Microbleeds in dementia with Lewy bodies

Introduction Microbleeds are associated with the development of dementia in older people and are common in Alzheimer’s disease (AD). Their prevalence and clinical importance in dementia with Lewy bodies (DLB) is unclear. The objective of this study was to compare the rates of microbleeds in DLB with...

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Veröffentlicht in:Journal of neurology 2020-05, Vol.267 (5), p.1491-1498
Hauptverfasser: Donaghy, Paul C., Firbank, Michael, Mitra, Dipayan, Petrides, George, Lloyd, Jim, Barnett, Nicola, Olsen, Kirsty, Thomas, Alan J., O’Brien, John T.
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container_end_page 1498
container_issue 5
container_start_page 1491
container_title Journal of neurology
container_volume 267
creator Donaghy, Paul C.
Firbank, Michael
Mitra, Dipayan
Petrides, George
Lloyd, Jim
Barnett, Nicola
Olsen, Kirsty
Thomas, Alan J.
O’Brien, John T.
description Introduction Microbleeds are associated with the development of dementia in older people and are common in Alzheimer’s disease (AD). Their prevalence and clinical importance in dementia with Lewy bodies (DLB) is unclear. The objective of this study was to compare the rates of microbleeds in DLB with those in AD and healthy older people, and investigate associations between microbleeds and amyloid deposition, vascular risk and disease severity in DLB. Methods DLB ( n  = 30), AD ( n  = 18) and control ( n  = 20) participants underwent clinical assessment at baseline and 1 year in this longitudinal observational study. 3T MRI (including T2* susceptibility weighted imaging) and florbetapir PET were carried out at baseline. Microbleeds were rated visually and a standardised uptake value ratio (SUVR) was calculated from florbetapir PET scans. Results 40% of DLB subjects had microbleeds compared with 50% of AD and 15% of controls. Compared to DLB without microbleeds, those with microbleeds had higher systolic BP (156 ± 26 v. 135 ± 19 mmHg; p  = 0.03), but did not have greater levels of vascular disease or amyloid deposition (SUVR 1.25 ± 0.24 v. 1.25 ± 0.22; p  = 0.33). There was evidence of less severe dementia in DLB participants with microbleeds, but these differences may have been driven by a shorter disease duration in those with microbleeds. Conclusion The presence of microbleeds in DLB is associated with higher blood pressure, but not with other measures of vascular disease or amyloid deposition. The relationship between microbleeds and clinical presentation remains unclear.
doi_str_mv 10.1007/s00415-020-09736-0
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Their prevalence and clinical importance in dementia with Lewy bodies (DLB) is unclear. The objective of this study was to compare the rates of microbleeds in DLB with those in AD and healthy older people, and investigate associations between microbleeds and amyloid deposition, vascular risk and disease severity in DLB. Methods DLB ( n  = 30), AD ( n  = 18) and control ( n  = 20) participants underwent clinical assessment at baseline and 1 year in this longitudinal observational study. 3T MRI (including T2* susceptibility weighted imaging) and florbetapir PET were carried out at baseline. Microbleeds were rated visually and a standardised uptake value ratio (SUVR) was calculated from florbetapir PET scans. Results 40% of DLB subjects had microbleeds compared with 50% of AD and 15% of controls. Compared to DLB without microbleeds, those with microbleeds had higher systolic BP (156 ± 26 v. 135 ± 19 mmHg; p  = 0.03), but did not have greater levels of vascular disease or amyloid deposition (SUVR 1.25 ± 0.24 v. 1.25 ± 0.22; p  = 0.33). There was evidence of less severe dementia in DLB participants with microbleeds, but these differences may have been driven by a shorter disease duration in those with microbleeds. Conclusion The presence of microbleeds in DLB is associated with higher blood pressure, but not with other measures of vascular disease or amyloid deposition. The relationship between microbleeds and clinical presentation remains unclear.