Evidence map›Paper›PMID 42798606›Full record

ArticleFrontiers in aging neuroscience2026

MAFF as a potential novel protective factor against Parkinson's disease: evidence from Mendelian randomization and single-cell RNA sequencing.

Xinyao Li, Qiuyan Wang, Guowen Min, Xiaoli Yuan, Yuling Tian

Abstract read
In one paragraph

Article in Frontiers in aging neuroscience, 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

What it found

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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

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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

5 authors.

Xinyao LiDepartment of Neurology, The First Hospital of Shanxi Medical University, Taiyuan, China.
Qiuyan WangDepartment of Neurology, The First Hospital of Shanxi Medical University, Taiyuan, China.
Guowen MinDepartment of Neurology, The First Hospital of Shanxi Medical University, Taiyuan, China.
Xiaoli YuanDepartment of Neurology, The First Hospital of Shanxi Medical University, Taiyuan, China.
Yuling TianDepartment of Neurology, The First Hospital of Shanxi Medical University, Taiyuan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Parkinson's disease (PD) is the second most prevalent neurodegenerative disorder. Although MAFF may be involved in PD, the mechanisms underlying this association remain unclear. This study aimed to investigate the potential mechanisms of MAFF in PD and identify novel therapeutic targets. Methods: PD-related datasets were obtained from public databases. The potential mechanisms of MAFF in PD were investigated using comprehensive gene expression profiling, receiver operating characteristic (ROC) analysis, Mendelian randomization (MR), functional enrichment analysis, immune infiltration analysis, drug prediction, molecular docking, and single-cell RNA sequencing (scRNA-seq). RT-qPCR and ELISA were then used to further validate MAFF expression in PD. Results: MAFF was significantly upregulated in PD samples across multiple datasets and in both mouse and clinical samples. ELISA showed significantly increased MAFF expression in serum samples from patients with PD. The area under the curve (AUC) values for MAFF exceeded 0.70 in both datasets, indicating good diagnostic potential. MR analysis suggested a potential causal association between MAFF and PD (OR = 0.9075, 95% CI = 0.8243-0.9990, Conclusion: Overall, this study demonstrated that MAFF may play an important role in PD. These findings provide insights into the molecular mechanisms of PD and may support the development of targeted therapeutic strategies.

Indexed as

MAFFMendelian randomizationParkinson’s diseaseprotective factorsingle-cell RNA sequencing

Identifiers

PMID42798606
PMCPMC13612465

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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.