Development of a Panel of Biomarkers for Differential Diagnosis of Multiple Sclerosis

Demyelinating diseases are a group of heterogeneous pathologies that affect the nervous system and reduce the quality of life. One of such diseases is multiple sclerosis (MS), an inflammatory autoimmune neurodegenerative disease of the central nervous system (CNS). At the initial stages, MS can mimic some infectious, neoplastic, genetic, metabolic, vascular, and other pathologies. Accurate differential diagnosis of this disease is important to improve the quality of life of patients and reduce possible irreversible damage to the central nervous system. In this work, we confirmed the possibility of using our previously proposed candidate panel of MS biomarkers to distinguish MS from neuromyelitis optica spectrum disorder (NMOSD) and amyotrophic lateral sclerosis (ALS). We have shown that our proposed panel (SPTAN1<sub>601-644</sub> + PRX<sub>451-494</sub> + PTK6<sub>301-344</sub> + LMP1<sub>285-330</sub>) allows us to distinguish MS from ALS (AUC = 0.796) and NMOSD (AUC = 0.779).

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Publication Details

Journal
Doklady Biochemistry and Biophysics
Published
2024-11-11
DOI
https://doi.org/10.1134/s160767292460060x
Primary Topic
Multiple Sclerosis Research Studies
Type
article
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article

Development of a Panel of Biomarkers for Differential Diagnosis of Multiple Sclerosis

Leyla A. Ovchinnikova, Yakov A. Lomakin, С. Н. Иллариошкин, М. Н. Захарова et al.
Doklady Biochemistry and Biophysics
Multiple Sclerosis Research Studies
article

Development of a Panel of Biomarkers for Differential Diagnosis of Multiple Sclerosis

Leyla A. Ovchinnikova, Yakov A. Lomakin, С. Н. Иллариошкин, М. Н. Захарова, Т. О. Simaniv, Samir S. Dzhelad, А. Г. Габибов
article en

Abstract

Demyelinating diseases are a group of heterogeneous pathologies that affect the nervous system and reduce the quality of life. One of such diseases is multiple sclerosis (MS), an inflammatory autoimmune neurodegenerative disease of the central nervous system (CNS). At the initial stages, MS can mimic some infectious, neoplastic, genetic, metabolic, vascular, and other pathologies. Accurate differential diagnosis of this disease is important to improve the quality of life of patients and reduce possible irreversible damage to the central nervous system. In this work, we confirmed the possibility of using our previously proposed candidate panel of MS biomarkers to distinguish MS from neuromyelitis optica spectrum disorder (NMOSD) and amyotrophic lateral sclerosis (ALS). We have shown that our proposed panel (SPTAN1<sub>601-644</sub> + PRX<sub>451-494</sub> + PTK6<sub>301-344</sub> + LMP1<sub>285-330</sub>) allows us to distinguish MS from ALS (AUC = 0.796) and NMOSD (AUC = 0.779).

Doklady Biochemistry and BiophysicsVol. 519(1)
Institute of Bioorganic Chemistry (RU), Moscow State University of Environmental Engineering (RU), Research Center of Neurology (RU)
Openalex Percentile: Top 68%
Multiple Sclerosis Research Studies
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