Evidence map›Paper›PMID 35663565›Full record

ArticleFrontiers in aging neuroscience2022

Synuclein Motor Dysfunction Composite Scale for the Discrimination of Dementia With Lewy Bodies From Alzheimer's Disease.

Ying-Tsung Chen, Satoshi Orimo, Cheng-Yu Wei, Guang-Uei Hung, Shieh-Yueh Yang, Pai-Yi Chiu

Open access · goldAbstract read
In one paragraph

Article in Frontiers in aging neuroscience, 2022. 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
0.1field-weighted citation impact, top 54% of its field
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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0 citing papers in PubMed, 1 citations in OpenAlex.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Ying-Tsung ChenDepartment of Psychiatry, Show Chwan Memorial Hospital, Changhua, Taiwan.
Satoshi OrimoDepartment of Neurology, Kamiyoga Setagaya Street Clinic, Tokyo, Japan.
Cheng-Yu WeiDepartment of Exercise and Health Promotion, College of Education, Chinese Culture University, Taipei, Taiwan.
Guang-Uei HungDepartment of Nuclear Medicine, Chang Bing Show Chwan Memorial Hospital, Changhua, Taiwan.
Shieh-Yueh YangMagQu Co., Ltd., New Taipei, Taiwan.
Pai-Yi ChiuDepartment of Neurology, Show Chwan Memorial Hospital, Changhua, Taiwan.
Chang Bing Show Chwan Memorial Hospital · TWChinese Culture University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: An abnormal increase of α-synuclein in the brain is the hallmark of dementia with Lewy bodies (DLB). However, the diagnostic power of plasma α-synuclein in DLB is not yet confirmed. Parkinsonism is highly associated with and is one of the core clinical features of DLB. We studied plasma α-synuclein and developed a novel tool that combined plasma α-synuclein level and Motor Dysfunction Questionnaire (MDQ), namely Synuclein Motor Dysfunction Composite Scale (SMDCS), for the clinical discrimination of DLB from Alzheimer's disease (AD). Methods: This cross-sectional study analyzed participants' demographical data, plasma α-synuclein level, MDQ, structured clinical history questionnaire, neuropsychological and motor function tests, and neuroimaging studies. The power of plasma α-synuclein level, MDQ, and SMDCS for discriminating DLB from non-demented controls (NC) or AD were compared. Results: Overall, 121 participants diagnosed as 58 DLB, 31 AD, and 31 NC were enrolled. Patients with DLB had significantly higher mean plasma α-synuclein level (0.24 ± 0.32 pg/ml) compared to the NC group (0.08 ± 0.05 pg/ml) and the AD group (0.08 ± 0.05 pg/ml). The DLB group demonstrated higher MDQ (2.95 ± 1.60) compared to the NC (0.42 ± 0.98) or AD (0.44 ± 0.99) groups. The sensitivity/specificity of plasma α-synuclein level, MDQ, and SMDCS for differentiating DLB from non-DLB were 0.80/0.64, 0.83/0.89, and 0.88/0.93, respectively. Conclusion: Both plasma α-synuclein and MDQ were significantly higher in patients with DLB compared to the NC or AD groups. The novel SMDCS, significantly improved accuracy for the clinical differentiation of DLB from AD or NC.

Indexed as

Alzheimer’s diseasedementia with Lewy bodiesMotor Dysfunction Questionnaireplasma α-synucleinSynuclein Motor Dysfunction Composite Scale

Identifiers

PMID35663565
PMCPMC9161692
OpenAlexW4280488586

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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.