Evidence map›Paper›PMID 35293156›Full record

ArticleAnnals of clinical and translational neurology2022

Quantitative evaluation of upper limb ataxia in spinocerebellar ataxias.

Yoshiyuki Kishimoto, Atsushi Hashizume, Yuta Imai, Masahiro Nakatochi, Shinichiro Yamada, Daisuke Ito, Ryota Torii, Yoshitaka Nagano, Hideo Fujimoto, Masahisa Katsuno

Open access · goldAbstract read
In one paragraph

Article in Annals of clinical and translational neurology, 2022. 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
0.7field-weighted citation impact, top 38% 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, 7 citations in OpenAlex.

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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

10 authors at 3 institutions in 1 country.

Yoshiyuki KishimotoDepartment of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Atsushi HashizumeDepartment of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Yuta ImaiDepartment of Basic Medicinal Sciences, Nagoya University Graduate School of Pharmaceutical Sciences, Nagoya, Japan.
Masahiro NakatochiPublic Health Informatics Unit, Department of Integrated Health Sciences, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Shinichiro YamadaDepartment of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Daisuke ItoDepartment of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Ryota ToriiDepartment of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Yoshitaka NaganoDepartment of Electronic Robot Engineering, Aichi University of Technology, Gamagori, Japan.
Hideo FujimotoDepartment of Computer Science and Engineering, Nagoya Institute of Technology Graduate School of Engineering, Nagoya, Japan.
Masahisa KatsunoDepartment of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan.ORCID 0000-0001-9453-9311
Nagoya University · JPAichi University of Technology · JPNagoya Institute of Technology · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo quantitatively evaluate upper limb ataxia using a novel pen-like sensor device in patients with spinocerebellar ataxia (SCA) and to assess its validity, reliability, and sensitivity to disease progression.

methodsWe designed a cross-sectional and longitudinal study of patients with SCA and healthy controls. Upper limb ataxia was evaluated using a device that measures the three-dimensional position every 10 msec. Participants were instructed to move a pen-like part of the device iteratively between two buttons. We evaluated the time, length, velocity, and variation coefficient of the stroke, and calculated the distortion index using the mean squared error. The following scales were also evaluated: Scale for the Assessment and Rating of Ataxia (SARA), the International Cooperative Ataxia Rating Scale (ICARS), and the nine-hole pegboard test. Subjects were followed 12 months after the baseline evaluation.

resultsA total of 42 patients with SCA and 33 healthy controls were enrolled and evaluated. For all ataxia indices measured using the device there were significant differences between healthy controls and patients with SCA. Among the ataxia indices, the distortion index showed the strongest correlation with the SARA and ICARS upper limb score (Pearson's r = 0.647 and 0.722, respectively). Test-retest reliability was high for most of the ataxia indices. In the longitudinal analysis, the distortion index showed high standardized response mean and adjusted effect size, regardless of disease severity.

interpretationOur study demonstrated that the distortion index is a reliable functional marker that is sensitive to longitudinal change in patients with SCA.

Indexed as

Cerebellar AtaxiaSpinocerebellar AtaxiasAtaxiaCross-Sectional StudiesHumansLongitudinal StudiesReproducibility of Results

Identifiers

PMID35293156
PMCPMC8994984
OpenAlexW4220893035

What OpenQuestion holds

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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.