Evidence map›Paper›PMID 35931783›Full record

ArticleNPJ Parkinson's disease2022

Pathophysiological evaluation of the LRRK2 G2385R risk variant for Parkinson's disease.

Toshiki Tezuka, Daisuke Taniguchi, Mariko Sano, Tomoyo Shimada, Yutaka Oji, Taiji Tsunemi, Aya Ikeda, Yuanzhe Li, Hiroyo Yoshino, Jun Ogata and 5 more

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 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.5field-weighted citation impact, top 9% 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, 24 citations in OpenAlex.

  1. Review
  2. Ex Vivo LRRK2 Activation in Asian G2385R and R1628P Variant Carriers and Idiopathic Parkinson's Disease.Movement disorders : official journal of the Movement Disorder Society · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Interpretable Machine Learning for Cross-Cohort Prediction of Motor Fluctuations in Parkinson's Disease.Movement disorders : official journal of the Movement Disorder Society · 2025
    Article
  7. Review
  8. Article
  9. Article
  10. Impairment of the Glial Phagolysosomal System Drives Prion-Like Propagation in aThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  11. Article
  12. Review
  13. ATP13A2 (PARK9) and basal ganglia function.Frontiers in neurology · 2023
    Review
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

15 authors at 3 institutions in 1 country.

Toshiki TezukaDepartment of Neurology, Juntendo University School of Medicine, Tokyo, 113-8421, Japan.
Daisuke TaniguchiDepartment of Neurology, Juntendo University School of Medicine, Tokyo, 113-8421, Japan.
Mariko SanoDepartment of Neurology, Juntendo University School of Medicine, Tokyo, 113-8421, Japan.
Tomoyo ShimadaDepartment of Neurology, Juntendo University School of Medicine, Tokyo, 113-8421, Japan.
Yutaka OjiDepartment of Neurology, Juntendo University School of Medicine, Tokyo, 113-8421, Japan.
Taiji TsunemiDepartment of Neurology, Juntendo University School of Medicine, Tokyo, 113-8421, Japan.
Aya IkedaDepartment of Neurology, Juntendo University School of Medicine, Tokyo, 113-8421, Japan.
Yuanzhe LiDepartment of Neurology, Juntendo University School of Medicine, Tokyo, 113-8421, Japan.
Hiroyo YoshinoResearch Institute for Diseases of Old Age, Juntendo University Graduate School of Medicine, Tokyo, 113-8421, Japan.
Jun OgataDepartment of Research for Parkinson's Disease, Juntendo University Graduate School of Medicine, Tokyo, 113-8421, Japan.
Kahori Shiba-FukushimaDepartment of Drug Development for Parkinson's Disease, Juntendo University Graduate School of Medicine, Tokyo, 113-8421, Japan.
Manabu FunayamaDepartment of Neurology, Juntendo University School of Medicine, Tokyo, 113-8421, Japan.ORCID http://orcid.org/0000-0002-7412-3631
Kenya NishiokaDepartment of Neurology, Juntendo University School of Medicine, Tokyo, 113-8421, Japan.
Yuzuru ImaiDepartment of Neurology, Juntendo University School of Medicine, Tokyo, 113-8421, Japan. yzimai@juntendo.ac.jp.ORCID http://orcid.org/0000-0003-2924-5231
Nobutaka HattoriDepartment of Neurology, Juntendo University School of Medicine, Tokyo, 113-8421, Japan. nhattori@juntendo.ac.jp.
Juntendo University · JPKeio University · JPRIKEN Center for Brain Science · JP

Funding

AbbVie (AbbVie Inc.) NAMEXT | Japan Society for the Promotion of Science (JSPS) 20H03453MEXT | Japan Society for the Promotion of Science (JSPS) 20K21531Otsuka Pharmaceutical (Otsuka Pharmaceutical Co., Ltd.) NATakeda Science Foundation NA
6 · The paper itself

Abstract

Missense variants in leucine-rich repeat kinase 2 (LRRK2) lead to familial and sporadic Parkinson's disease (PD). The pathological features of PD patients with LRRK2 variants differ. Here, we report an autopsy case harboring the LRRK2 G2385R, a risk variant for PD occurring mainly in Asian populations. The patient exhibited levodopa-responsive parkinsonism at the early stage and visual hallucinations at the advanced stage. The pathological study revealed diffuse Lewy bodies with neurofibrillary tangles, amyloid plaques, and mild signs of neuroinflammation. Biochemically, detergent-insoluble phospho-α-synuclein was accumulated in the frontal, temporal, entorhinal cortexes, and putamen, consistent with the pathological observations. Elevated phosphorylation of Rab10, a substrate of LRRK2, was also prominent in various brain regions. In conclusion, G2385R appears to increase LRRK2 kinase activity in the human brain, inducing a deleterious brain environment that causes Lewy body pathology.

Identifiers

PMID35931783
PMCPMC9355991
OpenAlexW4289866292

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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.