Cerebral Amyloid Positivity Prediction Models Using Clinical Data in Subjects With Mild Cognitive Impairment and Dementia

Objective Due to high cost of amyloid imaging, its use of amyloid imaging to confirm amyloid pathology is limited in clinical practice. It is of importance to develop a model to predict cerebral amyloid positivity using clinical data obtained from a memory clinic.Methods A total of 410 participants...

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Published inPsychiatry investigation Vol. 18; no. 9; pp. 864 - 870
Main Authors Joo, Soo Hyun, Lee, Chang Uk
Format Journal Article
LanguageEnglish
Published Korean Neuropsychiatric Association 01.09.2021
대한신경정신의학회
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ISSN1738-3684
1976-3026
DOI10.30773/pi.2021.0104

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Abstract Objective Due to high cost of amyloid imaging, its use of amyloid imaging to confirm amyloid pathology is limited in clinical practice. It is of importance to develop a model to predict cerebral amyloid positivity using clinical data obtained from a memory clinic.Methods A total of 410 participants who had symptom of subjective cognitive decline and underwent amyloid PET and apolipoprotein ε (APOE) genotyping were retrospectively enrolled from January 2016 to January 2019. Models for cerebral amyloid positivity prediction were developed in all subjects, mild cognitive impairment (MCI) subjects, and Alzheimer’s disease (AD) dementia subjects through multivariate logistic regression analysis. The performance of the models was assessed using receiver operating characteristic (ROC) curve analysis and the area under the curve (AUC) values.Results Age, sex, years of education, body mass index (BMI), APOE4, and mini mental state examination score (MMSE) were selected for the final model for all subjects. The AUC value of the ROC curve was 0.775. Age, sex, years of education, BMI, and APOE4 were selected for the final model for MCI subjects. The AUC value was 0.735. Age, sex, years of education, BMI, APOE4, MMSE, and history of hypertension were selected for the final model for AD dementia subjects. The AUC value was 0.845.Conclusion This study found that models using clinical data can predict cerebral amyloid positivity according to cognitive status. These models can be useful as a screening tool predict cerebral amyloid deposition in cognitively impaired patients in a memory clinic.
AbstractList Objective Due to high cost of amyloid imaging, its use of amyloid imaging to confirm amyloid pathology is limited in clinical practice. It is of importance to develop a model to predict cerebral amyloid positivity using clinical data obtained from a memory clinic.Methods A total of 410 participants who had symptom of subjective cognitive decline and underwent amyloid PET and apolipoprotein ε (APOE) genotyping were retrospectively enrolled from January 2016 to January 2019. Models for cerebral amyloid positivity prediction were developed in all subjects, mild cognitive impairment (MCI) subjects, and Alzheimer’s disease (AD) dementia subjects through multivariate logistic regression analysis. The performance of the models was assessed using receiver operating characteristic (ROC) curve analysis and the area under the curve (AUC) values.Results Age, sex, years of education, body mass index (BMI), APOE4, and mini mental state examination score (MMSE) were selected for the final model for all subjects. The AUC value of the ROC curve was 0.775. Age, sex, years of education, BMI, and APOE4 were selected for the final model for MCI subjects. The AUC value was 0.735. Age, sex, years of education, BMI, APOE4, MMSE, and history of hypertension were selected for the final model for AD dementia subjects. The AUC value was 0.845.Conclusion This study found that models using clinical data can predict cerebral amyloid positivity according to cognitive status. These models can be useful as a screening tool predict cerebral amyloid deposition in cognitively impaired patients in a memory clinic.
Due to high cost of amyloid imaging, its use of amyloid imaging to confirm amyloid pathology is limited in clinical practice. It is of importance to develop a model to predict cerebral amyloid positivity using clinical data obtained from a memory clinic.OBJECTIVEDue to high cost of amyloid imaging, its use of amyloid imaging to confirm amyloid pathology is limited in clinical practice. It is of importance to develop a model to predict cerebral amyloid positivity using clinical data obtained from a memory clinic.A total of 410 participants who had symptom of subjective cognitive decline and underwent amyloid PET and apolipoprotein ε (APOE) genotyping were retrospectively enrolled from January 2016 to January 2019. Models for cerebral amyloid positivity prediction were developed in all subjects, mild cognitive impairment (MCI) subjects, and Alzheimer's disease (AD) dementia subjects through multivariate logistic regression analysis. The performance of the models was assessed using receiver operating characteristic (ROC) curve analysis and the area under the curve (AUC) values.METHODSA total of 410 participants who had symptom of subjective cognitive decline and underwent amyloid PET and apolipoprotein ε (APOE) genotyping were retrospectively enrolled from January 2016 to January 2019. Models for cerebral amyloid positivity prediction were developed in all subjects, mild cognitive impairment (MCI) subjects, and Alzheimer's disease (AD) dementia subjects through multivariate logistic regression analysis. The performance of the models was assessed using receiver operating characteristic (ROC) curve analysis and the area under the curve (AUC) values.Age, sex, years of education, body mass index (BMI), APOE4, and mini mental state examination score (MMSE) were selected for the final model for all subjects. The AUC value of the