Cargando…
Regional brain amyloid-β accumulation associates with domain-specific cognitive performance in Parkinson disease without dementia
Parkinson disease patients develop clinically significant cognitive impairment at variable times over their disease course, which is often preceded by milder deficits in memory, visuo-spatial, and executive domains. The significance of amyloid-β accumulation to these problems is unclear. We hypothes...
Autores principales: | , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5444629/ https://www.ncbi.nlm.nih.gov/pubmed/28542444 http://dx.doi.org/10.1371/journal.pone.0177924 |
_version_ | 1783238735075213312 |
---|---|
author | Akhtar, Rizwan S. Xie, Sharon X. Chen, Yin J. Rick, Jacqueline Gross, Rachel G. Nasrallah, Ilya M. Van Deerlin, Vivianna M. Trojanowski, John Q. Chen-Plotkin, Alice S. Hurtig, Howard I. Siderowf, Andrew D. Dubroff, Jacob G. Weintraub, Daniel |
author_facet | Akhtar, Rizwan S. Xie, Sharon X. Chen, Yin J. Rick, Jacqueline Gross, Rachel G. Nasrallah, Ilya M. Van Deerlin, Vivianna M. Trojanowski, John Q. Chen-Plotkin, Alice S. Hurtig, Howard I. Siderowf, Andrew D. Dubroff, Jacob G. Weintraub, Daniel |
author_sort | Akhtar, Rizwan S. |
collection | PubMed |
description | Parkinson disease patients develop clinically significant cognitive impairment at variable times over their disease course, which is often preceded by milder deficits in memory, visuo-spatial, and executive domains. The significance of amyloid-β accumulation to these problems is unclear. We hypothesized that amyloid-β PET imaging by (18)F-florbetapir, a radiotracer that detects fibrillar amyloid-β plaque deposits, would identify subjects with global cognitive impairment or poor performance in individual cognitive domains in non-demented Parkinson disease patients. We assessed 61 non-demented Parkinson disease patients with detailed cognitive assessments and (18)F-florbetapir PET brain imaging. Scans were interpreted qualitatively (positive or negative) by two independent nuclear medicine physicians blinded to clinical data, and quantitatively by a novel volume-weighted method. The presence of mild cognitive impairment was determined through an expert consensus process using Level 1 criteria from the Movement Disorder Society. Nineteen participants (31.2%) were diagnosed with mild cognitive impairment and the remainder had normal cognition. Qualitative (18)F-florbetapir PET imaging was positive in 15 participants (24.6%). Increasing age and presence of an APOE ε4 allele were associated with higher composite (18)F-florbetapir binding. In multivariable models, an abnormal (18)F-florbetapir scan by expert rating was not associated with a diagnosis of mild cognitive impairment. However, (18)F-florbetapir retention values in the posterior cingulate gyrus inversely correlated with verbal memory performance. Retention values in the frontal cortex, precuneus, and anterior cingulate gyrus retention values inversely correlated with naming performance. Regional cortical amyloid-β amyloid, as measured by (18)F-florbetapir PET, may be a biomarker of specific cognitive deficits in non-demented Parkinson disease patients. |
format | Online Article Text |
id | pubmed-5444629 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-54446292017-06-12 Regional brain amyloid-β accumulation associates with domain-specific cognitive performance in Parkinson disease without dementia Akhtar, Rizwan S. Xie, Sharon X. Chen, Yin J. Rick, Jacqueline Gross, Rachel G. Nasrallah, Ilya M. Van Deerlin, Vivianna M. Trojanowski, John Q. Chen-Plotkin, Alice S. Hurtig, Howard I. Siderowf, Andrew D. Dubroff, Jacob G. Weintraub, Daniel PLoS One Research Article Parkinson disease patients develop clinically significant cognitive impairment at variable times over their disease course, which is often preceded by milder deficits in memory, visuo-spatial, and executive domains. The significance of amyloid-β accumulation to these problems is unclear. We hypothesized that amyloid-β PET imaging by (18)F-florbetapir, a radiotracer that detects fibrillar amyloid-β plaque deposits, would identify subjects with global cognitive impairment or poor performance in individual cognitive domains in non-demented Parkinson disease patients. We assessed 61 non-demented Parkinson disease patients with detailed cognitive assessments and (18)F-florbetapir PET brain imaging. Scans were interpreted qualitatively (positive or negative) by two independent nuclear