Clinical profile of PiB-positive corticobasal syndrome
Corticobasal syndrome (CBS) is a multifaceted neurodegenerative disorder characterized by a combination of motor and cognitive deficits. Several different pathological entities, including Alzheimer's pathology, have been described in association with CBS. The present study aimed to establish cl...
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description | Corticobasal syndrome (CBS) is a multifaceted neurodegenerative disorder characterized by a combination of motor and cognitive deficits. Several different pathological entities, including Alzheimer's pathology, have been described in association with CBS. The present study aimed to establish clinical, neuropsychological, and neuroimaging features that could be useful in the distinction of CBS due to AD pathology from other CBS cases in life based on [(11)C] Pittsburgh Compound B positron emission tomography (PiB-PET) status.
Patients with CBS were prospectively recruited from a specialized cognitive disorders clinic. All patients underwent detailed clinical and neuropsychological assessment, with structural imaging using voxel-based analysis of magnetic resonance imaging. Alzheimer's pathology was detected using PiB-PET imaging, and PiB-positive and PiB-negative groups were compared.
Fourteen CBS patients meeting defined criteria were included (7 male, 7 female; mean age 66.1+/-6.9 years; median symptom duration was 35.5+/-22.6 months) and compared to 20 matched control subjects. Of the 14 patients, 4 were PiB-positive and 10 PiB-negative. There were no significant differences between PiB-positive and PiB-negative CBS patients in age, gender, education, symptom duration, or motor features. PiB-positive patients had greater visuospatial deficits, a higher rate of sentence repetition impairment, and more functional decline. Voxel-based morphometry analyses demonstrated extensive peri-insular and post-central atrophy in both groups, but PiB-positive patients had atrophy that extended to include the posterior part of the left superior temporal gyrus.
Visuospatial function, aspects of language, and the pattern of cerebral atrophy may be useful in distinguishing patients with CBS due to underlying AD pathology. |
doi_str_mv | 10.1371/journal.pone.0061025 |
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Patients with CBS were prospectively recruited from a specialized cognitive disorders clinic. All patients underwent detailed clinical and neuropsychological assessment, with structural imaging using voxel-based analysis of magnetic resonance imaging. Alzheimer's pathology was detected using PiB-PET imaging, and PiB-positive and PiB-negative groups were compared.
Fourteen CBS patients meeting defined criteria were included (7 male, 7 female; mean age 66.1+/-6.9 years; median symptom duration was 35.5+/-22.6 months) and compared to 20 matched control subjects. Of the 14 patients, 4 were PiB-positive and 10 PiB-negative. There were no significant differences between PiB-positive and PiB-negative CBS patients in age, gender, education, symptom duration, or motor features. PiB-positive patients had greater visuospatial deficits, a higher rate of sentence repetition impairment, and more functional decline. Voxel-based morphometry analyses demonstrated extensive peri-insular and post-central atrophy in both groups, but PiB-positive patients had atrophy that extended to include the posterior part of the left superior temporal gyrus.
Visuospatial function, aspects of language, and the pattern of cerebral atrophy may be useful in distinguishing patients with CBS due to underlying AD pathology.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0061025</identifier><identifier>PMID: 23577184</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Advertising executives ; Aged ; Aging ; Alzheimer Disease - complications ; Alzheimer's disease ; Aniline Compounds ; Atrophy ; Behavior ; Biology ; Carbon Radioisotopes ; Cognition & reasoning ; Cognitive ability ; Cognitive impairment ; Dementia ; Female ; Humans ; Language ; Magnetic resonance ; Magnetic Resonance Imaging ; Male ; Medical imaging ; Medical research ; Medicine ; Medicine, Experimental ; Memory ; Middle Aged ; Morphometry ; Motor Activity ; Nervous system diseases ; Neurodegenerative diseases ; Neurodegenerative Diseases - complications ; Neurodegenerative Diseases - diagnostic imaging ; Neurodegenerative Diseases - physiopathology ; Neurodegenerative Diseases - psychology ; Neuroimaging ; Neurology ; Neuropsychological assessment ; Neuropsychological Tests ; Neurosciences ; Pathology ; Patients ; PET imaging ; Phonetics ; Positron emission ; Positron emission tomography ; Positron emission tomography (PET) ; Research subjects ; Social and Behavioral Sciences ; Superior temporal gyrus ; Temporal gyrus ; Thiazoles ; Tomography</subject><ispartof>PloS one, 2013-04, Vol.8 (4), p.e61025-e61025</ispartof><rights>COPYRIGHT 2013 Public Library of Science</rights><rights>2013 Burrell et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2013 Burrell et al 2013 Burrell et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c758t-2f102fa47ca9f78ee3bbea38b3de84dd8d582072848040711e56e379deae470b3</citedby><cites>FETCH-LOGICAL-c758t-2f102fa47ca9f78ee3bbea38b3de84dd8d582072848040711e56e379deae470b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3618463/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3618463/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,2096,2915,23845,27901,27902,53766,53768,79342,79343</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23577184$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Burrell, James R</creatorcontrib><creatorcontrib>Hornberger, Michael</creatorcontrib><creatorcontrib>Villemagne, Victor L</creatorcontrib><creatorcontrib>Rowe, Christopher C</creatorcontrib><creatorcontrib>Hodges, John R</creatorcontrib><title>Clinical profile of PiB-positive corticobasal syndrome</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Corticobasal syndrome (CBS) is a multifaceted neurodegenerative disorder characterized by a combination of motor and cognitive deficits. Several different pathological entities, including Alzheimer's pathology, have been described in association with CBS. The present study aimed to establish clinical, neuropsychological, and neuroimaging features that could be useful in the distinction of CBS due to AD pathology from other CBS cases in life based on [(11)C] Pittsburgh Compound B positron emission tomography (PiB-PET) status.
