Evidence map›Paper›PMID 40145120›Full record

ArticleJHLT open2024

Outcomes of lung transplantation in patients with telomere-related forms of progressive fibrosing interstitial lung disease pulmonary fibrosis: A systematic review.

Jaume Bordas-Martinez, Jelle R Miedema, Bas J Mathot, Leonard Seghers, Robert-Jan H Galjaard, Marc H G P Raaijmakers, Anna M Aalbers, Marlies Wijsenbeek, Maria Molina-Molina, Merel E Hellemons

Abstract read
In one paragraph

Article in JHLT open, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Review
  6. Lung transplantation for interstitial lung disease.Breathe (Sheffield, England) · 2025
    Review
  7. 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.

Jaume Bordas-MartinezErasmus MC Transplantation Institute, Department of Respiratory Medicine, Erasmus University Medical Center, Rotterdam, the Netherlands.
Jelle R MiedemaCentre of Excellence for Interstitial Lung Disease and Sarcoidosis, Department of Respiratory Medicine, Erasmus University Medical Center, Rotterdam, the Netherlands.
Bas J MathotErasmus MC Transplantation Institute, Department of Respiratory Medicine, Erasmus University Medical Center, Rotterdam, the Netherlands.
Leonard SeghersErasmus MC Transplantation Institute, Department of Respiratory Medicine, Erasmus University Medical Center, Rotterdam, the Netherlands.
Robert-Jan H GaljaardDepartment of Clinical Genetics, Erasmus MC University Medical Center, Rotterdam, the Netherlands.
Marc H G P RaaijmakersDepartment of Hematology, Erasmus MC Cancer Institute, Rotterdam, the Netherlands.
Anna M AalbersDepartment of Hematology, Erasmus MC Cancer Institute, Rotterdam, the Netherlands.
Marlies WijsenbeekCentre of Excellence for Interstitial Lung Disease and Sarcoidosis, Department of Respiratory Medicine, Erasmus University Medical Center, Rotterdam, the Netherlands.
Maria Molina-MolinaILD Unit, Department of Respiratory Medicine, Bellvitge University Hospital, IDIBELL, Barcelona University, Hospitalet de Llobregat, CIBERES, Barcelona, Spain.
Merel E HellemonsErasmus MC Transplantation Institute, Department of Respiratory Medicine, Erasmus University Medical Center, Rotterdam, the Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Lung transplantation (LTX) is the last life-extending option for patients with progressive fibrosing interstitial lung diseases (fILD). Between 12% and 71% of patients with fILD are patients with underlying telomere-dysfunction (trILD) related to pathogenic telomere-related gene (TRG) variants and/or short telomere length. TrILD patients tend to have earlier disease onset, faster progression, and worse prognosis causing them to be referred for LTX more often. Regarding LTX outcomes in trILD, there are contradictory reports on patient and graft survival, as well as numerous other outcomes. There is no consensus on whether trILD is associated with poorer outcomes after LTX and what considerations regarding candidacy are appropriate. Methods: We aimed to systematically review LTX outcomes of patients with trILD in comparison to those with non-trILD. Results: A systematic literature search yielded 13 studies that met the inclusion criteria including 933 LTX, 281 in trILD, and 652 in non-trILD. Despite large heterogeneity in the methodological study quality and reported outcomes among the studies, patient and graft survival after LTX in trILD did not evidently seem inferior to LTX in non-trILD. However, there may be increased risk of specific complications, such as cytopenias, airway complications, and cytomegalovirus-reactivation. Conclusions: In summary, due to large heterogeneity in methodological study quality and reported outcomes, no firm conclusions can be drawn. Patient and graft survival do not seem unequivocally inferior in patients with trILD

Indexed as

familial pulmonary fibrosisgeneticinterstitial lung diseaseslung transplantationoutcomestelomere

Identifiers

PMID40145120
PMCPMC11935452

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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.