Evidence map›Paper›PMID 35082326›Full record

SynthesisScientific reports2022

Identification of let-7f and miR-338 as plasma-based biomarkers for sporadic amyotrophic lateral sclerosis using meta-analysis and empirical validation.

Narges Daneshafrooz, Mohammad Taghi Joghataei, Mehdi Mehdizadeh, Afagh Alavi, Mahmood Barati, Bahman Panahi, Shahram Teimourian, Babak Zamani

Open access · goldAbstract readMeta-AnalysisSystematic Review
In one paragraph

Synthesis in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
3.7field-weighted citation impact, top 6% of its field
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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 30 citations in OpenAlex.

  1. Pooled it
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  5. IsomiR Utility in Amyotrophic Lateral Sclerosis Prognostication.medRxiv : the preprint server for health sciences · 2025
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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

8 authors at 5 institutions in 1 country.

Narges DaneshafroozCellular and Molecular Research Center, Department of Neuroscience, Faculty of Advanced Technologies in Medicine, Iran University of Medical Science, Tehran, Iran.
Mohammad Taghi JoghataeiCellular and Molecular Research Center, Department of Neuroscience, Faculty of Advanced Technologies in Medicine, Iran University of Medical Science, Tehran, Iran.
Mehdi MehdizadehReproductive Sciences and Technology Research Center, Department of Anatomy, School of Medicine, Iran University of Medical Science, Tehran, Iran.
Afagh AlaviGenetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
Mahmood BaratiDepartment of Medical Biotechnology, Faculty of Allied Medicine, Iran University of Medical Science, Tehran, Iran.
Bahman PanahiDepartment of Genomics, Branch for Northwest & West Region, Agricultural Biotechnology Research Institute of Iran (ABRII), Agricultural Research, Education and Extension Organization (AREEO), Tabriz, Iran.
Shahram TeimourianDepartment of Medical Genetics, School of Medicine, Iran University of Medical Science, Tehran, Iran.
Babak ZamaniDepartment of Neurology, Firoozgar Hospital, School of Medicine, Iran University of Medical Science, Tehran, Iran. zamaniba3@gmail.com.
Iran University of Medical Sciences · IRAgricultural Research & Education Organization · IRFiroozgar General Hospital · IRIran University of Science and Technology · IRUniversity of Social Welfare and Rehabilitation Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Amyotrophic lateral sclerosis (ALS) is a lethal neurodegenerative disease that in most cases occurs sporadic (sALS). The disease is not curable, and its pathogenesis mechanisms are not well understood yet. Given the intricacy of underlying molecular interactions and heterogeneity of ALS, the discovery of molecules contributing to disease onset and progression will open a new avenue for advancement in early diagnosis and therapeutic intervention. Here we conducted a meta-analysis of 12 circulating miRNA profiling studies using the robust rank aggregation (RRA) method, followed by enrichment analysis and experimental verification. We identified miR-451a and let-7f-5p as meta-signature miRNAs whose targets are involved in critical pathogenic pathways underlying ALS, including 'FoxO signaling pathway', 'MAPK signaling pathway', and 'apoptosis'. A systematic review of 7 circulating gene profiling studies elucidated that 241 genes up-regulated in sALS circulation with concomitant being targets of the meta-signature miRNAs. Protein-protein interaction (PPI) network analysis of the candidate targets using MCODE algorithm revealed the main subcluster is involved in multiple cascades eventually leads apoptosis, including 'positive regulation of neuron apoptosis. Besides, we validated the meta-analysis results using RT-qPCR. Indeed, relative expression analysis verified let-7f-5p and miR-338-3p as significantly down-regulated and up-regulated biomarkers in the plasma of sALS patients, respectively. Receiver operating characteristic (ROC) analysis also highlighted the let-7f-5p and miR-338-3p potential as robustness plasma biomarkers for diagnosis and potential therapeutic targets of sALS disease.

Indexed as

AlgorithmsAmyotrophic Lateral SclerosisBiomarkersCirculating MicroRNADown-RegulationEmpirical ResearchGene Expression ProfilingHigh-Throughput Nucleotide SequencingHumansMicroRNAsProtein Interaction MapsReal-Time Polymerase Chain ReactionReverse Transcriptase Polymerase Chain ReactionROC CurveTranscriptomeUp-RegulationBiomarkersCirculating MicroRNAMicroRNAsMIRN338 microRNA, human

Identifiers

PMID35082326
PMCPMC8791978
OpenAlexW4210475373

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.