Evidence map›Paper›PMID 38752411›Full record

ArticleThe European journal of neuroscience2024

A longitudinal evaluation of personalized intrinsic network topography and cognitive decline in Parkinson's disease.

Renxi Li, Vincent Pozorski, Kevin Dabbs, Maureen Haebig, Christopher R Cox, Colleen Pletcher, Alexandra Wey, Amy Barzgari, Frances Theisen, Ozioma Okonkwo and 1 more

Abstract read
In one paragraph

Article in The European journal of neuroscience, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
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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

11 authors.

Renxi LiWilliam S. Middleton V.A. Hospital, Madison, Wisconsin, USA.
Vincent PozorskiWilliam S. Middleton V.A. Hospital, Madison, Wisconsin, USA.ORCID 0000-0002-4597-0794
Kevin DabbsDepartment of Neurology, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA.
Maureen HaebigWilliam S. Middleton V.A. Hospital, Madison, Wisconsin, USA.
Christopher R CoxDepartment of Psychology, Louisiana State University, Baton Rouge, Louisiana, USA.
Colleen PletcherWilliam S. Middleton V.A. Hospital, Madison, Wisconsin, USA.
Alexandra WeyWilliam S. Middleton V.A. Hospital, Madison, Wisconsin, USA.
Amy BarzgariWilliam S. Middleton V.A. Hospital, Madison, Wisconsin, USA.
Frances TheisenWilliam S. Middleton V.A. Hospital, Madison, Wisconsin, USA.
Ozioma OkonkwoDepartment of Medicine, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA.
Catherine L GallagherWilliam S. Middleton V.A. Hospital, Madison, Wisconsin, USA.ORCID 0000-0002-1701-6362

Funding

Wisconsin Alzheimer's Disease Research CenterP50AG033514 · NIA · UNIVERSITY OF WISCONSIN-MADISON · PI ASTHANA, SANJAY · 2009 to 2018
$16.2M
Longitudinal MRI in Preclinical Parkinson DiseaseI01CX000555 · VA · WM S. MIDDLETON MEMORIAL VETERANS HOSP · PI GALLAGHER, CATHERINE L. · 2012 to 2023
–
CSRD VA I01 CX000555NIA NIH HHS P50 AG033514US Department of Veterans Affairs Clinical Sciences R&D I01-CX000555-01-05
6 · The paper itself

Abstract

Resting state functional magnetic resonance imaging (R-fMRI) offers insight into how synchrony within and between brain networks is altered in disease states. Individual and disease-related variability in intrinsic connectivity networks may influence our interpretation of R-fMRI data. We used a personalized approach designed to account for individual variation in the spatial location of correlation maxima to evaluate R-fMRI differences between Parkinson's disease (PD) patients who showed cognitive decline, those who remained cognitively stable and cognitively stable controls. We compared fMRI data from these participant groups, studied at baseline and 18 months later, using both network-based statistics (NBS) and calculations of mean inter- and intra-network connectivity within pre-defined functional networks. The NBS analysis showed that PD participants who remained cognitively stable showed exclusively (at baseline) or predominantly (at follow-up) increased intra-network connectivity, whereas decliners showed exclusively reduced intra-network and inter- (ventral attention and default mode) connectivity, in comparison with the control group. Evaluation of mean connectivity between all regions of interest (ROIs) within a priori networks showed that decliners had consistently reduced inter-network connectivity for ventral attention, somatomotor, visual and striatal networks and reduced intra-network connectivity for ventral attention network to striatum and cerebellum. These findings suggest that specific functional connectivity covariance patterns differentiate PD cognitive subtypes and may predict cognitive decline. Further, increased intra and inter-network synchrony may support cognitive function in the face of PD-related network disruptions.

Indexed as

Cognitive DysfunctionMagnetic Resonance ImagingNerve NetParkinson DiseaseAgedBrainFemaleHumansLongitudinal StudiesMaleMiddle Agedageingfunctional MRIhumansmagnetic resonance imagingneurodegenerative disease

Identifiers

PMID38752411
PMCPMC11638918

What OpenQuestion holds

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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.