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Abstract
Mitochondrial dysfunction linked to Down syndrome is characterized by energy metabolism disruption and increased oxidative stress.
- Down syndrome is caused by having an extra copy of chromosome 21, which is associated with neurodevelopmental challenges and early-onset Alzheimer's disease.
- Mitochondrial imbalance in Down syndrome is marked by disrupted energy production, heightened oxidative stress, and impaired cellular maintenance processes.
- These mitochondrial abnormalities contribute to increased vulnerability of neurons, leading to cognitive decline and neurodegeneration.
- The review examines how genes located on chromosome 21 may influence mitochondrial dysfunction in individuals with Down syndrome.
- Interactions between mitochondrial dysfunction, oxidative stress, and cellular aging processes may accelerate Alzheimer's-like brain aging in this population.
- Emerging therapies aimed at targeting mitochondrial pathways could potentially reduce neurodegeneration and improve health outcomes in individuals with Down syndrome.
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