medicine physicians blinded to clinical data, and quantitatively by a novel volume-weighted method. The presence of mild cognitive impairment was determined through an expert consensus process using Level 1 criteria from the Movement Disorder Society. Nineteen participants (31.2%) were diagnosed with mild cognitive impairment and the remainder had normal cognition. Qualitative (18)F-florbetapir PET imaging was positive in 15 participants (24.6%). Increasing age and presence of an APOE ε4 allele were associated with higher composite (18)F-florbetapir binding. In multivariable models, an abnormal (18)F-florbetapir scan by expert rating was not associated with a diagnosis of mild cognitive impairment. However, (18)F-florbetapir retention values in the posterior cingulate gyrus inversely correlated with verbal memory performance. Retention values in the frontal cortex, precuneus, and anterior cingulate gyrus retention values inversely correlated with naming performance. Regional cortical amyloid-β amyloid, as measured by (18)F-florbetapir PET, may be a biomarker of specific cognitive deficits in non-demented Parkinson disease patients. Public Library of Science 2017-05-25 /pmc/articles/PMC5444629/ /pubmed/28542444 http://dx.doi.org/10.1371/journal.pone.0177924 Text en © 2017 Akhtar et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Akhtar, Rizwan S. Xie, Sharon X. Chen, Yin J. Rick, Jacqueline Gross, Rachel G. Nasrallah, Ilya M. Van Deerlin, Vivianna M. Trojanowski, John Q. Chen-Plotkin, Alice S. Hurtig, Howard I. Siderowf, Andrew D. Dubroff, Jacob G. Weintraub, Daniel Regional brain amyloid-β accumulation associates with domain-specific cognitive performance in Parkinson disease without dementia |
title | Regional brain amyloid-β accumulation associates with domain-specific cognitive performance in Parkinson disease without dementia |
title_full | Regional brain amyloid-β accumulation associates with domain-specific cognitive performance in Parkinson disease without dementia |
title_fullStr | Regional brain amyloid-β accumulation associates with domain-specific cognitive performance in Parkinson disease without dementia |
title_full_unstemmed | Regional brain amyloid-β accumulation associates with domain-specific cognitive performance in Parkinson disease without dementia |
title_short | Regional brain amyloid-β accumulation associates with domain-specific cognitive performance in Parkinson disease without dementia |
title_sort | regional brain amyloid-β accumulation associates with domain-specific cognitive performance in parkinson disease without dementia |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5444629/ https://www.ncbi.nlm.nih.gov/pubmed/28542444 http://dx.doi.org/10.1371/journal.pone.0177924 |
work_keys_str_mv | AT akhtarrizwans regionalbrainamyloidbaccumulationassociateswithdomainspecificcognitiveperformanceinparkinsondiseasewithoutdementia AT xiesharonx regionalbrainamyloidbaccumulationassociateswithdomainspecificcognitiveperformanceinparkinsondiseasewithoutdementia AT chenyinj regionalbrainamyloidbaccumulationassociateswithdomainspecificcognitiveperformanceinparkinsondiseasewithoutdementia AT rickjacqueline regionalbrainamyloidbaccumulationassociateswithdomainspecificcognitiveperformanceinparkinsondiseasewithoutdementia AT grossrachelg regionalbrainamyloidbaccumulationassociateswithdomainspecificcognitiveperformanceinparkinsondiseasewithoutdementia AT nasrallahilyam regionalbrainamyloidbaccumulationassociateswithdomainspecificcognitiveperformanceinparkinsondiseasewithoutdementia AT vandeerlinviviannam regionalbrainamyloidbaccumulationassociateswithdomainspecificcognitiveperformanceinparkinsondiseasewithoutdementia AT trojanowskijohnq regionalbrainamyloidbaccumulationassociateswithdomainspecificcognitiveperformanceinparkinsondiseasewithoutdementia AT chenplotkinalices regionalbrainamyloidbaccumulationassociateswithdomainspecificcognitiveperformanceinparkinsondiseasewithoutdementia AT hurtighowardi regionalbrainamyloidbaccumulationassociateswithdomainspecificcognitiveperformanceinparkinsondiseasewithoutdementia AT siderowfandrewd regionalbrainamyloidbaccumulationassociateswithdomainspecificcognitiveperformanceinparkinsondiseasewithoutdementia AT dubroffjacobg regionalbrainamyloidbaccumulationassociateswithdomainspecificcognitiveperformanceinparkinsondiseasewithoutdementia AT weintraubdaniel regionalbrainamyloidbaccumulationassociateswithdomainspecificcognitiveperformanceinparkinsondiseasewithoutdementia |