Ross Mary Kay, Raji Cyrus, Lokken Kristine L, Bredesen Dale E, Roach Jared C, Funk Cory C, Price Nathan, Rappaport Noa, Hood Leroy, Heath James R
Brain Health and Research Institute, Seattle, WA, USA.
Washington University School of Medicine, St. Louis, MO, USA.
J Alzheimers Dis Parkinsonism. 2021;11(Suppl 5). Epub 2021 Aug 25.
We report a case of a patient with mixed dementia successfully treated with a personalized multimodal therapy. Monotherapeutics are inadequate for the treatment of Alzheimer's disease (AD) and mixed dementia; therefore, we approach treatment through an adaptive personalized multimodal program. Many multimodal programs are pre-determined, and thus may not address the underlying contributors to cognitive decline in each particular individual. The combination of a targeted, personalized, precision medicine approach using a multimodal program promises advantages over monotherapies and untargeted multimodal therapies for multifactorial dementia. In this case study, we describe successful treatment for a patient diagnosed with AD, using a multimodal, programmatic, precision medicine intervention encompassing therapies targeting multiple dementia diastheses. We describe specific interventions used in this case that are derived from a comprehensive protocol for AD precision medicine. After treatment, our patient demonstrated improvements in quantitative neuropsychological testing, volumetric neuroimaging, PET scans, and serum chemistries, accompanied by symptomatic improvement over a 3.5-year period. This case outcome supports the need for rigorous trials of comprehensive, targeted combination therapies to stabilize, restore, and prevent cognitive decline in individuals with potentially many underlying causes of such decline and dementia. Our multimodal therapy included personalized treatments to address each potential perturbation to neuroplasticity. In particular, neuroinflammation and metabolic subsystems influence cognitive function and hippocampal volume. In this patient with a primary biliary cholangitis (PBC) multimorbidity component, we introduced a personalized diet that helped reduce liver inflammation. Together, all these components of multimodal therapy showed a sustained functional and cognitive benefit. Multimodal therapies may have systemwide benefits on all dementias, particularly in the context of multimorbidity. Furthermore, these therapies provide generalized health benefits, as many of the factors - such as inflammation - that impact cognitive function also impact other systems.
我们报告了一例通过个性化多模式疗法成功治疗的混合性痴呆患者。单一疗法不足以治疗阿尔茨海默病(AD)和混合性痴呆;因此,我们通过适应性个性化多模式方案进行治疗。许多多模式方案是预先确定的,因此可能无法解决每个特定个体认知衰退的潜在因素。使用多模式方案的靶向、个性化、精准医学方法相结合,有望比单一疗法和非靶向多模式疗法在治疗多因素痴呆方面具有优势。在本病例研究中,我们描述了对一名被诊断为AD的患者的成功治疗,采用了一种多模式、程序化、精准医学干预,包括针对多种痴呆诊断的疗法。我们描述了该病例中使用的特定干预措施,这些措施源自AD精准医学的综合方案。治疗后,我们的患者在定量神经心理学测试、容积神经成像、PET扫描和血清化学方面均有改善,同时在3.5年期间症状也有所改善。该病例结果支持有必要对全面、靶向联合疗法进行严格试验,以稳定、恢复和预防可能有多种潜在病因导致认知衰退和痴呆的个体的认知衰退。我们的多模式疗法包括个性化治疗,以应对对神经可塑性的每一个潜在干扰。特别是,神经炎症和代谢子系统会影响认知功能和海马体积。在这名患有原发性胆汁性胆管炎(PBC)合并症的患者中,我们引入了有助于减轻肝脏炎症的个性化饮食。总之,多模式疗法的所有这些组成部分都显示出持续的功能和认知益处。多模式疗法可能对所有痴呆症都有全系统的益处,特别是在合并症的情况下。此外,这些疗法还能带来广泛的健康益处,因为许多影响认知功能的因素,如炎症,也会影响其他系统。