Evidence map›Paper›PMID 38896976›Full record

ArticleParkinsonism & related disorders2024

Neuropathological findings and in vivo imaging correlates of the red nucleus compared to those of the substantia nigra pars compacta in parkinsonisms.

Melinda L Johnson, Mechelle M Lewis, Ernest W Wang, Leslie C Jellen, Guangwei Du, Sol De Jesus, Lan Kong, Cunfeng Pu, Xuemei Huang

Abstract read
In one paragraph

Article in Parkinsonism & related disorders, 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

9 authors.

Melinda L JohnsonDepartment of Neurology, Pennsylvania State University-Milton S. Hershey Medical Center, Hershey, PA, USA; Translational Brain Research Center, Pennsylvania State University-Milton S. Hershey Medical Center, Hershey, PA, USA.
Mechelle M LewisDepartment of Neurology, Pennsylvania State University-Milton S. Hershey Medical Center, Hershey, PA, USA; Department of Pharmacology, Pennsylvania State University-Milton S. Hershey Medical Center, Hershey, PA, USA; Translational Brain Research Center, Pennsylvania State University-Milton S. Hershey Medical Center, Hershey, PA, USA.
Ernest W WangDepartment of Neurology, Pennsylvania State University-Milton S. Hershey Medical Center, Hershey, PA, USA; Translational Brain Research Center, Pennsylvania State University-Milton S. Hershey Medical Center, Hershey, PA, USA.
Leslie C JellenDepartment of Neurology, Pennsylvania State University-Milton S. Hershey Medical Center, Hershey, PA, USA; Translational Brain Research Center, Pennsylvania State University-Milton S. Hershey Medical Center, Hershey, PA, USA.
Guangwei DuDepartment of Neurology, Pennsylvania State University-Milton S. Hershey Medical Center, Hershey, PA, USA; Department of Radiology, Pennsylvania State University-Milton S. Hershey Medical Center, Hershey, PA, USA; Translational Brain Research Center, Pennsylvania State University-Milton S. Hershey Medical Center, Hershey, PA, USA.
Sol De JesusDepartment of Neurology, Pennsylvania State University-Milton S. Hershey Medical Center, Hershey, PA, USA.
Lan KongDepartment of Public Health Science, Pennsylvania State University-Milton S. Hershey Medical Center, Hershey, PA, USA.
Cunfeng PuDepartment of Pathology and Laboratory Medicine, Pennsylvania State University-Milton S. Hershey Medical Center, Hershey, PA, USA.
Xuemei HuangDepartment of Neurology, Pennsylvania State University-Milton S. Hershey Medical Center, Hershey, PA, USA; Department of Pharmacology, Pennsylvania State University-Milton S. Hershey Medical Center, Hershey, PA, USA; Department of Radiology, Pennsylvania State University-Milton S. Hershey Medical Center, Hershey, PA, USA; Department of Neurosurgery, Pennsylvania State University-Milton S. Hershey Medical Center, Hershey, PA, USA; Translational Brain Research Center, Pennsylvania State University-Milton S. Hershey Medical Center, Hershey, PA, USA; Department of Kinesiology, Penn State University, University Park, PA, USA. Electronic address: Xuemei@psu.edu.

Funding

Penn State Clinical and Translational Science InstituteUL1TR002014 · NCATS · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI KRASCHNEWSKI, JENNIFER L. · 2016 to 2025
$33.7M
Regional Brain Manganese Accumulation and Functional Consequences in WeldersR01ES019672 · NIEHS · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI HUANG, XUEMEI · 2011 to 2021
$5.9M
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
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
Effects of HFE H63D on Brain Mn Accumulation and NeurotoxicityF30ES030607 · NIEHS · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI WANG, ERNEST W · 2019 to 2024
$181k
NCATS NIH HHS UL1 TR002014NIEHS NIH HHS F30 ES030607NIEHS NIH HHS R01 ES019672NINDS NIH HHS R01 NS060722NINDS NIH HHS U01 NS082151NINDS NIH HHS U01 NS112008
6 · The paper itself

Abstract

introductionThe substantia nigra pars compacta (SNc) is the key pathologic locus in neurodegenerative parkinsonian disorders. Recently, in vivo susceptibility MRI metrics were associated with postmortem glial cell density and tau burden in the SNc of parkinsonism subjects. This study investigated the red nucleus (RN), another iron-rich region adjacent to the SNc and a potential site of higher functionality in parkinsonisms.

methodsIn vivo MRI and postmortem data were obtained from 34 parkinsonism subjects and 3 controls. Neuron density, glial cell density, and percentages of area occupied by α-synuclein and tau were quantified using digitized midbrain slides. R2* and quantitative susceptibility mapping (QSM) metrics in the RN and SNc were derived from multi-gradient echo images. Histopathology data were compared between the RN and SNc using paired t-tests. MRI-histology associations were analyzed using partial Pearson correlations.

resultsThe RN had greater neuron (t

conclusionsThe RN is resilient to parkinsonian-related pathological processes compared to the SNc, and susceptibility MRI captured glial cell density in both regions. These findings help to further our understanding of the underlying pathophysiological processes in parkinsonisms.

Indexed as

Magnetic Resonance ImagingParkinsonian DisordersPars CompactaRed NucleusSubstantia NigraAgedAged, 80 and overalpha-SynucleinFemaleHumansMaleMiddle AgedNeurogliaNeuronstau Proteinsalpha-Synucleintau ProteinsMultiple system atrophyParkinson's diseaseProgressive supranuclear palsyRed nucleusSusceptibility magnetic resonance imaging

Identifiers

PMID38896976
PMCPMC11283947

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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.