Evidence map›Paper›PMID 28299644›Full record

ReviewGeroScience2017

Neuroprotective mechanisms of astaxanthin: a potential therapeutic role in preserving cognitive function in age and neurodegeneration.

Bethany Grimmig, Seol-Hee Kim, Kevin Nash, Paula C Bickford, R Douglas Shytle

Abstract readReview
In one paragraph

Review in GeroScience, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 91 papers.

0numbers the graph read from it
0cells of the map it votes in
91citing 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

91 citing papers in PubMed.

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  5. The Ubiquitin-Proteasome System in Brain Disorders: Pathogenic Pathways, Post-Translational Tweaks, and Therapeutic Frontiers.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2025
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31 more citing papers are in PubMed but not listed here.

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

5 authors.

Bethany GrimmigDepartment of Neurosurgery and Brain Repair, Center of Excellence for Aging and Brain Repair, Morsani College of Medicine, University of South Florida, Tampa, FL, USA.
Seol-Hee KimDepartment of Neurosurgery and Brain Repair, Center of Excellence for Aging and Brain Repair, Morsani College of Medicine, University of South Florida, Tampa, FL, USA.
Kevin NashByrd Alzheimer's Institute, Department of Molecular Pharmacology and Physiology, Morsani College of Medicine, University of South Florida, Tampa, FL, USA.
Paula C BickfordDepartment of Neurosurgery and Brain Repair, Center of Excellence for Aging and Brain Repair, Morsani College of Medicine, University of South Florida, Tampa, FL, USA. pbickfor@health.usf.edu.
R Douglas ShytleDepartment of Neurosurgery and Brain Repair, Center of Excellence for Aging and Brain Repair, Morsani College of Medicine, University of South Florida, Tampa, FL, USA.

Funding

STATISTICAL COREP01AG004418 · NIA · UNIVERSITY OF SOUTH FLORIDA · PI BICKFORD, PAULA C · 1985 to 2010
$11.6M
Neuron - glial communication and brain agingR01AG044919 · NIA · UNIVERSITY OF SOUTH FLORIDA · PI BICKFORD, PAULA C · 2012 to 2016
$1.7M
Aging and Microglial PolarizationI01BX003421 · VA · JAMES A. HALEY VA MEDICAL CENTER · PI BICKFORD, PAULA C · 2016 to 2020
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BLRD VA I01 BX003231BLRD VA I01 BX003421NIA NIH HHS P01 AG004418NIA NIH HHS R01 AG044919
6 · The paper itself

Abstract

Astaxanthin (AXT) is a carotenoid with multiple health benefits. It is currently marketed as a health supplement and is well known for its antioxidant capacity. Recent evidence has emerged to suggest a broad range of biological activities. The interest in this compound has increased dramatically over the last few years and many studies are now applying this molecule across many disease models. Results from the current research are beginning to come together to suggest neuroprotective properties including anti-inflammatory, anti-apoptotic, and antioxidant effects, as well as the potential to promote or maintain neural plasticity. These emergent mechanisms of actions implicate AXT as a promising therapeutic agent for neurodegenerative disease. This review will examine and extrapolate from the recent literature to build support for the use of AXT in mitigating neuropathy in normal aging and neurodegenerative disease.

Indexed as

AgingAnimalsDietary SupplementsHumansNeurodegenerative DiseasesNeuroprotectionNeuroprotective AgentsPrognosisRisk AssessmentTreatment OutcomeXanthophyllsastaxanthineNeuroprotective AgentsXanthophyllsAgingAstaxanthinMicroglial functionNeural plasticityNeuroprotection

Identifiers

PMID28299644
PMCPMC5352583

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.