Tobeh Nour S, Bruce Kimberley D
Division of Endocrinology, Metabolism and Diabetes, Department of Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO, United States.
Skaggs School of Pharmacy and Pharmaceutical Sciences, University of Colorado Anschutz Medical Campus, Aurora, CO, United States.
Front Aging Neurosci. 2023 Oct 25;15:1259012. doi: 10.3389/fnagi.2023.1259012. eCollection 2023.
More than 55 million people suffer from dementia, with this number projected to double every 20 years. In the United States, 1 in 3 aged individuals dies from Alzheimer's disease (AD) or another type of dementia and AD kills more individuals than breast cancer and prostate cancer combined. AD is a complex and multifactorial disease involving amyloid plaque and neurofibrillary tangle formation, glial cell dysfunction, and lipid droplet accumulation (among other pathologies), ultimately leading to neurodegeneration and neuronal death. Unfortunately, the current FDA-approved therapeutics do not reverse nor halt AD. While recently approved amyloid-targeting antibodies can slow AD progression to improve outcomes for some patients, they are associated with adverse side effects, may have a narrow therapeutic window, and are expensive. In this review, we evaluate current and emerging AD therapeutics in preclinical and clinical development and provide insight into emerging strategies that target brain lipid metabolism and microglial function - an approach that may synergistically target multiple mechanisms that drive AD neuropathogenesis. Overall, we evaluate whether these disease-modifying emerging therapeutics hold promise as interventions that may be able to reverse or halt AD progression.
超过5500万人患有痴呆症,预计这一数字每20年将翻一番。在美国,三分之一的老年人死于阿尔茨海默病(AD)或其他类型的痴呆症,AD导致的死亡人数超过乳腺癌和前列腺癌的总和。AD是一种复杂的多因素疾病,涉及淀粉样斑块和神经原纤维缠结的形成、胶质细胞功能障碍和脂滴积累(以及其他病理情况),最终导致神经退行性变和神经元死亡。不幸的是,目前美国食品药品监督管理局(FDA)批准的治疗方法既不能逆转也不能阻止AD。虽然最近批准的靶向淀粉样蛋白的抗体可以减缓AD的进展,改善一些患者的预后,但它们会产生不良副作用,治疗窗口可能较窄,而且价格昂贵。在这篇综述中,我们评估了处于临床前和临床开发阶段的现有及新兴AD治疗方法,并深入探讨了针对脑脂质代谢和小胶质细胞功能的新兴策略——这种方法可能协同靶向驱动AD神经病理发生的多种机制。总体而言,我们评估这些疾病修饰性新兴治疗方法是否有望成为能够逆转或阻止AD进展的干预措施。