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ABSTRACT: Background
Certain peripheral proteins are involved in the development of Neuromyelitis optica spectrum disorders (NMOSD), such as IL-6, complement proteins, and MHC class II molecules. However, the roles of other new protein biomarkers are unclear. Current NMOSD treatments (e.g., intravenous pulse methylprednisolone, or satralizumab for IL-6 receptor inhibition) can only manage symptoms, necessitating the identification of new drug targets to treat NMOSD. The objective of this study is to identify potential drug targets for NMOSD through Mendelian randomization (MR) analysis, thereby addressing the limitations of current treatments and providing better clinical options for patients.Methods
NMOSD potential drug targets were evaluated via MR. Data was obtained from a genome-
SUBMITTER: Meng H
PROVIDER: S-EPMC12083898 | biostudies-literature | 2025
REPOSITORIES: biostudies-literature