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Alzheimer’s disease diagnosis based on the Hippocampal Unified Multi-Atlas Network (HUMAN) algorithm

BACKGROUND: Hippocampal atrophy is a supportive feature for the diagnosis of probable Alzheimer’s disease (AD). However, even for an expert neuroradiologist, tracing the hippocampus and measuring its volume is a time consuming and extremely challenging task. Accordingly, the development of reliable...

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Autores principales: Amoroso, Nicola, Rocca, Marianna La, Bellotti, Roberto, Fanizzi, Annarita, Monaco, Alfonso, Tangaro, Sabina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5778685/
https://www.ncbi.nlm.nih.gov/pubmed/29357893
http://dx.doi.org/10.1186/s12938-018-0439-y
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author Amoroso, Nicola
Rocca, Marianna La
Bellotti, Roberto
Fanizzi, Annarita
Monaco, Alfonso
Tangaro, Sabina
author_facet Amoroso, Nicola
Rocca, Marianna La
Bellotti, Roberto
Fanizzi, Annarita
Monaco, Alfonso
Tangaro, Sabina
author_sort Amoroso, Nicola
collection PubMed
description BACKGROUND: Hippocampal atrophy is a supportive feature for the diagnosis of probable Alzheimer’s disease (AD). However, even for an expert neuroradiologist, tracing the hippocampus and measuring its volume is a time consuming and extremely challenging task. Accordingly, the development of reliable fully-automated segmentation algorithms is of paramount importance. MATERIALS AND METHODS: The present study evaluates (i) the precision and the robustness of the novel Hippocampal Unified Multi-Atlas Network (HUMAN) segmentation algorithm and (ii) its clinical reliability for AD diagnosis. For these purposes, we used a mixed cohort of 456 subjects and their T1 weighted magnetic resonance imaging (MRI) brain scans. The cohort included 145 controls (CTRL), 217 mild cognitive impairment (MCI) subjects and 94 AD patients from Alzheimer’s Disease Neuroimaging Initiative (ADNI). For each subject the baseline, repeat, 12 and 24 month follow-up scans were available. RESULTS: HUMAN provides hippocampal volumes with a 3% precision; volume measurements effectively reveal AD, with an area under the curve (AUC) AUC(1) = 0.08 ± 0.02. Segmented volumes can also reveal the subtler effects present in MCI subjects, AUC(2) = 0.76 ± 0.05. The algorithm is stable and reproducible over time, even for 24 month follow-up scans. CONCLUSIONS: The experimental results demonstrate HUMAN is a precise segmentation algorithm, besides hippocampal volumes, provided by HUMAN, can effectively support the diagnosis of Alzheimer’s disease and become a useful tool for other neuroimaging applications.
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spelling pubmed-57786852018-01-31 Alzheimer’s disease diagnosis based on the Hippocampal Unified Multi-Atlas Network (HUMAN) algorithm Amoroso, Nicola Rocca, Marianna La Bellotti, Roberto Fanizzi, Annarita Monaco, Alfonso Tangaro, Sabina Biomed Eng Online Research BACKGROUND: Hippocampal atrophy is a supportive feature for the diagnosis of probable Alzheimer’s disease (AD). However, even for an expert neuroradiologist, tracing the hippocampus and measuring its volume is a time consuming and extremely challenging task. Accordingly, the development of reliable fully-automated segmentation algorithms is of paramount importance. MATERIALS AND METHODS: The present study evaluates (i) the precision and the robustness of the novel Hippocampal Unified Multi-Atlas Network (HUMAN) segmentation algorithm and (ii) its clinical reliability for AD diagnosis. For these purposes, we used a mixed cohort of 456 subjects and their T1 weighted magnetic resonance imaging (MRI) brain scans. The cohort included 145 controls (CTRL), 217 mild cognitive impairment (MCI) subjects and 94 AD patients from Alzheimer’s Disease Neuroimaging Initiative (ADNI). For each subject the baseline, repeat, 12 and 24 month follow-up scans were available. RESULTS: HUMAN provides hippocampal volumes with a 3% precision; volume measurements effectively reveal AD, with an area under the curve (AUC) AUC(1) = 0.08 ± 0.02. Segmented volumes can also reveal the subtler effects present in MCI subjects, AUC(2) = 0.76 ± 0.05. The algorithm is stable and reproducible over time, even for 24 month follow-up scans. CONCLUSIONS: The experimental results demonstrate HUMAN is a precise segmentation algorithm, besides hippocampal volumes, provided by HUMAN, can effectively support the diagnosis of Alzheimer’s disease and become a useful tool for other neuroimaging applications. BioMed Central 2018-01-22 /pmc/articles/PMC5778685/ /pubmed/29357893 http://dx.doi.org/10.1186/s12938-018-0439-y Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Amoroso, Nicola
Rocca, Marianna La
Bellotti, Roberto
Fanizzi, Annarita
Monaco, Alfonso
Tangaro, Sabina
Alzheimer’s disease diagnosis based on the Hippocampal Unified Multi-Atlas Network (HUMAN) algorithm
title Alzheimer’s disease diagnosis based on the Hippocampal Unified Multi-Atlas Network (HUMAN) algorithm
title_full Alzheimer’s disease diagnosis based on the Hippocampal Unified Multi-Atlas Network (HUMAN) algorithm
title_fullStr Alzheimer’s disease diagnosis based on the Hippocampal Unified Multi-Atlas Network (HUMAN) algorithm
title_full_unstemmed Alzheimer’s disease diagnosis based on the Hippocampal Unified Multi-Atlas Network (HUMAN) algorithm
title_short Alzheimer’s disease diagnosis based on the Hippocampal Unified Multi-Atlas Network (HUMAN) algorithm
title_sort alzheimer’s disease diagnosis based on the hippocampal unified multi-atlas network (human) algorithm
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5778685/
https://www.ncbi.nlm.nih.gov/pubmed/29357893
http://dx.doi.org/10.1186/s12938-018-0439-y
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