Evidence map›Paper›PMID 41455880›Full record

ArticleBMC neurology2025

Integrative analysis of mRNA and LncRNA profiles from small extracellular vesicles identifies apoptosis-related biomarkers in patients with Parkinson's disease after rehabilitation.

Yixuan Wang, Yonghong Liu, Boyan Fang, Cui Liu, Keke Chen, Detao Meng, Zhaohui Jin

Abstract read
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Article in BMC neurology, 2025. 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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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

7 authors.

Yixuan Wang *Beijing Rehabilitation Hospital, Parkinson Medical Center, Capital Medical University, Beijing, China.
Yonghong Liu *Beijing Rehabilitation Hospital, Parkinson Medical Center, Capital Medical University, Beijing, China.
Boyan FangBeijing Rehabilitation Hospital, Parkinson Medical Center, Capital Medical University, Beijing, China.
Cui LiuBeijing Rehabilitation Hospital, Parkinson Medical Center, Capital Medical University, Beijing, China.
Keke ChenBeijing Rehabilitation Hospital, Parkinson Medical Center, Capital Medical University, Beijing, China.
Detao MengBeijing Rehabilitation Hospital, Parkinson Medical Center, Capital Medical University, Beijing, China.
Zhaohui JinBeijing Rehabilitation Hospital, Parkinson Medical Center, Capital Medical University, Beijing, China. bestvin2004010201@163.com.

Funding

The Science and Technology Development Fund of Beijing Rehabilitation Hospital, Capital Medical University 2019-023The Science and Technology Development Fund of Beijing Rehabilitation Hospital, Capital Medical University 2022R-001
6 · The paper itself

Abstract

backgroundIncreasing evidence has highlighted the crucial role of long noncoding RNAs (lncRNAs) and messenger RNAs (mRNAs) in the development and progression of Parkinson’s disease (PD). Investigating which lncRNA and mRNA biomarkers are associated with PD rehabilitation is valuable.

methodsSix patients with PD (PWP, Hoehn & Yahr stages 1.5–2.5) and age- and sex-matched healthy controls (HCs) were recruited. Total RNA was extracted from extracellular vesicles (EVs) from peripheral blood samples collected before and after 14 days of rehabilitation in the hospital. Differentially expressed mRNAs (DEmRNAs) and differentially expressed lncRNAs (DElncRNAs) were identified via next-generation sequencing (NGS), and a coexpression network was constructed.

resultsOverall, 3038 DEmRNAs (2337 upregulated/701 downregulated) and 1723 DElncRNAs (1278 upregulated/445 downregulated) were identified between prerehabilitation (prerehab) PWPs and HCs, whereas 3117 DEmRNAs (2490 upregulated/629 downregulated) and 1931 DElncRNAs (1561 upregulated/370 downregulated) were identified between postrehabilitation (postrehab) PWPs and HCs. Moreover, 1662 DEmRNAs (606 upregulated/1056 downregulated) and 1729 DElncRNAs (593 upregulated/1136 downregulated) were identified between prerehab PWPs and postrehab PWPs. Four DEmRNAs and 19 DElncRNAs were found in the blood EVs of both pre- and postrehab PWPs. GO and KEGG enrichment analyses revealed significant enrichment of the DEGs associated with the apoptotic process, mitogen-activated protein kinase (MAPK) signaling pathway, and Wnt signaling pathway. Coexpression network analysis revealed one DEmRNA (ENSG00000168646, AXIN2) and one positively related DElncRNA (ENST00000577329). The expression of the DEGs was validated in human samples via quantitative reverse transcription polymerase chain reaction (qRT‒PCR).

conclusionsThese findings suggest that the apoptotic pathway-related biomarker AXIN2 may be involved in PD rehabilitation, which should be further confirmed in clinical evaluations after PD rehabilitation.

Indexed as

ApoptosisExtracellular VesiclesParkinson DiseaseRNA, Long NoncodingRNA, MessengerAgedBiomarkersFemaleGene Expression ProfilingHumansMaleMiddle AgedBiomarkersRNA, Long NoncodingRNA, MessengerApoptotic pathwayAXIN2Extracellular vesicleLong noncoding RNAMessenger RNAParkinson's diseaseRehabilitation

Identifiers

PMID41455880
PMCPMC12860165

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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.