Benatar, M., Wuu, J., Andersen, P. M., Lombardi, V., & Malaspina, A. (2018). Neurofilament light: A candidate biomarker of presymptomatic amyotrophic lateral sclerosis and phenoconversion. Annals of Neurology, 84(1), 130–139. https://doi.org/10.1002/ana.25276
Article CAS PubMed Google Scholar
Ceccanti, M., Pozzilli, V., Cambieri, C., Libonati, L., Onesti, E., Frasca, V., Fiorini, I., Petrucci, A., Garibaldi, M., Palma, E., Bendotti, C., Fabbrizio, P., Trolese, M. C., Nardo, G., & Inghilleri, M. (2020). Creatine kinase and progression rate in amyotrophic lateral sclerosis. Cells, 9(5), 1174. https://doi.org/10.3390/cells9051174
Article CAS PubMed PubMed Central Google Scholar
Cheng, Y., Chen, Y., & Shang, H. (2021). Aberrations of biochemical indicators in amyotrophic lateral sclerosis: A systematic review and meta-analysis. Translational Neurodegeneration, 10(1), 3. https://doi.org/10.1186/s40035-020-00228-9
Article CAS PubMed PubMed Central Google Scholar
Chio, A., Logroscino, G., Hardiman, O., Swingler, R., Mitchell, D., Beghi, E., Traynor, B. G., Eurals Consortium. (2009). Prognostic factors in ALS: A critical review. Amyotrophic Lateral Sclerosis: Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases, 10(5–6), 310–323. https://doi.org/10.3109/17482960802566824
Cohen, T. J., Waddell, D. S., Barrientos, T., Lu, Z., Feng, G., Cox, G. A., Bodine, S. C., & Yao, T.-P. (2007). The histone deacetylase HDAC4 connects neural activity to muscle transcriptional reprogramming. The Journal of Biological Chemistry, 282(46), 33752–33759. https://doi.org/10.1074/jbc.M706268200
Article CAS PubMed Google Scholar
de Andrade, H. M. T., de Albuquerque, M., Avansini, S. H., Rocha, Cd. S., Dogini, D. B., Nucci, A., Carvalho, B., Lopes-Cendes, I., & França, M. C. (2016). MicroRNAs-424 and 206 are potential prognostic markers in spinal onset amyotrophic lateral sclerosis. Journal of the Neurological Sciences, 368, 19–24. https://doi.org/10.1016/j.jns.2016.06.046
Article CAS PubMed Google Scholar
De Schaepdryver, M., Jeromin, A., Gille, B., Claeys, K. G., Herbst, V., Brix, B., Van Damme, P., & Poesen, K. (2018). Comparison of elevated phosphorylated neurofilament heavy chains in serum and cerebrospinal fluid of patients with amyotrophic lateral sclerosis. Journal of Neurology, Neurosurgery, and Psychiatry, 89(4), 367–373. https://doi.org/10.1136/jnnp-2017-316605
Dobrowolny, G., Martone, J., Lepore, E., Casola, I., Petrucci, A., Inghilleri, M., Morlando, M., Colantoni, A., Scicchitano, B. M., Calvo, A., Bisogni, G., Chiò, A., Sabatelli, M., Bozzoni, I., & Musarò, A. (2021). A longitudinal study defined circulating microRNAs as reliable biomarkers for disease prognosis and progression in ALS human patients. Cell Death Discovery, 7(1), 4. https://doi.org/10.1038/s41420-020-00397-6
Article CAS PubMed PubMed Central Google Scholar
Elia, A. E., Lalli, S., Monsurrò, M. R., Sagnelli, A., Taiello, A. C., Reggiori, B., La Bella, V., Tedeschi, G., & Albanese, A. (2016). Tauroursodeoxycholic acid in the treatment of patients with amyotrophic lateral sclerosis. European Journal of Neurology, 23(1), 45–52. https://doi.org/10.1111/ene.12664
Article CAS PubMed Google Scholar
