Evidence map›Paper›PMID 28864907›Full record

ArticleJournal of neural transmission (Vienna, Austria : 1996)2018

Alterations in the reduced pteridine contents in the cerebrospinal fluids of LRRK2 mutation carriers and patients with Parkinson's disease.

Hiroshi Ichinose, Ken-Ichi Inoue, Shinobu Arakawa, Yuki Watanabe, Hiroki Kurosaki, Shoko Koshiba, Eldbjorg Hustad, Masahiko Takada, Jan O Aasly

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of neural transmission (Vienna, Austria : 1996), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

12 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Long-Term Outcomes of Genetic Parkinson's Disease.Journal of movement disorders · 2020
    Article
  11. Review
  12. 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

9 authors at 3 institutions in 2 countries.

Hiroshi IchinoseSchool of Life Science and Technology, Tokyo Institute of Technology, 4259-B7, Nagatsuta, Midori-ku, Yokohama, 226-8501, Japan. hichinos@bio.titech.ac.jp.ORCID 0000-0001-6008-6860
Ken-Ichi InoueSystems Neuroscience Section, Primate Research Institute, Kyoto University, Inuyama, Aichi, 484-8506, Japan.
Shinobu ArakawaSchool of Life Science and Technology, Tokyo Institute of Technology, 4259-B7, Nagatsuta, Midori-ku, Yokohama, 226-8501, Japan.
Yuki WatanabeSchool of Life Science and Technology, Tokyo Institute of Technology, 4259-B7, Nagatsuta, Midori-ku, Yokohama, 226-8501, Japan.
Hiroki KurosakiSchool of Life Science and Technology, Tokyo Institute of Technology, 4259-B7, Nagatsuta, Midori-ku, Yokohama, 226-8501, Japan.
Shoko KoshibaSchool of Life Science and Technology, Tokyo Institute of Technology, 4259-B7, Nagatsuta, Midori-ku, Yokohama, 226-8501, Japan.
Eldbjorg HustadDepartment of Neurology, St. Olavs Hospital, Norwegian University of Science and Technology (NTNU), 7030, Trondheim, Norway.
Masahiko TakadaSystems Neuroscience Section, Primate Research Institute, Kyoto University, Inuyama, Aichi, 484-8506, Japan.
Jan O AaslyDepartment of Neurology, St. Olavs Hospital, Norwegian University of Science and Technology (NTNU), 7030, Trondheim, Norway.
Tokyo Institute of Technology · JPKyoto University · JPNorwegian University of Science and Technology · NO

Funding

Ministry of Education, Culture, Sports, Science and Technology 15H01422Ministry of Health, Labour and Welfare H22-nanchi-ippan-123Ministry of Health, Labour and Welfare H23-nanchi-ippan-096
6 · The paper itself

Abstract

Tetrahydrobiopterin (BH4) is a cofactor for tyrosine hydroxylase that is essential for the biosynthesis of dopamine. Parkinson's disease (PD) is characterized by a progressive degeneration of nigrostriatal dopaminergic neurons, and biomarkers reflecting the degree of neurodegeneration are important not only for basic research but also for clinical diagnosis and the treatment of the disease. Although the total neopterin and biopterin levels in the cerebrospinal fluids (CSF) of the patients with PD were reported, alterations in the composition of reduced and oxidized forms of pteridine compounds have not been examined. In this study, we first examined the time-dependent alterations in BH4 and other reduced pteridine compounds in the CSF of an MPTP-treated monkey as a primate PD model. We found that the CSF levels of BH4 and dihydroneopterin, an intermittent metabolite of BH4-biosynthesis, altered inversely with progression of neurodegeneration, whereas those of dihydrobiopterin and neopterin were relatively low and constant. Next, we assayed the amounts of reduced pteridine compounds in the CSF of 36 pre-symptomatic LRRK2-mutation (N1437H or G2019S) carriers (LRRK2-carrier), 13 patients with PD symptoms (LRRK2-PD), 46 patients with sporadic PD (sPD), and 26 non-PD individuals. The BH4 levels were significantly lower in both the LRRK2-PD and sPD patients, and the LRRK2-carriers exhibited higher BH4 levels compared with the sPD patients. The total neopterin levels in the CSF of the LRRK2-PD were significantly higher than those in the sPD and non-PD individuals, which indicated greater inflammatory responses in the brains of LRRK2-PD patients. The present results suggest that detailed analyses of pteridine levels in the CSF might be useful for understanding the pathophysiology of familial PD and for monitoring PD progression.

Indexed as

HeterozygoteAdultAgedAged, 80 and overAnimalsBiomarkersFemaleHumansLeucine-Rich Repeat Serine-Threonine Protein Kinase-2MacacaMaleMiddle AgedMPTP PoisoningMutationParkinson DiseasePteridinesBiomarkersLeucine-Rich Repeat Serine-Threonine Protein Kinase-2LRRK2 protein, humanPteridinesLRRK2NeopterinPARK8Parkinson’s diseaseTetrahydrobiopterin

Identifiers

PMID28864907
OpenAlexW2751779016

What OpenQuestion holds

Textmetadata
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.