Evidence map›Paper›PMID 39915090›Full record

ArticleJournal of neurology, neurosurgery, and psychiatry2025

miRNA-214 to predict progression and survival in ALS.

Min-Young Noh, Min-Soo Kwon, Ki-Wook Oh, Minyeop Nahm, Jinseok Park, Hee Kyung Jin, Jae-Sung Bae, Bugyeong Son, Seung Hyun Kim

Abstract read
In one paragraph

Article in Journal of neurology, neurosurgery, and psychiatry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

  1. miR-214-3p and NCKAP1: A microglial functional dimension of Alzheimer's progression.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2026
    Article
  2. Article
  3. Extracellular RNAs as Messengers and Early Biomarkers in Neurodegeneration.International journal of molecular sciences · 2025
    Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Min-Young Noh *Department of Neurology, College of Medicine, Hanyang University, Seoul, South Korea.ORCID http://orcid.org/0000-0002-2746-0686
Min-Soo Kwon *Department of Pharmacology, Research Institute of Basic Medical Science, School of Medicine, CHA University, Pangyo, Gyeonggi-do, South Korea.
Ki-Wook OhDepartment of Neurology, College of Medicine, Hanyang University, Seoul, South Korea.ORCID http://orcid.org/0000-0001-6011-629X
Minyeop NahmDementia Research Group, Korea Brain Research Institute, Daegu, South Korea.
Jinseok ParkDepartment of Neurology, College of Medicine, Hanyang University, Seoul, South Korea.
Hee Kyung JinDepartment of Laboratory Animal Medicine, College of Veterinary Medicine, Kyungpook National University, Daegu, South Korea.
Jae-Sung BaeDepartment of Physiology, School of Medicine, Kyungpook National University, Daegu, South Korea.
Bugyeong SonCell Therapy Center, Hanyang University Medical Center, Seoul, South Korea.
Seung Hyun KimDepartment of Neurology, College of Medicine, Hanyang University, Seoul, South Korea kimsh1@hanyang.ac.kr.ORCID http://orcid.org/0000-0001-9644-9598

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundReliable biomarkers are essential for predicting the progression speed and prognosis of patients with amyotrophic lateral sclerosis (ALS). We previously identified NCK-associated protein 1 (NCKAP1) as a critical factor in the defective phagocytosis observed in induced microglia-like cells (iMGs) from patients with rapidly progressive sporadic ALS. This study explored the roles of microRNA (miRNA)-214, which targets the

methodsThe discovery cohort (n=29) was used to identify miR-214 targeting

resultsIn the discovery cohort, miR-214 levels were increased in plasma and iMGs from rapidly progressive ALS participants. This finding was validated in another cohort of 132 ALS participants and 30 age-matched healthy volunteers. Plasma miR-214 levels correlated with disease progression, severity and survival, distinguishing between rapidly progressive and slowly progressive ALS. In addition, miR-214 levels also correlated with plasma neurofilament light chain (NfL) and cerebrospinal fluid inflammatory cytokines, showing specific associations with increased NfL and monocyte chemoattractant protein 1 (MCP-1). Survival prediction accuracy improved when miR-214 levels were considered with NfL or MCP-1 levels.

conclusionsPlasma miRNA-214 could serve as a novel biomarker for predicting the progression and prognosis of ALS.

Indexed as

Amyotrophic Lateral SclerosisMicroRNAsAdaptor Proteins, Signal TransducingAdultAgedBiomarkersCohort StudiesCytokinesDisease ProgressionFemaleHumansMaleMicrogliaMiddle AgedNeurofilament ProteinsPrognosisAdaptor Proteins, Signal TransducingBiomarkersCytokinesMicroRNAsMIRN214 microRNA, humanneurofilament protein LNeurofilament ProteinsALSPersonal Satisfaction

Identifiers

PMID39915090
PMCPMC12322380

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Registered trials

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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.