Evidence map›Paper›PMID 37100802›Full record

ArticleNPJ Parkinson's disease2023

Clinico-imaging features of subjects at risk of Lewy body disease in NaT-PROBE baseline analysis.

Makoto Hattori, Keita Hiraga, Yuki Satake, Takashi Tsuboi, Daigo Tamakoshi, Maki Sato, Katsunori Yokoi, Keisuke Suzuki, Yutaka Arahata, Akihiro Hori and 6 more

Open access · goldAbstract read
In one paragraph

Article in NPJ Parkinson's disease, 2023. 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
3.2field-weighted citation impact, top 8% 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, 14 citations in OpenAlex.

  1. Review
  2. 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

16 authors at 4 institutions in 1 country.

Makoto HattoriDepartment of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Keita HiragaDepartment of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan.ORCID http://orcid.org/0000-0002-0134-2956
Yuki SatakeDepartment of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Takashi TsuboiDepartment of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan.ORCID http://orcid.org/0000-0001-5042-3181
Daigo TamakoshiDepartment of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Maki SatoDepartment of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Katsunori YokoiDepartment of Neurology and Center for Comprehensive Care and Research Center on Memory Disorders, National Center for Geriatrics and Gerontology, Obu, Aichi, Japan.
Keisuke SuzukiInnovation Center for Translational Research, National Center for Geriatrics and Gerontology, Obu, Aichi, Japan.
Yutaka ArahataDepartment of Neurology and Center for Comprehensive Care and Research Center on Memory Disorders, National Center for Geriatrics and Gerontology, Obu, Aichi, Japan.
Akihiro HoriKumiai Kosei Hospital, Takayama, Gifu, Japan.
Motoshi KawashimaMedical Examination Center, Daido Clinic, Nagoya, Japan.
Hideaki ShimizuMedical Examination Center, Daido Clinic, Nagoya, Japan.
Hiroshi MatsudaDepartment of Biofunctional Imaging, Fukushima Medical University, Fukushima, Japan.ORCID http://orcid.org/0000-0002-6297-9897
Katsuhiko KatoFunctional Medical Imaging, Biomedical Imaging Sciences, Division of Advanced Information Health Sciences, Department of Integrated Health Sciences, Nagoya University Graduate School of Medicine, Nagoya, Japan.ORCID http://orcid.org/0000-0002-2083-9319
Yukihiko WashimiDepartment of Neurology and Center for Comprehensive Care and Research Center on Memory Disorders, National Center for Geriatrics and Gerontology, Obu, Aichi, Japan.
Masahisa KatsunoDepartment of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan. ka2no@med.nagoya-u.ac.jp.ORCID http://orcid.org/0000-0001-9453-9311
Nagoya University · JPNational Center for Geriatrics and Gerontology · JPDaido University · JPFukushima Medical University · JP

Funding

Japan Agency for Medical Research and Development (AMED) JP20dm0107155Japan Agency for Medical Research and Development (AMED) JP22ae0101077Japan Agency for Medical Research and Development (AMED) JP22dk0207052Japan Agency for Medical Research and Development (AMED) JP22lk0201124MEXT | Japan Society for the Promotion of Science (JSPS) JP21K19443
6 · The paper itself

Abstract

Individuals with prodromal symptoms of Lewy body disease (LBD), such as rapid eye movement sleep behavior disorder (RBD), often showed imaging defects similar to patients with Parkinson's disease and dementia with Lewy bodies. We examined dopamine transporter (DaT) single-photon-emission computed tomography (SPECT) and metaiodobenzylguanidine (MIBG) scintigraphy in 69 high-risk subjects with ≥2 prodromal symptoms (dysautonomia, hyposmia, and probable RBD) and 32 low-risk subjects without prodromal symptoms, whom were identified through a questionnaire survey of health checkup examinees. The high-risk subjects had significantly worse scores on Stroop test, line orientation test, and the Odor Stick Identification Test for Japanese than the low-risk subjects. The prevalence of abnormalities on DaT-SPECT was higher in the high-risk group than in the low-risk group (24.6% vs. 6.3%, p = 0.030). A decreased uptake on DaT-SPECT was associated with motor impairment, and MIBG scintigraphy defects were associated with hyposmia. The simultaneous evaluation of DaT-SPECT and MIBG scintigraphy may capture a wide range of individuals with prodromal LBD.

Identifiers

PMID37100802
PMCPMC10133289
OpenAlexW4367051984

What OpenQuestion holds

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LicenceCC BY
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.