Patients with CBS were prospectively recruited from a specialized cognitive disorders clinic. All patients underwent detailed clinical and neuropsychological assessment, with structural imaging using voxel-based analysis of magnetic resonance imaging. Alzheimer's pathology was detected using PiB-PET imaging, and PiB-positive and PiB-negative groups were compared.
Fourteen CBS patients meeting defined criteria were included (7 male, 7 female; mean age 66.1+/-6.9 years; median symptom duration was 35.5+/-22.6 months) and compared to 20 matched control subjects. Of the 14 patients, 4 were PiB-positive and 10 PiB-negative. There were no significant differences between PiB-positive and PiB-negative CBS patients in age, gender, education, symptom duration, or motor features. PiB-positive patients had greater visuospatial deficits, a higher rate of sentence repetition impairment, and more functional decline. Voxel-based morphometry analyses demonstrated extensive peri-insular and post-central atrophy in both groups, but PiB-positive patients had atrophy that extended to include the posterior part of the left superior temporal gyrus.
Visuospatial function, aspects of language, and the pattern of cerebral atrophy may be useful in distinguishing patients with CBS due to underlying AD pathology.</description><subject>Advertising executives</subject><subject>Aged</subject><subject>Aging</subject><subject>Alzheimer Disease - complications</subject><subject>Alzheimer's disease</subject><subject>Aniline Compounds</subject><subject>Atrophy</subject><subject>Behavior</subject><subject>Biology</subject><subject>Carbon Radioisotopes</subject><subject>Cognition & reasoning</subject><subject>Cognitive ability</subject><subject>Cognitive impairment</subject><subject>Dementia</subject><subject>Female</subject><subject>Humans</subject><subject>Language</subject><subject>Magnetic resonance</subject><subject>Magnetic Resonance Imaging</subject><subject>Male</subject><subject>Medical imaging</subject><subject>Medical research</subject><subject>Medicine</subject><subject>Medicine, Experimental</subject><subject>Memory</subject><subject>Middle Aged</subject><subject>Morphometry</subject><subject>Motor Activity</subject><subject>Nervous system diseases</subject><subject>Neurodegenerative diseases</subject><subject>Neurodegenerative Diseases - complications</subject><subject>Neurodegenerative Diseases - diagnostic imaging</subject><subject>Neurodegenerative Diseases - physiopathology</subject><subject>Neurodegenerative Diseases - psychology</subject><subject>Neuroimaging</subject><subject>Neurology</subject><subject>Neuropsychological assessment</subject><subject>Neuropsychological Tests</subject><subject>Neurosciences</subject><subject>Pathology</subject><subject>Patients</subject><subject>PET imaging</subject><subject>Phonetics</subject><subject>Positron emission</subject><subject>Positron emission tomography</subject><subject>Positron emission tomography (PET)</subject><subject>Research subjects</subject><subject>Social and Behavioral 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a combination of motor and cognitive deficits. Several different pathological entities, including Alzheimer's pathology, have been described in association with CBS. The present study aimed to establish clinical, neuropsychological, and neuroimaging features that could be useful in the distinction of CBS due to AD pathology from other CBS cases in life based on [(11)C] Pittsburgh Compound B positron emission tomography (PiB-PET) status.
Patients with CBS were prospectively recruited from a specialized cognitive disorders clinic. All patients underwent detailed clinical and neuropsychological assessment, with structural imaging using voxel-based analysis of magnetic resonance imaging. Alzheimer's pathology was detected using PiB-PET imaging, and PiB-positive and PiB-negative groups were compared.
Fourteen CBS patients meeting defined criteria were included (7 male, 7 female; mean age 66.1+/-6.9 years; median symptom duration was 35.5+/-22.6 months) and compared to 20 matched control subjects. Of the 14 patients, 4 were PiB-positive and 10 PiB-negative. There were no significant differences between PiB-positive and PiB-negative CBS patients in age, gender, education, symptom duration, or motor features. PiB-positive patients had greater visuospatial deficits, a higher rate of sentence repetition impairment, and more functional decline. Voxel-based morphometry analyses demonstrated extensive peri-insular and post-central atrophy in both groups, but PiB-positive patients had atrophy that extended to include the posterior part of the left superior temporal gyrus.
Visuospatial function, aspects of language, and the pattern of cerebral atrophy may be useful in distinguishing patients with CBS due to underlying AD pathology.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>23577184</pmid><doi>10.1371/journal.pone.0061025</doi><tpages>e61025</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Advertising executives Aged Aging Alzheimer Disease - complications Alzheimer's disease Aniline Compounds Atrophy Behavior Biology Carbon Radioisotopes Cognition & reasoning Cognitive ability Cognitive impairment Dementia Female Humans Language Magnetic resonance Magnetic Resonance Imaging Male Medical imaging Medical research Medicine Medicine, Experimental Memory Middle Aged Morphometry Motor Activity Nervous system diseases Neurodegenerative diseases Neurodegenerative Diseases - complications Neurodegenerative Diseases - diagnostic imaging Neurodegenerative Diseases - physiopathology Neurodegenerative Diseases - psychology Neuroimaging Neurology Neuropsychological assessment Neuropsychological Tests Neurosciences Pathology Patients PET imaging Phonetics Positron emission Positron emission tomography Positron emission tomography (PET) Research subjects Social and Behavioral Sciences Superior temporal gyrus Temporal gyrus Thiazoles Tomography |
title | Clinical profile of PiB-positive corticobasal syndrome |
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