This analysis explores pathogenic mechanisms and therapeutic strategies in neurodegenerative diseases, suggesting potential for personalized treatments.
Neurodegenerative diseases are characterized by progressive and irreversible damage to the central nervous system, representing a major global health challenge. This article analyzes the pathogenesis, molecular mechanisms, and current therapeutic strategies for Alzheimer's disease and Parkinson's disease. In Alzheimer’s disease, key pathogenic factors include β-amyloid plaque accumulation, tau protein hyperphosphorylation, synaptic dysfunction, and neuroinflammation. In Parkinson’s disease, degeneration of nigrostriatal dopaminergic neurons, α-synuclein aggregation, and mitochondrial dysfunction are primary mechanisms. Recently, biomarkers (cerebrospinal fluid and plasma Aβ42, phosphorylated tau, neurofilament light chain, and α-synuclein) have gained importance for early diagnosis and disease monitoring. Current treatments go beyond symptomatic therapy and include disease-modifying approaches, such as monoclonal antibodies, neuroprotective strategies, and gene therapy. Gene therapy using adeno-associated viral (AAV) vectors to deliver neurotrophic factors or modulate pathological protein expression is considered a promising avenue. Analyses suggest that molecular biomarkers and gene-based therapies may play a key role in developing individualized treatment concepts in the future.
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Choriyev et al. (2026) studied this question.
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