Evidence map›Paper›PMID 32660119›Full record

ReviewMarine drugs2020

Impact of Astaxanthin on Diabetes Pathogenesis and Chronic Complications.

Rebecca Landon, Virginie Gueguen, Hervé Petite, Didier Letourneur, Graciela Pavon-Djavid, Fani Anagnostou

Open access · goldAbstract readReview
In one paragraph

Review in Marine drugs, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed
6.7field-weighted citation impact, top 2% of its field
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

68 citing papers in PubMed, 137 citations in OpenAlex.

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  14. International journal of endocrinology · 2025
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8 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

6 authors at 2 institutions in 1 country.

Rebecca LandonCNRS UMR7052-INSERM U1271, Laboratory of Osteoarticular Biology, Bioengineering and Bioimaging, Paris Diderot University, 10 av.de Verdun, 75010 Paris, France.
Virginie GueguenINSERM U1148, Laboratory for Vascular Translational Science, Cardiovascular Bioengineering, Sorbonne University Paris Nord, 99 Av. Jean-Baptiste Clément, 93430 Villetaneuse, France.
Hervé PetiteCNRS UMR7052-INSERM U1271, Laboratory of Osteoarticular Biology, Bioengineering and Bioimaging, Paris Diderot University, 10 av.de Verdun, 75010 Paris, France.
Didier LetourneurINSERM U1148, Laboratory for Vascular Translational Science, Cardiovascular Bioengineering, Sorbonne University Paris Nord, 99 Av. Jean-Baptiste Clément, 93430 Villetaneuse, France.ORCID 0000-0003-2197-9468
Graciela Pavon-DjavidINSERM U1148, Laboratory for Vascular Translational Science, Cardiovascular Bioengineering, Sorbonne University Paris Nord, 99 Av. Jean-Baptiste Clément, 93430 Villetaneuse, France.ORCID 0000-0001-5819-1071
Fani AnagnostouCNRS UMR7052-INSERM U1271, Laboratory of Osteoarticular Biology, Bioengineering and Bioimaging, Paris Diderot University, 10 av.de Verdun, 75010 Paris, France.
Centre National de la Recherche Scientifique · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oxidative stress (OS) plays a pivotal role in diabetes mellitus (DM) onset, progression, and chronic complications. Hyperglycemia-induced reactive oxygen species (ROS) have been shown to reduce insulin secretion from pancreatic β-cells, to impair insulin sensitivity and signaling in insulin-responsive tissues, and to alter endothelial cells function in both type 1 and type 2 DM. As a powerful antioxidant without side effects, astaxanthin (ASX), a xanthophyll carotenoid, has been suggested to contribute to the prevention and treatment of DM-associated pathologies. ASX reduces inflammation, OS, and apoptosis by regulating different OS pathways though the exact mechanism remains elusive. Based on several studies conducted on type 1 and type 2 DM animal models, orally or parenterally administrated ASX improves insulin resistance and insulin secretion; reduces hyperglycemia; and exerts protective effects against retinopathy, nephropathy, and neuropathy. However, more experimental support is needed to define conditions for its use. Moreover, its efficacy in diabetic patients is poorly explored. In the present review, we aimed to identify the up-to-date biological effects and underlying mechanisms of ASX on the ROS-induced DM-associated metabolic disorders and subsequent complications. The development of an in-depth research to better understand the biological mechanisms involved and to identify the most effective ASX dosage and route of administration is deemed necessary.

Indexed as

AntioxidantsDiabetes Mellitus, Type 2HumansOxidative StressXanthophyllsAntioxidantsastaxanthineXanthophyllsantioxidantastaxanthindiabetes complicationdiabetes mellitusdiabetic nephropathydiabetic neuropathydiabetic retinopathyhyperglycemiainsulin resistanceoxidative stressROS

Identifiers

PMID32660119
PMCPMC7401277
OpenAlexW3041018901

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.