Evidence map›Paper›PMID 31590338›Full record

ReviewInternational journal of molecular sciences2019

Metabolomic Perspectives in Antiblastic Cardiotoxicity and Cardioprotection.

Martino Deidda, Valentina Mercurio, Alessandra Cuomo, Antonio Noto, Giuseppe Mercuro, Christian Cadeddu Dessalvi

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 15% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 18 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. Review
  8. Metabolic Aspects of Anthracycline Cardiotoxicity.Current treatment options in oncology · 2021
    Review
  9. Article
  10. Article
  11. Article
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.

Martino DeiddaDepartment of Medical Sciences and Public Health, University of Cagliari, 09042 Monserrato-Cagliari, Italy. martino.deidda@tiscali.it.ORCID 0000-0002-3725-7614
Valentina MercurioDepartment of Translational Medical Sciences, Federico II University, 80131 Naples, Italy. valentina.mercurio@unina.it.
Alessandra CuomoDepartment of Translational Medical Sciences, Federico II University, 80131 Naples, Italy. alebcuomo@gmail.com.ORCID 0000-0002-5781-2865
Antonio NotoDepartment of Medical Sciences and Public Health, University of Cagliari, 09042 Monserrato-Cagliari, Italy. antonionoto@unica.it.
Giuseppe MercuroDepartment of Medical Sciences and Public Health, University of Cagliari, 09042 Monserrato-Cagliari, Italy. giuseppemercuro@gmail.com.
Christian Cadeddu DessalviDepartment of Medical Sciences and Public Health, University of Cagliari, 09042 Monserrato-Cagliari, Italy. cadedduc@unica.it.ORCID 0000-0002-2823-1797
University of Cagliari · ITFederico II University Hospital · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite advances in supportive and protective therapy for myocardial function, cardiovascular diseases due to antineoplastic therapy-primarily cardiomyopathy associated with contractile dysfunction-remain a major cause of morbidity and mortality. Because of the limitations associated with current therapies, investigators are searching for alternative strategies that can timely recognise cardiovascular damage-thus permitting a quick therapeutic approach-or prevent the development of the disease. Damage to the heart can result from both traditional chemotherapeutic agents, such as anthracyclines, and new targeted therapies, such as tyrosine kinase inhibitors. In recent years, metabolomics has proved to be a practical tool to highlight fundamental changes in the metabolic state in several pathological conditions. In this article, we present the state-of-the-art technology with regard to the metabolic mechanisms underlying cardiotoxicity and cardioprotection.

Indexed as

MetabolomeAnimalsAntineoplastic AgentsCardiotonic AgentsCardiotoxicityDrug DiscoveryHeart FailureHumansMetabolomicsAntineoplastic AgentsCardiotonic Agentscardiotoxicityheart failuremetabolismmetabolomics

Identifiers

PMID31590338
PMCPMC6801977
OpenAlexW2978447526

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.