Evidence map›Paper›PMID 32071288›Full record

ArticleCell death & disease2020

Nutritional intervention with cyanidin hinders the progression of muscular dystrophy.

Marielle Saclier, Chiara Bonfanti, Stefania Antonini, Giuseppe Angelini, Giada Mura, Federica Zanaglio, Valentina Taglietti, Vanina Romanello, Marco Sandri, Chiara Tonelli and 3 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 23% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 22 citations in OpenAlex.

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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

13 authors at 2 institutions in 1 country.

Marielle SaclierDepartment of Biosciences, University of Milan, via Celoria 26, 20133, Milan, Italy.
Chiara BonfantiDepartment of Biosciences, University of Milan, via Celoria 26, 20133, Milan, Italy.
Stefania AntoniniDepartment of Biosciences, University of Milan, via Celoria 26, 20133, Milan, Italy.
Giuseppe AngeliniDepartment of Biosciences, University of Milan, via Celoria 26, 20133, Milan, Italy.
Giada MuraDepartment of Biosciences, University of Milan, via Celoria 26, 20133, Milan, Italy.
Federica ZanaglioDepartment of Biosciences, University of Milan, via Celoria 26, 20133, Milan, Italy.
Valentina TagliettiDepartment of Biosciences, University of Milan, via Celoria 26, 20133, Milan, Italy.
Vanina RomanelloVenetian Institute of Molecular Medicine (VIMM), Department of Biomedical Sciences, University of Padova, Padova, Italy.
Marco SandriVenetian Institute of Molecular Medicine (VIMM), Department of Biomedical Sciences, University of Padova, Padova, Italy.
Chiara TonelliDepartment of Biosciences, University of Milan, via Celoria 26, 20133, Milan, Italy.ORCID http://orcid.org/0000-0002-9505-3118
Katia Petroni *Department of Biosciences, University of Milan, via Celoria 26, 20133, Milan, Italy.ORCID http://orcid.org/0000-0003-3318-0442
Marco Cassano *Department of Biosciences, University of Milan, via Celoria 26, 20133, Milan, Italy.
Graziella Messina *Department of Biosciences, University of Milan, via Celoria 26, 20133, Milan, Italy. graziella.messina@unimi.it.ORCID http://orcid.org/0000-0001-8189-0727
University of Milan · ITVeneto Institute of Molecular Medicine · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Muscular Dystrophies are severe genetic diseases due to mutations in structural genes, characterized by progressive muscle wasting that compromises patients' mobility and respiratory functions. Literature underlined oxidative stress and inflammation as key drivers of these pathologies. Interestingly among different myofiber classes, type I fibers display a milder dystrophic phenotype showing increased oxidative metabolism. This work shows the benefits of a cyanidin-enriched diet, that promotes muscle fiber-type switch and reduced inflammation in dystrophic alpha-sarcoglyan (Sgca) null mice having, as a net outcome, morphological and functional rescue. Notably, this benefit is achieved also when the diet is administered in dystrophic animals when the signs of the disease are seriously evident. Our work provides compelling evidence that a cyanidin-rich diet strongly delays the progression of muscular dystrophies, paving the way for a combinatorial approach where nutritional-based reduction of muscle inflammation and oxidative stress facilitate the successful perspectives of definitive treatments.

Indexed as

Dietary SupplementsOxidative StressAnimalsAnthocyaninsDisease Models, AnimalDisease ProgressionFemaleInflammation MediatorsMaleMice, KnockoutMitochondria, MuscleMuscle, SkeletalOrganelle BiogenesisPhenotypeProtein CarbonylationSarcoglycanopathiesAnthocyaninscyanidin-3-O-beta-glucopyranosideInflammation MediatorsSarcoglycans

Identifiers

PMID32071288
PMCPMC7028923
OpenAlexW3008294575

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.