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. 2021 Nov;24(11):1534-1541.
doi: 10.1038/s41593-021-00936-z. Epub 2021 Oct 28.

Circulating miR-181 is a prognostic biomarker for amyotrophic lateral sclerosis

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Circulating miR-181 is a prognostic biomarker for amyotrophic lateral sclerosis

Iddo Magen et al. Nat Neurosci. 2021 Nov.

Abstract

Amyotrophic lateral sclerosis (ALS) is a relentless neurodegenerative disease of the human motor neuron system, where variability in progression rate limits clinical trial efficacy. Therefore, better prognostication will facilitate therapeutic progress. In this study, we investigated the potential of plasma cell-free microRNAs (miRNAs) as ALS prognostication biomarkers in 252 patients with detailed clinical phenotyping. First, we identified, in a longitudinal cohort, miRNAs whose plasma levels remain stable over the course of disease. Next, we showed that high levels of miR-181, a miRNA enriched in neurons, predicts a greater than two-fold risk of death in independent discovery and replication cohorts (126 and 122 patients, respectively). miR-181 performance is similar to neurofilament light chain (NfL), and when combined together, miR-181 + NfL establish a novel RNA-protein biomarker pair with superior prognostication capacity. Therefore, plasma miR-181 alone and a novel miRNA-protein biomarker approach, based on miR-181 + NfL, boost precision of patient stratification. miR-181-based ALS biomarkers encourage additional validation and might enhance the power of clinical trials.

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References

    1. Munsat, T. L., Andres, P. L., Finison, L., Conlon, T. & Thibodeau, L. The natural history of motoneuron loss in amyotrophic lateral sclerosis. Neurology 38, 409–413 (1988). - PubMed - DOI
    1. Ravits, J. M. & La Spada, A. R. ALS motor phenotype heterogeneity, focality, and spread: deconstructing motor neuron degeneration. Neurology 73, 805–811 (2009). - PubMed - PMC - DOI
    1. Benatar, M. et al. ALS biomarkers for therapy development: state of the field and future directions. Muscle Nerve 53, 169–182 (2016). - PubMed - DOI
    1. Chipika, R. H., Finegan, E., Li Hi Shing, S., Hardiman, O. & Bede, P. Tracking a fast-moving disease: longitudinal markers, monitoring, and clinical trial endpoints in ALS. Front. Neurol. 10, 229 (2019). - PubMed - PMC - DOI
    1. Verber, N. S. et al. Biomarkers in motor neuron disease: a state of the art review. Front. Neurol. 10, 291 (2019). - PubMed - PMC - DOI

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