Evidence map›Paper›PMID 37576589›Full record

ArticleCurrent transplantation reports2023

Cellular Senescence and Frailty in Transplantation.

Elizabeth C Lorenz, LaTonya J Hickson, Pascale Khairallah, Bijan Najafi, Cassie C Kennedy

Abstract read
In one paragraph

Article in Current transplantation reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. Article
  2. Clinical outcomes of solid organ transplant patients after total joint arthroplasty: a propensity-matched analysis.European journal of orthopaedic surgery & traumatology : orthopedie traumatologie · 2026
    Article
  3. Review
  4. Article
  5. Article
  6. Observational
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.

Elizabeth C LorenzSection of Nephrology, Baylor College of Medicine, Houston, Texas.
LaTonya J HicksonDivision of Nephrology and Hypertension, Mayo Clinic, Jacksonville, Florida.
Pascale KhairallahSection of Nephrology, Baylor College of Medicine, Houston, Texas.
Bijan NajafiDivision of Vascular Surgery and Endovascular Therapy, Baylor College of Medicine, Houston, Texas.
Cassie C KennedyDivision of Pulmonary, Critical Care, and Sleep Medicine, Mayo Clinic, Rochester, Minnesota.

Funding

Extracellular vesicle-based senotherapeutics for aging diabetic kidneydiseaseR01AG076537 · NIA · MAYO CLINIC JACKSONVILLE · PI LaTonya J Hickson · 2023 to 2026
$2.3M
Pre-transplant health coaching to improve patient-reported outcomes in lung transplant candidatesR33HL158811 · NHLBI · MAYO CLINIC ROCHESTER · PI Cassie Colleen Kennedy · 2023 to 2026
$2.1M
Mesenchymal stem cell senescence in diabetic nephropathy (K23 COVID Admin Supplement)K23DK109134 · NIDDK · MAYO CLINIC ROCHESTER · PI HICKSON, LATONYA J · 2016 to 2021
$1.0M
Exploring the Unmeasured Risk and Treating the Untreated Prognostic Factor: Towards Candidate Optimization in Heart and Lung TransplantK23HL128859 · NHLBI · MAYO CLINIC ROCHESTER · PI KENNEDY, CASSIE COLLEEN · 2016 to 2020
$854k
Improving frailty and long-term outcomes after kidney transplantationK23DK123313 · NIDDK · MAYO CLINIC ROCHESTER · PI LORENZ, ELIZABETH C. · 2019 to 2023
$795k
Pre-transplant health coaching to improve patient-reported outcomes in lung transplant candidatesR61HL158811 · NHLBI · MAYO CLINIC ROCHESTER · PI KENNEDY, CASSIE COLLEEN · 2022 to 2022
$484k
Renal repair effects of senolytic preconditioned mesenchymal stromal PP #o20-111cells in diabetic kidney diseaseR03DK123492 · NIDDK · MAYO CLINIC ROCHESTER · PI HICKSON, LATONYA J · 2020 to 2021
$467k
NHLBI NIH HHS K23 HL128859NHLBI NIH HHS R33 HL158811NHLBI NIH HHS R61 HL158811NIA NIH HHS R01 AG076537NIDDK NIH HHS K23 DK109134NIDDK NIH HHS K23 DK123313NIDDK NIH HHS R03 DK123492
6 · The paper itself

Abstract

Purpose of review: To summarizes the literature on cellular senescence and frailty in solid-organ transplantation and highlight the emerging role of senotherapeutics as a treatment for cellular senescence. Recent findings: Solid-organ transplant patients are aging. Many factors contribute to aging acceleration in this population, including cellular senescence. Senescent cells accumulate in tissues and secrete proinflammatory and profibrotic proteins which result in tissue damage. Cellular senescence contributes to age-related diseases and frailty. Our understanding of the role cellular senescence plays in transplant-specific complications such as allograft immunogenicity and infections is expanding. Promising treatments, including senolytics, senomorphics, cell-based regenerative therapies, and behavioral interventions, may reduce cellular senescence abundance and frailty in patients with solid-organ transplants. Summary: Cellular senescence and frailty contribute to adverse outcomes in solid-organ transplantation. Continued pursuit of understanding the role cellular senescence plays in transplantation may lead to improved senotherapeutic approaches and better graft and patient outcomes.

Indexed as

AgingBiomarkersFrailtySenescenceSenolyticsTransplantation

Identifiers

PMID37576589
PMCPMC10414789

What Socratic holds

Textmetadata
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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 Socratic graph.