Evidence map›Paper›PMID 41776198›Full record

Articlenpj aging2026

A hierarchy of causes of death in senescent C. elegans.

Hongyuan Wang, Carina C Kern, Chiminh Nguyen Hong, Alis Saez Allende, Jiayi Qiao, Aihan Zhang, Yimu Fan, Marina Ezcurra, David Gems

Abstract read
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In one paragraph

Article in npj aging, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Hongyuan WangInstitute of Healthy Ageing, and Research Department of Genetics, Evolution and Environment, University College London, London, UK.
Carina C KernInstitute of Healthy Ageing, and Research Department of Genetics, Evolution and Environment, University College London, London, UK.
Chiminh Nguyen HongInstitute of Healthy Ageing, and Research Department of Genetics, Evolution and Environment, University College London, London, UK.
Alis Saez AllendeInstitute of Healthy Ageing, and Research Department of Genetics, Evolution and Environment, University College London, London, UK.
Jiayi QiaoInstitute of Healthy Ageing, and Research Department of Genetics, Evolution and Environment, University College London, London, UK.
Aihan ZhangInstitute of Healthy Ageing, and Research Department of Genetics, Evolution and Environment, University College London, London, UK.
Yimu FanInstitute of Healthy Ageing, and Research Department of Genetics, Evolution and Environment, University College London, London, UK.
Marina EzcurraSchool of Biosciences, Stacey Building, University of Kent, Canterbury, UK.
David GemsInstitute of Healthy Ageing, and Research Department of Genetics, Evolution and Environment, University College London, London, UK. david.gems@ucl.ac.uk.

Funding

Wellcome Trust Investigator Award 215574/Z/19/Z
6 · The paper itself

Abstract

Interventions that extend lifespan in animal models could, in principle, decelerate the aging process as a whole. Alternatively, they could act by suppressing one or more individual late-life pathologies that contribute to mortality. Here we show how, in the nematode Caenorhabditis elegans, late-life pathologies can compete in a hierarchical fashion to cause death, such that removal of one cause of death can unmask another. Under standard culture conditions, a major cause of death in elderly C. elegans is infection by their bacterial food source. We report that only when such infection is prevented is lifespan extended by suppression of a second senescent pathology, teratoma-like uterine tumors. Thus, as in mammals, lifespan in wild-type C. elegans can be limited by naturally-occurring neoplasia. By contrast, blocking bacterial infection attenuated the life-shortening effects of vitellogenesis, and did not unmask a life-shortening effect of distal gonad degeneration. Thus, depending on the masking or unmasking of competing causes of mortality in the hierarchy of causes of death, nematode lifespan limitation in different contexts can reflect action of distinct life-limiting senescent pathologies. This underscores how increases in lifespan do not necessarily reflect a reduction in overall aging rate.

Identifiers

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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.