Evidence map›Paper›PMID 33110151›Full record

ArticleScientific reports2020

Cyclocreatine treatment ameliorates the cognitive, autistic and epileptic phenotype in a mouse model of Creatine Transporter Deficiency.

Francesco Cacciante, Mariangela Gennaro, Giulia Sagona, Raffaele Mazziotti, Leonardo Lupori, Elisa Cerri, Elena Putignano, Mark Butt, Minh-Ha T Do, John C McKew and 5 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

9 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Creatine deficiency and heart failure.Heart failure reviews · 2022
    Review
  5. Article
  6. Article
  7. Article
  8. Visual Cortex Engagement in Retinitis Pigmentosa.International journal of molecular sciences · 2021
    Article
  9. Review
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

15 authors at 5 institutions in 2 countries.

Francesco CaccianteInstitute of Neuroscience, National Research Council (CNR), Via Moruzzi 1, 56124, Pisa, Italy.
Mariangela GennaroInstitute of Neuroscience, National Research Council (CNR), Via Moruzzi 1, 56124, Pisa, Italy.
Giulia SagonaDepartment of Neuroscience, Psychology, Drug Research and Child Health NEUROFARBA, University of Florence, 50135, Florence, Italy.
Raffaele MazziottiInstitute of Neuroscience, National Research Council (CNR), Via Moruzzi 1, 56124, Pisa, Italy.
Leonardo LuporiBIO@SNS Lab, Scuola Normale Superiore di Pisa, 56125, Pisa, Italy.
Elisa CerriInstitute of Neuroscience, National Research Council (CNR), Via Moruzzi 1, 56124, Pisa, Italy.
Elena PutignanoInstitute of Neuroscience, National Research Council (CNR), Via Moruzzi 1, 56124, Pisa, Italy.
Mark ButtTox Path Specialists, Frederick, MD, 21701, USA.
Minh-Ha T DoLumos Pharma, Austin, TX, 78756, USA.
John C McKewLumos Pharma, Austin, TX, 78756, USA.
Maria Grazia AlessandrìDepartment of Developmental Neuroscience, IRCCS Stella Maris Foundation, 56128, Pisa, Italy.
Roberta BattiniDepartment of Developmental Neuroscience, IRCCS Stella Maris Foundation, 56128, Pisa, Italy.
Giovanni CioniDepartment of Developmental Neuroscience, IRCCS Stella Maris Foundation, 56128, Pisa, Italy.
Tommaso PizzorussoInstitute of Neuroscience, National Research Council (CNR), Via Moruzzi 1, 56124, Pisa, Italy.
Laura BaroncelliInstitute of Neuroscience, National Research Council (CNR), Via Moruzzi 1, 56124, Pisa, Italy. baroncelli@in.cnr.it.
National Research Council · ITFondazione Stella Maris · ITLumos Pharma (United States) · USAtlas Copco (United States) · USScuola Normale Superiore · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Creatine Transporter Deficiency (CTD) is an inborn error of metabolism presenting with intellectual disability, behavioral disturbances and epilepsy. There is currently no cure for this disorder. Here, we employed novel biomarkers for monitoring brain function, together with well-established behavioral readouts for CTD mice, to longitudinally study the therapeutic efficacy of cyclocreatine (cCr) at the preclinical level. Our results show that cCr treatment is able to partially correct hemodynamic responses and EEG abnormalities, improve cognitive deficits, revert autistic-like behaviors and protect against seizures. This study provides encouraging data to support the potential therapeutic benefit of cyclocreatine or other chemically modified lipophilic analogs of Cr.

Indexed as

AnimalsAutistic DisorderBlood-Brain BarrierBrain Diseases, Metabolic, InbornCerebrovascular CirculationCognition DisordersCreatineCreatinineDisease Models, AnimalElectroencephalographyEpilepsyHemodynamicsMaleMiceMice, Inbred C57BLPhenotypeCreatineCreatininecyclocreatinePlasma Membrane Neurotransmitter Transport Proteins

Identifiers

PMID33110151
PMCPMC7591530
OpenAlexW3096281450

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.