Evidence map›Paper›PMID 42027317›Full record

ArticleResearch and practice in thrombosis and haemostasis2026

Resistance to age-related hypercoagulability: insights from the naked mole rat.

Véronique Regnault, Jeremy Lagrange, Chris G Faulkes, J Kennedy Cruickshank, Cécile Lakomy, Athanase Benetos, Cécile V Denis, Patrick Lacolley

Abstract readComparative Study
In one paragraph

Article in Research and practice in thrombosis and haemostasis, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Véronique RegnaultUniversité de Lorraine, INSERM, DCAC, Nancy, France.
Jeremy LagrangeUniversité de Lorraine, INSERM, DCAC, Nancy, France.
Chris G FaulkesSchool of Biological and Chemical Sciences, Queen Mary University of London, London, United Kingdom.
J Kennedy CruickshankCardiovascular Medicine-Diabetes Group, School of Life Course-Nutritional Sciences Division, King's College London, London, United Kingdom.
Cécile LakomyUniversité de Lorraine, INSERM, DCAC, Nancy, France.
Athanase BenetosUniversité de Lorraine, INSERM, DCAC, Nancy, France.
Cécile V DenisUniversité Paris-Saclay, Inserm, HITh, Le Kremlin-Bicêtre, France.
Patrick LacolleyUniversité de Lorraine, INSERM, DCAC, Nancy, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Human aging is characterized by endothelial dysfunction that drives a systemic prothrombotic shift. In contrast, the long-lived naked mole rat (NMR) represents a unique model of delayed aging, exhibiting a notable resistance to age-related pathologies. However, while its cardiovascular stability is well-documented, the NMR hemostatic profile across its lifespan remains unexplored. Objectives: To assess whether NMRs undergo age-related hypercoagulability and to compare their hemostatic trajectory with that of humans. Methods: We compared young (2-year-old) and aged (20-year-old) NMRs. Assessments included clotting factor quantification, endothelial markers, and integrative thrombin generation assays. Plasma from human volunteers (20-year-old vs 80-year-old NMRs) were used as a reference point for typical hemostatic aging. Results: NMRs maintained cellular blood composition and showed no age-related increase in markers of endothelial activation (including von Willebrand factor, factor VIII, tissue factor pathway inhibitor, soluble thrombomodulin, and tissue plasminogen activator). While aged NMRs showed a modest increase in fibrinogen and D-dimer, this rise was significantly lower than the 2- to 5-fold elevations seen in elderly humans. Most notably, thrombin generation potential remained identical between young and aged NMRs. In contrast, humans exhibited a marked age-dependent shift toward accelerated and heightened thrombin production. Conclusion: NMRs possess the ability to bypass the pathologic clotting shifts that drive thrombotic events in humans, effectively decoupling chronologic aging from prothrombotic risk. By maintaining stable endothelial coagulation markers and an unchanged thrombin-forming capacity throughout their lifespan, NMRs appear naturally protected against age-dependent hypercoagulability.

Indexed as

AgingBlood CoagulationThrombophiliaAged, 80 and overAge FactorsAnimalsBiomarkersChild, PreschoolFemaleFibrin Fibrinogen Degradation ProductsHemostasisHumansMaleMole RatsThrombinYoung AdultBiomarkersFibrin Fibrinogen Degradation Productsfibrin fragment DThrombinagingcoagulationendothelial markersnaked mole ratthrombin generation

Identifiers

PMID42027317
PMCPMC13099443

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