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Diagnostic Value of Subjective Memory Complaints Assessed with a Single Item in Dominantly Inherited Alzheimer's Disease: Results of the DIAN Study.
Laske, Christoph; Sohrabi, Hamid R; Jasielec, Mateusz S; Müller, Stephan; Koehler, Niklas K; Gräber, Susanne; Förster, Stefan; Drzezga, Alexander; Mueller-Sarnowski, Felix; Danek, Adrian; Jucker, Mathias; Bateman, Randall J; Buckles, Virginia; Saykin, Andrew J; Martins, Ralph N; Morris, John C.
Afiliação
  • Laske C; German Center for Neurodegenerative Diseases (DZNE), 72076 Tübingen, Germany ; Section for Dementia Research, Department of Cellular Neurology, Hertie Institute for Clinical Brain Research and Department of Psychiatry and Psychotherapy, University of Tübingen, 72076 Tübingen, Germany ; Department of
  • Sohrabi HR; Centre of Excellence for Alzheimer's Disease Research and Care, School of Medical Sciences, Edith Cowan University, Perth, WA 6027, Australia ; School of Psychiatry and Clinical Neurosciences, University of Western Australia, Nedlands, WA 6009, Australia.
  • Jasielec MS; Division of Biostatistics, Washington University School of Medicine, St. Louis, MO 63108, USA.
  • Müller S; Department of Psychiatry and Psychotherapy, University of Tübingen, 72076 Tübingen, Germany.
  • Koehler NK; Department of Psychiatry and Psychotherapy, University of Tübingen, 72076 Tübingen, Germany.
  • Gräber S; German Center for Neurodegenerative Diseases (DZNE), 72076 Tübingen, Germany ; Department of Neurodegeneration, Hertie Institute for Clinical Brain Research, University of Tübingen, 72076 Tübingen, Germany.
  • Förster S; Department of Nuclear Medicine & TUM Neuroimaging Center (TUM-NIC), Klinikum Rechts der Isar, Technical University Munich, 80333 Munich, Germany.
  • Drzezga A; Department of Nuclear Medicine, University of Cologne, 50937 Cologne, Germany.
  • Mueller-Sarnowski F; Deutsches Zentrum für Neurodegenerative Erkrankungen, 81377 München, Germany ; Neurologische Klinik und Poliklinik, Ludwig-Maximilians-Universität, 81377 München, Germany.
  • Danek A; Deutsches Zentrum für Neurodegenerative Erkrankungen, 81377 München, Germany ; Neurologische Klinik und Poliklinik, Ludwig-Maximilians-Universität, 81377 München, Germany.
  • Jucker M; German Center for Neurodegenerative Diseases (DZNE), 72076 Tübingen, Germany ; Department of Cellular Neurology, Hertie Institute for Clinical Brain Research, University of Tübingen, 72076 Tübingen, Germany.
  • Bateman RJ; Department of Neurology, Knight Alzheimer's Disease Research Center, Washington University School of Medicine, St. Louis, MO 63108, USA.
  • Buckles V; Department of Neurology, Knight Alzheimer's Disease Research Center, Washington University School of Medicine, St. Louis, MO 63108, USA.
  • Saykin AJ; Indiana Alzheimer Disease Center, Indiana University School of Medicine, Indianapolis, IN 46202, USA.
  • Martins RN; Centre of Excellence for Alzheimer's Disease Research and Care, School of Medical Sciences, Edith Cowan University, Perth, WA 6027, Australia ; School of Psychiatry and Clinical Neurosciences, University of Western Australia, Nedlands, WA 6009, Australia.
  • Morris JC; Department of Neurology, Knight Alzheimer's Disease Research Center, Washington University School of Medicine, St. Louis, MO 63108, USA.
  • Dominantly Inherited Alzheimer Network Dian; Department of Neurology, Washington University in St. Louis, MO 63108, USA.
Biomed Res Int ; 2015: 828120, 2015.
Article em En | MEDLINE | ID: mdl-25922840
ABSTRACT

OBJECTIVE:

We examined the diagnostic value of subjective memory complaints (SMCs) assessed with a single item in a large cross-sectional cohort consisting of families with autosomal dominant Alzheimer's disease (ADAD) participating in the Dominantly Inherited Alzheimer Network (DIAN).

METHODS:

The baseline sample of 183 mutation carriers (MCs) and 117 noncarriers (NCs) was divided according to Clinical Dementia Rating (CDR) scale into preclinical (CDR 0; MCs n = 107; NCs n = 109), early symptomatic (CDR 0.5; MCs n = 48; NCs n = 8), and dementia stage (CDR ≥ 1; MCs n = 28; NCs n = 0). These groups were subdivided by the presence or absence of SMCs.

RESULTS:

At CDR 0, SMCs were present in 12.1% of MCs and 9.2% of NCs (P = 0.6). At CDR 0.5, SMCs were present in 66.7% of MCs and 62.5% of NCs (P = 1.0). At CDR ≥ 1, SMCs were present in 96.4% of MCs. SMCs in MCs were significantly associated with CDR, logical memory scores, Geriatric Depression Scale, education, and estimated years to onset.

CONCLUSIONS:

The present study shows that SMCs assessed by a single-item scale have no diagnostic value to identify preclinical ADAD in asymptomatic individuals. These results demonstrate the need of further improvement of SMC measures that should be examined in large clinical trials.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Alzheimer / Doenças Genéticas Inatas / Memória / Mutação Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Alzheimer / Doenças Genéticas Inatas / Memória / Mutação Idioma: En Ano de publicação: 2015 Tipo de documento: Article