Evidence map›Paper›PMID 37880106›Full record

ArticleCirculation journal : official journal of the Japanese Circulation Society2024

Potential Clinical Implications of Senotherapies for Cardiovascular Disease.

Masayoshi Suda, Goro Katsuumi, Tamar Tchkonia, James L Kirkland, Tohru Minamino

Open access · diamondAbstract read
In one paragraph

Article in Circulation journal : official journal of the Japanese Circulation Society, 2024. 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
4.7field-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.

  1. Article
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  7. Role of Vascular Niche in Cardiac Aging.Circulation research · 2025
    Article
  8. Review
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  13. Article
  14. Cardiovascular aging: spotlight on mitochondria.American journal of physiology. Heart and circulatory physiology · 2024
    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

5 authors at 2 institutions in 2 countries.

Masayoshi SudaDepartment of Cardiovascular Biology and Medicine, Juntendo University Graduate School of Medicine.
Goro KatsuumiDepartment of Cardiovascular Biology and Medicine, Juntendo University Graduate School of Medicine.
Tamar TchkoniaDepartment of Medicine and Physiology and Biomedical Engineering, Mayo Clinic.
James L KirklandDepartment of Medicine and Physiology and Biomedical Engineering, Mayo Clinic.
Tohru MinaminoDepartment of Cardiovascular Biology and Medicine, Juntendo University Graduate School of Medicine.
Mayo Clinic in Arizona · USJuntendo University · JP

Funding

Targeting Cellular Senescence to Extend HealthspanP01AG062413 · NIA · MAYO CLINIC ROCHESTER · PI Sundeep Khosla, Nathan K LeBrasseur · 2019 to 2026
$28.7M
ConProject-001UH3AG056933 · NIA · JOHNS HOPKINS UNIVERSITY · PI BANDEEN-ROCHE, KAREN J., VARADHAN, RAVI · 2019 to 2021
$7.0M
Effect of Aging on Preadipocyte DifferentiationR37AG013925 · NIA · MAYO CLINIC ROCHESTER · PI KIRKLAND, JAMES L. · 2016 to 2025
$6.6M
Translational Geroscience NetworkR33AG061456 · NIA · MAYO CLINIC ROCHESTER · PI JAMES L. KIRKLAND, STEPHEN B. KRITCHEVSKY · 2019 to 2026
$6.2M
Characterizing Resiliencies to Physical Stressors in Older Adults: A Dynamical Physiological Systems ApproachUH2AG056933 · NIA · JOHNS HOPKINS UNIVERSITY · PI BANDEEN-ROCHE, KAREN J., VARADHAN, RAVI · 2017 to 2018
$3.5M
Obesity-induced mesenchymal stem cell senescenceR01DK120292 · NIDDK · MAYO CLINIC ROCHESTER · PI LERMAN, LILACH O · 2019 to 2022
$2.6M
Senescent cells drive mt-DNA accumulation and inflamm-agingR01AG064165 · NIA · BRIGHAM AND WOMEN'S HOSPITAL · PI TULLIUS, STEFAN GUNTHER · 2020 to 2024
$2.6M
The role of sub-lethal mitochondrial apoptotic stress in cellular senescenceR01AG068048 · NIA · MAYO CLINIC ROCHESTER · PI PASSOS, JOAO · 2020 to 2024
$2.2M
COVID-FIS: A PHASE 2 PLACEBO-CONTROLLED PILOT STUDY IN COVID-19 OF FISETIN TO ALLEVIATE DYSFUNCTION AND EXCESSIVE INFLAMMATORY RESPONSE IN OLDER ADULTS IN NURSING HOMESR01AG072301 · NIA · MAYO CLINIC ROCHESTER · PI PIGNOLO, ROBERT JOHN · 2020 to 2024
$1.9M
Senescence cells as a source of pro-aging miR-146aR56AG061414 · NIA · UNIVERSITY OF CENTRAL FLORIDA · PI KIRKLAND, JAMES L., MASTERNAK, MICHAL MATEUSZ · 2019 to 2019
$406k
NIA NIH HHS P01 AG062413NIA NIH HHS R01 AG064165NIA NIH HHS R01 AG068048NIA NIH HHS R01 AG072301NIA NIH HHS R33 AG061456NIA NIH HHS R37 AG013925NIA NIH HHS R56 AG061414NIA NIH HHS UH2 AG056933NIA NIH HHS UH3 AG056933NIDDK NIH HHS R01 DK120292
6 · The paper itself

Abstract

Aging is a major risk factor for cardiovascular diseases (CVDs) and accumulating evidence indicates that biological aging has a significant effect on the onset and progression of CVDs. In recent years, therapies targeting senescent cells (senotherapies), particularly senolytics that selectively eliminate senescent cells, have been developed and show promise for treating geriatric syndromes and age-associated diseases, including CVDs. In 2 pilot studies published in 2019 the senolytic combination, dasatinib plus quercetin, improved physical function in patients with idiopathic pulmonary fibrosis and eliminated senescent cells from adipose tissue in patients with diabetic kidney disease. More than 30 clinical trials using senolytics are currently underway or planned. In preclinical CVD models, senolytics appear to improve heart failure, ischemic heart disease, valvular heart disease, atherosclerosis, aortic aneurysm, vascular dysfunction, dialysis arteriovenous fistula patency, and pre-eclampsia. Because senotherapies are completely different strategies from existing treatment paradigms, they might alleviate diseases for which there are no current effective treatments or they could be used in addition to current therapies to enhance efficacy. Moreover, senotherapies might delay, prevent, alleviate or treat multiple diseases in the elderly and reduce polypharmacy, because senotherapies target fundamental aging mechanisms. We comprehensively summarize the preclinical evidence about senotherapies for CVDs and discuss future prospects for their clinical application.

Indexed as

Cardiovascular DiseasesCellular SenescenceAgedAgingHumansRenal DialysisSenotherapeuticsSenotherapeuticsAtherosclerosisCellular senescenceDiabetesSenescence-associated secretory phenotype (SASP)Senolytics

Identifiers

PMID37880106
PMCPMC10922738
OpenAlexW4387933183

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.