Evidence map›Paper›PMID 42791197›Full record

ArticleAnnals of clinical and translational neurology2026

microRNA-7-5p and α-Synuclein SAA Predict Parkinson's Disease Phenoconversion.

Shayan Zadegan, Praveen Velammal, Kanmani Muthiah, Madhu Jatty, Christopher Adams

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Article in Annals of clinical and translational neurology, 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

5 authors.

Shayan ZadeganDepartment of Neurology, The University of Tennessee Health Science Center, Memphis, Tennessee, USA.
Praveen VelammalDepartment of Neurology, The University of Tennessee Health Science Center, Memphis, Tennessee, USA.
Kanmani MuthiahDepartment of Neurology, The University of Tennessee Health Science Center, Memphis, Tennessee, USA.
Madhu JattyDepartment of Neurology, The University of Tennessee Health Science Center, Memphis, Tennessee, USA.
Christopher AdamsDepartment of Neurology, The University of Tennessee Health Science Center, Memphis, Tennessee, USA.ORCID https://orcid.org/0000-0001-8847-2501

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveCorroborate blood neuron-derived extracellular vesicle (NDEV) alpha-synuclein (αSyn), the CSF αSyn seed amplification assay (αSyn-SAA), and blood microRNA-7-5p (miR-7-5p) as markers for Parkinson's disease (PD) phenoconversion and determine if combining these markers would help select subjects who would be more likely to phenoconvert.

methodsUsing Parkinson Progression Marker Initiative data, time to PD phenoconversion was determined by Hoehn and Yahr scores. Log-rank analysis was used to find cutpoints. Cox regression analysis was used with log[miR-7-5p], log[NDEV αSyn], and the αSyn-SAA. Models included age and sex.

resultsIn a Cox model with baseline log[miR-7-5p], for each unit increase in log[miR-7-5p], there was 1.57 times increased PD phenoconversion (p = 0.003). In a model with baseline log[NDEV αSyn], only baseline age was associated with increased phenoconversion (p < 0.05). Using Cox regression analysis, the cutpoints for miR-7-5p and NDEV αSyn were 27.39 reads per million mapped (p < 0.01) and 18.36 pg/mL (p = 0.01), respectively. In separate models using log[miR-7-5p] and log[NDEV αSyn] cutpoints, higher levels of log[miR-7-5p] and log[NDEV αSyn] resulted in 2.26 (p < 0.001) and 4.46 (p < 0.05) times increased PD phenoconversion, respectively. A positive αSyn-SAA was associated with 3.62 times increased phenoconversion (p < 0.001). Having log[miR-7-5p] higher than its cutpoint and a positive αSyn-SAA was associated with 4.31 times phenoconversion (p < 0.001).

interpretationBlood miR-7-5p, NDEV αSyn, and αSyn-SAA could be used to enrich for prodromal patients likely to develop PD earlier in disease-modifying clinical trials and combining them could further enrich for this population.

Indexed as

alpha‐synuclein seed amplification assaymicroRNA‐7‐5pneuron‐derived extracellular vesicle alpha‐synucleinParkinson's diseaseprodromal Parkinson's disease

Identifiers

PMID42791197
PMCPMC13614880

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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.