Feneberg, E., Oeckl, P., Steinacker, P., Verde, F., Barro, C., Van Damme, P., Gray, E., Grosskreutz, J., Jardel, C., Kuhle, J., & Koerner, S. (2018). Multicenter evaluation of neurofilaments in early symptom onset amyotrophic lateral sclerosis. Neurology, 90(1), e22–e30. https://doi.org/10.1212/WNL.0000000000004761
Article CAS PubMed Google Scholar
Filipowicz, W., Jaskiewicz, L., Kolb, F. A., & Pillai, R. S. (2005). Post-transcriptional gene silencing by siRNAs and miRNAs. Current Opinion in Structural Biology, 15(3), 331–341. https://doi.org/10.1016/j.sbi.2005.05.006
Article CAS PubMed Google Scholar
Gille, B., De Schaepdryver, M., Goossens, J., Dedeene, L., De Vocht, J., Oldoni, E., Goris, A., Van Den Bosch, L., Depreitere, B., Claeys, K. G., Tournoy, J., Van Damme, P., & Poesen, K. (2019). Serum neurofilament light chain levels as a marker of upper motor neuron degeneration in patients with amyotrophic lateral sclerosis. Neuropathology and Applied Neurobiology, 45(3), 291–304. https://doi.org/10.1111/nan.12511
Article CAS PubMed Google Scholar
Guo, Q.-F., Hu, W., Xu, L.-Q., Luo, H., Wang, N., & Zhang, Q.-J. (2021). Decreased serum creatinine levels predict short survival in amyotrophic lateral sclerosis. Annals of Clinical and Translational Neurology, 8(2), 448–455. https://doi.org/10.1002/acn3.51299
Article CAS PubMed PubMed Central Google Scholar
Kovanda, A., Leonardis, L., Zidar, J., Koritnik, B., Dolenc-Groselj, L., Kovacic, S. R., Curk, T., & Rogelj, B. (2018). Differential expression of microRNAs and other small RNAs in muscle tissue of patients with ALS and healthy age-matched controls. Scientific Reports, 8(1), 5609. https://doi.org/10.1038/s41598-018-23139-2
Article ADS CAS PubMed PubMed Central Google Scholar
Li, S., Ren, Y., Zhu, W., Yang, F., Zhang, X., & Huang, X. (2016). Phosphorylated neurofilament heavy chain levels in paired plasma and CSF of amyotrophic lateral sclerosis. Journal of the Neurological Sciences, 367, 269–274. https://doi.org/10.1016/j.jns.2016.05.062
Article CAS PubMed Google Scholar
Li, X., Wang, H., Liu, Z., & Abudureyimu, A. (2021). CircSETD3 (Hsa_circ_0000567) suppresses hepatoblastoma pathogenesis via targeting the miR-423-3p/Bcl-2-interacting mediator of cell death axis. Frontiers in Genetics, 12, 724197. https://doi.org/10.3389/fgene.2021.724197
Article CAS PubMed PubMed Central Google Scholar
Livak, K. J., & Schmittgen, T. D. (2001). Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) method. Methods (san Diego, Calif.), 25(4), 402–408. https://doi.org/10.1006/meth.2001.1262
Article CAS PubMed Google Scholar
Lu, C.-H., Macdonald-Wallis, C., Gray, E., Pearce, N., Petzold, A., Norgren, N., Giovannoni, G., Fratta, P., Sidle, K., Fish, M., Orrell, R., Howard, R., Talbot, K., Greensmith, L., Kuhle, J., Turner, M. R., & Malaspina, A. (2015). Neurofilament light chain: A prognostic biomarker in amyotrophic lateral sclerosis. Neurology, 84(22), 2247–2257. https://doi.org/10.1212/WNL.0000000000001642
Article CAS PubMed PubMed Central Google Scholar
Maia, L. F., Maceski, A., Conceição, I., Obici, L., Magalhães, R., Cortese, A., Leppert, D., Merlini, G., Kuhle, J., & Saraiva, M. J. (2020). Plasma neurofilament light chain: An early biomarker for hereditary ATTR amyloid polyneuropathy. Amyloid: the International Journal of Experimental and Clinical Investigation: the Official Journal of the International Society of Amyloidosis, 27(2), 97–102. https://doi.org/10.1080/13506129.2019.1708716
