Xu Mengying, Li Tianjiao, Liu Xuan, Islam Binish, Xiang Yuyue, Zou Xiyan, Wang Jianwu
Xiangya School of Public Health, Central South University, Changsha, 410078, China.
Neurochem Res. 2024 Dec 14;50(1):61. doi: 10.1007/s11064-024-04311-9.
Mitochondrial dysfunction is well recognized as a critical component of the complicated pathogenesis of neurodegenerative diseases such as Alzheimer's disease, Parkinson's disease, and Huntington's disease. This review investigates the influence of mitochondrial DNA single nucleotide polymorphisms on mitochondrial function, as well as their role in the onset and progression of these neurodegenerative diseases. Furthermore, the contemporary approaches to mitochondrial regulation in these disorders are discussed. Our objective is to uncover early diagnostic targets and formulate precision medicine strategies for neurodegenerative diseases, thereby offering new paths for preventing and treating these conditions.
线粒体功能障碍是阿尔茨海默病、帕金森病和亨廷顿病等神经退行性疾病复杂发病机制的关键组成部分,这一点已得到广泛认可。本综述探讨了线粒体DNA单核苷酸多态性对线粒体功能的影响,以及它们在这些神经退行性疾病的发生和发展中的作用。此外,还讨论了针对这些疾病的线粒体调节的当代方法。我们的目标是发现神经退行性疾病的早期诊断靶点并制定精准医学策略,从而为预防和治疗这些疾病提供新途径。