Evidence map›Paper›PMID 32979174›Full record

ReviewCardiovascular drugs and therapy2022

Therapeutic Potential of Senolytics in Cardiovascular Disease.

Emily Dookun, João F Passos, Helen M Arthur, Gavin D Richardson

Open access · hybridAbstract readReview
In one paragraph

Review in Cardiovascular drugs and therapy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
4.9field-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

48 citing papers in PubMed, 62 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Neurovascular interactions in the ageing heart.Nature reviews. Cardiology · 2026
    Review
  5. Review
  6. Review
  7. Review
  8. Review
  9. Review
  10. Review
  11. Weight of time: exploring the link between obesity and aging.Aging clinical and experimental research · 2025
    Review
  12. Review
  13. Article
  14. The role of T cells in vascular aging, hypertension, and atherosclerosis.American journal of physiology. Heart and circulatory physiology · 2024
    Review
  15. Review
  16. Article
  17. The Senescent Heart-"Age Doth Wither Its Infinite Variety".International journal of molecular sciences · 2024
    Review
  18. Potential Clinical Implications of Senotherapies for Cardiovascular Disease.Circulation journal : official journal of the Japanese Circulation Society · 2024
    Article
  19. Review
  20. 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

4 authors at 2 institutions in 2 countries.

Emily DookunBiosciences Institute, Newcastle University, Newcastle upon Tyne, NE1 3BZ, UK.ORCID 0000-0002-4999-4427
João F PassosDepartment of Physiology and Biomedical Engineering, Mayo Clinic, Rochester, MN, USA.ORCID 0000-0001-8765-1890
Helen M ArthurBiosciences Institute, Newcastle University, Newcastle upon Tyne, NE1 3BZ, UK.ORCID 0000-0001-6522-1363
Gavin D RichardsonBiosciences Institute, Newcastle University, Newcastle upon Tyne, NE1 3BZ, UK. Gavin.Richardson@ncl.ac.uk.ORCID 0000-0002-2310-9987
Newcastle University · GBMayo Clinic in Florida · US

Funding

The role of sub-lethal mitochondrial apoptotic stress in cellular senescenceR01AG068048 · NIA · MAYO CLINIC ROCHESTER · PI PASSOS, JOAO · 2020 to 2024
$2.2M
Development of machine learning software to quantitatively map telomere induced senescence in tissue sections during agingUG3CA268103 · NCI · MAYO CLINIC ROCHESTER · PI PASSOS, JOAO · 2021 to 2022
$1.1M
British Heart Foundation PG/19/15/34269NCI NIH HHS UG3 CA268103NIA NIH HHS R01 AG068048
6 · The paper itself

Abstract

Ageing is the biggest risk factor for impaired cardiovascular health, with cardiovascular disease being the leading cause of death in 40% of individuals over 65 years old. Ageing is associated with both an increased prevalence of cardiovascular disease including heart failure, coronary artery disease, and myocardial infarction. Furthermore, ageing is associated with a poorer prognosis to these diseases. Genetic models allowing the elimination of senescent cells revealed that an accumulation of senescence contributes to the pathophysiology of cardiovascular ageing and promotes the progression of cardiovascular disease through the expression of a proinflammatory and profibrotic senescence-associated secretory phenotype. These studies have resulted in an effort to identify pharmacological therapeutics that enable the specific elimination of senescent cells through apoptosis induction. These senescent cell apoptosis-inducing compounds are termed senolytics and their potential to ameliorate age-associated cardiovascular disease is the focus of this review.

Indexed as

AgedAgingAnimalsApoptosisCardiovascular DiseasesCellular SenescenceDisease ProgressionHumansPrognosisRisk FactorsSenescence-Associated Secretory PhenotypeSenotherapeuticsSenotherapeuticsAtherosclerosisCardiovascularInflammationRemodellingSenescenceSenolytic

Identifiers

PMID32979174
PMCPMC8770386
OpenAlexW3089255423

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.