</description><identifier>ISSN: 0340-5354</identifier><identifier>EISSN: 1432-1459</identifier><identifier>DOI: 10.1007/s00415-020-09736-0</identifier><identifier>PMID: 32016624</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Aged ; Aged, 80 and over ; Alzheimer Disease - diagnostic imaging ; Alzheimer Disease - metabolism ; Alzheimer Disease - pathology ; Alzheimer Disease - physiopathology ; Alzheimer's disease ; Amyloid beta-Peptides - metabolism ; Blood pressure ; Blood Pressure - physiology ; Cerebral Hemorrhage - diagnostic imaging ; Cerebral Hemorrhage - metabolism ; Cerebral Hemorrhage - pathology ; Cerebral Hemorrhage - physiopathology ; Dementia ; Dementia disorders ; Female ; Humans ; Lewy bodies ; Lewy Body Disease - diagnostic imaging ; Lewy Body Disease - metabolism ; Lewy Body Disease - pathology ; Lewy Body Disease - physiopathology ; Longitudinal Studies ; Magnetic Resonance Imaging ; Male ; Medicine ; Medicine &amp; Public Health ; Neurodegenerative diseases ; Neurology ; Neuroradiology ; Neurosciences ; Older people ; Original Communication ; Positron-Emission Tomography ; Vascular diseases</subject><ispartof>Journal of neurology, 2020-05, Vol.267 (5), p.1491-1498</ispartof><rights>The Author(s) 2020</rights><rights>The Author(s) 2020. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c474t-7b49fbb2d59c0ecf564e8ec6a98271cc512ef4764b100b7810dafa74f6eff8da3</citedby><cites>FETCH-LOGICAL-c474t-7b49fbb2d59c0ecf564e8ec6a98271cc512ef4764b100b7810dafa74f6eff8da3</cites><orcidid>0000-0001-7195-4846</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00415-020-09736-0$$EPDF$$P50$$Gspringer$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00415-020-09736-0$$EHTML$$P50$$Gspringer$$Hfree_for_read</linktohtml><link.rule.ids>230,314,780,784,885,27922,27923,41486,42555,51317</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32016624$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Donaghy, Paul C.</creatorcontrib><creatorcontrib>Firbank, Michael</creatorcontrib><creatorcontrib>Mitra, Dipayan</creatorcontrib><creatorcontrib>Petrides, George</creatorcontrib><creatorcontrib>Lloyd, Jim</creatorcontrib><creatorcontrib>Barnett, Nicola</creatorcontrib><creatorcontrib>Olsen, Kirsty</creatorcontrib><creatorcontrib>Thomas, Alan J.</creatorcontrib><creatorcontrib>O’Brien, John T.</creatorcontrib><title>Microbleeds in dementia with Lewy bodies</title><title>Journal of neurology</title><addtitle>J Neurol</addtitle><addtitle>J Neurol</addtitle><description>Introduction Microbleeds are associated with the development of dementia in older people and are common in Alzheimer’s disease (AD). Their prevalence and clinical importance in dementia with Lewy bodies (DLB) is unclear. The objective of this study was to compare the rates of microbleeds in DLB with those in AD and healthy older people, and investigate associations between microbleeds and amyloid deposition, vascular risk and disease severity in DLB. Methods DLB ( n  = 30), AD ( n  = 18) and control ( n  = 20) participants underwent clinical assessment at baseline and 1 year in this longitudinal observational study. 3T MRI (including T2* susceptibility weighted imaging) and florbetapir PET were carried out at baseline. Microbleeds were rated visually and a standardised uptake value ratio (SUVR) was calculated from florbetapir PET scans. Results 40% of DLB subjects had microbleeds compared with 50% of AD and 15% of controls. Compared to DLB without microbleeds, those with microbleeds had higher systolic BP (156 ± 26 v. 135 ± 19 mmHg; p  = 0.03), but did not have greater levels of vascular disease or amyloid deposition (SUVR 1.25 ± 0.24 v. 1.25 ± 0.22; p  = 0.33). There was evidence of less severe dementia in DLB participants with microbleeds, but these differences may have been driven by a shorter disease duration in those with microbleeds. Conclusion The presence of microbleeds in DLB is associated with higher blood pressure, but not with other measures of vascular disease or amyloid deposition. 