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Subjective Cognitive Impairment Subjects in Our Clinical Practice
BACKGROUND: The clinical challenge in subjective cognitive impairment (SCI) is to identify which individuals will present cognitive decline. We created a statistical model to determine which variables contribute to SCI and mild cognitive impairment (MCI) versus Alzheimer's disease (AD) diagnose...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
S. Karger AG
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4264484/ https://www.ncbi.nlm.nih.gov/pubmed/25538726 http://dx.doi.org/10.1159/000366270 |
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author | Garcia-Ptacek, Sara Cavallin, Lena Kåreholt, Ingemar Kramberger, Milica Gregoric Winblad, Bengt Jelic, Vesna Eriksdotter, Maria |
author_facet | Garcia-Ptacek, Sara Cavallin, Lena Kåreholt, Ingemar Kramberger, Milica Gregoric Winblad, Bengt Jelic, Vesna Eriksdotter, Maria |
author_sort | Garcia-Ptacek, Sara |
collection | PubMed |
description | BACKGROUND: The clinical challenge in subjective cognitive impairment (SCI) is to identify which individuals will present cognitive decline. We created a statistical model to determine which variables contribute to SCI and mild cognitive impairment (MCI) versus Alzheimer's disease (AD) diagnoses. METHODS: A total of 993 subjects diagnosed at a memory clinic (2007-2009) were included retrospectively: 433 with SCI, 373 with MCI and 187 with AD. Descriptive statistics were provided. A logistic regression model analyzed the likelihood of SCI and MCI patients being diagnosed with AD, using age, gender, Mini-Mental State Examination score, the ratio of β-amyloid 42 divided by total tau, and phosphorylated tau as independent variables. RESULTS: The SCI subjects were younger (57.8 ± 8 years) than the MCI (64.2 ± 10.6 years) and AD subjects (70.1 ± 9.7 years). They were more educated, had less medial temporal lobe atrophy (MTA) and frequently normal cerebrospinal fluid biomarkers. Apolipoprotein E4/E4 homozygotes and apolipoprotein E3/E4 heterozygotes were significantly less frequent in the SCI group (6 and 36%) than in the AD group (28 and 51%). Within the regression model, cardiovascular risk factors, confluent white matter lesions, MTA and central atrophy increased the AD likelihood for SCI subjects. CONCLUSIONS: SCI patients form a distinct group. In our model, factors suggesting cardiovascular risk, MTA and central atrophy increased the AD likelihood for SCI subjects. |
format | Online Article Text |
id | pubmed-4264484 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | S. Karger AG |
record_format | MEDLINE/PubMed |
spelling | pubmed-42644842014-12-23 Subjective Cognitive Impairment Subjects in Our Clinical Practice Garcia-Ptacek, Sara Cavallin, Lena Kåreholt, Ingemar Kramberger, Milica Gregoric Winblad, Bengt Jelic, Vesna Eriksdotter, Maria Dement Geriatr Cogn Dis Extra Original Research Article BACKGROUND: The clinical challenge in subjective cognitive impairment (SCI) is to identify which individuals will present cognitive decline. We created a statistical model to determine which variables contribute to SCI and mild cognitive impairment (MCI) versus Alzheimer's disease (AD) diagnoses. METHODS: A total of 993 subjects diagnosed at a memory clinic (2007-2009) were included retrospectively: 433 with SCI, 373 with MCI and 187 with AD. Descriptive statistics were provided. A logistic regression model analyzed the likelihood of SCI and MCI patients being diagnosed with AD, using age, gender, Mini-Mental State Examination score, the ratio of β-amyloid 42 divided by total tau, and phosphorylated tau as independent variables. RESULTS: The SCI subjects were younger (57.8 ± 8 years) than the MCI (64.2 ± 10.6 years) and AD subjects (70.1 ± 9.7 years). They were more educated, had less medial temporal lobe atrophy (MTA) and frequently normal cerebrospinal fluid biomarkers. Apolipoprotein E4/E4 homozygotes and apolipoprotein E3/E4 heterozygotes were significantly less frequent in the SCI group (6 and 36%) than in the AD group (28 and 51%). Within the regression model, cardiovascular risk factors, confluent white matter lesions, MTA and central atrophy increased the AD likelihood for SCI subjects. CONCLUSIONS: SCI patients form a distinct group. In our model, factors suggesting cardiovascular risk, MTA and central atrophy increased the AD likelihood for SCI subjects. S. Karger AG 2014-11-11 /pmc/articles/PMC4264484/ /pubmed/25538726 http://dx.doi.org/10.1159/000366270 Text en Copyright © 2014 by S. Karger AG, Basel http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article licensed under the terms of the Creative Commons Attribution-NonCommercial 3.0 Unported license (CC BY-NC) (www.karger.com/OA-license), applicable to the online version of the article only. Users may download, print and share this work on the Internet for noncommercial purposes only, provided the original work is properly cited, and a link to the original work on http://www.karger.com and the terms of this license are included in any shared versions. |
spellingShingle | Original Research Article Garcia-Ptacek, Sara Cavallin, Lena Kåreholt, Ingemar Kramberger, Milica Gregoric Winblad, Bengt Jelic, Vesna Eriksdotter, Maria Subjective Cognitive Impairment Subjects in Our Clinical Practice |
title | Subjective Cognitive Impairment Subjects in Our Clinical Practice |
title_full | Subjective Cognitive Impairment Subjects in Our Clinical Practice |
title_fullStr | Subjective Cognitive Impairment Subjects in Our Clinical Practice |
title_full_unstemmed | Subjective Cognitive Impairment Subjects in Our Clinical Practice |
title_short | Subjective Cognitive Impairment Subjects in Our Clinical Practice |
title_sort | subjective cognitive impairment subjects in our clinical practice |
topic | Original Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4264484/ https://www.ncbi.nlm.nih.gov/pubmed/25538726 http://dx.doi.org/10.1159/000366270 |
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