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Consensus classification of posterior cortical atrophy

Title: Consensus classification of posterior cortical atrophy
Authors: Crutch, SJ; Schott, JM; Rabinovici, GD; Murray, M; Snowden, JS; van der Flier, WM; Dickerson, BC; Vandenberghe, R; Ahmed, S; Bak, TH; Boeve, BF; Butler, C; Cappa, SF; Ceccaldi, M; de Souza, LC; Dubois, B; Felician, O; Galasko, D; Graff-Radford, J; Graff-Radford, NR; Hof, PR; Krolak-Salmon, P; Lehmann, M; Magnin, E; Mendez, MF; Nestor, PJ; Onyike, CU; Pelak, VS; Pijnenburg, Y; Primativo, S; Rossor, MN; Ryan, NS; Scheltens, P; Shakespeare, TJ; Suárez González, A; Tang-Wai, DF; Yong, KX; Carrillo, M; Fox, NC; Alzheimer's Association ISTAART Atypical Alzheimer's Disease and, .
Source: Alzheimer's & Dementia (2017) (In press).
Publication Year: 2017
Collection: University College London: UCL Discovery
Subject Terms: Alzheimer's disease; Biomarker; Clinico-radiological syndrome; Pathophysiology; Posterior cortical atrophy
Description: INTRODUCTION: A classification framework for posterior cortical atrophy (PCA) is proposed to improve the uniformity of definition of the syndrome in a variety of research settings. METHODS: Consensus statements about PCA were developed through a detailed literature review, the formation of an international multidisciplinary working party which convened on four occasions, and a Web-based quantitative survey regarding symptom frequency and the conceptualization of PCA. RESULTS: A three-level classification framework for PCA is described comprising both syndrome- and disease-level descriptions. Classification level 1 (PCA) defines the core clinical, cognitive, and neuroimaging features and exclusion criteria of the clinico-radiological syndrome. Classification level 2 (PCA-pure, PCA-plus) establishes whether, in addition to the core PCA syndrome, the core features of any other neurodegenerative syndromes are present. Classification level 3 (PCA attributable to AD [PCA-AD], Lewy body disease [PCA-LBD], corticobasal degeneration [PCA-CBD], prion disease [PCA-prion]) provides a more formal determination of the underlying cause of the PCA syndrome, based on available pathophysiological biomarker evidence. The issue of additional syndrome-level descriptors is discussed in relation to the challenges of defining stages of syndrome severity and characterizing phenotypic heterogeneity within the PCA spectrum. DISCUSSION: There was strong agreement regarding the definition of the core clinico-radiological syndrome, meaning that the current consensus statement should be regarded as a refinement, development, and extension of previous single-center PCA criteria rather than any wholesale alteration or redescription of the syndrome. The framework and terminology may facilitate the interpretation of research data across studies, be applicable across a broad range of research scenarios (e.g., behavioral interventions, pharmacological trials), and provide a foundation for future collaborative work.
Document Type: article in journal/newspaper
File Description: text
Language: English
Relation: https://discovery.ucl.ac.uk/id/eprint/1544187/
Availability: https://discovery.ucl.ac.uk/id/eprint/1544187/1/1-s2.0-S1552526017300407-main.pdf; https://discovery.ucl.ac.uk/id/eprint/1544187/
Rights: open
Accession Number: edsbas.717400D6
Database: BASE