Omega-3 Fatty Acids Increase Amyloid-β Immunity, Energy, and Circadian Rhythm for Cognitive Protection of Alzheimer's Disease Patients Beyond Cholinesterase Inhibitors

Omega-3 脂肪酸可增强淀粉样蛋白 β 的免疫力、能量和昼夜节律,从而为阿尔茨海默病患者提供认知保护,效果远超胆碱酯酶抑制剂

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作者:Milan Fiala, Yik Chai Charles Lau, Anthony Aghajani, Sneha Bhargava, Eli Aminpour, Karolina Elżbieta Kaczor-Urbanowicz, Hayk Mirzoyan, India Nichols, Meng-Wei Ko, Marco Morselli, Joslyn Santana, Johnny Dang, James Sayre, Ketema Paul, Matteo Pellegrini

Background

The cholinesterase inhibitor therapeutics (CI) approved for use in Alzheimer's disease (AD) are palliative for a limited time.

Conclusion

Add-on ω-3 therapy to CI may delay dementia in certain patients who had failed single CI therapy.

Methods

We performed a prospective study using Mini-Mental State Examination, amyloid-β (Aβ) phagocytosis blood assay, and RNA-seq of peripheral blood mononuclear cells in 28 neurodegenerative patients who had failed their therapies, including 8 subjective cognitive impairment (SCI), 8 mild cognitive impairment (MCI), 2 AD dementia, 1 frontotemporal dementia (FTD), 2 vascular cognitive impairment, and 3 dementia with Lewy bodies (DLB) patients.

Objective

To examine the outcome of AD patients with add-on therapy of the omega-3 fatty acid drink Smartfish.

Results

MCI, FTD, and DLB patients patients volunteered for the addition of a ω-3 fatty acid drink Smartfish protected by anti-oxidants to failing CI therapy. On this therapy, all MCI patients improved in the first year energy transcripts, Aβ phagocytosis, cognition, and activities of daily living; in the long term, they remained in MCI status two to 4.5 years. All FTD and DLB patients rapidly progressed to dementia. On in vivo or in vitroω-3 treatments, peripheral blood mononuclear cells of MCI patients upregulated energy enzymes for glycolysis and citric acid cycle, as well as the anti-inflammatory circadian genes CLOCK and ARNTL2.

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