Evidence map›Paper›PMID 29751799›Full record

ArticleRespiratory research2018

The aging lung: tissue telomere shortening in health and disease.

Stephanie Everaerts, Elise J Lammertyn, Dries S Martens, Laurens J De Sadeleer, Karen Maes, Aernoud A van Batenburg, Roel Goldschmeding, Coline H M van Moorsel, Lieven J Dupont, Wim A Wuyts and 10 more

Open access · goldAbstract read
In one paragraph

Article in Respiratory research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 1 pooled it
4.6field-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

31 citing papers in PubMed, 1 synthesis or guideline pooled it, 57 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Short airway telomeres are associated with primary graft dysfunction and chronic lung allograft dysfunction.The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation · 2023
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Lung Microenvironments and Disease Progression in Fibrotic Hypersensitivity Pneumonitis.American journal of respiratory and critical care medicine · 2022
    Article
  17. Review
  18. Th17/IL-17 induces endothelial cell senescence via activation of NF-κB/p53/Rb signaling pathway.Laboratory investigation; a journal of technical methods and pathology · 2021
    Article
  19. Review
  20. Article
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

20 authors at 6 institutions in 4 countries.

Stephanie EveraertsLaboratory of Respiratory Diseases, Department of Chronic Diseases, Metabolism & Aging (CHROMETA), KU Leuven, Herestraat 49, O&NI, box 706, B-3000, Leuven, Belgium. stephanie.everaerts@kuleuven.be.ORCID 0000-0003-2646-4770
Elise J LammertynLaboratory of Respiratory Diseases, Department of Chronic Diseases, Metabolism & Aging (CHROMETA), KU Leuven, Herestraat 49, O&NI, box 706, B-3000, Leuven, Belgium.
Dries S MartensCentre for Environmental Sciences, Hasselt University, Hasselt, Belgium.
Laurens J De SadeleerLaboratory of Respiratory Diseases, Department of Chronic Diseases, Metabolism & Aging (CHROMETA), KU Leuven, Herestraat 49, O&NI, box 706, B-3000, Leuven, Belgium.
Karen MaesLaboratory of Respiratory Diseases, Department of Chronic Diseases, Metabolism & Aging (CHROMETA), KU Leuven, Herestraat 49, O&NI, box 706, B-3000, Leuven, Belgium.
Aernoud A van BatenburgDepartment of Pulmonology, St Antonius ILD Center of Excellence, St Antonius Hospital, Nieuwegein, the Netherlands.
Roel GoldschmedingDepartment of Pathology, University Medical Center Utrecht, Utrecht, the Netherlands.
Coline H M van MoorselDepartment of Pulmonology, St Antonius ILD Center of Excellence, St Antonius Hospital, Nieuwegein, the Netherlands.
Lieven J DupontLaboratory of Respiratory Diseases, Department of Chronic Diseases, Metabolism & Aging (CHROMETA), KU Leuven, Herestraat 49, O&NI, box 706, B-3000, Leuven, Belgium.
Wim A WuytsLaboratory of Respiratory Diseases, Department of Chronic Diseases, Metabolism & Aging (CHROMETA), KU Leuven, Herestraat 49, O&NI, box 706, B-3000, Leuven, Belgium.
Robin VosLaboratory of Respiratory Diseases, Department of Chronic Diseases, Metabolism & Aging (CHROMETA), KU Leuven, Herestraat 49, O&NI, box 706, B-3000, Leuven, Belgium.
Ghislaine Gayan-RamirezLaboratory of Respiratory Diseases, Department of Chronic Diseases, Metabolism & Aging (CHROMETA), KU Leuven, Herestraat 49, O&NI, box 706, B-3000, Leuven, Belgium.
Naftali KaminskiSection of Pulmonary, Critical Care, and Sleep Medicine, Yale University, New Haven, CT, USA.
James C HoggUniversity of British Columbia James Hogg Research Centre, St. Paul's Hospital, Vancouver, BC, Canada.
Wim JanssensLaboratory of Respiratory Diseases, Department of Chronic Diseases, Metabolism & Aging (CHROMETA), KU Leuven, Herestraat 49, O&NI, box 706, B-3000, Leuven, Belgium.
Geert M VerledenLaboratory of Respiratory Diseases, Department of Chronic Diseases, Metabolism & Aging (CHROMETA), KU Leuven, Herestraat 49, O&NI, box 706, B-3000, Leuven, Belgium.
Tim S NawrotCentre for Environmental Sciences, Hasselt University, Hasselt, Belgium.
Stijn E VerledenLaboratory of Respiratory Diseases, Department of Chronic Diseases, Metabolism & Aging (CHROMETA), KU Leuven, Herestraat 49, O&NI, box 706, B-3000, Leuven, Belgium.
John E McDonoughLaboratory of Respiratory Diseases, Department of Chronic Diseases, Metabolism & Aging (CHROMETA), KU Leuven, Herestraat 49, O&NI, box 706, B-3000, Leuven, Belgium.
Bart M VanaudenaerdeLaboratory of Respiratory Diseases, Department of Chronic Diseases, Metabolism & Aging (CHROMETA), KU Leuven, Herestraat 49, O&NI, box 706, B-3000, Leuven, Belgium.
KU Leuven · BEHasselt University · BEUniversity Medical Center Utrecht · NLSt. Antonius Ziekenhuis · NLUniversity of British Columbia · CAYale University · US

