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Prediction of Disability in Multiple System Atrophy Based on Machine Learning Algorithm: A Prospective Cohort Study

21 Pages Posted: 31 Mar 2022

See all articles by Lingyu Zhang

Lingyu Zhang

Sichuan University - Rare Disease Center; Sichuan University - Department of Neurology

Yan-Bing Hou

Sichuan University - Rare Disease Center; Sichuan University - Laboratory of Neurodegenerative Disorders

Xiaojing Gu

Sichuan University - Mental Health Center

Bei Cao

Sichuan University - Rare Disease Center

Qianqian Wei

Sichuan University - Rare Disease Center; Sichuan University - Laboratory of Neurodegenerative Disorders

Ru-Wei Ou

Sichuan University - Laboratory of Neurodegenerative Disorders; Sichuan University - Rare Disease Center

Kuncheng Liu

Sichuan University - Laboratory of Neurodegenerative Disorders

Jun-Yu Lin

Sichuan University - Laboratory of Neurodegenerative Disorders

Tianmi Yang

Sichuan University - Rare Disease Center

Yi Xiao

Sichuan University - Rare Disease Center

Yongping Chen

Sichuan University - Rare Disease Center

Bi Zhao

Sichuan University - Laboratory of Neurodegenerative Disorders

Huifang Shang

Sichuan University - Laboratory of Neurodegenerative Disorders

More...

Abstract

Background: The predictive factors for disability in patients with multiple system atrophy (MSA) are unclear. We aimed to explore the predictive factors for disability in patients with MSA focusing on clinical features and blood biomarkers.

Methods: This prospective cohort study included patients diagnosed with MSA between January 2014 and December 2019. At the deadline of October 2021, patients met the diagnosis of probable MSA were included in the analysis. Random forest (RF) was used to establish a predictive model for disability. Accuracy, sensitivity, specificity, and area under the receiver operating characteristic curve (AUC) were used to evaluate the performance of the model.

Findings: Altogether, 100 patients with MSA including 49 with disability and 51 without disability were enrolled in the RF model. Baseline plasma neurofilament light chain (NFL) levels were higher in patients with disability than in those without disability ( P =0.037). According to the Gini index, the five major predictive factors were disease duration, age of onset, Unified MSA Rating Scale (UMSARS)-II score, NFL, and UMSARS-I score, followed by C-reactive protein (CRP) levels, neutrophil-to-lymphocyte ratio (NLR), UMSARS-IV score, symptom onset, orthostatic hypotension, sex, urinary incontinence, and diagnosis subtype. The sensitivity, specificity, accuracy, and AUC of the RF model were 70.82%, 74.55%, 72.29%, and 0.72, respectively.

Interpretation: Besides clinical features, baseline features including NFL, CRP, and NLR were potential predictive biomarkers of disability in MSA. These findings provide new insights into the trials regarding early intervention in MSA.

Funding: The present study was supported by the funding of 1.3.5 project for disciplines of excellence, West China Hospital, Sichuan University (Grant No. ZYJC18038), 1.3.5 project for disciplines of excellence–Clinical Research Incubation Project, West China Hospital, Sichuan University (Grant No. 2019HXFH016), and Sichuan Science and Technology Program (Grant No. 2022ZDZX0023).

Declaration of Interest: The authors declare that they have no competing interests.

Ethical Approval: Approval was obtained from the Ethics Committee of West China Hospital of Sichuan University. Informed consent was obtained from all participates.

Keywords: multiple system atrophy, disability, random forest, machine learning algorithm

Suggested Citation

Zhang, Lingyu and Hou, Yan-Bing and Gu, Xiaojing and Cao, Bei and Wei, Qianqian and Ou, Ru-Wei and Liu, Kuncheng and Lin, Jun-Yu and Yang, Tianmi and Xiao, Yi and Chen, Yongping and Zhao, Bi and Shang, Huifang, Prediction of Disability in Multiple System Atrophy Based on Machine Learning Algorithm: A Prospective Cohort Study. Available at SSRN: https://ssrn.com/abstract=4071373 or http://dx.doi.org/10.2139/ssrn.4071373

Lingyu Zhang

Sichuan University - Rare Disease Center ( email )

Sichuan University - Department of Neurology ( email )

Yan-Bing Hou

Sichuan University - Rare Disease Center ( email )

Chengdu, Sichuan
China

Sichuan University - Laboratory of Neurodegenerative Disorders ( email )

Xiaojing Gu

Sichuan University - Mental Health Center ( email )

Bei Cao

Sichuan University - Rare Disease Center ( email )

Qianqian Wei

Sichuan University - Rare Disease Center ( email )

Sichuan University - Laboratory of Neurodegenerative Disorders ( email )

Ru-Wei Ou

Sichuan University - Laboratory of Neurodegenerative Disorders ( email )

Sichuan University - Rare Disease Center ( email )

Chengdu, Sichuan
China

Kuncheng Liu

Sichuan University - Laboratory of Neurodegenerative Disorders ( email )

Jun-Yu Lin

Sichuan University - Laboratory of Neurodegenerative Disorders ( email )

Tianmi Yang

Sichuan University - Rare Disease Center ( email )

Yi Xiao

Sichuan University - Rare Disease Center ( email )

Yongping Chen

Sichuan University - Rare Disease Center ( email )

Bi Zhao

Sichuan University - Laboratory of Neurodegenerative Disorders ( email )

Huifang Shang (Contact Author)

Sichuan University - Laboratory of Neurodegenerative Disorders ( email )

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