Island Medical Program, University of British Columbia, Victoria, BC, Canada.
Division of Medical Sciences, University of Victoria, Victoria, BC, Canada.
Neurosci Biobehav Rev. 2019 Jul;102:56-84. doi: 10.1016/j.neubiorev.2019.04.002. Epub 2019 Apr 15.
Major depressive disorder (MDD) is a highly prevalent psychiatric disorder and a major cause of disability worldwide. This neurological condition is commonly associated with neurodegenerative diseases such as Alzheimer's disease (AD), Parkinson's disease (PD) and Huntington's disease (HD), and has a significant impact on the increasing burden of these neuropathologies. Over the past decades, some of the pathophysiological and molecular mechanisms that contribute to these diseases have been elucidated and these findings indicate that, despite presenting distinct features, there are several similarities between the neurobiological alterations that lead to MDD and neurodegeneration in AD, PD, and HD. For instance, disturbances in monoaminergic transmission and the hypothalamic-pituitary-adrenal (HPA) axis, increased oxidative and neuroinflammatory events, and impaired trophic support are thought to contribute to neuronal atrophy and death in all these diseases. In addition, neuroimaging findings have helped elucidate the structural and functional changes implicated in the relationship between depression and neurodegeneration, thus establishing a neuroanatomical signature to explain, at least in part, the comorbidity between MDD and AD, PD, and HD. The present review summarizes these findings and the current evidence regarding the effectiveness of common antidepressant therapies for the treatment of MDD in patients with these neurodegenerative diseases. This population is particularly vulnerable to the drawdowns of conventional antidepressant therapy (namely inadequate response and high risk of side effects), and the development of emerging therapeutic approaches to treat MDD in patients with AD, PD, and HD is thus of paramount importance to improve the quality of life of these individuals.
重度抑郁症(MDD)是一种高发性精神疾病,也是全球范围内导致残疾的主要原因。这种神经疾病通常与神经退行性疾病如阿尔茨海默病(AD)、帕金森病(PD)和亨廷顿病(HD)有关,对这些神经病理学疾病负担的增加有重大影响。在过去几十年中,一些导致这些疾病的病理生理和分子机制已经被阐明,这些发现表明,尽管表现出不同的特征,但导致 MDD 的神经生物学改变与 AD、PD 和 HD 中的神经退行性变之间存在一些相似之处。例如,单胺能传递和下丘脑-垂体-肾上腺(HPA)轴的紊乱、氧化和神经炎症事件的增加以及营养支持受损,被认为导致了所有这些疾病中的神经元萎缩和死亡。此外,神经影像学的发现有助于阐明与抑郁症和神经退行性变之间关系相关的结构和功能变化,从而建立一个神经解剖学特征,以部分解释 MDD 与 AD、PD 和 HD 之间的共病性。本综述总结了这些发现以及关于在这些神经退行性疾病患者中使用常见抗抑郁治疗来治疗 MDD 的有效性的现有证据。这些患者特别容易受到常规抗抑郁治疗的影响(即反应不足和副作用风险高),因此,开发针对 AD、PD 和 HD 患者的治疗 MDD 的新兴治疗方法对于提高这些患者的生活质量至关重要。