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Evaluating the causal association between microRNAs and amyotrophic lateral sclerosis.

Authors :
Zhu Y
Li M
He Z
Pang X
Du R
Yu W
Zhang J
Bai J
Wang J
Huang X
Source :
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology [Neurol Sci] 2023 Oct; Vol. 44 (10), pp. 3567-3575. Date of Electronic Publication: 2023 Jun 01.
Publication Year :
2023

Abstract

Background: Currently, miRNAs are involved in the development of amyotrophic lateral sclerosis (ALS), and identifying circulating miRNAs that are causally associated with ALS risk as biomarkers is imperative.<br />Methods: We performed a two-sample Mendelian randomization study to evaluate the causal relationship between miRNAs and ALS. Our analysis was conducted using summary statistics from miRNA expression quantitative loci (eQTL) data of the Framingham Heart Study and ALS genome-wide association studies data. Another independent miRNA data was used to further validate.<br />Results: We identified eight unique miRNAs that were causally associated with ALS risk. Using expression data of miRNAs from an independent study, we validated three high-confidence miRNAs, namely hsa-miR-27b-3p, hsa-miR-139-5p, and hsa-miR-152-3p, which might have a potential causal effect on ALS risk.<br />Conclusion: We suggested that higher levels of hsa-miR-27b-3p and hsa-miR-139-5p had protective effects on ALS, whereas higher levels of hsa-miR-152-3p might act as a risk factor for ALS. The analytical framework presented in this study helps to understand the role of miRNAs in the development of ALS and to identify the biomarkers for ALS risk.<br /> (© 2023. Fondazione Società Italiana di Neurologia.)

Details

Language :
English
ISSN :
1590-3478
Volume :
44
Issue :
10
Database :
MEDLINE
Journal :
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Publication Type :
Academic Journal
Accession number :
37261630
Full Text :
https://doi.org/10.1007/s10072-023-06860-3