Evidence map›Paper›PMID 33871046›Full record

ReviewClinical genetics2021

The genetic underpinnings of anthracycline-induced cardiomyopathy predisposition.

Amy M Berkman, Michelle A T Hildebrandt, Andrew P Landstrom

Open access · greenAbstract readReview
In one paragraph

Review in Clinical genetics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 2 pooled it
1.9field-weighted citation impact, top 13% 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

12 citing papers in PubMed, 2 syntheses or guidelines pooled it, 17 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Review
  5. Review
  6. Genetic factors in the pathogenesis of cardio-oncology.Journal of translational medicine · 2024
    Review
  7. Review
  8. Article
  9. Article
  10. Uncovering the Genetic Etiology of the (Posttherapy) Broken Heart.Journal of the National Cancer Institute · 2022
    Article
  11. Review
  12. Pharmaceutics · 2021
    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

3 authors at 2 institutions in 1 country.

Amy M BerkmanDepartment of Pediatrics, Division of Cardiology, Duke University School of Medicine, Durham, North Carolina, USA.
Michelle A T HildebrandtDepartment of Lymphoma/Myeloma, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Andrew P LandstromDepartment of Pediatrics, Division of Cardiology, Duke University School of Medicine, Durham, North Carolina, USA.
Duke University Hospital · USThe University of Texas MD Anderson Cancer Center · US

Funding

Stimulating Access to Research in Residency (StARR) - NHLBIR38HL143612 · NHLBI · DUKE UNIVERSITY · PI Mai ElMallah, David H. Harpole · 2018 to 2026
$2.6M
The Role of Junctophilin Type 2 in Cardiac Node AutomaticityK08HL136839 · NHLBI · DUKE UNIVERSITY · PI LANDSTROM, ANDREW P. · 2017 to 2021
$769k
NHLBI NIH HHS K08 HL136839NHLBI NIH HHS R38 HL143612
6 · The paper itself

Abstract

Anthracyclines, chemotherapeutic agents that have contributed to significant improvements in cancer survival, also carry risk of both acute and chronic cardiotoxicity. This has led to significantly elevated risks of cardiac morbidity and mortality among cancer survivors treated with these agents. Certain treatment related, demographic, and medical factors increase an individual's risk of anthracycline induced cardiotoxicity; however, significant variability among those affected suggests that there is an underlying genetic predisposition to anthracycline induced cardiotoxicity. The current narrative review seeks to summarize the literature to date that has identified genetic variants associated with anthracycline induced cardiotoxicity. These include variants found in genes that encode proteins associated with anthracycline transportation and metabolism, those that encode proteins associated with the generation of reactive oxygen species, and those known to be associated with cardiac disease. While there is strong evidence that susceptibility to anthracycline induced cardiotoxicity has genetic underpinnings, the majority of work to date has been candidate gene analyses. Future work should focus on genome-wide analyses including genome-wide association and sequencing-based studies to confirm and expand these findings.

Indexed as

Genetic Predisposition to DiseaseAlcohol OxidoreductasesAnthracyclinesAntibiotics, AntineoplasticATP Binding Cassette Transporter, Subfamily BCardiomyopathiesCardiotoxicityHumansNADPH OxidasesNitric Oxide Synthase Type IIIOrganic Anion Transport Protein 1Alcohol OxidoreductasesAnthracyclinesAntibiotics, AntineoplasticATP Binding Cassette Transporter, Subfamily BCBR3 protein, humanmultidrug resistance protein 3NADPH OxidasesNCF4 protein, humanNitric Oxide Synthase Type IIINOS3 protein, humanOrganic Anion Transport Protein 1SLC22A6 protein, humananthracyclinescancercardiotoxicitySNPs

Identifiers

PMID33871046
PMCPMC9902211
OpenAlexW3156604581

What OpenQuestion holds

Textmetadata
LicenceTDM
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.