Evidence map›Paper›PMID 33958996›Full record

ArticleFrontiers in aging neuroscience2021

Potential Fluid Biomarkers and a Prediction Model for Better Recognition Between Multiple System Atrophy-Cerebellar Type and Spinocerebellar Ataxia.

Shuo Guo, Bi Zhao, Yunfei An, Yu Zhang, Zirui Meng, Yanbing Zhou, Mingxue Zheng, Dan Yang, Minjin Wang, Binwu Ying

Abstract read
In one paragraph

Article in Frontiers in aging neuroscience, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
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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.

Shuo GuoDepartment of Laboratory Medicine, West China Hospital of Sichuan University, Chengdu, China.
Bi ZhaoDepartment of Neurology, West China Hospital of Sichuan University, Chengdu, China.
Yunfei AnDepartment of Laboratory Medicine, West China Hospital of Sichuan University, Chengdu, China.
Yu ZhangDepartment of Neurology, West China Hospital of Sichuan University, Chengdu, China.
Zirui MengDepartment of Laboratory Medicine, West China Hospital of Sichuan University, Chengdu, China.
Yanbing ZhouDepartment of Laboratory Medicine, West China Hospital of Sichuan University, Chengdu, China.
Mingxue ZhengDepartment of Laboratory Medicine, West China Hospital of Sichuan University, Chengdu, China.
Dan YangDepartment of Radiology, West China Hospital of Sichuan University, Chengdu, China.
Minjin WangDepartment of Laboratory Medicine, West China Hospital of Sichuan University, Chengdu, China.
Binwu YingDepartment of Laboratory Medicine, West China Hospital of Sichuan University, Chengdu, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThis study screened potential fluid biomarkers and developed a prediction model based on the easily obtained information at initial inspection to identify ataxia patients more likely to have multiple system atrophy-cerebellar type (MSA-C).

methodsWe established a retrospective cohort with 125 ataxia patients from southwest China between April 2018 and June 2020. Demographic and laboratory variables obtained at the time of hospital admission were screened using Least Absolute Shrinkage and Selection Operator (LASSO) regression and logistic regression to construct a diagnosis score. The receiver operating characteristic (ROC) and decision curve analyses were performed to assess the accuracy and net benefit of the model. Also, independent validation using 25 additional ataxia patients was carried out to verify the model efficiency. Then the model was translated into a visual and operable web application using the R studio and Shiny package.

resultsFrom 47 indicators, five variables were selected and integrated into the prediction model, including the age of onset (AO), direct bilirubin (DBIL), aspartate aminotransferase (AST), eGFR, and synuclein-alpha. The prediction model exhibited an area under the curve (AUC) of 0.929 for the training cohort and an AUC of 0.917 for the testing cohort. The decision curve analysis (DCA) plot displayed a good net benefit for this model, and external validation confirmed its reliability. The model also was translated into a web application that is freely available to the public.

conclusionThe prediction model that was developed based on laboratory and demographic variables obtained from ataxia patients at admission to the hospital might help improve the ability to differentiate MSA-C from spinocerebellar ataxia clinically.

Indexed as

LASSOliquid biomarkersmultiple system atrophyprediction modelspinocerebellar ataxia

Identifiers

PMID33958996
PMCPMC8093568

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