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(11)C-PIB PET imaging reveals that amyloid deposition in cases with early-onset Alzheimer’s disease in the absence of known mutations retains higher levels of PIB in the basal ganglia
PURPOSE: Early-onset Alzheimer’s disease (EOAD) has a different pathologic burden and clinical features compared with late-onset Alzheimer’s disease (LOAD). We examined the effects of age at onset on the burden and distribution of β-amyloid in patients with EOAD, in whom well-characterized mutations...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Dove Medical Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5500536/ https://www.ncbi.nlm.nih.gov/pubmed/28721032 http://dx.doi.org/10.2147/CIA.S132884 |
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author | Youn, Young Chul Jang, Jae-Won Han, Su-Hyun Kim, HyeRyoun Seok, Ju-Won Byun, Jun Soo Park, Kwang-Yeol An, Seong Soo A Chun, In Kook Kim, SangYun |
author_facet | Youn, Young Chul Jang, Jae-Won Han, Su-Hyun Kim, HyeRyoun Seok, Ju-Won Byun, Jun Soo Park, Kwang-Yeol An, Seong Soo A Chun, In Kook Kim, SangYun |
author_sort | Youn, Young Chul |
collection | PubMed |
description | PURPOSE: Early-onset Alzheimer’s disease (EOAD) has a different pathologic burden and clinical features compared with late-onset Alzheimer’s disease (LOAD). We examined the effects of age at onset on the burden and distribution of β-amyloid in patients with EOAD, in whom well-characterized mutations associated with Alzheimer’s disease were absent. METHODS: We genotyped ApoE, APP, PSEN1 and PSEN2 in the patients with Alzheimer’s disease: 9 patients with EOAD (age <65), 11 with LOAD (age >70) and 8 normal controls (NCs), all of whom had undergone (11)C-labeled Pittsburgh compound B-positron emission tomography imaging. RESULTS: Patients with EOAD exhibited higher z scores and larger cluster sizes, and retained higher levels of Pittsburgh compound B in the bilateral thalamus and in some parts of the globus pallidus (P<0.05, false discovery rate). CONCLUSION: Distribution of amyloid deposition in EOAD outside the context of genetic mutations topographically showed some differences from that in LOAD. |
format | Online Article Text |
id | pubmed-5500536 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-55005362017-07-18 (11)C-PIB PET imaging reveals that amyloid deposition in cases with early-onset Alzheimer’s disease in the absence of known mutations retains higher levels of PIB in the basal ganglia Youn, Young Chul Jang, Jae-Won Han, Su-Hyun Kim, HyeRyoun Seok, Ju-Won Byun, Jun Soo Park, Kwang-Yeol An, Seong Soo A Chun, In Kook Kim, SangYun Clin Interv Aging Original Research PURPOSE: Early-onset Alzheimer’s disease (EOAD) has a different pathologic burden and clinical features compared with late-onset Alzheimer’s disease (LOAD). We examined the effects of age at onset on the burden and distribution of β-amyloid in patients with EOAD, in whom well-characterized mutations associated with Alzheimer’s disease were absent. METHODS: We genotyped ApoE, APP, PSEN1 and PSEN2 in the patients with Alzheimer’s disease: 9 patients with EOAD (age <65), 11 with LOAD (age >70) and 8 normal controls (NCs), all of whom had undergone (11)C-labeled Pittsburgh compound B-positron emission tomography imaging. RESULTS: Patients with EOAD exhibited higher z scores and larger cluster sizes, and retained higher levels of Pittsburgh compound B in the bilateral thalamus and in some parts of the globus pallidus (P<0.05, false discovery rate). CONCLUSION: Distribution of amyloid deposition in EOAD outside the context of genetic mutations topographically showed some differences from that in LOAD. Dove Medical Press 2017-06-29 /pmc/articles/PMC5500536/ /pubmed/28721032 http://dx.doi.org/10.2147/CIA.S132884 Text en © 2017 Youn et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Youn, Young Chul Jang, Jae-Won Han, Su-Hyun Kim, HyeRyoun Seok, Ju-Won Byun, Jun Soo Park, Kwang-Yeol An, Seong Soo A Chun, In Kook Kim, SangYun (11)C-PIB PET imaging reveals that amyloid deposition in cases with early-onset Alzheimer’s disease in the absence of known mutations retains higher levels of PIB in the basal ganglia |
title | (11)C-PIB PET imaging reveals that amyloid deposition in cases with early-onset Alzheimer’s disease in the absence of known mutations retains higher levels of PIB in the basal ganglia |
title_full | (11)C-PIB PET imaging reveals that amyloid deposition in cases with early-onset Alzheimer’s disease in the absence of known mutations retains higher levels of PIB in the basal ganglia |
title_fullStr | (11)C-PIB PET imaging reveals that amyloid deposition in cases with early-onset Alzheimer’s disease in the absence of known mutations retains higher levels of PIB in the basal ganglia |
title_full_unstemmed | (11)C-PIB PET imaging reveals that amyloid deposition in cases with early-onset Alzheimer’s disease in the absence of known mutations retains higher levels of PIB in the basal ganglia |
title_short | (11)C-PIB PET imaging reveals that amyloid deposition in cases with early-onset Alzheimer’s disease in the absence of known mutations retains higher levels of PIB in the basal ganglia |
title_sort | (11)c-pib pet imaging reveals that amyloid deposition in cases with early-onset alzheimer’s disease in the absence of known mutations retains higher levels of pib in the basal ganglia |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5500536/ https://www.ncbi.nlm.nih.gov/pubmed/28721032 http://dx.doi.org/10.2147/CIA.S132884 |
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