Evidence map›Paper›PMID 28158466›Full record

ArticleThe journals of gerontology. Series A, Biological sciences and medical sciences2017

Assessing Health Span in Caenorhabditis elegans: Lessons From Short-Lived Mutants.

Jarod A Rollins, Amber C Howard, Sarah K Dobbins, Elsie H Washburn, Aric N Rogers

Abstract read
In one paragraph

Article in The journals of gerontology. Series A, Biological sciences and medical sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing 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

42 citing papers in PubMed.

  1. Article
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  11. Characterizing the Role of daf-16/C. elegans FOXO in Lifespan and Healthspan.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  12. Miquelianin and spiraeoside fromFrontiers in pharmacology · 2025
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  15. Beneficial Effects ofAntioxidants (Basel, Switzerland) · 2024
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  16. ConsideringCells · 2024
    Review
  17. Article
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  19. Article
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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

5 authors.

Jarod A RollinsDavis Center for Regenerative Biology and Medicine, Mount Desert Island Biological Laboratory, Bar Harbor, Maine.
Amber C HowardCollege of Arts and Sciences, University of Maine at Augusta.
Sarah K DobbinsDepartment of Engineering, Stanford University, California.
Elsie H WashburnCollege of Math and Science, California Polytechnic University, San Luis Obispo.
Aric N RogersDavis Center for Regenerative Biology and Medicine, Mount Desert Island Biological Laboratory, Bar Harbor, Maine.

Funding

The Maine Biomedical Research Network (INBRE)P20GM103423 · NIGMS · MOUNT DESERT ISLAND BIOLOGICAL LAB · PI Dustin Lynn Updike · 2012 to 2026
$60.0M
Understanding the role of thyroid hormone signaling during axolotl limb regenerationP20GM104318 · NIGMS · MOUNT DESERT ISLAND BIOLOGICAL LAB · PI DRUMMOND, IAIN A. · 2013 to 2023
$23.0M
Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Aric L Daul, Ann E. Rougvie · 2012 to 2026
$7.5M
Lifespan extension by differential translation mediated by eIF-4G in C. elegansR00AG037621 · NIA · MOUNT DESERT ISLAND BIOLOGICAL LAB · PI ROGERS, ARIC N · 2013 to 2015
$739k
NIA NIH HHS R00 AG037621NIGMS NIH HHS P20 GM103423NIGMS NIH HHS P20 GM104318NIH HHS P40 OD010440
6 · The paper itself

Abstract

Genetic changes resulting in increased life span are often positively associated with enhanced stress resistance and somatic maintenance. A recent study found that certain long-lived Caenorhabditis elegans mutants spent a decreased proportion of total life in a healthy state compared with controls, raising concerns about how the relationship between health and longevity is assessed. We evaluated seven markers of health and two health-span models for their suitability in assessing age-associated health in invertebrates using C elegans strains not expected to outperform wild-type animals. Additionally, we used an empirical method to determine the transition point into failing health based on the greatest rate of change with age for each marker. As expected, animals with mutations causing sickness or accelerated aging had reduced health span when compared chronologically to wild-type animals. Physiological health span, the proportion of total life spent healthy, was reduced for locomotion markers in chronically ill mutants, but, surprisingly, was extended for thermotolerance. In contrast, all short-lived mutants had reduced "quality-of-life" in another model recently employed for assessing invertebrate health. Results suggest that the interpretation of physiological health span is not straightforward, possibly because it factors out time and thus does not account for the added cost of extrinsic forces on longer-lived strains.

Indexed as

AgingAnimalsCaenorhabditis elegansFeeding BehaviorFertilityFluorescenceGenotypeLocomotionLongevityMuscle ContractionMutationOxidative StressPharyngeal MusclesStress, PhysiologicalThermotoleranceHealthInvertebrateLife-span measurementPhenotypeSarcopenia

Identifiers

PMID28158466
PMCPMC6075462

What OpenQuestion holds

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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.