Evidence map›Paper›PMID 42858219›Full record

ArticleCerebellum (London, England)2026

Three-dimensional Motion Capture Discriminates Extremely Mild Cerebellar Ataxia from Parkinsonism in the Upper Limbs.

Naohisa Ueda, Katsuya Abe, Erena Kobayashi, Noriko Hayashi, Yuichi Higashiyama, Yosuke Miyaji, Yu Kitazawa, Hideyuki Takeuchi, Katsuo Kimura, Hitaru Kishida and 2 more

Abstract read
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In one paragraph

Article in Cerebellum (London, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

Naohisa UedaDepartment of Neurology, Yokohama City University Medical Center, 4-57 Urafune-cho, Minami-ku, Yokohama, Kanagawa, 232-0024, Japan. uedandan@yokohama-cu.ac.jp.ORCID http://orcid.org/0000-0001-6610-058X
Katsuya AbeDepartment of Neurology, Yokohama City University Medical Center, 4-57 Urafune-cho, Minami-ku, Yokohama, Kanagawa, 232-0024, Japan.
Erena KobayashiDepartment of Neurology and Stroke Medicine, Yokohama City University Graduate School of Medicine, 3-9 Fukuura, Kanazawa-ku, Yokohama, Kanagawa, 236-0004, Japan.ORCID http://orcid.org/0000-0002-2378-2493
Noriko HayashiDepartment of Neurology, Yokohama City University Medical Center, 4-57 Urafune-cho, Minami-ku, Yokohama, Kanagawa, 232-0024, Japan.ORCID http://orcid.org/0000-0001-5346-9193
Yuichi HigashiyamaDepartment of Neurology and Stroke Medicine, Yokohama City University Graduate School of Medicine, 3-9 Fukuura, Kanazawa-ku, Yokohama, Kanagawa, 236-0004, Japan.ORCID http://orcid.org/0009-0002-7495-5048
Yosuke MiyajiDepartment of Neurology and Stroke Medicine, Yokohama City University Graduate School of Medicine, 3-9 Fukuura, Kanazawa-ku, Yokohama, Kanagawa, 236-0004, Japan.ORCID http://orcid.org/0000-0002-4482-965X
Yu KitazawaDepartment of Neurology and Stroke Medicine, Yokohama City University Graduate School of Medicine, 3-9 Fukuura, Kanazawa-ku, Yokohama, Kanagawa, 236-0004, Japan.ORCID http://orcid.org/0000-0002-3253-0810
Hideyuki TakeuchiDepartment of Neurology and Stroke Medicine, Yokohama City University Graduate School of Medicine, 3-9 Fukuura, Kanazawa-ku, Yokohama, Kanagawa, 236-0004, Japan.ORCID http://orcid.org/0000-0001-5912-7581
Katsuo KimuraDepartment of Neurology, Yokohama City University Medical Center, 4-57 Urafune-cho, Minami-ku, Yokohama, Kanagawa, 232-0024, Japan.ORCID http://orcid.org/0000-0002-3339-8743
Hitaru KishidaDepartment of Neurology, Yokohama City University Medical Center, 4-57 Urafune-cho, Minami-ku, Yokohama, Kanagawa, 232-0024, Japan.ORCID http://orcid.org/0009-0004-5690-2721
Hiroshi DoiDepartment of Neurology and Stroke Medicine, Yokohama City University Graduate School of Medicine, 3-9 Fukuura, Kanazawa-ku, Yokohama, Kanagawa, 236-0004, Japan.ORCID http://orcid.org/0000-0001-5807-2523
Fumiaki TanakaDepartment of Neurology and Stroke Medicine, Yokohama City University Graduate School of Medicine, 3-9 Fukuura, Kanazawa-ku, Yokohama, Kanagawa, 236-0004, Japan. ftanaka@yokohama-cu.ac.jp.ORCID http://orcid.org/0000-0002-9961-2693

Funding

AMED JP23ek0109648JSPS KAKENHI 21K07440JSPS KAKENHI 24K14300Ministry of Health, Labour and Welfare of Japan 20FC1041Strategic Research Promotion from Yokohama City University SK2804
6 · The paper itself

Abstract

Upper-limb motor symptoms in spinocerebellar degeneration (SCD) and Parkinson's disease (PD) frequently overlap, making clinical differentiation challenging in mild cases using the finger-to-nose test (FNT) or the diadochokinesis test (DDKT). This study aimed to identify quantitative kinematic markers that distinguish mild SCD from mild PD using three-dimensional motion capture. Twenty-six individuals per group-mild SCD, mild PD, and normal controls (NCs)--underwent motion analysis during FNT forward, FNT backward, and DDKT. Key parameters including segmental velocity ratios during FNT and rotational angle parameters during DDKT were analyzed. Significant parameters were validated in an additional cohort of 20 patients with moderate-to-severe SCD and 23 with moderate-to-severe PD, and their associations with motor rating scores were examined. During FNT-forward, the velocity ratio in the final third of the movement was significantly higher in patients with mild SCD than in those with mild PD and NCs and correlated with dysmetria scores in the moderate-to-severe SCD group. During DDKT, patients with mild PD showed smaller rotation angles and a greater decline over time than did patients with mild SCD and NCs. This reduction correlated with the akinesia scores in the moderate-to-severe PD group. Three-dimensional motion capture identified disease-specific kinematic features that were undetectable by visual inspection. Mild SCD was characterized by an increased terminal velocity during FNT-forward, reflecting subtle dysmetria, whereas mild PD showed reduced rotation amplitude during DDKT, reflecting early akinesia. These markers may support the early differential diagnosis and upper-limb motor assessment.

Indexed as

Cerebellar AtaxiaParkinsonian DisordersUpper ExtremityAgedBiomechanical PhenomenaDiagnosis, DifferentialFemaleHumansImaging, Three-DimensionalMaleMiddle AgedMotion CaptureMovementParkinson DiseaseSeverity of Illness Index3D motion captureEarly-stage differentiationMild motor dysfunctionParkinson’s diseaseSpinocerebellar ataxia

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Read underepoch 390

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.