Evidence map›Paper›PMID 41498878›Full record

ArticleJournal of molecular neuroscience : MN2026

Mendelian Randomization Analysis of the Brain, Cerebrospinal Fluid, and Plasma Proteome Identifies a Potential Peripheral Biomarker for Isolated REM Sleep Behavior Disorder.

Hong Ye, Zhenzhen Liu, Yajing Huang, Na Xu, Chaoya Jiang, Qiuhan Xu, Xuxia Zhou

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Article in Journal of molecular neuroscience : MN, 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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5 · Who and what money

Authors and funding

7 authors.

Hong Ye *Xiangshan Hospital of TCM Medical and Health Group, Ningbo City, Zhejiang Province, China. yehong1354861@163.com.
Zhenzhen Liu *Department of Obstetrics and Gynecology, Tongji Hospital Affiliated to Tongji University, Putuo District, Shanghai, China.
Yajing Huang *Department of Obstetrics and Gynecology, Tongji Hospital Affiliated to Tongji University, Putuo District, Shanghai, China.
Na XuXiangshan Hospital of TCM Medical and Health Group, Ningbo City, Zhejiang Province, China.
Chaoya JiangDepartment of Gastroenterology, Affliated Xiangshan Hospital of Wenzhou Medical University, Ningbo, Zhejiang, China.
Qiuhan XuDepartment of Neurosurgey, the First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China. xuqiuhan@zju.edu.cn.
Xuxia ZhouXiangshan Hospital of TCM Medical and Health Group, Ningbo City, Zhejiang Province, China. xszyy2006@126.com.

Funding

Zhejiang Provincial Traditional Chinese Medicine Science and Technology Program No. 2024ZL986
6 · The paper itself

Abstract

backgroundIsolated REM sleep behavior disorder (iRBD) is among the strongest clinical markers of prodromal α-synucleinopathies. Pinpointing causal proteins may open the door to early diagnosis and disease-modifying therapies.

methodsWe performed a proteome-wide Mendelian randomization (MR) using protein QTLs from brain, cerebrospinal fluid, and plasma, with GWAS data from 1,061 iRBD cases and 8,386 controls. The findings were validated in an independent cohort of 35,559 individuals from Iceland, utilizing plasma proteome data. To assess the directionality and robustness of the association, we additionally performed Steiger filtering and Bayesian colocalization analyses. PheWAS was applied to explore pleiotropy and safety.

resultsAmong hundreds of proteins screened, only plasma SPOCK3 (SPARC/Osteonectin, Cwcv and Kazal-like Domains Proteoglycan 3) showed a significant causal link to iRBD (OR = 2.07, 95% CI = 1.50-2.84, P = 7.45 × 10⁻⁶). No brain or CSF proteins met significance. In the independent cohort, MR confirmed the association between SPOCK3 and iRBD risk (OR = 1.39, 95% CI: 1.03-1.88, P = 0.029). Steiger filtering supported the inferred causal direction (P < 0.05), and colocalization analysis revealed a high posterior probability of a shared causal variant between SPOCK3 levels and iRBD risk (PPH4 = 0.96). PheWAS revealed no major off-target associations.

conclusionsPlasma SPOCK3 emerges as a candidate peripheral biomarker for iRBD. While Mendelian randomization supports a potential causal association, the underlying mechanisms-such as extracellular matrix involvement-require further experimental validation.

Indexed as

BrainProteoglycansProteomeREM Sleep Behavior DisorderBiomarkersHumansMaleMendelian Randomization AnalysisBiomarkersProteoglycansProteomeIsolated REM sleep behavior disorderMendelian randomizationPlasma biomarkerSPOCK3

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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.