Evidence map›Paper›PMID 27002861›Full record

ArticleScientific reports2016

Two phases of aging separated by the Smurf transition as a public path to death.

E Dambroise, L Monnier, L Ruisheng, H Aguilaniu, J-S Joly, H Tricoire, M Rera

Registry-linked trialAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06845865 (Measurement of Intestinal Permeability in Intensive Care Patients With Single or Multiple Organ Failure), which is not on this map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing 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.

NCT06845865 recruitingnot on this mapstarted 2025, after this paper: background citation

Measurement of Intestinal Permeability in Intensive Care Patients With Single or Multiple Organ Failure

TypeobservationalSponsorDirection Centrale du Service de Santé des ArméesRan2025 to 2029Enrolled126ConditionsMultivisceral Failure Syndrome, Monovisceral Failure, Infection in ICUArmsenteric dyed solution
3 · Its place in the literature

Who cites it

58 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
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  5. Article
  6. Molecular evolution of animal aging.The EMBO journal · 2026
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Network analysis andFrontiers in pharmacology · 2025
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Trametinib ameliorates aging-associated gut pathology inProceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  18. Article
  19. Article
  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

7 authors.

E DambroiseEquipe CASBAH "Comparative Analysis of Stem cells, Brain Anatomy and Homeostasis", Neuroscience Paris-Saclay Institute (Neuro-PSI), UMR 9197, CNRS, Gif-sur-Yvette, France.
L MonnierEcole Normale Supérieure de Lyon - CNRS - Université de Lyon Claude Bernard - Institut de Génomique Fonctionnelle de Lyon /UMR5262 46, Allée d'Italie, 69364 Lyon, France.
L RuishengEcole Normale Supérieure de Lyon - CNRS - Université de Lyon Claude Bernard - Institut de Génomique Fonctionnelle de Lyon /UMR5262 46, Allée d'Italie, 69364 Lyon, France.
H AguilaniuEcole Normale Supérieure de Lyon - CNRS - Université de Lyon Claude Bernard - Institut de Génomique Fonctionnelle de Lyon /UMR5262 46, Allée d'Italie, 69364 Lyon, France.
J-S JolyEquipe CASBAH "Comparative Analysis of Stem cells, Brain Anatomy and Homeostasis", Neuroscience Paris-Saclay Institute (Neuro-PSI), UMR 9197, CNRS, Gif-sur-Yvette, France.
H TricoireUnité de Biologie Fonctionnelle et Adaptative (BFA) UMR8251 - CNRS - Université Diderot, Sorbonne Paris Cité, 4 Rue Marie Andrée Lagroua Weill Hallé, 75013, Paris, France.
M ReraUnité de Biologie Fonctionnelle et Adaptative (BFA) UMR8251 - CNRS - Université Diderot, Sorbonne Paris Cité, 4 Rue Marie Andrée Lagroua Weill Hallé, 75013, Paris, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aging's most obvious characteristic is the time dependent increase of an individual's probability to die. This lifelong process is accompanied by a large number of molecular and physiological changes. Although numerous genes involved in aging have been identified in the past decades its leading factors have yet to be determined. To identify the very processes driving aging we have developed in the past years an assay to identify physiologically old individuals in a synchronized population of Drosophila melanogaster. Those individuals show an age-dependent increase of intestinal permeability followed by a high risk of death. Here we show that this physiological marker of aging is conserved in 3 invertebrate species Drosophila mojavensis, Drosophila virilis, Caenorhabditis elegans as well as in 1 vertebrate species Danio rerio. Our findings suggest that intestinal barrier dysfunction may be an important event in the aging process conserved across a broad range of species, thus raising the possibility that it may also be the case in Homo sapiens.

Indexed as

Biological EvolutionAgingAnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsConserved SequenceDeathDrosophilaDrosophila ProteinsFemaleGene Expression RegulationIntestinesMaleUbiquitin-Protein LigasesZebrafishZebrafish ProteinsCaenorhabditis elegans ProteinsDrosophila ProteinsSmurf protein, DrosophilaUbiquitin-Protein LigasesZebrafish Proteins

Identifiers

PMID27002861
PMCPMC4802314

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Registered trials

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.