Evidence map›Paper›PMID 35821533›Full record

ArticleCellular and molecular life sciences : CMLS2022

SIRT1 pharmacological activation rescues vascular dysfunction and prevents thrombosis in MTHFR deficiency.

Albino Carrizzo, Concetta Iside, Angela Nebbioso, Vincenzo Carafa, Antonio Damato, Sebastiano Sciarretta, Giacomo Frati, Flavio Di Nonno, Valentina Valenti, Michele Ciccarelli and 15 more

Open access · hybridAbstract read
In one paragraph

Article in Cellular and molecular life sciences : CMLS, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
4.6field-weighted citation impact, top 4% 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

14 citing papers in PubMed, 27 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

25 authors at 5 institutions in 1 country.

Albino CarrizzoDepartment of Medicine, Surgery and Dentistry, "Scuola Medica Salernitana" University of Salerno, Via S. Allende, 84081, Baronissi, Italy.
Concetta IsideIRCCS Synlab SDN, Via E. Gianturco 113, 80143, Naples, Italy.
Angela NebbiosoDepartment of Precision Medicine, University of Campania "Luigi Vanvitelli", Vico L. De Crecchio, 80138, Naples, Italy.
Vincenzo CarafaDepartment of Precision Medicine, University of Campania "Luigi Vanvitelli", Vico L. De Crecchio, 80138, Naples, Italy.
Antonio DamatoIRCCS Neuromed, Vascular Physiopathology Unit, 86077, Pozzilli, Italy.
Sebastiano SciarrettaIRCCS Neuromed, Vascular Physiopathology Unit, 86077, Pozzilli, Italy.
Giacomo FratiIRCCS Neuromed, Vascular Physiopathology Unit, 86077, Pozzilli, Italy.
Flavio Di NonnoIRCCS Neuromed, Vascular Physiopathology Unit, 86077, Pozzilli, Italy.
Valentina ValentiDepartment of Cardiology, Santa Maria Goretti Hospital, 04100, Latina, Italy.
Michele CiccarelliDepartment of Medicine, Surgery and Dentistry, "Scuola Medica Salernitana" University of Salerno, Via S. Allende, 84081, Baronissi, Italy.
Eleonora VenturiniIRCCS Neuromed, Vascular Physiopathology Unit, 86077, Pozzilli, Italy.
Mariarosaria ScioliIRCCS Neuromed, Vascular Physiopathology Unit, 86077, Pozzilli, Italy.
Paola Di PietroDepartment of Medicine, Surgery and Dentistry, "Scuola Medica Salernitana" University of Salerno, Via S. Allende, 84081, Baronissi, Italy.
Tommaso BucciDepartment of Medicine, Surgery and Dentistry, "Scuola Medica Salernitana" University of Salerno, Via S. Allende, 84081, Baronissi, Italy.
Valentina GiudiceDepartment of Medicine, Surgery and Dentistry, "Scuola Medica Salernitana" University of Salerno, Via S. Allende, 84081, Baronissi, Italy.
Marianna StortoDepartment of Medicine, Surgery and Dentistry, "Scuola Medica Salernitana" University of Salerno, Via S. Allende, 84081, Baronissi, Italy.
Bianca SerioUniversity Hospital, San Giovanni di Dio e Ruggi D'Aragona, 84125, Salerno, Italy.
Annibale Alessandro PucaDepartment of Medicine, Surgery and Dentistry, "Scuola Medica Salernitana" University of Salerno, Via S. Allende, 84081, Baronissi, Italy.
Giuseppe GiuglianoDepartment of Advanced Biomedical Sciences, "Federico II" University, Via Pansini 5, 80131, Naples, Italy.
Valentina TrimarcoDepartment of Neuroscience, Reproductive Sciences and Dentistry, "Federico II" University, Via Pansini 5, 80131, Naples, Italy.
Raffaele IzzoDepartment of Advanced Biomedical Sciences, "Federico II" University, Via Pansini 5, 80131, Naples, Italy.
Bruno TrimarcoInternational Translational Research and Medical Education (ITME) Consortium and Department of Advanced Biomedical Sciences, "Federico II" University, 80131, Naples, Italy.
Carmine SelleriDepartment of Medicine, Surgery and Dentistry, "Scuola Medica Salernitana" University of Salerno, Via S. Allende, 84081, Baronissi, Italy.
Lucia AltucciDepartment of Precision Medicine, University of Campania "Luigi Vanvitelli", Vico L. De Crecchio, 80138, Naples, Italy.
Carmine VecchioneDepartment of Medicine, Surgery and Dentistry, "Scuola Medica Salernitana" University of Salerno, Via S. Allende, 84081, Baronissi, Italy. cvecchione@unisa.it.ORCID http://orcid.org/0000-0002-2473-4565
University of Salerno · ITIstituto Neurologico Mediterraneo · ITFederico II University Hospital · ITUniversity of Campania "Luigi Vanvitelli" · ITOspedali Riuniti San Giovanni di Dio e Ruggi d'Aragona · IT

Funding

Ministero della Salute GR-2018- 12366268
6 · The paper itself

Abstract

Beyond well-assessed risk factors, cardiovascular events could be also associated with the presence of epigenetic and genetic alterations, such as the methylenetetrahydrofolate-reductase (MTHFR) C677T polymorphism. This gene variant is related to increased circulating levels of homocysteine (Hcy) and cardiovascular risk. However, heterozygous carriers have an augmented risk of cardiovascular accidents independently from normal Hcy levels, suggesting the presence of additional deregulated processes in MTHFR C677T carriers. Here, we hypothesize that targeting Sirtuin 1 (SIRT1) could be an alternative mechanism to control the cardiovascular risk associated to MTHFR deficiency condition. Flow Mediated Dilatation (FMD) and light transmission aggregometry assay were performed in subjects carrying MTHFR C677T allele after administration of resveratrol, the most powerful natural clinical usable compound that owns SIRT1 activating properties. MTHFR C677T carriers with normal Hcy levels revealed endothelial dysfunction and enhanced platelet aggregation associated with SIRT1 downregulation. SIRT1 activity stimulation by resveratrol intake was able to override these abnormalities without affecting Hcy levels. Impaired endothelial function, bleeding time, and wire-induced thrombus formation were rescued in a heterozygous Mthfr-deficient (Mthfr

Indexed as

HomocystinuriaMethylenetetrahydrofolate Reductase (NADPH2)Sirtuin 1ThrombosisAnimalsGenotypeHumansMiceMuscle SpasticityPsychotic DisordersResveratrolMethylenetetrahydrofolate Reductase (NADPH2)MTHFR protein, mouseResveratrolSirt1 protein, mouseSirtuin 1EndotheliumMTHFRNitric oxideSIRT1Vascular function

Identifiers

PMID35821533
PMCPMC9276577
OpenAlexW4285094944

What OpenQuestion holds

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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.