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DOI 10.1007/s11011-024-01368-x

Медицинская библиотека · Metabolic brain disease · 2024

Blood-based therapies to combat neurodegenerative diseases.

Lee Jia Yee, Lim Mervyn Chen Xi, Koh Rhun Yian, Tsen Min Tze, Chye Soi Moi

СтатьяОбзорПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

Neurodegeneration, known as the progressive loss of neurons in terms of their structure and function, is the principal pathophysiological change found in the majority of brain-related disorders. Ageing has been considered the most well-established risk factor in most common neurodegenerative diseases, such as Parkinson's disease (PD) and Alzheimer's disease (AD). There is currently no effective treatment or cure for these diseases; the approved therapeutic options to date are only for palliative care. Ageing and neurodegenerative diseases are closely intertwined; reversing the aspects of brain ageing could theoretically mitigate age-related neurodegeneration. Ever since the regenerative properties of young blood on aged tissues came to light, substantial efforts have been focused on identifying and characterizing the circulating factors in the young and old systemic milieu that may attenuate or accentuate brain ageing and neurodegeneration. Later studies discovered the superiority of old plasma dilution in tissue rejuvenation, which is achieved through a molecular reset of the systemic proteome. These findings supported the use of therapeutic blood exchange for the treatment of degenerative diseases in older individuals. The first objective of this article is to explore the rejuvenating properties of blood-based therapies in the ageing brains and their therapeutic effects on AD. Then, we also look into the clinical applications, various limitations, and challenges associated with blood-based therapies for AD patients.

Для цитирования: Lee Jia Yee, Lim Mervyn Chen Xi, Koh Rhun Yian, Tsen Min Tze, Chye Soi Moi. Blood-based therapies to combat neurodegenerative diseases.. Metabolic brain disease. 2024. DOI: 10.1007/s11011-024-01368-x.

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