Article CAS PubMed Google Scholar
Matus, S., Lopez, E., Valenzuela, V., Nassif, M., & Hetz, C. (2013). Functional contribution of the transcription factor ATF4 to the pathogenesis of amyotrophic lateral sclerosis. PLoS ONE, 8(7), e66672. https://doi.org/10.1371/journal.pone.0066672
Article ADS CAS PubMed PubMed Central Google Scholar
Petzold, A. (2005). Neurofilament phosphoforms: Surrogate markers for axonal injury, degeneration and loss. Journal of the Neurological Sciences, 233(1–2), 183–198. https://doi.org/10.1016/j.jns.2005.03.015
Article CAS PubMed Google Scholar
Poesen, K., De Schaepdryver, M., Stubendorff, B., Gille, B., Muckova, P., Wendler, S., Prell, T., Ringer, T. M., Rhode, H., Stevens, O., Claeys, K. G., Couwelier, G., D’Hondt, A., Lamaire, N., Tilkin, P., Van Reijen, D., Gourmaud, S., Fedtke, N., Heiling, B., … Van Damme, P. (2017). Neurofilament markers for ALS correlate with extent of upper and lower motor neuron disease. Neurology, 88(24), 2302–2309. https://doi.org/10.1212/WNL.0000000000004029
Article CAS PubMed Google Scholar
Pun, S., Santos, A. F., Saxena, S., Xu, L., & Caroni, P. (2006). Selective vulnerability and pruning of phasic motoneuron axons in motoneuron disease alleviated by CNTF. Nature Neuroscience, 9(3), 408–419. https://doi.org/10.1038/nn1653
Article CAS PubMed Google Scholar
Quinlan, S., Kenny, A., Medina, M., Engel, T., & Jimenez-Mateos, E. M. (2017). MicroRNAs in neurodegenerative diseases. International Review of Cell and Molecular Biology, 334, 309–343. https://doi.org/10.1016/bs.ircmb.2017.04.002
Article CAS PubMed Google Scholar
Rafiq, M. K., Lee, E., Bradburn, M., McDermott, C. J., & Shaw, P. J. (2016). Creatine kinase enzyme level correlates positively with serum creatinine and lean body mass, and is a prognostic factor for survival in amyotrophic lateral sclerosis. European Journal of Neurology, 23(6), 1071–1078. https://doi.org/10.1111/ene.12995
Article CAS PubMed Google Scholar
Romano, A., Primiano, G., Antonini, G., Ceccanti, M., Fenu, S., Forcina, F., Gentile, L., Inghilleri, M., Leonardi, L., Manganelli, F., & Obici, L. (2024). Serum neurofilament light chain: a promising early diagnostic biomarker for hereditary transthyretin amyloidosis? European Journal of Neurology, 31(1), e16070. https://doi.org/10.1111/ene.16070
Rowland, L. P., & Shneider, N. A. (2001). Amyotrophic lateral sclerosis. The New England Journal of Medicine, 344(22), 1688–1700. https://doi.org/10.1056/NEJM200105313442207
Article CAS PubMed Google Scholar
Saliminejad, K., KhorramKhorshid, H. R., SoleymaniFard, S., & Ghaffari, S. H. (2019). An overview of microRNAs: Biology, functions, therapeutics, and analysis methods. Journal of Cellular Physiology, 234(5), 5451–5465. https://doi.org/10.1002/jcp.27486
Article CAS PubMed Google Scholar
Shefner, J., Heiman-Patterson, T., Pioro, E. P., Wiedau-Pazos, M., Liu, S., Zhang, J., Agnese, W., & Apple, S. (2020). Long-term edaravone efficacy in amyotrophic lateral sclerosis: Post-hoc analyses of Study 19 (MCI186-19). Muscle & Nerve, 61(2), 218–221. https://doi.org/10.1002/mus.26740
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