Literature DB >> 27283329

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

Roberta Diehl Rodriguez1, Claudia Kimie Suemoto1, Mariana Molina1, Camila Fernandes Nascimento1, Renata Elaine Paraizo Leite1, Renata Eloah de Lucena Ferretti-Rebustini1, José Marcelo Farfel1, Helmut Heinsen1, Ricardo Nitrini1, Kenji Ueda1, Carlos Augusto Pasqualucci1, Wilson Jacob-Filho1, Kristine Yaffe1, Lea Tenenholz Grinberg2.   

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 São 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.
© 2016 American Association of Neuropathologists, Inc. All rights reserved.

Entities:  

Keywords:  Dementia; Neurodegeneration; Neuropathology; Postmortem; Tauopathy

Mesh:

Year:  2016        PMID: 27283329      PMCID: PMC4913431          DOI: 10.1093/jnen/nlw034

Source DB:  PubMed          Journal:  J Neuropathol Exp Neurol        ISSN: 0022-3069            Impact factor:   3.685


  67 in total

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Journal:  Acta Neuropathol       Date:  2013-01-31       Impact factor: 17.088

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Review 9.  Argyrophilic grain disease.

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Journal:  Clinics (Sao Paulo)       Date:  2013       Impact factor: 2.365

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2.  Mixed TDP-43 proteinopathy and tauopathy in frontotemporal lobar degeneration: nine case series.

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3.  Neuropathological correlates of structural and functional imaging biomarkers in 4-repeat tauopathies.

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Review 4.  A review on shared clinical and molecular mechanisms between bipolar disorder and frontotemporal dementia.

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5.  Characteristic asymmetric limbic and anterior temporal atrophy in demented patients with pathologically confirmed argyrophilic grain disease.

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6.  Neuropathological lesions in the very old: results from a large Brazilian autopsy study.

Authors:  Claudia K Suemoto; Renata E P Leite; Renata E L Ferretti-Rebustini; Roberta D Rodriguez; Ricardo Nitrini; Carlos A Pasqualucci; Wilson Jacob-Filho; Lea T Grinberg
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Review 7.  RNA Binding Proteins and the Pathogenesis of Frontotemporal Lobar Degeneration.

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Review 8.  Hippocampal Sclerosis, Argyrophilic Grain Disease, and Primary Age-Related Tauopathy.

Authors:  Gregory A Jicha; Peter T Nelson
Journal:  Continuum (Minneap Minn)       Date:  2019-02

9.  Astrocytic Tau Deposition Is Frequent in Typical and Atypical Alzheimer Disease Presentations.

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Journal:  J Neuropathol Exp Neurol       Date:  2019-12-01       Impact factor: 3.685

Review 10.  Tau at the interface between neurodegeneration and neuroinflammation.

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