Posterior cortical atrophy

被引:401
作者
Crutch, Sebastian J. [1 ]
Lehmann, Manja [1 ,2 ]
Schott, Jonathan M. [1 ]
Rabinovici, Gil D. [2 ]
Rossor, Martin N. [1 ]
Fox, Nick C. [1 ]
机构
[1] UCL, Inst Neurol, Dementia Res Ctr, London, England
[2] Univ Calif San Francisco, Memory & Aging Ctr, San Francisco, CA 94143 USA
基金
英国医学研究理事会; 美国国家卫生研究院;
关键词
APOLIPOPROTEIN-E GENOTYPE; ALZHEIMERS-DISEASE; VISUAL VARIANT; CORTICOBASAL DEGENERATION; METABOLIC DEFICITS; BALINTS SYNDROME; APOE GENOTYPE; ASSOCIATION; DEMENTIA; PATHWAYS;
D O I
10.1016/S1474-4422(11)70289-7
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Posterior cortical atrophy (PCA) is a neurodegenerative syndrome that is characterised by progressive decline in visuospatial, visuoperceptual, literacy, and praxic skills. The progressive neurodegeneration affecting parietal, occipital, and occipitotemporal cortices that underlies PCA is attributable to Alzheimer's disease in most patients. However, alternative underlying causes, including dementia with Lewy bodies, corticobasal degeneration, and prion disease, have also been identified, and not all patients with PCA have atrophy on clinical imaging. This heterogeneity has led to inconsistencies in diagnosis and terminology and difficulties in comparing studies from different centres, and has restricted the generalisability of findings from clinical trials and investigations of factors that drive phenotypic variability. Important challenges remain, including the identification of factors associated not only with the selective vulnerability of posterior cortical regions but also with the young age of onset of PCA. Greater awareness of the syndrome and agreement over the correspondence between syndrome-level and disease-level classifications are needed to improve diagnostic accuracy, clinical management, and the design of research studies.
引用
收藏
页码:170 / 178
页数:9
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