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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

d Argyrophilic Grain Disease: Demographics, Clinical, and Neuropathological Features From a Large Autopsy Study

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Rodriguez, Roberta Diehl ; Suemoto, Claudia Kimie ; Molina, Mariana ; Nascimento, Camila Fernandes ; Leite, Renata Elaine Paraizo ; de Lucena Ferretti-Rebustini, Renata Eloah ; Farfel, Jose Marcelo ; Heinsen, Helmut ; Nitrini, Ricardo ; Ueda, Kenji ; Pasqualucci, Carlos Augusto ; Jacob-Filho, Wilson ; Yaffe, Kristine ; Grinberg, Lea Tenenholz
Total Authors: 14
Document type: Journal article
Source: JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY; v. 75, n. 7, p. 628-635, JUL 2016.
Web of Science Citations: 13
Abstract

Argyrophilic grain disease (AGD) is a frequent late-onset, 4 repeat tauopathy reported in Caucasians with high educational attainment. Little is known about AGD in non-Caucasians or in those with low educational attainment. We describe AGD demographics, clinical, and neuropathological features in a multiethnic cohort of 983 subjects >50 years of age from Sao Paulo, Brazil. Clinical data were collected through semistructured interviews with an informant and included in the Informant Questionnaire on Cognitive Decline in the Elderly, the Clinical Dementia Rating, and the Neuropsychiatric Inventory. Neuropathologic assessment relied on internationally accepted criteria. AGD was frequent (15.2%) and was the only neuropathological diagnosis in 8.9% of all cases (mean, 78.9 +/- 9.4 years); it rarely occurred as an isolated neuropathological finding. AGD was associated with older age, lower socioeconomic status (SES), and appetite disorders. This is the first study of demographic, clinical, and neuropathological aspects of AGD in different ethnicities and subjects from all socioeconomic strata. The results suggest that prospective studies of AGD patients include levels of hormones related to appetite control as possible antemortem markers. Moreover, understanding the mechanisms behind higher susceptibility to AGD of low SES subjects may disclose novel environmental risk factors for AGD and other neurodegenerative diseases. (AU)

FAPESP's process: 11/19833-7 - Characterization of TDP-43 changes during normal aging: a postmortem study
Grantee:Camila Nascimento Mantelli
Support Opportunities: Scholarships in Brazil - Doctorate
FAPESP's process: 10/06521-4 - Proteomic analysis of neuromelanin granules in normal aging and Parkinson disease
Grantee:Renata Elaine Paraizo Leite
Support Opportunities: Scholarships in Brazil - Post-Doctoral
FAPESP's process: 12/07526-5 - Argyrophilic grain disease
Grantee:Roberta Diehl Rodriguez
Support Opportunities: Scholarships in Brazil - Doctorate (Direct)