Department of Neurochemistry, Inge Grundke-Iqbal Research Floor, New York State Institute for Basic Research in Developmental Disabilities, Staten Island, NY, USA.
J Alzheimers Dis. 2018;64(s1):S107-S117. doi: 10.3233/JAD-179921.
The amyloid cascade hypothesis has been dominating drug discovery for Alzheimer's disease (AD) for the last two decades. The failure of the development of effective drugs for slowing down or reversing the progression of AD warrants the AD field to consider out-of-the-box thinking and therapeutic approaches. We propose the multifactorial hypothesis of AD, emphasizing that AD is caused by multiple etiological factors, which may result in common brain pathology and functional consequences through several separate but integrated molecular pathways. More than one etiological factor and mechanistic pathway may be involved in a single individual with sporadic AD, and different individuals may have different etiological factors, involving different mechanisms/pathways. We urge the recognition of the multifactorial nature of AD and the paradigm shift of AD drug development from a single target to multiple targets, either with the multitarget-directed ligands approach or the cocktail therapy approach. We believe that patient stratification and the use of the precision medicine model will also benefit AD drug discovery.
淀粉样蛋白级联假说主导了过去二十年中阿尔茨海默病(AD)的药物研发。开发出有效药物来减缓或逆转 AD 的进展的失败,使得 AD 领域需要考虑非常规的思维和治疗方法。我们提出 AD 的多因素假说,强调 AD 是由多种病因引起的,这些病因可能通过几个独立但又相互关联的分子途径导致共同的大脑病理和功能后果。在单个散发 AD 患者中,可能涉及不止一个病因因素和机制途径,不同的个体可能具有不同的病因因素,涉及不同的机制/途径。我们敦促人们认识到 AD 的多因素性质,并将 AD 药物研发的范式从单一靶点转变为多个靶点,无论是采用多靶点定向配体方法还是鸡尾酒疗法。我们相信,患者分层和使用精准医学模型也将有益于 AD 药物的发现。