Evidence map›Paper›PMID 31330843›Full record

ReviewMolecules (Basel, Switzerland)2019

The Neuroprotective Effects of Astaxanthin: Therapeutic Targets and Clinical Perspective.

Sajad Fakhri, Ina Yosifova Aneva, Mohammad Hosein Farzaei, Eduardo Sobarzo-Sánchez

Registry-linked trialAbstract readReview
In one paragraph

Review in Molecules (Basel, Switzerland), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04689984 (The Benefits of Astaxanthin as Add on Therapy in the Management of Painful Diabetic Neuropathy Patient), which is not on this map. Cited by 79 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
79citing papers in PubMed, 1 pooled it
–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.

NCT04689984 phase2 / phase3unknown statusnot on this mapstarted 2020, after this paper: background citation

The Benefits of Astaxanthin as Add on Therapy in the Management of Painful Diabetic Neuropathy Patient: Randomized Clinical Trial

TypeinterventionalSponsorDuta Wacana Christian UniversityRan2020 to 2021Enrolled60ConditionsPainful Diabetic NeuropathyArmsStandard therapy, Astaxanthin
3 · Its place in the literature

Who cites it

79 citing papers in PubMed, 1 synthesis or guideline pooled it.

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19 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

4 authors.

Sajad FakhriPharmaceutical Sciences Research Center, Health Institute, Kermanshah University of Medical Sciences, Kermanshah, Iran.
Ina Yosifova AnevaInstitute of Biodiversity and Ecosystem Research, Bulgarian Academy of Sciences, 1113 Sofia, Bulgaria.
Mohammad Hosein FarzaeiPharmaceutical Sciences Research Center, Health Institute, Kermanshah University of Medical Sciences, Kermanshah, Iran. mh.farzaei@gmail.com.
Eduardo Sobarzo-SánchezLaboratory of Pharmaceutical Chemistry, Department of Organic Chemistry, Faculty of Pharmacy, University of Santiago de Compostela, 15782 Santiago de Compostela, Spain. e.sobarzo@usc.es.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As the leading causes of human disability and mortality, neurological diseases affect millions of people worldwide and are on the rise. Although the general roles of several signaling pathways in the pathogenesis of neurodegenerative disorders have so far been identified, the exact pathophysiology of neuronal disorders and their effective treatments have not yet been precisely elucidated. This requires multi-target treatments, which should simultaneously attenuate neuronal inflammation, oxidative stress, and apoptosis. In this regard, astaxanthin (AST) has gained growing interest as a multi-target pharmacological agent against neurological disorders including Parkinson's disease (PD), Alzheimer's disease (AD), brain and spinal cord injuries, neuropathic pain (NP), aging, depression, and autism. The present review highlights the neuroprotective effects of AST mainly based on its anti-inflammatory, antioxidative, and anti-apoptotic properties that underlies its pharmacological mechanisms of action to tackle neurodegeneration. The need to develop novel AST delivery systems, including nanoformulations, targeted therapy, and beyond, is also considered.

Indexed as

AgingAnimalsDrug Delivery SystemsHumansNanoparticlesNeurodegenerative DiseasesNeuroprotective AgentsStructure-Activity RelationshipTheranostic NanomedicineXanthophyllsastaxanthineNeuroprotective AgentsXanthophyllsapoptosisastaxanthindrug delivery systemneurodegenerative diseasesneuroinflammationneuroprotective agentoxidative stresspharmacology

Identifiers

PMID31330843
PMCPMC6680436

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Registered trials

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.