Neurosurgery Research Group (NRG), Student Research Committee, Hamadan University of Medical Sciences, Hamadan, Iran.
NeuroImaging Network (NIN), Universal Scientific Education and Research Network (USERN), Tehran, Iran.
J Alzheimers Dis. 2022;87(4):1433-1449. doi: 10.3233/JAD-215680.
Alzheimer's disease (AD) is the most common cause of dementia globally. There is increasing evidence showing AD has no single pathogenic mechanism, and thus treatment approaches focusing only on one mechanism are unlikely to be meaningfully effective. With only one potentially disease modifying treatment approved, targeting amyloid-β (Aβ), AD is underserved regarding effective drug treatments. Combining multiple drugs or designing treatments that target multiple pathways could be an effective therapeutic approach. Considering the distinction between added and combination therapies, one can conclude that most trials fall under the category of added therapies. For combination therapy to have an actual impact on the course of AD, it is likely necessary to target multiple mechanisms including but not limited to Aβ and tau pathology. Several challenges have to be addressed regarding combination therapy, including choosing the correct agents, the best time and stage of AD to intervene, designing and providing proper protocols for clinical trials. This can be achieved by a cooperation between the pharmaceutical industry, academia, private research centers, philanthropic institutions, and the regulatory bodies. Based on all the available information, the success of combination therapy to tackle complicated disorders such as cancer, and the blueprint already laid out on how to implement combination therapy and overcome its challenges, an argument can be made that the field has to move cautiously but quickly toward designing new clinical trials, further exploring the pathological mechanisms of AD, and re-examining the previous studies with combination therapies so that effective treatments for AD may be finally found.
阿尔茨海默病(AD)是全球最常见的痴呆症病因。越来越多的证据表明,AD 不存在单一的发病机制,因此仅针对一种机制的治疗方法不太可能产生有意义的效果。由于只有一种潜在的疾病修饰治疗方法(针对淀粉样蛋白-β[Aβ])获得批准,AD 在有效的药物治疗方面还远远不够。联合使用多种药物或设计针对多种途径的治疗方法可能是一种有效的治疗方法。考虑到附加治疗和联合治疗之间的区别,可以得出结论,大多数试验都属于附加治疗类别。为了使联合治疗对 AD 的病程产生实际影响,很可能需要针对多种机制进行治疗,包括但不限于 Aβ 和 tau 病理学。关于联合治疗,需要解决几个挑战,包括选择正确的药物、在 AD 的最佳时间和阶段进行干预、设计和提供临床试验的适当方案。这可以通过制药行业、学术界、私人研究中心、慈善机构和监管机构之间的合作来实现。基于所有可用信息,联合治疗在攻克癌症等复杂疾病方面的成功,以及已经制定的实施联合治疗和克服其挑战的蓝图,可以认为该领域必须谨慎但迅速地设计新的临床试验,进一步探索 AD 的病理机制,并重新检查以前的联合治疗研究,以便最终找到 AD 的有效治疗方法。