Evidence map›Paper›PMID 36501121›Full record

ArticleNutrients2022

How Alpha Linolenic Acid May Sustain Blood-Brain Barrier Integrity and Boost Brain Resilience against Alzheimer's Disease.

Alicia Leikin-Frenkel, Michal Schnaider Beeri, Itzik Cooper

Abstract read
In one paragraph

Article in Nutrients, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed.

  1. Gut microbes · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Alicia Leikin-FrenkelBert Strassburger Lipid Center, Sheba Medical Center, Tel-Hashomer 52621, Israel.ORCID 0000-0002-6156-0533
Michal Schnaider BeeriThe Joseph Sagol Neuroscience Center, Sheba Medical Center, Ramat-Gan 52621, Israel.ORCID 0000-0002-4254-9742
Itzik CooperThe Joseph Sagol Neuroscience Center, Sheba Medical Center, Ramat-Gan 52621, Israel.ORCID 0000-0003-0723-5542

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cognitive decline, the primary clinical phenotype of Alzheimer's disease (AD), is currently attributed mainly to amyloid and tau protein deposits. However, a growing body of evidence is converging on brain lipids, and blood-brain barrier (BBB) dysfunction, as crucial players involved in AD development. The critical role of lipids metabolism in the brain and its vascular barrier, and its constant modifications particularly throughout AD development, warrants investigation of brain lipid metabolism as a high value therapeutic target. Yet, there is limited knowledge on the biochemical and structural roles of lipids in BBB functionality in AD. Within this framework, we hypothesize that the ApoE4 genotype, strongly linked to AD risk and progression, may be related to altered fatty acids composition in the BBB. Interestingly, alpha linolenic acid (ALA), the precursor of the majoritarian brain component docosahexaenoic acid (DHA), emerges as a potential novel brain savior, acting via BBB functional improvements, and this may be primarily relevant to ApoE4 carriers.

Indexed as

Alzheimer Diseasealpha-Linolenic AcidApolipoprotein E4Blood-Brain BarrierBrainHumansalpha-Linolenic AcidApolipoprotein E4alpha linolenic acidAlzheimer’s dementiaAlzheimer’s diseaseblood–brain barriercardiocerebrovascular diseasesfatty acidsvascular cognitive impairment

Identifiers

PMID36501121
PMCPMC9737216

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.