From the Centre d'Imagerie Médicale de Cornavin, Place de Cornavin 18, 1201 Geneva, Switzerland (S.H.); Department of Surgical Sciences, Radiology, Uppsala University, Uppsala, Sweden (S.H.); Faculty of Medicine of the University of Geneva, Geneva, Switzerland (S.H.); Department of Radiology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China (S.H.); Tanta University, Faculty of Medicine, Tanta, Egypt (S.H.); Neuroradiological Academic Unit, Department of Brain Repair and Rehabilitation, Queen Square Institute of Neurology (H.R.J., F.B.), and Centre for Medical Image Computing, Institute of Healthcare Engineering (F.B.), University College London, London, England; Lysholm Department of Neuroradiology, The National Hospital for Neurology and Neurosurgery, London, England (H.R.J.); Departments of Epidemiology and Radiology & Nuclear Medicine, Erasmus MC, Rotterdam, the Netherlands (M.W.V.); and Department of Radiology and Nuclear Medicine, Amsterdam University Medical Centre, Amsterdam, the Netherlands (F.B.).
Radiology. 2023 Sep;308(3):e230173. doi: 10.1148/radiol.230173.
Alzheimer disease (AD) is the most common cause of dementia. The prevailing theory of the underlying pathology assumes amyloid accumulation followed by tau protein aggregation and neurodegeneration. However, the current antiamyloid and antitau treatments show only variable clinical efficacy. Three relevant points are important for the radiologic assessment of dementia. First, besides various dementing disorders (including AD, frontotemporal dementia, and dementia with Lewy bodies), clinical variants and imaging subtypes of AD include both typical and atypical AD. Second, atypical AD has overlapping radiologic and clinical findings with other disorders. Third, the diagnostic process should consider mixed pathologies in neurodegeneration, especially concurrent cerebrovascular disease, which is frequent in older age. Neuronal loss is often present at, or even before, the onset of cognitive decline. Thus, for effective emerging treatments, early diagnosis before the onset of clinical symptoms is essential to slow down or stop subsequent neuronal loss, requiring molecular imaging or plasma biomarkers. Neuroimaging, particularly MRI, provides multiple imaging parameters for neurodegenerative and cerebrovascular disease. With emerging treatments for AD, it is increasingly important to recognize AD variants and other disorders that mimic AD. Describing the individual composition of neurodegenerative and cerebrovascular disease markers while considering overlapping and mixed diseases is necessary to better understand AD and develop efficient individualized therapies.
阿尔茨海默病(AD)是痴呆症最常见的病因。目前普遍认为,淀粉样蛋白的积累会导致tau 蛋白聚集和神经退行性变。然而,目前的抗淀粉样蛋白和抗 tau 治疗方法仅显示出不同的临床疗效。对于痴呆症的影像学评估,有三个相关要点很重要。首先,除了各种痴呆症(包括 AD、额颞叶痴呆和路易体痴呆)外,AD 的临床变异型和影像学亚型包括典型 AD 和非典型 AD。其次,非典型 AD 与其他疾病具有重叠的影像学和临床表现。第三,诊断过程应考虑神经退行性变中的混合病理学,尤其是在老年人群中经常发生的并发脑血管病。神经元丢失通常发生在认知能力下降之前,甚至在其之前。因此,对于有效的新兴治疗方法,在出现临床症状之前进行早期诊断对于减缓或阻止随后的神经元丢失至关重要,这需要进行分子影像学或血浆生物标志物检查。神经影像学,特别是 MRI,为神经退行性疾病和脑血管病提供了多种影像学参数。随着 AD 治疗方法的不断涌现,识别 AD 变异型和其他类似 AD 的疾病变得越来越重要。在考虑重叠和混合疾病的情况下,描述神经退行性疾病和脑血管疾病标志物的个体组成对于更好地理解 AD 并开发有效的个体化治疗方法是必要的。