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肌萎缩侧索硬化症的营养干预:从生酮饮食和神经保护营养素到微生物群-肠-脑轴调节

Nutritional Interventions in Amyotrophic Lateral Sclerosis: From Ketogenic Diet and Neuroprotective Nutrients to the Microbiota-Gut-Brain Axis Regulation.

作者信息

Nabakhteh Samira, Lotfi Anahita, Afsartaha Arman, Khodadadi Elaheh Sadat, Abdolghaderi Siavash, Mohammadpour Mozhdeh, Shokri Yasaman, Kiani Pouria, Ehtiati Sajad, Khakshournia Sara, Khatami Seyyed Hossein

机构信息

Department of Biochemistry, School of Basic Sciences, Tehran Medical Branch, Islamic Azad University, Tehran, Iran.

Department of Food Sciences and Industry, School of Agricultural Sciences and Natural Resources, Islamic Azad University, Khorasgan Branch, Isfahan, Iran.

出版信息

Mol Neurobiol. 2025 Mar 17. doi: 10.1007/s12035-025-04830-8.

Abstract

Amyotrophic lateral sclerosis (ALS) is a complex neurodegenerative disease with significant challenges in diagnosis and treatment. Recent research has highlighted the complex nature of ALS, encompassing behavioral impairments in addition to its neurological manifestations. While several medications have been approved to slow disease progression, ongoing research is focused on identifying new therapeutic targets. The current review focuses on emerging therapeutic strategies and personalized approaches aimed at improving patient outcomes. Recent advancements highlight the importance of targeting additional pathways such as mitochondrial dysfunction and neuroinflammation to develop more effective treatments. Personalized medicine, including genetic testing and biomarkers, is proving valuable in stratifying patients and tailoring treatment options. Complementary therapies, such as nutritional interventions like the ketogenic diet and microbiome modulation, also show promise. This review emphasizes the need for a multidisciplinary approach that integrates early diagnosis, targeted treatments, and supportive care to address the multisystemic nature of ALS and improve the quality of life for patients.

摘要

肌萎缩侧索硬化症(ALS)是一种复杂的神经退行性疾病,在诊断和治疗方面面临重大挑战。最近的研究突出了ALS的复杂性质,除了神经学表现外,还包括行为障碍。虽然已有几种药物被批准用于减缓疾病进展,但正在进行的研究集中在确定新的治疗靶点。本综述重点关注旨在改善患者预后的新兴治疗策略和个性化方法。最近的进展凸显了针对线粒体功能障碍和神经炎症等其他途径以开发更有效治疗方法的重要性。包括基因检测和生物标志物在内的个性化医疗在对患者进行分层和定制治疗方案方面正证明具有价值。补充疗法,如生酮饮食等营养干预措施和微生物群调节,也显示出前景。本综述强调需要采取多学科方法,将早期诊断、靶向治疗和支持性护理结合起来,以应对ALS的多系统性质并改善患者的生活质量。

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