentrations were measured serially at baseline (1992/1993), 6 years, and 13 years later. Cognitive decline and impairment were assessed using the 100-point Modified Mini-Mental State Examination (3MSE) up to 7 times. Clinical dementia was identified using adjudicated neuropsychological tests, and ICD-9 codes. Results: Among 3,564 older adults free of stroke and dementia at baseline, cognitive function declined annually by approximately -0.5 3MSE points; 507 participants developed cognitive impairment and 499 dementia over up to 23 years of follow-up. In multivariable models, higher circulating arachidonic acid (AA) concentrations were associated with slower cognitive decline and lower dementia risk, with associations growing stronger with greater length of follow-up (hazard ratio [HR,95% CI] of dementia per interquintile range, 0.74 [0.56-0.97] at 5 years, and 0.53 [0.37-0.77] at 15 years). Circulating docosapentaenoic (DPA) concentrations were associated with slower cognitive decline and lower risk of cognitive impairment (extreme-quintile HR, 0.72 [95% CI: 0.55, 0.95]). Findings were generally null or inconsistent for other omega-3 or omega-6 PUFA. Conclusion: Circulating AA and DPA, but not other PUFA, are associated with slower rate of cognitive decline and lower risk of dementia or cognitive impairment later in life.

Publisher

IOS Press

Subject

Psychiatry and Mental health,Geriatrics and Gerontology,Clinical Psychology,General Medicine,General Neuroscience

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