Evidence map›Paper›PMID 32828029›Full record

ArticleNeuroImage. Clinical2020

Cortical thinning pattern according to differential nigrosome involvement in patients with Parkinson's disease.

Na-Young Shin, Bo-Hyun Kim, Eunkyeong Yun, Uicheul Yoon, Jong-Min Lee, Young Hee Sung, Eung Yeop Kim

Open access · goldAbstract read
In one paragraph

Article in NeuroImage. Clinical, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 45% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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

7 authors at 4 institutions in 1 country.

Na-Young ShinDepartment of Radiology, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul 06591, Republic of Korea.
Bo-Hyun KimDepartment of Biomedical Engineering, Hanyang University, Seoul 04763, Republic of Korea.
Eunkyeong YunDepartment of Biomedical Engineering, College of Bio and Medical Sciences, Daegu Catholic University, Gyeongbuk 38430, Republic of Korea.
Uicheul YoonDepartment of Biomedical Engineering, College of Bio and Medical Sciences, Daegu Catholic University, Gyeongbuk 38430, Republic of Korea.
Jong-Min LeeDepartment of Biomedical Engineering, Hanyang University, Seoul 04763, Republic of Korea.
Young Hee SungDepartment of Neurology, Gil Medical Center, Gachon University College of Medicine, Incheon 21565, Republic of Korea.
Eung Yeop KimDepartment of Radiology, Gil Medical Center, Gachon University College of Medicine, Incheon 21565, Republic of Korea. Electronic address: neuroradkim@gmail.com.
Catholic University of Daegu · KRGachon University · KRHanyang University · KRSeoul St. Mary's Hospital · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The pathological hallmark of Parkinson's disease (PD) is the progressive degeneration of dopaminergic neurons in the substantia nigra pars compacta, where the dopaminergic neurons form five clusters called nigrosomes 1-5 (N1-N5). N1 is the largest and considered to be the most affected by PD, followed by N2, N4, N3, and N5. Recently, an MRI study suggested a sequential progression of loss from N1 to N4. As the extent of cortical thinning widens as PD progresses, we aimed to define cortical thinning patterns according to the differential involvement of N1 and N4 in PD patients. Cortical thickness was analyzed in 83 PD patients (29 with N1 loss on at least one side of the brain, but no N4 loss; and 54 with N4 loss on at least one side) and 35 healthy subjects with age, sex, disease duration, and intracranial volume as covariates. On patient-wise analysis, for areas with more cortical thinning than the controls, PD patients with N4 loss had wider cortical thinning involving more dorsolateral prefrontal cortex and temporal areas than PD patients with only N1 loss, but cortical thinning did not significantly differ between these two patient groups. However, cortical thinning was more apparent in hemisphere-level analysis with statistically significant clusters being found more in hemispheres with N4 loss than hemispheres with N1 loss in PD patients compared to normal hemispheres of the controls. Cortical thinning occurred in a similar propagation pattern to that seen with PD progression, supporting past hypotheses on the sequential progression of nigrosome loss from N1 to N4.

Indexed as

Parkinson DiseaseCerebral CortexCerebral Cortical ThinningHumansMagnetic Resonance ImagingPrefrontal CortexAtrophyCerebral cortexMagnetic resonance imagingParkinson diseaseSubstantia nigra

Identifiers

PMID32828029
PMCPMC7451416
OpenAlexW3048554868

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.