Evidence map›Paper›PMID 31926111›Full record

ArticleAging2020

Association of adult lung function with accelerated biological aging.

Faisal I Rezwan, Medea Imboden, Andre F S Amaral, Matthias Wielscher, Ayoung Jeong, Kai Triebner, Francisco Gómez Real, Marjo-Riitta Jarvelin, Deborah Jarvis, Nicole M Probst-Hensch and 1 more

Open access · greenAbstract read
In one paragraph

Article in Aging, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.8field-weighted citation impact, top 8% 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

18 citing papers in PubMed, 42 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. 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

11 authors at 5 institutions in 3 countries.

Faisal I RezwanHuman Development and Health, Faculty of Medicine, University of Southampton, Southampton, United Kingdom.
Medea ImbodenChronic Disease Epidemiology Unit, Department of Epidemiology and Public Health, Swiss Tropical and Public Health Institute, Basel, Switzerland.
Andre F S AmaralPopulation Health and Occupational Disease, NHLI, Imperial College London, London, United Kingdom.
Matthias WielscherDepartment of Epidemiology and Biostatistics, MRC-PHE Centre for Environment and Health, School of Public Health, Imperial College London, London, United Kingdom.
Ayoung JeongChronic Disease Epidemiology Unit, Department of Epidemiology and Public Health, Swiss Tropical and Public Health Institute, Basel, Switzerland.
Kai TriebnerDepartment of Clinical Science, University of Bergen, Bergen, Norway.
Francisco Gómez RealDepartment of Clinical Science, University of Bergen, Bergen, Norway.
Marjo-Riitta JarvelinPopulation Health and Occupational Disease, NHLI, Imperial College London, London, United Kingdom.
Deborah JarvisPopulation Health and Occupational Disease, NHLI, Imperial College London, London, United Kingdom.
Nicole M Probst-HenschChronic Disease Epidemiology Unit, Department of Epidemiology and Public Health, Swiss Tropical and Public Health Institute, Basel, Switzerland.
John W HollowayHuman Development and Health, Faculty of Medicine, University of Southampton, Southampton, United Kingdom.
Imperial College London · GBSwiss Tropical and Public Health Institute · CHUniversity of Bergen · NOUniversity of Southampton · GBUniversity of Basel · CH

Funding

Medical Research Council G0901214Medical Research Council MR/S019669/1
6 · The paper itself

Abstract

Lung function, strongly associated with morbidity and mortality, decreases with age. This study examines whether poor adult lung function is associated with age accelerations (AAs). DNA methylation (DNAm) based AAs, lifespan predictors (GrimAge and plasminogen activator inhibitor 1-PAI1) and their related age-adjusted measures were estimated from peripheral blood at two time points (8-to-11 years apart) in adults from two cohorts: SAPALDIA (n=987) and ECRHS (n=509). Within each cohort and stratified by gender (except for estimators from GrimAge and PAI1), AAs were used as predictors in multivariate linear regression with cross-sectional lung function parameters, and in covariate-adjusted mixed linear regression with longitudinal change in lung function and meta-analysed.AAs were found cross-sectionally associated with lower mean FEV1 (Forced Expiratory Volume in one second) (AA-residuals:P-value=4x10

Indexed as

AdultAge FactorsAgingBiomarkersCross-Sectional StudiesEpigenesis, GeneticFemaleHumansLungMaleMeta-Analysis as TopicMiddle AgedRespiratory Function TestsSex FactorsBiomarkersage accelerationDNA methylationepigenetic clocklung functionrespiratory health

Identifiers

PMID31926111
PMCPMC6977706
OpenAlexW3000301202

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.