Evidence map›Paper›PMID 30597973›Full record

ArticleCells2018

Zonisamide Administration Improves Fatty Acid β-Oxidation in Parkinson's Disease.

Shin-Ichi Ueno, Shinji Saiki, Motoki Fujimaki, Haruka Takeshige-Amano, Taku Hatano, Genko Oyama, Kei-Ichi Ishikawa, Akihiro Yamaguchi, Shuko Nojiri, Wado Akamatsu and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cells, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

6 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
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  3. Article
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  6. 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

11 authors at 1 institution in 1 country.

Shin-Ichi UenoDepartment of Neurology, Juntendo University School of Medicine, Bunkyo-ku, Tokyo 113-8421, Japan. sueno@juntendo.ac.jp.
Shinji SaikiDepartment of Neurology, Juntendo University School of Medicine, Bunkyo-ku, Tokyo 113-8421, Japan. ssaiki@juntendo.ac.jp.ORCID 0000-0002-9732-8488
Motoki FujimakiDepartment of Neurology, Juntendo University School of Medicine, Bunkyo-ku, Tokyo 113-8421, Japan. mtfujima@juntendo.ac.jp.
Haruka Takeshige-AmanoDepartment of Neurology, Juntendo University School of Medicine, Bunkyo-ku, Tokyo 113-8421, Japan. h-amano@juntendo.ac.jp.
Taku HatanoDepartment of Neurology, Juntendo University School of Medicine, Bunkyo-ku, Tokyo 113-8421, Japan. thatano@juntendo.ac.jp.ORCID 0000-0002-6808-0444
Genko OyamaDepartment of Neurology, Juntendo University School of Medicine, Bunkyo-ku, Tokyo 113-8421, Japan. g_oyama@juntendo.ac.jp.
Kei-Ichi IshikawaDepartment of Neurology, Juntendo University School of Medicine, Bunkyo-ku, Tokyo 113-8421, Japan. kishikaw@juntendo.ac.jp.
Akihiro YamaguchiCenter for Genomic and Regenerative Medicine, Juntendo University School of Medicine, Bunkyo-ku, Tokyo 113-8421, Japan. akihiro0781@gmail.com.
Shuko NojiriMedical Technology Innovation Center, Juntendo University, Bunkyo-ku, Tokyo 113-8421, Japan. s-nojiri@juntendo.ac.jp.
Wado AkamatsuCenter for Genomic and Regenerative Medicine, Juntendo University School of Medicine, Bunkyo-ku, Tokyo 113-8421, Japan. awado@juntendo.ac.jp.
Nobutaka HattoriDepartment of Neurology, Juntendo University School of Medicine, Bunkyo-ku, Tokyo 113-8421, Japan. nhattori@juntendo.ac.jp.
Juntendo University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although many experimental studies have shown the favorable effects of zonisamide on mitochondria using models of Parkinson's disease (PD), the influence of zonisamide on metabolism in PD patients remains unclear. To assess metabolic status under zonisamide treatment in PD, we performed a pilot study using a comprehensive metabolome analysis. Plasma samples were collected for at least one year from 30 patients with PD: 10 without zonisamide medication and 20 with zonisamide medication. We performed comprehensive metabolome analyses of plasma with capillary electrophoresis time-of-flight mass spectrometry and liquid chromatography time-of-flight mass spectrometry. We also measured disease severity using Hoehn and Yahr (H&Y) staging and the Unified Parkinson's Disease Rating Scale (UPDRS) motor section, and analyzed blood chemistry. In PD with zonisamide treatment, 15 long-chain acylcarnitines (LCACs) tended to be increased, of which four (AC(12:0), AC(12:1)-1, AC(16:1), and AC(16:2)) showed statistical significance. Of these, two LCACs (AC(16:1) and AC(16:2)) were also identified by partial least squares analysis. There was no association of any LCAC with age, disease severity, levodopa daily dose, or levodopa equivalent dose. Because an upregulation of LCACs implies improvement of mitochondrial β-oxidation, zonisamide might be beneficial for mitochondrial β-oxidation, which is suppressed in PD.

Indexed as

AgedAged, 80 and overAntiparkinson AgentsCarnitineFatty AcidsFemaleHumansLevodopaMaleMental Status and Dementia TestsMetabolomeMiddle AgedMitochondriaOxidation-ReductionParkinson DiseasePilot ProjectsacylcarnitineAntiparkinson AgentsCarnitineFatty AcidsLevodopaZonisamidefatty acid β-oxidationlong-chain acylcarnitineParkinson’s disease

Identifiers

PMID30597973
PMCPMC6356654
OpenAlexW2908511124

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.