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Enhancing Diagnostic Accuracy of aMCI in the Elderly: Combination of Olfactory Test, Pupillary Response Test, BDNF Plasma Level, and APOE Genotype

Background. Amnestic Mild Cognitive Impairment (aMCI) often progresses to Alzheimer's disease. There are clinical markers and biomarkers to identify the degenerative process in the brain. Objectives. To obtain the diagnostic values of olfactory test, pupillary response to tropicamide 0.01%, BDN...

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Autores principales: Turana, Yuda, Ranakusuma, Teguh Asaat S., Purba, Jan Sudir, Amir, Nurmiati, Ahmad, Siti Airiza, Machfoed, Moh. Hasan, Handayani, Yvonne Suzy, Asmarinah, Waspadji, Sarwono
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3929508/
https://www.ncbi.nlm.nih.gov/pubmed/24639912
http://dx.doi.org/10.1155/2014/912586
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author Turana, Yuda
Ranakusuma, Teguh Asaat S.
Purba, Jan Sudir
Amir, Nurmiati
Ahmad, Siti Airiza
Machfoed, Moh. Hasan
Handayani, Yvonne Suzy
Asmarinah,
Waspadji, Sarwono
author_facet Turana, Yuda
Ranakusuma, Teguh Asaat S.
Purba, Jan Sudir
Amir, Nurmiati
Ahmad, Siti Airiza
Machfoed, Moh. Hasan
Handayani, Yvonne Suzy
Asmarinah,
Waspadji, Sarwono
author_sort Turana, Yuda
collection PubMed
description Background. Amnestic Mild Cognitive Impairment (aMCI) often progresses to Alzheimer's disease. There are clinical markers and biomarkers to identify the degenerative process in the brain. Objectives. To obtain the diagnostic values of olfactory test, pupillary response to tropicamide 0.01%, BDNF plasma level, and APOE ε4 in diagnosing aMCI. Methods. Cross-sectional, comparative analysis. Results. There were 109 subjects enrolled (aMCI: 51, normal cognition: 58) with age 64 ± 5.54 years. For diagnosing aMCI, cut-off point for the olfactory score was <7 out of 10 and >22% for pupil dilatation response. Low BDNF plasma level was related significantly with olfactory deficits and aMCI (P < 0.05). Four of five subjects with homozygote e4 presented with multiple-domain aMCI. This group displayed the lowest means of olfactory score and the highest means of pupillary hypersensitivity response (P < 0.0001). Combination of olfactory deficit and pupillary hypersensitivity response in detection of aMCI was beneficial with Sp 91% and PPV 87%. In conjunction with clinical markers, BDNF plasma level and presence of APOE e4+ improved Sp and PPV. Conclusions. Combination of olfactory test and pupillary response test was useful as diagnostic tool in aMCI. In conjunction with clinical markers, low level of BDNF plasma and presence of APOE e4 improved the diagnostic value.
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spelling pubmed-39295082014-03-17 Enhancing Diagnostic Accuracy of aMCI in the Elderly: Combination of Olfactory Test, Pupillary Response Test, BDNF Plasma Level, and APOE Genotype Turana, Yuda Ranakusuma, Teguh Asaat S. Purba, Jan Sudir Amir, Nurmiati Ahmad, Siti Airiza Machfoed, Moh. Hasan Handayani, Yvonne Suzy Asmarinah, Waspadji, Sarwono Int J Alzheimers Dis Research Article Background. Amnestic Mild Cognitive Impairment (aMCI) often progresses to Alzheimer's disease. There are clinical markers and biomarkers to identify the degenerative process in the brain. Objectives. To obtain the diagnostic values of olfactory test, pupillary response to tropicamide 0.01%, BDNF plasma level, and APOE ε4 in diagnosing aMCI. Methods. Cross-sectional, comparative analysis. Results. There were 109 subjects enrolled (aMCI: 51, normal cognition: 58) with age 64 ± 5.54 years. For diagnosing aMCI, cut-off point for the olfactory score was <7 out of 10 and >22% for pupil dilatation response. Low BDNF plasma level was related significantly with olfactory deficits and aMCI (P < 0.05). Four of five subjects with homozygote e4 presented with multiple-domain aMCI. This group displayed the lowest means of olfactory score and the highest means of pupillary hypersensitivity response (P < 0.0001). Combination of olfactory deficit and pupillary hypersensitivity response in detection of aMCI was beneficial with Sp 91% and PPV 87%. In conjunction with clinical markers, BDNF plasma level and presence of APOE e4+ improved Sp and PPV. Conclusions. Combination of olfactory test and pupillary response test was useful as diagnostic tool in aMCI. In conjunction with clinical markers, low level of BDNF plasma and presence of APOE e4 improved the diagnostic value. Hindawi Publishing Corporation 2014 2014-02-02 /pmc/articles/PMC3929508/ /pubmed/24639912 http://dx.doi.org/10.1155/2014/912586 Text en Copyright © 2014 Yuda Turana et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Turana, Yuda
Ranakusuma, Teguh Asaat S.
Purba, Jan Sudir
Amir, Nurmiati
Ahmad, Siti Airiza
Machfoed, Moh. Hasan
Handayani, Yvonne Suzy
Asmarinah,
Waspadji, Sarwono
Enhancing Diagnostic Accuracy of aMCI in the Elderly: Combination of Olfactory Test, Pupillary Response Test, BDNF Plasma Level, and APOE Genotype
title Enhancing Diagnostic Accuracy of aMCI in the Elderly: Combination of Olfactory Test, Pupillary Response Test, BDNF Plasma Level, and APOE Genotype
title_full Enhancing Diagnostic Accuracy of aMCI in the Elderly: Combination of Olfactory Test, Pupillary Response Test, BDNF Plasma Level, and APOE Genotype
title_fullStr Enhancing Diagnostic Accuracy of aMCI in the Elderly: Combination of Olfactory Test, Pupillary Response Test, BDNF Plasma Level, and APOE Genotype
title_full_unstemmed Enhancing Diagnostic Accuracy of aMCI in the Elderly: Combination of Olfactory Test, Pupillary Response Test, BDNF Plasma Level, and APOE Genotype
title_short Enhancing Diagnostic Accuracy of aMCI in the Elderly: Combination of Olfactory Test, Pupillary Response Test, BDNF Plasma Level, and APOE Genotype
title_sort enhancing diagnostic accuracy of amci in the elderly: combination of olfactory test, pupillary response test, bdnf plasma level, and apoe genotype
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3929508/
https://www.ncbi.nlm.nih.gov/pubmed/24639912
http://dx.doi.org/10.1155/2014/912586
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