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Prediction of Cerebral Amyloid With Common Information Obtained From Memory Clinic Practice

Background: Given the barriers prohibiting the broader utilization of amyloid imaging and high screening failure rate in clinical trials, an easily available and valid screening method for identifying cognitively impaired patients with cerebral amyloid deposition is needed. Therefore, we developed a...

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Autores principales: Lee, Jun Ho, Byun, Min Soo, Yi, Dahyun, Sohn, Bo Kyung, Jeon, So Yeon, Lee, Younghwa, Lee, Jun-Young, Kim, Yu Kyeong, Lee, Yun-Sang, Lee, Dong Young
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6178978/
https://www.ncbi.nlm.nih.gov/pubmed/30337868
http://dx.doi.org/10.3389/fnagi.2018.00309
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author Lee, Jun Ho
Byun, Min Soo
Yi, Dahyun
Sohn, Bo Kyung
Jeon, So Yeon
Lee, Younghwa
Lee, Jun-Young
Kim, Yu Kyeong
Lee, Yun-Sang
Lee, Dong Young
author_facet Lee, Jun Ho
Byun, Min Soo
Yi, Dahyun
Sohn, Bo Kyung
Jeon, So Yeon
Lee, Younghwa
Lee, Jun-Young
Kim, Yu Kyeong
Lee, Yun-Sang
Lee, Dong Young
author_sort Lee, Jun Ho
collection PubMed
description Background: Given the barriers prohibiting the broader utilization of amyloid imaging and high screening failure rate in clinical trials, an easily available and valid screening method for identifying cognitively impaired patients with cerebral amyloid deposition is needed. Therefore, we developed a prediction model for cerebral amyloid positivity in cognitively impaired patients using variables that are routinely obtained in memory clinics. Methods: Six hundred and fifty two cognitively impaired subjects from the Korean Brain Aging Study for the Early diagnosis and prediction of Alzheimer disease (KBASE) and the Alzheimer’s Disease Neuroimaging Initiative-2 (ADNI-2) cohorts were included in this study (107 amnestic mild cognitive impairment (MCI) and 69 Alzheimer’s disease (AD) dementia patients for KBASE cohort, and 332 MCI and 144 AD dementia patients for ADNI-2 cohort). Using the cross-sectional dataset from the KBASE cohort, a multivariate stepwise logistic regression analysis was conducted to develop a cerebral amyloid prediction model using variables commonly obtained in memory clinics. For each participant, the logit value derived from the final model was calculated, and the probability for being amyloid positive, which was calculated from the logit value, was named the amyloid prediction index. The final model was validated using an independent dataset from the ADNI-2 cohort. Results: The final model included age, sex, years of education, history of hypertension, apolipoprotein ε4 positivity, and score from a word list recall test. The model predicted that younger age, female sex, higher educational level, absence of hypertension history, presence of apolipoprotein ε4 allele, and lower score of word list recall test are associated with higher probability for being amyloid positive. The amyloid prediction index derived from the model was proven to be valid across the two cohorts. The area under the curve was 0.873 (95% confidence interval 0.815 to 0.918) for the KBASE cohort, and 0.808 (95% confidence interval = 0.769 to 0.842) for ADNI-2 cohort. Conclusion: The amyloid prediction index, which was based on commonly available clinical information, can be useful for screening cognitively impaired individuals with a high probability of amyloid deposition in therapeutic trials for early Alzheimer’s disease as well as in clinical practice.
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spelling pubmed-61789782018-10-18 Prediction of Cerebral Amyloid With Common Information Obtained From Memory Clinic Practice Lee, Jun Ho Byun, Min Soo Yi, Dahyun Sohn, Bo Kyung Jeon, So Yeon Lee, Younghwa Lee, Jun-Young Kim, Yu Kyeong Lee, Yun-Sang Lee, Dong Young Front Aging Neurosci Aging Neuroscience Background: Given the barriers prohibiting the broader utilization of amyloid imaging and high screening failure rate in clinical trials, an easily available and valid screening method for identifying cognitively impaired patients with cerebral amyloid deposition is needed. Therefore, we developed a prediction model for cerebral amyloid positivity in cognitively impaired patients using variables that are routinely obtained in memory clinics. Methods: Six hundred and fifty two cognitively impaired subjects from the Korean Brain Aging Study for the Early diagnosis and prediction of Alzheimer disease (KBASE) and the Alzheimer’s Disease Neuroimaging Initiative-2 (ADNI-2) cohorts were included in this study (107 amnestic mild cognitive impairment (MCI) and 69 Alzheimer’s disease (AD) dementia patients for KBASE cohort, and 332 MCI and 144 AD dementia patients for ADNI-2 cohort). Using the cross-sectional dataset from the KBASE cohort, a multivariate stepwise logistic regression analysis was conducted to develop a cerebral amyloid prediction model using variables commonly obtained in memory clinics. For each participant, the logit value derived from the final model was calculated, and the probability for being amyloid positive, which was calculated from the logit value, was named the amyloid prediction index. The final model was validated using an independent dataset from the ADNI-2 cohort. Results: The final model included age, sex, years of education, history of hypertension, apolipoprotein ε4 positivity, and score from a word list recall test. The model predicted that younger age, female sex, higher educational level, absence of hypertension history, presence of apolipoprotein ε4 allele, and lower score of word list recall test are associated with higher probability for being amyloid positive. The amyloid prediction index derived from the model was proven to be valid across the two cohorts. The area under the curve was 0.873 (95% confidence interval 0.815 to 0.918) for the KBASE cohort, and 0.808 (95% confidence interval = 0.769 to 0.842) for ADNI-2 cohort. Conclusion: The amyloid prediction index, which was based on commonly available clinical information, can be useful for screening cognitively impaired individuals with a high probability of amyloid deposition in therapeutic trials for early Alzheimer’s disease as well as in clinical practice. Frontiers Media S.A. 2018-10-03 /pmc/articles/PMC6178978/ /pubmed/30337868 http://dx.doi.org/10.3389/fnagi.2018.00309 Text en Copyright © 2018 Lee, Byun, Yi, Sohn, Jeon, Lee, Lee, Kim, Lee and Lee. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Aging Neuroscience
Lee, Jun Ho
Byun, Min Soo
Yi, Dahyun
Sohn, Bo Kyung
Jeon, So Yeon
Lee, Younghwa
Lee, Jun-Young
Kim, Yu Kyeong
Lee, Yun-Sang
Lee, Dong Young
Prediction of Cerebral Amyloid With Common Information Obtained From Memory Clinic Practice
title Prediction of Cerebral Amyloid With Common Information Obtained From Memory Clinic Practice
title_full Prediction of Cerebral Amyloid With Common Information Obtained From Memory Clinic Practice
title_fullStr Prediction of Cerebral Amyloid With Common Information Obtained From Memory Clinic Practice
title_full_unstemmed Prediction of Cerebral Amyloid With Common Information Obtained From Memory Clinic Practice
title_short Prediction of Cerebral Amyloid With Common Information Obtained From Memory Clinic Practice
title_sort prediction of cerebral amyloid with common information obtained from memory clinic practice
topic Aging Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6178978/
https://www.ncbi.nlm.nih.gov/pubmed/30337868
http://dx.doi.org/10.3389/fnagi.2018.00309
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