Evidence map›Paper›PMID 41360820›Full record

ArticleNPJ Parkinson's disease2025

Classifying the risk of cognitive impairment in Parkinson's disease using serum bile acid profiles and machine learning.

Tong Shen, Can Cui, Ruiqi Liu, Xin Yin, Jie Zu, Wei Zhang, Liguo Dong, Chuanying Xu, Hailong Lu, Guiyun Cui and 2 more

Abstract read
In one paragraph

Article in NPJ Parkinson's disease, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

12 authors.

Tong Shen *Department of Neurology, The Affiliated Hospital of Xuzhou Medical University, Xuzhou, Jiangsu Province, China.
Can Cui *Jiangsu Key Laboratory of Brain Disease and Bioinformation, Xuzhou Medical University, Xuzhou, China.
Ruiqi Liu *Department of Neurology and Cell Biology, School of Life Science, Xuzhou Medical University, Xuzhou, China.
Xin YinDepartment of Genetic Medicine, Xuzhou Maternity and Child Health Care Hospital Affiliated to Xuzhou Medical University, Xuzhou, Jiangsu, China.
Jie ZuDepartment of Neurology, The Affiliated Hospital of Xuzhou Medical University, Xuzhou, Jiangsu Province, China.
Wei ZhangDepartment of Neurology, The Affiliated Hospital of Xuzhou Medical University, Xuzhou, Jiangsu Province, China.
Liguo DongDepartment of Neurology, The Affiliated Hospital of Xuzhou Medical University, Xuzhou, Jiangsu Province, China.
Chuanying XuDepartment of Neurology, The Affiliated Hospital of Xuzhou Medical University, Xuzhou, Jiangsu Province, China.
Hailong LuDepartment of Neurology, The Affiliated Hospital of Xuzhou Medical University, Xuzhou, Jiangsu Province, China.
Guiyun CuiDepartment of Neurology, The Affiliated Hospital of Xuzhou Medical University, Xuzhou, Jiangsu Province, China. guiyuncui@foxmail.com.
Xuebin QuDepartment of Basic Medical Science, Jiangsu Medical College, Yancheng, Jiangsu, China. xuebinqu@jsmc.edu.cn.
Chu ZhangDepartment of Neurology and Cell Biology, School of Life Science, Xuzhou Medical University, Xuzhou, China. zhangchu@xzhmu.edu.cn.

Funding

Affiliated Hospital of Xuzhou Medical University 2021ZA24Construction Project of High Level Hospital of Jiangsu Province GSPSJ20240804Construction Project of High Level Hospital of Jiangsu Province LCZX202514Jiangsu Provincial Geriatric Health Research Project LKM2024016Jiangsu Provincial Health Commission Scientific Research Project ZQ2024018Science and Technology Project of Xuzhou Health Commission XWKYHT20230062
6 · The paper itself

Abstract

Cognitive impairment (CI) is a common and early non-motor manifestation of Parkinson's disease (PD), yet its biochemical basis remains poorly understood. Given the emerging link between bile acids (BAs) and neurodegeneration, we investigated whether serum BA profiles differ by cognitive status in PD and whether they can classify CI. A total of 363 participants were enrolled, including 63 healthy controls, 154 PD patients with normal cognition, and 146 with CI. Serum BA concentrations were quantified by ultra-performance liquid chromatography-tandem mass spectrometry, and multivariate as well as machine learning analyses were applied. Compared with cognitively normal PD patients, those with CI exhibited distinct BA alterations, characterized by elevated deoxycholic and cholic acids and reduced glyco- and tauro-conjugated species. Deoxycholic acid showed the strongest negative correlations with cognitive scores. Machine learning models based on combined BA profiles, particularly the random forest classifier, achieved robust discrimination between PD-CI and PD-NC groups (AUC up to 0.90). These findings indicate that BA dysregulation is closely linked to cognitive impairment in PD and may serve as a promising metabolic biomarker for early detection. Clinical trial number. Not applicable.

Identifiers

PMID41360820
PMCPMC12800191

What Socratic holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

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 Socratic graph.