Evidence map›Paper›PMID 35545633›Full record

ArticleNPJ Parkinson's disease2022

Effects of Alzheimer's genetic risk scores and CSF biomarkers in de novo Parkinson's Disease.

Young-Gun Lee, Seong Ho Jeong, Mincheol Park, Sung Woo Kang, Kyoungwon Baik, Seun Jeon, Phil Hyu Lee, Young Ho Sohn, Byoung Seok Ye

Open access · goldAbstract read
In one paragraph

Article in NPJ Parkinson's disease, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 35% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Evaluation of ATNNeurology · 2024
    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

9 authors at 2 institutions in 1 country.

Young-Gun LeeDepartment of Neurology, Yonsei University College of Medicine, Seoul, South Korea.ORCID http://orcid.org/0000-0003-0460-455X
Seong Ho JeongDepartment of Neurology, Sanggye Paik Hospital, Inje University College of Medicine, Seoul, South Korea.
Mincheol ParkDepartment of Neurology, Yonsei University College of Medicine, Seoul, South Korea.
Sung Woo KangDepartment of Neurology, Yonsei University College of Medicine, Seoul, South Korea.
Kyoungwon BaikDepartment of Neurology, Yonsei University College of Medicine, Seoul, South Korea.
Seun JeonBrain Research Institute, Yonsei University College of Medicine, Seoul, South Korea.ORCID http://orcid.org/0000-0003-2817-3352
Phil Hyu LeeDepartment of Neurology, Yonsei University College of Medicine, Seoul, South Korea.
Young Ho SohnDepartment of Neurology, Yonsei University College of Medicine, Seoul, South Korea.
Byoung Seok YeDepartment of Neurology, Yonsei University College of Medicine, Seoul, South Korea. romel79@gmail.com.
Yonsei University · KRInje University Sanggye Paik Hospital · KR

Funding

Yonsei University | Yonsei University College of Medicine (YUCM) 6-2018-0052
6 · The paper itself

Abstract

Coexisting Alzheimer's disease (AD) pathology is common in Parkinson's disease (PD). However, the implications of genetic risk scores (GRS) for AD have not been elucidated in PD. In 413 de novo PD and 195 healthy controls from the Parkinson's Progression Marker Initiative database, the effects of GRS for AD (GRS-AD) and PD (GRS-PD) on the risk of PD and longitudinal CSF biomarkers and clinical outcomes were explored. Higher GRS-PD and lower baseline CSF α-synuclein were associated with an increased risk of PD. In the PD group, GRS-AD was correlated positively with CSF p-tau/Aβ and negatively with CSF α-synuclein. Higher GRS-PD was associated with faster CSF p-tau/Aβ increase, and GRS-AD and GRS-PD were interactively associated with CSF α-synuclein. In the PD group, higher GRS-AD was associated with poor visuospatial function, and baseline CSF p-tau/Aβ was associated with faster cognitive decline. Higher GRS-PD was associated with better semantic fluency and frontal-related cognition and motor function given the same levels of CSF biomarkers and dopamine transporter uptake. Taken together, our results suggest that higher GRS-AD and CSF p-tau/Aβ, reflecting AD-related pathophysiology, may be associated with cognitive decline in PD patients.

Identifiers

PMID35545633
PMCPMC9095668
OpenAlexW4280495207

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.