Evidence map›Paper›PMID 39756432›Full record

ArticleCerebral cortex (New York, N.Y. : 1991)2025

Aging-related losses in dopamine D2/3 receptor availability are linked to working-memory decline across five years.

Goran Papenberg, Nina Karalija, Alireza Salami, Jarkko Johansson, Anders Wåhlin, Micael Andersson, Jan Axelsson, Douglas D Garrett, Katrine Riklund, Ulman Lindenberger and 2 more

Abstract read
In one paragraph

Article in Cerebral cortex (New York, N.Y. : 1991), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. 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

12 authors.

Goran PapenbergAging Research Center, Karolinska Institutet and Stockholm University, Tomtebodavägen 18 A, SE-171 65 Solna, Sweden.
Nina KaralijaDepartment of Medical and Translational Biology, Umeå University, Johan Bures väg 12, SE-90187 Umeå, Sweden.
Alireza SalamiAging Research Center, Karolinska Institutet and Stockholm University, Tomtebodavägen 18 A, SE-171 65 Solna, Sweden.ORCID 0000-0002-4675-8437
Jarkko JohanssonUmeå Center for Functional Brain Imaging (UFBI), Umeå University, Johan Bures väg 12, SE-90187 Umeå, Sweden.
Anders WåhlinUmeå Center for Functional Brain Imaging (UFBI), Umeå University, Johan Bures väg 12, SE-90187 Umeå, Sweden.
Micael AnderssonUmeå Center for Functional Brain Imaging (UFBI), Umeå University, Johan Bures väg 12, SE-90187 Umeå, Sweden.
Jan AxelssonUmeå Center for Functional Brain Imaging (UFBI), Umeå University, Johan Bures väg 12, SE-90187 Umeå, Sweden.
Douglas D GarrettCenter for Lifespan Psychology, Max Planck Institute for Human Development, Lentzeallee 94, DE-14195 Berlin, Germany.ORCID 0000-0002-0629-7672
Katrine RiklundUmeå Center for Functional Brain Imaging (UFBI), Umeå University, Johan Bures väg 12, SE-90187 Umeå, Sweden.
Ulman LindenbergerCenter for Lifespan Psychology, Max Planck Institute for Human Development, Lentzeallee 94, DE-14195 Berlin, Germany.
Lars NybergDepartment of Medical and Translational Biology, Umeå University, Johan Bures väg 12, SE-90187 Umeå, Sweden.
Lars BäckmanAging Research Center, Karolinska Institutet and Stockholm University, Tomtebodavägen 18 A, SE-171 65 Solna, Sweden.

Funding

2010 Leibniz Research Award from the German Research FoundationAlexander von Humboldt ResearchInnovation Fund of the Max Planck SocietyJochnick FoundationKnut and Alice Wallenberg FoundationSwedish Brain FoundationSwedish Brain PowerSwedish Research CouncilTorsten and Ragnar Söderberg FoundationUmeå UniversityUmeå University-Karolinska Institute Strategic Neuroscience ProgramVästerbotten County Council
6 · The paper itself

Abstract

Although age differences in the dopamine system have been suggested to contribute to age-related cognitive decline based on cross-sectional data, recent large-scale cross-sectional studies reported only weak evidence for a correlation among aging, dopamine receptor availability, and cognition. Regardless, longitudinal data remain essential to make robust statements about dopamine losses as a basis for cognitive aging. We present correlations between changes in D2/3 dopamine receptor availability and changes in working memory measured over 5 yr in healthy, older adults (n = 128, ages 64 to 68 yr at baseline). Greater decline in D2/3 dopamine receptor availability in working memory-relevant regions (caudate, middle frontal cortex, hippocampus) was related to greater decline in working memory performance in individuals who exhibited working memory reductions across time (n = 43; caudate: rs = 0.494; middle frontal cortex: rs = 0.506; hippocampus; rs = 0.423), but not in individuals who maintained performance (n = 41; caudate: rs = 0.052; middle frontal cortex: rs = 0.198; hippocampus; rs = 0.076). The dopamine-working memory link in decliners was not observed in the orbitofrontal cortex, which does not belong to the core working memory network. Our longitudinal analyses support the notion that aging-related changes in the dopamine system contribute to working memory decline in aging.

Indexed as

AgingBrainMemory DisordersMemory, Short-TermReceptors, Dopamine D2Receptors, Dopamine D3AgedFemaleHippocampusHumansLongitudinal StudiesMagnetic Resonance ImagingMaleMiddle AgedNeuropsychological TestsDRD2 protein, humanDRD3 protein, humanReceptors, Dopamine D2Receptors, Dopamine D3agingcognitive declinedopamine 2/3-receptor availabilitylongitudinalworking memory

Identifiers

PMID39756432
PMCPMC11795306

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.