Evidence map›Paper›PMID 27990481›Full record

ArticleTransplantation direct2016

Increased Telomere Attrition After Renal Transplantation-Impact of Antimetabolite Therapy.

Karin Luttropp, Louise Nordfors, Dagmara McGuinness, Lars Wennberg, Hannah Curley, Tara Quasim, Helena Genberg, John Sandberg, Isabella Sönnerborg, Martin Schalling and 4 more

Abstract read
In one paragraph

Article in Transplantation direct, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Selective decrease of donor-reactive TScience translational medicine · 2022
    Trial
  2. Article
  3. Telomere Attrition in Chronic Kidney Diseases.Antioxidants (Basel, Switzerland) · 2023
    Review
  4. Review
  5. Review
  6. Review
  7. Article
  8. The role of epigenetics in renal ageing.Nature reviews. Nephrology · 2017
    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

14 authors.

Karin LuttroppNeurogenetics Division, Department of Molecular Medicine and Surgery, Karolinska Institutet, Sweden.
Louise Nordfors
Dagmara McGuinnessWolfson Wohl Translational Research Centre, Institute of Cancer Sciences, University of Glasgow, United Kingdom.
Lars WennbergDivision of Transplantation, Department of Clinical Science, Intervention and Technology, Karolinska Institutet, Sweden.
Hannah CurleyWolfson Wohl Translational Research Centre, Institute of Cancer Sciences, University of Glasgow, United Kingdom.
Tara QuasimNHS Greater Glasgow and Clyde, Glasgow Royal Infirmary, United Kingdom.
Helena GenbergDivision of Transplantation, Department of Clinical Science, Intervention and Technology, Karolinska Institutet, Sweden.
John SandbergDivision of Transplantation, Department of Clinical Science, Intervention and Technology, Karolinska Institutet, Sweden.
Isabella SönnerborgDivision of Transplantation, Department of Clinical Science, Intervention and Technology, Karolinska Institutet, Sweden.
Martin SchallingNeurogenetics Division, Department of Molecular Medicine and Surgery, Karolinska Institutet, Sweden.
Abdul Rashid QureshiDivision of Renal Medicine, Department of Clinical Science, Intervention and Technology, Karolinska Institutet, Sweden.
Peter BárányDivision of Renal Medicine, Department of Clinical Science, Intervention and Technology, Karolinska Institutet, Sweden.
Paul G ShielsWolfson Wohl Translational Research Centre, Institute of Cancer Sciences, University of Glasgow, United Kingdom.
Peter StenvinkelDivision of Renal Medicine, Department of Clinical Science, Intervention and Technology, Karolinska Institutet, Sweden.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe uremic milieu exposes chronic kidney disease (CKD) patients to premature ageing processes. The impact of renal replacement therapy (dialysis and renal transplantation [RTx]) or immunosuppressive treatment regimens on ageing biomarkers has scarcely been studied.

methodsIn this study telomere length in whole blood cells was measured in 49 dialysis patients and 47 RTx patients close to therapy initiation and again after 12 months. Forty-three non-CKD patients were included as controls.

resultsNon-CKD patients had significantly (

conclusionsThe associations between immunosuppressive therapy, telomere attrition, and changes in folate indicate a link between methyl donor potential, immunosuppressive drugs, and biological ageing. The hypothesis that the increased telomere attrition, observed in the MMF group after RTx, is driven by the immunosuppressive treatment, deserves further attention.

Identifiers

PMID27990481
PMCPMC5142370

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Registered trials

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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.