Evidence map›Paper›PMID 42270657›Full record

Articlenpj aging2026

Low circulating adropin concentrations identify vulnerability in learning-dependent cognitive performance in aged rhesus macaques.

Andrew A Butler, James L Graham, Lesly C Ceniceros, Ashlee M Cruz, Ashley D Cunningham, Riya Subedi, Anthony P Brown, Nicholas Dai, Giovanne B Diniz, Peter J Havel and 2 more

Abstract read
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. Not yet cited in PubMed.

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

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

12 authors.

Andrew A ButlerDepartment of Pharmacology and Physiology and the Institute for Translational Neuroscience, Saint Louis University School of Medicine, St. Louis, MO, USA. andrew.butler@health.slu.edu.
James L GrahamDepartment of Molecular Biosciences, School of Veterinary Medicine, University of California, Davis, CA, USA.
Lesly C CenicerosCalifornia National Primate Research Center, University of California, Davis, CA, USA.
Ashlee M CruzCalifornia National Primate Research Center, University of California, Davis, CA, USA.
Ashley D CunninghamCalifornia National Primate Research Center, University of California, Davis, CA, USA.
Riya SubediCalifornia National Primate Research Center, University of California, Davis, CA, USA.
Anthony P BrownCalifornia National Primate Research Center, University of California, Davis, CA, USA.
Nicholas DaiCalifornia National Primate Research Center, University of California, Davis, CA, USA.
Giovanne B DinizCalifornia National Primate Research Center, University of California, Davis, CA, USA.
Peter J HavelDepartment of Molecular Biosciences, School of Veterinary Medicine, University of California, Davis, CA, USA.
John H MorrisonCalifornia National Primate Research Center, University of California, Davis, CA, USA.
Erin L KinnallyCalifornia National Primate Research Center, University of California, Davis, CA, USA. elkinnally@ucdavis.edu.

Funding

National Institute on Aging (NIA) ColonyP51OD011107 · OD · UNIVERSITY OF CALIFORNIA AT DAVIS · PI Simon J. Atkinson · 2012 to 2026
$191.5M
Neuropathology and inflammation in a nonhuman primate model of insulin resistance/metabolic syndromeR01AG085572 · NIA · UNIVERSITY OF CALIFORNIA AT DAVIS · PI STEPHEN D GINSBERG, PETER J HAVEL · 2024 to 2026
$3.8M
Coordinating Center for Primate Aging ResearchR61AG087970 · NIA · TULANE UNIVERSITY OF LOUISIANA · PI MORRISON, JOHN H, RAPPAPORT, JAY · 2024 to 2025
$1.9M
Exceptional Longevity and Biobehavioral Aging in Rhesus MacaquesR21AG081998 · NIA · UNIVERSITY OF CALIFORNIA AT DAVIS · PI KINNALLY, ERIN LORAINE · 2023 to 2024
$434k
An investigation of the response of preclinical mouse models of dementia to adropin therapyR21AG083451 · NIA · SAINT LOUIS UNIVERSITY · PI BUTLER, ANDREW ALISTAIR, FARR, SUSAN A · 2024 to 2024
$417k
Methods for treating aging-related cognitive decline and reducing risk of AD/ADRD by enhancing the endogenous expression of adropinR21AG087308 · NIA · SAINT LOUIS UNIVERSITY · PI BUTLER, ANDREW ALISTAIR, NGUYEN, ANDREW D. · 2024 to 2024
$417k
NIA NIH HHS R01 AG085572NIA NIH HHS R21 AG081998NIA NIH HHS R21 AG083451NIA NIH HHS R21 AG087308NIA NIH HHS R61 AG087970NIH HHS P51 OD011107
6 · The paper itself

Abstract

Identifying biomarkers that identify vulnerability to age-related cognitive decline is a major priority in aging research. Adropin, a circulating peptide that regulates metabolic and vascular homeostasis, has been associated with cognitive performance in humans, but its relevance across species has remained unclear. Here we report low plasma adropin concentrations associate with poor decision-making in aged rhesus macaques subject to an increasing food choice test paradigm. Animals with higher adropin levels exhibited faster improvement in reaction time and reductions of variability in reaction time, whereas intrinsic performance on simple tasks was preserved. These associations were most apparent under conditions requiring adaptation to novelty or stress, suggesting that adropin may signal cognitive resilience rather than baseline executive capacity. The findings parallel mechanistic data from rodent models linking adropin signaling to mitochondrial function, resistance to oxidative stress, and hippocampal-dependent learning. Together, these results support measurements of circulating adropin as a conserved, translational biomarker of cognitive aging and a potential therapeutic target.

Identifiers

PMID42270657
PMCPMC13639007

What Socratic holds

Textmetadata
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 Socratic graph.