Evidence map›Paper›PMID 34695606›Full record

ReviewTranslational research : the journal of laboratory and clinical medicine2022

Role of senescence in the chronic health consequences of COVID-19.

Erin O Wissler Gerdes, Greg Vanichkachorn, Brandon P Verdoorn, Gregory J Hanson, Avni Y Joshi, M Hassan Murad, Stacey A Rizza, Ryan T Hurt, Tamar Tchkonia, James L Kirkland

Open access · bronzeAbstract readReview
In one paragraph

Review in Translational research : the journal of laboratory and clinical medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

22 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Observational
  12. COVID-19 and cellular senescence.Nature reviews. Immunology · 2023
    Review
  13. Neutrophil extracellular traps and long COVID.Frontiers in immunology · 2023
    Review
  14. Article
  15. Review
  16. Article
  17. Review
  18. Immunosenescence and COVID-19.Mechanisms of ageing and development · 2022
    Review
  19. Article
  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

10 authors at 5 institutions in 1 country.

Erin O Wissler GerdesRobert and Arlene Kogod Center on Aging, Mayo Clinic, Rochester, Minnesota.
Greg VanichkachornDivision of Preventive, Occupational, and Aerospace Medicine, Mayo Clinic, Rochester, Minnesota.
Brandon P VerdoornRobert and Arlene Kogod Center on Aging, Mayo Clinic, Rochester, Minnesota; Division of Community Internal Medicine, Geriatrics, and Palliative Care; Mayo Clinic, Rochester, Minnesota.
Gregory J HansonRobert and Arlene Kogod Center on Aging, Mayo Clinic, Rochester, Minnesota; Division of Community Internal Medicine, Geriatrics, and Palliative Care; Mayo Clinic, Rochester, Minnesota.
Avni Y JoshiDivision of Allergic Diseases, Mayo Clinic College of Medicine, Rochester, Minnesota; Department of Pediatric and Adolescent Medicine, Mayo Clinic Children's Center, Rochester, Minnesota.
M Hassan MuradDivision of Community Internal Medicine, Geriatrics, and Palliative Care; Mayo Clinic, Rochester, Minnesota.
Stacey A RizzaDivision of Infectious Diseases, Department of Medicine, Mayo Clinic, Rochester, Minnesota.
Ryan T HurtDivision of General Internal Medicine, Mayo Clinic, Rochester, Minnesota.
Tamar TchkoniaRobert and Arlene Kogod Center on Aging, Mayo Clinic, Rochester, Minnesota; Department of Physiology and Biomedical Engineering, Mayo Clinic, Rochester, Minnesota.
James L KirklandRobert and Arlene Kogod Center on Aging, Mayo Clinic, Rochester, Minnesota; Department of Physiology and Biomedical Engineering, Mayo Clinic, Rochester, Minnesota; Division of Geriatrics and Gerontology, Mayo Clinic, Rochester, Minnesota. Electronic address: kirkland.james@mayo.edu.
Mayo Clinic · USMayo Clinic in Florida · USWinnMed · USChildren's Center · USCommunity Care · US

Funding

Targeting Cellular Senescence to Extend HealthspanP01AG062413 · NIA · MAYO CLINIC ROCHESTER · PI Sundeep Khosla, Nathan K LeBrasseur · 2019 to 2026
$28.7M
Systems Biology and Bioinformatics CoreP01AG041122 · NIA · MAYO CLINIC ROCHESTER · PI CAMPISI, JUDITH · 2012 to 2016
$9.8M
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
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
NIA NIH HHS P01 AG041122NIA NIH HHS P01 AG062413NIA NIH HHS R01 AG072301NIA NIH HHS R33 AG061456NIA NIH HHS R37 AG013925
6 · The paper itself

Abstract

While the full impact of COVID-19 is not yet clear, early studies have indicated that upwards of 10% of patients experience COVID-19 symptoms longer than 3 weeks, known as Long-Hauler's Syndrome or PACS (postacute sequelae of SARS-CoV-2 infection). There is little known about risk factors or predictors of susceptibility for Long-Hauler's Syndrome, but older adults are at greater risk for severe outcomes and mortality from COVID-19. The pillars of aging (including cellular senescence, telomere dysfunction, impaired proteostasis, mitochondrial dysfunction, deregulated nutrient sensing, genomic instability, progenitor cell exhaustion, altered intercellular communication, and epigenetic alterations) that contribute to age-related dysfunction and chronic diseases (the "Geroscience Hypothesis") may interfere with defenses against viral infection and consequences of these infections. Heightening of the low-grade inflammation that is associated with aging may generate an exaggerated response to an acute COVID-19 infection. Innate immune system dysfunction that leads to decreased senescent cell removal and/or increased senescent cell formation could contribute to accumulation of senescent cells with both aging and viral infections. These processes may contribute to increased risk for long-term COVID-19 sequelae in older or chronically ill patients. Hence, senolytics and other geroscience interventions that may prolong healthspan and alleviate chronic diseases and multimorbidity linked to fundamental aging processes might be an option for delaying, preventing, or alleviating Long-Hauler's Syndrome.

Indexed as

AgedAgingChronic DiseaseCOVID-19HumansSARS-CoV-2

Identifiers

PMID34695606
PMCPMC8532377
OpenAlexW3209376120

What OpenQuestion holds

Textmetadata
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.