Funding

FP7 Ideas: European Research Council 603038KU Leuven C24/15/030
6 · The paper itself

Abstract

backgroundTelomere shortening has been associated with several lung diseases. However, telomere length is generally measured in peripheral blood leucocytes rather than in lung tissue, where disease occurs. Consequently, telomere dynamics have not been established for the normal human lung nor for diseased lung tissue. We hypothesized an age- and disease-dependent shortening of lung tissue telomeres.

methodsAt time of (re-)transplantation or autopsy, 70 explant lungs were collected: from unused donors (normal, n = 13) and patients with cystic fibrosis (CF, n = 12), chronic obstructive pulmonary disease (COPD, n = 11), chronic hypersensitivity pneumonitis (cHP, n = 9), bronchiolitis obliterans syndrome (BOS) after prior transplantation (n = 11) and restrictive allograft syndrome (RAS) after prior transplantation (n = 14). Lungs were inflated, frozen and then scanned using CT. Four tissue cores from distinct lung regions were sampled for analysis. Disease severity was evaluated using CT and micro CT imaging. DNA was extracted from the samples and average relative telomere length (RTL) was determined using real-time qPCR.

resultsThe normal lungs showed a decrease in RTL with age (p < 0.0001). Of the diseased lungs, only BOS and RAS showed significant RTL decrease with increasing lung age (p = 0.0220 and p = 0.0272 respectively). Furthermore, we found that RTL showed considerable variability between samples within both normal and diseased lungs. cHP, BOS and RAS lungs had significant shorter RTL in comparison with normal lungs, after adjustment for lung age, sex and BMI (p < 0.0001, p = 0.0051 and p = 0.0301 respectively). When investigating the relation between RTL and regional disease severity in CF, cHP and RAS, no association was found.

conclusionThese results show a progressive decline in telomere length with age in normal, BOS and RAS lungs. cHP, BOS and RAS lungs demonstrated shorter RTL compared to normal lungs. Lung tissue RTL does not associate with regional disease severity within the lung. Therefore, tissue RTL does not seem to fully reflect peripheral blood telomere length.

Indexed as

Health StatusAdolescentAdultAgedChildFemaleHumansLungLung DiseasesMaleMiddle AgedTelomere ShorteningYoung AdultBOSCellular senescenceChronic hypersensitivity pneumonitisChronic lung allograft dysfunctionChronic obstructive pulmonary diseaseCystic fibrosisRASTelomere length

Identifiers

PMID29751799
PMCPMC5948770
OpenAlexW2807310339

What OpenQuestion holds

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LicenceCC BY
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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.