Evidence map›Paper›PMID 36068704›Full record

ArticleJournal of neuroimaging : official journal of the American Society of Neuroimaging2023

Frontostriatal and limbic contributions to cognitive decline in Parkinson's disease.

Gregory Brown, Jonathan Hakun, Mechelle M Lewis, Sol De Jesus, Guangwei Du, Paul J Eslinger, Lan Kong, Xuemei Huang

Open access · greenAbstract read
In one paragraph

Article in Journal of neuroimaging : official journal of the American Society of Neuroimaging, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 10% of its field
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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 20 citations in OpenAlex.

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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

8 authors at 1 institution in 1 country.

Gregory BrownDepartment of Neurology, Penn State University Milton S. Hershey Medical Center, Hershey, Pennsylvania, USA.ORCID 0000-0002-4013-8405
Jonathan HakunDepartment of Neurology, Penn State University Milton S. Hershey Medical Center, Hershey, Pennsylvania, USA.
Mechelle M LewisDepartment of Neurology, Penn State University Milton S. Hershey Medical Center, Hershey, Pennsylvania, USA.
Sol De JesusDepartment of Neurology, Penn State University Milton S. Hershey Medical Center, Hershey, Pennsylvania, USA.
Guangwei DuDepartment of Pharmacology, Penn State University Milton S. Hershey Medical Center, Hershey, Pennsylvania, USA.
Paul J EslingerDepartment of Neurology, Penn State University Milton S. Hershey Medical Center, Hershey, Pennsylvania, USA.
Lan KongDepartment of Public Health Sciences, Penn State University Milton S. Hershey Medical Center, Hershey, Pennsylvania, USA.
Xuemei HuangDepartment of Neurology, Penn State University Milton S. Hershey Medical Center, Hershey, Pennsylvania, USA.
Penn State Milton S. Hershey Medical Center · US

Funding

Penn State Clinical and Translational Science InstituteUL1TR002014 · NCATS · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI KRASCHNEWSKI, JENNIFER L. · 2016 to 2025
$33.7M
Penn State Clinical and Translational Science InstituteUL1TR000127 · NCATS · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI SINOWAY, LAWRENCE I · 2012 to 2015
$17.1M
Discovery of Multimodal Biomarkers for Parkinsonian Syndromes, Their Progression, and Pathological RelevanceU01NS112008 · NINDS · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI HUANG, XUEMEI, KANTHASAMY, ANUMANTHA GOUNDER · 2019 to 2023
$5.5M
PENN STATE CLINICAL AND TRANSLATIONAL SCIENCE INSTITUTEUL1RR033184 · NCRR · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI SINOWAY, LAWRENCE I · 2011 to 2011
$4.5M
Multimodal MRI Markers of Nigrostriatal Pathology in Parkinson's DiseaseU01NS082151 · NINDS · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI HUANG, XUEMEI · 2012 to 2016
$4.2M
Structural MRI marker(s) of Parkinson's Disease's ProgressionR01NS060722 · NINDS · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI HUANG, XUEMEI · 2009 to 2013
$2.9M
Self-regulation of Health Promotion: the Roles of Momentary Variability in Working Memory Capacity and Neurocognitive AgingR00AG056670 · NIA · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI HAKUN, JONATHAN G. · 2019 to 2021
$721k
The Striatum and Hippocampus: "Hubs" of White Matter Connections in Parkinson's Disease Cognitive DeclineF30AG067651 · NIA · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI BROWN, GREGORY L · 2020 to 2024
$153k
Alzheimer's AssociationNCATS NIH HHS UL1 TR000127NCATS NIH HHS UL1 TR002014NCRR NIH HHS UL1 RR033184NIA NIH HHS F30 AG067651NIA NIH HHS R00 AG056670NINDS NIH HHS NS060722NINDS NIH HHS NS082151NINDS NIH HHS NS112008NINDS NIH HHS R01 NS060722NINDS NIH HHS U01 NS082151NINDS NIH HHS U01 NS112008
6 · The paper itself

Abstract

background and purposeThe circuitry underlying heterogenous cognitive profiles in Parkinson's disease (PD) remains unclear. The purpose of this study is to investigate whether structural changes in frontostriatal and limbic pathways contribute to different cognitive trajectories in PD.

methodsWe obtained clinical and multimodal MRI data from 120 control and 122 PD subjects without dementia or severe motor disability. T1/T2-weighted images estimated volume, and diffusion imaging evaluated fractional anisotropy (FA) of frontostriatal (striatum and frontostriatal white matter [FSWM]) and limbic (hippocampus and fornix) structures. Montreal Cognitive Assessment (MoCA) gauged total and domain-specific (attention/executive and memory) cognitive function. Linear mixed-effects models were used to compare MRI and cognitive progression over 4.5 years between controls and PD and evaluate associations between baseline MRI and cognitive changes in PD.

resultsAt baseline, control and PD groups were comparable, except PD participants had smaller striatal volume (p < 0.001). Longitudinally, PD showed faster decline in hippocampal volume, FSWM FA, and fornix FA (ps < .016), but not striatal volume (p = .218). Total and domain-specific MoCA scores declined faster in PD (ps < .030). In PD, lower baseline hippocampal volume (p = .005) and fornix FA (p = .032), but not striatal volume (p = .662) or FSWM FA (p = .143), were associated with faster total MoCA decline. Baseline frontostriatal metrics of striatal volume and FSWM FA were associated with faster attention/executive decline (p < .038), whereas lower baseline hippocampal volume was associated with faster memory decline (p = .005).

conclusionIn PD, frontostriatal structural metrics are associated with attention/executive tasks, whereas limbic changes correlated with faster global cognitive decline, particularly in memory tasks.

Indexed as

Cognitive DysfunctionMotor DisordersParkinson DiseasePersons with DisabilitiesCognitionHumansNeuropsychological TestscognitionfornixhippocampuslongitudinalMRIParkinson's disease

Identifiers

PMID36068704
PMCPMC9840678
OpenAlexW4294916296

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.