From, The Columbus Memory Center, Columbus, GA, USA.
US Medical Affairs - Neuroscience, Genentech, A Member of the Roche Group, South San Francisco, CA, USA.
J Intern Med. 2021 Aug;290(2):310-334. doi: 10.1111/joim.13244. Epub 2021 Mar 31.
The critical role of primary care clinicians (PCCs) in Alzheimer's disease (AD) prevention, diagnosis and management must evolve as new treatment paradigms and disease-modifying therapies (DMTs) emerge. Our understanding of AD has grown substantially: no longer conceptualized as a late-in-life syndrome of cognitive and functional impairments, we now recognize that AD pathology builds silently for decades before cognitive impairment is detectable. Clinically, AD first manifests subtly as mild cognitive impairment (MCI) due to AD before progressing to dementia. Emerging optimism for improved outcomes in AD stems from a focus on preventive interventions in midlife and timely, biomarker-confirmed diagnosis at early signs of cognitive deficits (i.e. MCI due to AD and mild AD dementia). A timely AD diagnosis is particularly important for optimizing patient care and enabling the appropriate use of anticipated DMTs. An accelerating challenge for PCCs and AD specialists will be to respond to innovations in diagnostics and therapy for AD in a system that is not currently well positioned to do so. To overcome these challenges, PCCs and AD specialists must collaborate closely to navigate and optimize dynamically evolving AD care in the face of new opportunities. In the spirit of this collaboration, we summarize here some prominent and influential models that inform our current understanding of AD. We also advocate for timely and accurate (i.e. biomarker-defined) diagnosis of early AD. In doing so, we consider evolving issues related to prevention, detecting emerging cognitive impairment and the role of biomarkers in the clinic.
初级保健临床医生(PCCs)在阿尔茨海默病(AD)预防、诊断和管理方面的关键作用必须随着新的治疗模式和疾病修饰疗法(DMT)的出现而发展。我们对 AD 的理解有了很大的提高:不再将其概念化为认知和功能障碍的晚年综合征,我们现在认识到 AD 病理在认知障碍可检测之前已经默默地发展了几十年。临床上,AD 首先表现为由于 AD 引起的轻度认知障碍(MCI),然后发展为痴呆。AD 预后改善的新希望源于对中年预防干预的关注以及在认知缺陷(即由于 AD 引起的 MCI 和轻度 AD 痴呆)的早期出现时通过生物标志物确认的及时诊断。及时进行 AD 诊断对于优化患者护理和启用预期 DMT 非常重要。对于 PCC 和 AD 专家来说,一个加速的挑战将是在目前尚未做好准备的系统中对 AD 的诊断和治疗创新做出响应。为了克服这些挑战,PCC 和 AD 专家必须密切合作,在面对新机遇时动态优化 AD 护理。本着这种合作精神,我们在此总结了一些告知我们当前对 AD 理解的突出和有影响力的模型。我们还主张及时进行准确(即基于生物标志物的)AD 早期诊断。在这样做的过程中,我们考虑与预防、检测新出现的认知障碍以及生物标志物在临床中的作用相关的不断发展的问题。
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