Effects of Docosahexaenoic Acid Supplementation on Aggressive Behavior Among People With Dementia

We tested the efficacy of docosahexaenoic acid (DHA) supplementation on aggressive behavior among people with dementia. We used secondary data from a randomized, double-blind, placebo-controlled trial. Analyses included 402 individuals with dementia. We compared group differences in mean aggressive behavior change at baseline vs six (primary), 12, and 18 months (secondary outcome). We used independent samples t-tests with the aggressive behavior item from the Neuropsychiatric Inventory Questionnaire. We stratified group differences by ApoE-ε4 status, gender, baseline aggressive behavior, and dementia severity. All tests favored DHA but no differences reached statistical significance. For example, the group differences between baseline and month 6 aggressive behavior were 0.11 (p=0.22). Group differences nearly reached statistical significance with clinically important effect sizes when excluding participants without baseline aggressive behavior. Despite obtaining null results, these trends suggest avenues for future research that includes participants with higher baseline aggressive behavior levels and more sensitive outcome scales.

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Publication Details

Journal
Alzheimer Disease & Associated Disorders
Published
2025-04-01
DOI
https://doi.org/10.1097/wad.0000000000000674
Primary Topic
Fatty Acid Research and Health
Type
article
Field-Weighted Citation Impact
0.00
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article

Effects of Docosahexaenoic Acid Supplementation on Aggressive Behavior Among People With Dementia

Frances M. Yang, Ryan Townley, Jaime Perales‐Puchalt
Alzheimer Disease & Associated Disorders
Fatty Acid Research and Health
article

Effects of Docosahexaenoic Acid Supplementation on Aggressive Behavior Among People With Dementia

Frances M. Yang, Ryan Townley, Jaime Perales‐Puchalt
article en

Abstract

We tested the efficacy of docosahexaenoic acid (DHA) supplementation on aggressive behavior among people with dementia. We used secondary data from a randomized, double-blind, placebo-controlled trial. Analyses included 402 individuals with dementia. We compared group differences in mean aggressive behavior change at baseline vs six (primary), 12, and 18 months (secondary outcome). We used independent samples t-tests with the aggressive behavior item from the Neuropsychiatric Inventory Questionnaire. We stratified group differences by ApoE-ε4 status, gender, baseline aggressive behavior, and dementia severity. All tests favored DHA but no differences reached statistical significance. For example, the group differences between baseline and month 6 aggressive behavior were 0.11 (p=0.22). Group differences nearly reached statistical significance with clinically important effect sizes when excluding participants without baseline aggressive behavior. Despite obtaining null results, these trends suggest avenues for future research that includes participants with higher baseline aggressive behavior levels and more sensitive outcome scales.

Alzheimer Disease & Associated DisordersVol. 39(2)
University of Kansas Medical Center (US)
Openalex Percentile: Top 88%
Fatty Acid Research and Health
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