Ghobadi Mojtaba, Heidari Mohammad Foad, Farhadi Arezoo, Shakerimoghaddam Ali, Ghorbani Mahdi, Hami Zahra, Ehtesham Naeim, Behroozi Javad
Cancer Epidemiology Research Center, Aja University of Medical Sciences, Tehran, Iran.
Department of Medical Laboratory Sciences, School of Allied Health Medicine, AJA Univers.
Bioimpacts. 2025 Apr 21;15:30795. doi: 10.34172/bi.30795. eCollection 2025.
Dementia is an umbrella term describing different types of diseases that lead to cognitive impairment and memory dysfunction, predominantly affecting older adults. The most common forms include Alzheimer's disease (AD), vascular dementia (VaD), dementia with Lewy bodies (DLB), and frontotemporal dementia (FTD). Despite extensive research, there is no definitive cure for dementia, primarily due to its complex and multifactorial nature, particularly the role of genetic abnormalities. Gene therapy, a novel therapeutic approach, aims to correct defective genes or introduce functional gene products by delivering specific DNA sequences to patients, and is often considered for individuals unresponsive to conventional treatments, such as those with dementia. Over the past decade, significant research has explored the potential of gene therapy in dementia, offering new hope for more effective treatments. However, several challenges remain in its practical application. One key challenge is developing safe and efficient gene delivery methods, as the brain's intricate structure and protective barriers present significant obstacles. Furthermore, ensuring the long-term expression and stability of therapeutic genes is crucial for sustained benefit. Future studies should focus on identifying genes implicated in different types of dementia, optimizing gene delivery systems, improving gene-targeting specificity, and conducting comprehensive clinical trials to assess the safety and efficacy of these therapies. Addressing these challenges could pave the way for novel treatment strategies, ultimately improving the quality of life for individuals with dementia.
痴呆症是一个概括性术语,描述导致认知障碍和记忆功能障碍的不同类型疾病,主要影响老年人。最常见的形式包括阿尔茨海默病(AD)、血管性痴呆(VaD)、路易体痴呆(DLB)和额颞叶痴呆(FTD)。尽管进行了广泛研究,但痴呆症尚无确切治愈方法,主要因其性质复杂且具有多因素性,尤其是基因异常的作用。基因治疗是一种新型治疗方法,旨在通过向患者递送特定DNA序列来纠正缺陷基因或引入功能性基因产物,常用于对传统治疗无反应的个体,如痴呆症患者。在过去十年中,大量研究探索了基因治疗在痴呆症中的潜力,为更有效的治疗带来了新希望。然而,其实际应用仍存在一些挑战。一个关键挑战是开发安全有效的基因递送方法,因为大脑复杂的结构和保护屏障构成了重大障碍。此外,确保治疗基因的长期表达和稳定性对于持续获益至关重要。未来研究应专注于识别与不同类型痴呆症相关的基因、优化基因递送系统、提高基因靶向特异性,并开展全面的临床试验以评估这些疗法的安全性和有效性。应对这些挑战可为新型治疗策略铺平道路,最终改善痴呆症患者的生活质量。