Evidence map›Paper›PMID 35107705›Full record

ArticleGeroScience2022

Naked mole-rats maintain cardiac function and body composition well into their fourth decade of life.

Emine Can, Megan Smith, Bastiaan J Boukens, Ruben Coronel, Rochelle Buffenstein, Johannes Riegler

Open access · hybridAbstract read
In one paragraph

Article in GeroScience, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
5.6field-weighted citation impact, top 3% 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

15 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Article
  3. Resistance to age-related hypercoagulability: insights from the naked mole rat.Research and practice in thrombosis and haemostasis · 2026
    Article
  4. Article
  5. Article
  6. Article
  7. The Fourth Annual Symposium of the Midwest Aging Consortium.The journals of gerontology. Series A, Biological sciences and medical sciences · 2024
    Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. The mTOR signaling pathway in cardiac aging.The journal of cardiovascular aging · 2023
    Article
  15. 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

6 authors at 4 institutions in 2 countries.

Emine CanCalico Life Sciences LLC, 1170 Veterans Blvd, South San Francisco, CA, 94080, USA.
Megan SmithCalico Life Sciences LLC, 1170 Veterans Blvd, South San Francisco, CA, 94080, USA.
Bastiaan J BoukensDepartment of Medical Biology, Amsterdam University Medical Centers, University of Amsterdam, 1105, AZ, Amsterdam, The Netherlands.
Ruben CoronelDepartment of Experimental Cardiology, Heart Center, Academic University Medical Centers, University of Amsterdam, 1105, AZ, Amsterdam, The Netherlands.
Rochelle BuffensteinCalico Life Sciences LLC, 1170 Veterans Blvd, South San Francisco, CA, 94080, USA. rbuffen@gmail.com.
Johannes RieglerCalico Life Sciences LLC, 1170 Veterans Blvd, South San Francisco, CA, 94080, USA. riegler@calicolabs.com.ORCID 0000-0002-4713-7392
Enzo Life Sciences (United States) · USSan Francisco VA Medical Center · USAmsterdam University Medical Centers · NLMaastricht University Medical Centre · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The prevalence of cardiovascular disease increases exponentially with age, highlighting the contribution of aging mechanisms to cardiac diseases. Although model organisms which share human disease pathologies can elucidate mechanisms driving disease, they do not provide us with innate examples how cardiac aging might be slowed or attenuated. The identification of animal models that preserve cardiac function throughout most of life offers an alternative approach to study mechanisms which might slow cardiac aging. One such species may be the naked mole-rat (NMR), a mouse-sized (40 g) rodent with extraordinary longevity (> 37 years), and constant mortality hazard over its four decades of life. We used a cross-sectional study design to measure a range of physiological parameters in NMRs between 2 and 34 years of age and compared these findings with those of mice aged between 3 months and 2.5 years. We observed a rapid decline in body fat content and bone mineral density in old mice, but no changes in NMRs. Similarly, rhythm disorders (premature atrial and ventricular complexes) occurred in aged mice but not in NMRs. Magnetic resonance and ultrasound imaging showed age-dependent increases in cardiac hypertrophy and diastolic dysfunction in mice which were absent in NMRs. Finally, cardiac stress tests showed an age-dependent decline in normalized cardiac output in mice, which was absent in NMRs. Unlike mice, that manifest several aspects of human cardiac aging, NMRs maintain cardiac function and reserve capacity throughout their long lives and may offer insights on how to delay or prevent cardiac aging.

Indexed as

LongevityMole RatsAgingAnimalsBody CompositionCross-Sectional StudiesMiceAgingArrhythmiaCardiac functionEchocardiographyElectrocardiogramMagnetic resonance imagingMouseNaked mole rat

Identifiers

PMID35107705
PMCPMC9135933
OpenAlexW4210756881

What OpenQuestion holds

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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.