Evidence map›Paper›PMID 41606618›Full record

ArticleJournal of translational medicine2026

Cerebrospinal fluid dopamine 3-O-sulfate as a novel biomarker for predicting motor complications in Parkinson's disease: insights from the PPMI cohort.

Jieshan Chi, Rui Yang, Piao Zhang, Siming Rong, Mengfei Cai, Yuhu Zhang

Abstract read
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Article in Journal of translational medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Jieshan ChiDepartment of Neurology, Guangdong Neuroscience Institute, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Southern Medical University, No. 106 Zhongshan Er Road, Guangzhou, Guangdong Province, 510080, China.
Rui YangDepartment of Neurology, Guangdong Neuroscience Institute, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Southern Medical University, No. 106 Zhongshan Er Road, Guangzhou, Guangdong Province, 510080, China.
Piao ZhangDepartment of Neurology, Guangdong Neuroscience Institute, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Southern Medical University, No. 106 Zhongshan Er Road, Guangzhou, Guangdong Province, 510080, China.
Siming RongDepartment of Neurology, Guangdong Neuroscience Institute, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Southern Medical University, No. 106 Zhongshan Er Road, Guangzhou, Guangdong Province, 510080, China.
Mengfei CaiDepartment of Neurology, Guangdong Neuroscience Institute, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Southern Medical University, No. 106 Zhongshan Er Road, Guangzhou, Guangdong Province, 510080, China.
Yuhu ZhangDepartment of Neurology, Guangdong Neuroscience Institute, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Southern Medical University, No. 106 Zhongshan Er Road, Guangzhou, Guangdong Province, 510080, China. zhangyuhu@gdph.org.cn.ORCID 0000-0003-3492-4669

Funding

Leading Innovation Specialist Support Program of Guangdong Province No.0820250119National Natural Science Foundation of China No.82301420National Natural Science Foundation of China No.82301663Natural Science Foundation of Guangdong Province No.2025A1515010666State Key Laboratory of Neurology and Oncology Drug Development No. SKLSIM-20250174
6 · The paper itself

Abstract

backgroundLong-term levodopa treatment for Parkinson’s disease (PD) is often complicated by motor fluctuations and dyskinesia. Predictive biomarkers for these debilitating side effects are currently lacking, hindering personalized treatment.

objectivesThis study aimed to characterize the cerebrospinal fluid (CSF) metabolome across the PD continuum, distinguish disease-related from medication-related changes, and identify predictive biomarkers for levodopa-induced motor complications.

methodsWe analyzed targeted CSF metabolomic data from the Parkinson’s Progression Markers Initiative (PPMI) cohort, which included healthy controls, prodromal, and PD participants. Statistical analyses revealed differentially abundant metabolites. The association of the metabolite dopamine 3-O-sulfate (DA3S) with motor complications was assessed using logistic regression and decision tree models.

resultsDA3S was the most significantly altered metabolite in PD patients, with its elevation exclusively driven by levodopa treatment. DA3S levels were strongly correlated with levodopa exposure (LEDD) and demonstrated a significant independent association with the development of motor complications. A multivariable model combining DA3S, disease duration, and LEDD was used to predict motor complications, with an AUC of 0.806. A decision tree further confirmed the value of DA3S for risk stratification in specific patient subgroups.

conclusionsCSF DA3S is a pharmacodynamic marker of central levodopa metabolism and a robust, independent predictor of the onset of motor complications in PD patients. When combined with clinical variables, it facilitates effective risk stratification, providing a novel tool for personalizing therapy to mitigate treatment-related adverse effects.

Indexed as

DopamineMotor ActivityParkinson DiseaseAgedBiomarkersCohort StudiesFemaleHumansLevodopaMaleMiddle AgedMultivariate AnalysisBiomarkersDopamineLevodopaDopamine 3-O-sulfateLevodopaMetabolomicsMotor complicationsParkinson’s disease

Identifiers

PMID41606618
PMCPMC12895786

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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.