Evidence map›Paper›PMID 42732056›Full record

ArticleJournal of neuroinflammation2026

Neuroinflammation-associated thalamocortical functional connectivity and cognition in older adults.

Jeffrey Browndyke, Tyler Reekes, Mary C Wright, Melody R Smith, Michael Devinney, Piper Boykin, Vinith R Upadhya, Daphne Zhu, Katherine T Martucci, Leslie M Shaw and 11 more

Abstract read
In one paragraph

Article in Journal of neuroinflammation, 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

21 authors.

Jeffrey BrowndykeDepartment of Psychiatry & Behavioral Sciences, Division of Behavioral Medicine & Neurosciences, Duke University Medical Center, 1830 Hillandale Road, Rm 205, Durham, NC, 27705, USA. j.browndyke@duke.edu.ORCID https://orcid.org/0000-0002-8573-7073
Tyler ReekesDepartment of Anesthesiology, Duke University Medical Center, Durham, NC, USA.
Mary C WrightDepartment of Anesthesiology, Duke University Medical Center, Durham, NC, USA.
Melody R SmithDepartment of Anesthesiology, Perioperative and Pain Medicine, Stanford University School of Medicine, Stanford, CA, USA.
Michael DevinneyDepartment of Anesthesiology, Duke University Medical Center, Durham, NC, USA.
Piper BoykinDepartment of Anesthesiology, Duke University Medical Center, Durham, NC, USA.
Vinith R UpadhyaDuke Trinity College of Arts & Sciences, Duke University, Durham, NC, USA.
Daphne ZhuDuke University School of Medicine, Durham, NC, USA.
Katherine T MartucciDuke Institute for Brain Sciences, Duke University, Durham, NC, USA.
Leslie M ShawDepartment of Pathology & Laboratory Medicine, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.
Teresa WaligorskaDepartment of Pathology & Laboratory Medicine, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.
Charlotte HerberDepartment of Anesthesiology, Perioperative and Pain Medicine, Stanford University School of Medicine, Stanford, CA, USA.
Connie Tian YuDepartment of Anesthesiology, Perioperative and Pain Medicine, Stanford University School of Medicine, Stanford, CA, USA.
Henrik ZetterbergDepartment of Psychiatry & Neurochemistry, Institute of Neuroscience & Physiology, Sahlgrenska Academy, University of Gothenburg, Mölndal, Sweden.
Kaj BlennowDepartment of Psychiatry & Neurochemistry, Institute of Neuroscience & Physiology, Sahlgrenska Academy, University of Gothenburg, Mölndal, Sweden.
Janet L HuebnerDuke Molecular Physiology Institute, Duke University, Durham, NC, USA.
Harvey J CohenCenter for the Study of Aging & Human Development, Duke University Medical Center, Durham, NC, USA.
Heather WhitsonCenter for the Study of Aging & Human Development, Duke University Medical Center, Durham, NC, USA.
Joseph P MathewDepartment of Anesthesiology, Duke University Medical Center, Durham, NC, USA.
Miles BergerCenter for the Study of Aging & Human Development, Duke University Medical Center, Durham, NC, USA.
INTUIT & MADCO-PC Trial Investigators

Funding

Research Education Component CoreP30AG072958 · NIA · DUKE UNIVERSITY · PI Maria Marquine · 2021 to 2026
$24.1M
INTEGRATED TRAINING IN ANESTHESIOLOGY RESEARCHT32GM008600 · NIGMS · DUKE UNIVERSITY · PI Miriam Treggiari · 1996 to 2026
$6.6M
Cognitive Effects of Body Temperature During Hypothermic Circulatory ArrestR01HL130443 · NHLBI · DUKE UNIVERSITY · PI HUGHES, G. CHAD, MATHEW, JOSEPH P · 2016 to 2020
$3.5M
The role of cerebrospinal fluid complement activation in delirium and post-intensive care unit long-term cognitive impairmentK23AG084898 · NIA · DUKE UNIVERSITY · PI Michael Joseph Devinney · 2024 to 2026
$537k
NHLBI NIH HHS R01 HL130443NHLBI NIH HHS R01-HL130443NIA NIH HHS K23 AG084898NIA NIH HHS K23AG084898NIA NIH HHS P30 AG072958NIA NIH HHS P30-AG072958NIGMS NIH HHS T32 GM008600NIGMS NIH HHS T32-GM08600Swedish Research Council (#2023-00356, #2022-01018 and #2019-02397
6 · The paper itself

Abstract

Neuroinflammation has detrimental neurocognitive effects in patients with systemic and neuropsychiatric diseases. Yet, outside of these conditions, it is unclear to what extent neuroinflammation modulates brain network-level function in older adults in the general population and, what, if any cognitive performance issues arise as a result. To evaluate these questions, we compared cerebrospinal fluid (CSF) inflammatory cytokine levels, resting-state functional magnetic resonance imaging, and cognitive performance data in 96 community-dwelling older adults (age ≥ 60 yrs). Principal component analysis yielded three components, accounting for > 50% of the variance in CSF cytokine levels; of which, the first principal component (PC1) accounted for 32% of the overall variance. A multivariate pattern analysis regression model, adjusted for age, sex and in-scanner movement, revealed cytokine PC1 values were inversely associated with functional connectivity between the mediodorsal thalamus and multiple cortical regions associated with the frontoparietal, default mode and dorsal attention functional brain networks (p-FWE = 0.037). For the majority of these cortical regions, functional connectivity with the mediodorsal thalamus was not associated with cognitive performance. In a robust multivariable model, narrative memory performances were positively associated with thalamocortical connectivity to a posterior parietal hub region of the frontoparietal and dorsal attention networks [beta = 0.25 (95% CI; 0.01, 0.49); p = 0.040], but this association did not survive correction for the number of evaluated cognitive domains (Bonferroni-adjusted p < 0.01). Study results reveal that neuroinflammatory CSF cytokine levels were inversely associated with functional connectivity between the mediodorsal thalamus and cortical regions largely involved in frontoparietal, dorsal attention and default mode networks, but the functional consequences of this relationship remain to be determined and will require further investigation to determine if reduced corticothalamic functional connectivity may help account, in part, for common illness-related cognitive complaints.

Indexed as

AgingCerebral CortexCognitionNeuroinflammatory DiseasesThalamusAgedAged, 80 and overCytokinesFemaleHumansMagnetic Resonance ImagingMaleMiddle AgedNeural PathwaysNeuropsychological TestsCytokinesBrainCerebrospinal fluidCytokineFMRIFunctional connectivityNeuroinflammationThalamocorticalThalamus

Identifiers

PMID42732056
PMCPMC13570534

What OpenQuestion holds

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Registered trials

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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.