ROC curve was 0.775. Age, sex, years of education, BMI, and APOE4 were selected for the final model for MCI subjects. The AUC value was 0.735. Age, sex, years of education, BMI, APOE4, MMSE, and history of hypertension were selected for the final model for AD dementia subjects. The AUC value was 0.845.RESULTSAge, sex, years of education, body mass index (BMI), APOE4, and mini mental state examination score (MMSE) were selected for the final model for all subjects. The AUC value of the ROC curve was 0.775. Age, sex, years of education, BMI, and APOE4 were selected for the final model for MCI subjects. The AUC value was 0.735. Age, sex, years of education, BMI, APOE4, MMSE, and history of hypertension were selected for the final model for AD dementia subjects. The AUC value was 0.845.This study found that models using clinical data can predict cerebral amyloid positivity according to cognitive status. These models can be useful as a screening tool predict cerebral amyloid deposition in cognitively impaired patients in a memory clinic.CONCLUSIONThis study found that models using clinical data can predict cerebral amyloid positivity according to cognitive status. These models can be useful as a screening tool predict cerebral amyloid deposition in cognitively impaired patients in a memory clinic.
Objective Due to high cost of amyloid imaging, its use of amyloid imaging to confirm amyloid pathology is limited in clinical practice. It is of importance to develop a model to predict cerebral amyloid positivity using clinical data obtained from a memory clinic.Methods A total of 410 participants who had symptom of subjective cognitive decline and underwent amyloid PET and apolipoprotein ε (APOE) genotyping were retrospectively enrolled from January 2016 to January 2019. Models for cerebral amyloid positivity prediction were developed in all subjects, mild cognitive impairment (MCI) subjects, and Alzheimer’s disease (AD) dementia subjects through multivariate logistic regression analysis. The performance of the models was assessed using receiver operating characteristic (ROC) curve analysis and the area under the curve (AUC) values.Results Age, sex, years of education, body mass index (BMI), APOE4, and mini mental state examination score (MMSE) were selected for the final model for all subjects. The AUC value of the ROC curve was 0.775. Age, sex, years of education, BMI, and APOE4 were selected for the final model for MCI subjects. The AUC value was 0.735. Age, sex, years of education, BMI, APOE4, MMSE, and history of hypertension were selected for the final model for AD dementia subjects. The AUC value was 0.845.Conclusion This study found that models using clinical data can predict cerebral amyloid positivity according to cognitive status. These models can be useful as a screening tool predict cerebral amyloid deposition in cognitively impaired patients in a memory clinic. KCI Citation Count: 0
Author Joo, Soo Hyun
Lee, Chang Uk
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10.3233/jad-2012-121315
10.1016/j.nbd.2020.104784
10.1016/j.jalz.2013.02.003
10.1038/mp.2013.40
10.1016/j.neurobiolaging.2011.02.012
10.1002/mds.21507
10.1056/nejmoa1202753
10.2967/jnumed.113.120618
10.1016/j.jalz.2011.03.005
10.1016/j.jalz.2016.03.012
10.1007/s40336-015-0102-6
10.1111/j.1365-2796.2004.01380.x
10.1038/nature25456
10.1016/j.jalz.2012.07.003
10.1093/geronb/57.1.p47
10.1212/wnl.65.12.1992-a
10.3233/jad-140705
10.3389/fnagi.2018.00309
10.1212/01.wnl.0000144280.59178.78
10.1097/nen.0b013e31824b211b
10.1212/wnl.43.2.250
10.1001/jamaneurol.2017.0244
10.3346/jkms.2010.25.7.1071
10.1016/j.jalz.2017.06.2266
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References ref12
ref15
ref14
ref11
ref10
ref2
ref1
ref17
ref16
ref19
ref18
(ref13) 2013
ref24
ref23
ref26
ref25
ref20
ref22
ref21
ref28
ref27
ref7
ref9
ref4
ref3
ref6
ref5
Rascovsky (ref8) 2011
References_xml – ident: ref20
  doi: 10.1186/s13195-017-0248-8
– ident: ref17
  doi: 10.3233/jad-2012-121315
– ident: ref24
  doi: 10.1016/j.nbd.2020.104784
– ident: ref1
  doi: 10.1016/j.jalz.2013.02.003
– ident: ref18
  doi: 10.1038/mp.2013.40
– ident: ref27
  doi: 10.1016/j.neurobiolaging.2011.02.012
– ident: ref12
  doi: 10.1002/mds.21507
– start-page: 2456
  volume-title: Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia
  year: 2011
  ident: ref8
– ident: ref2
  doi: 10.1056/nejmoa1202753
– ident: ref5
  doi: 10.2967/jnumed.113.120618
– ident: ref14
  doi: 10.1016/j.jalz.2011.03.005
– ident: ref26
  doi: 10.1016/j.jalz.2016.03.012
– ident: ref15
  doi: 10.1007/s40336-015-0102-6
– ident: ref11
  doi: 10.1111/j.1365-2796.2004.01380.x
– ident: ref19
  doi: 10.1038/nature25456
– year: 2013
  ident: ref13
– ident: ref4
  doi: 10.1016/j.jalz.2012.07.003
– ident: ref7
  doi: 10.1093/geronb/57.1.p47
– ident: ref9
  doi: 10.1212/wnl.65.12.1992-a
– ident: ref22
  doi: 10.3233/jad-140705
– ident: ref23
  doi: 10.3389/fnagi.2018.00309
– volume-title: VizamylTM Flutemetamol F 18 Injection
  ident: ref16
– ident: ref28
  doi: 10.1212/01.wnl.0000144280.59178.78
– ident: ref3
  doi: 10.1097/nen.0b013e31824b211b
– ident: ref10
  doi: 10.1212/wnl.43.2.250
– ident: ref25
  doi: 10.1001/jamaneurol.2017.0244
– ident: ref6
  doi: 10.3346/jkms.2010.25.7.1071
– ident: ref21
  doi: 10.1016/j.jalz.2017.06.2266
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Snippet Objective Due to high cost of amyloid imaging, its use of amyloid imaging to confirm amyloid pathology is limited in clinical practice. It is of importance to...
Due to high cost of amyloid imaging, its use of amyloid imaging to confirm amyloid pathology is limited in clinical practice. It is of importance to develop a...
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Title Cerebral Amyloid Positivity Prediction Models Using Clinical Data in Subjects With Mild Cognitive Impairment and Dementia
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