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Public Health</topic><topic>Neurodegenerative diseases</topic><topic>Neurology</topic><topic>Neuroradiology</topic><topic>Neurosciences</topic><topic>Older people</topic><topic>Original Communication</topic><topic>Positron-Emission Tomography</topic><topic>Vascular diseases</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Donaghy, Paul C.</creatorcontrib><creatorcontrib>Firbank, Michael</creatorcontrib><creatorcontrib>Mitra, Dipayan</creatorcontrib><creatorcontrib>Petrides, George</creatorcontrib><creatorcontrib>Lloyd, Jim</creatorcontrib><creatorcontrib>Barnett, Nicola</creatorcontrib><creatorcontrib>Olsen, Kirsty</creatorcontrib><creatorcontrib>Thomas, Alan J.</creatorcontrib><creatorcontrib>O’Brien, John T.</creatorcontrib><collection>Springer</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>ProQuest Health &amp; 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Their prevalence and clinical importance in dementia with Lewy bodies (DLB) is unclear. The objective of this study was to compare the rates of microbleeds in DLB with those in AD and healthy older people, and investigate associations between microbleeds and amyloid deposition, vascular risk and disease severity in DLB. Methods DLB ( n  = 30), AD ( n  = 18) and control ( n  = 20) participants underwent clinical assessment at baseline and 1 year in this longitudinal observational study. 3T MRI (including T2* susceptibility weighted imaging) and florbetapir PET were carried out at baseline. Microbleeds were rated visually and a standardised uptake value ratio (SUVR) was calculated from florbetapir PET scans. Results 40% of DLB subjects had microbleeds compared with 50% of AD and 15% of controls. Compared to DLB without microbleeds, those with microbleeds had higher systolic BP (156 ± 26 v. 135 ± 19 mmHg; p  = 0.03), but did not have greater levels of vascular disease or amyloid deposition (SUVR 1.25 ± 0.24 v. 1.25 ± 0.22; p  = 0.33). There was evidence of less severe dementia in DLB participants with microbleeds, but these differences may have been driven by a shorter disease duration in those with microbleeds. Conclusion The presence of microbleeds in DLB is associated with higher blood pressure, but not with other measures of vascular disease or amyloid deposition. The relationship between microbleeds and clinical presentation remains unclear.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>32016624</pmid><doi>10.1007/s00415-020-09736-0</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0001-7195-4846</orcidid><oa>free_for_read</oa></addata></record>
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subjects Aged
Aged, 80 and over
Alzheimer Disease - diagnostic imaging
Alzheimer Disease - metabolism
Alzheimer Disease - pathology
Alzheimer Disease - physiopathology
Alzheimer's disease
Amyloid beta-Peptides - metabolism
Blood pressure
Blood Pressure - physiology
Cerebral Hemorrhage - diagnostic imaging
Cerebral Hemorrhage - metabolism
Cerebral Hemorrhage - pathology
Cerebral Hemorrhage - physiopathology
Dementia
Dementia disorders
Female
Humans
Lewy bodies
Lewy Body Disease - diagnostic imaging
Lewy Body Disease - metabolism
Lewy Body Disease - pathology
Lewy Body Disease - physiopathology
Longitudinal Studies
Magnetic Resonance Imaging
Male
Medicine
Medicine & Public Health
Neurodegenerative diseases
Neurology
Neuroradiology
Neurosciences
Older people
Original Communication
Positron-Emission Tomography
Vascular diseases
title Microbleeds in dementia with Lewy bodies
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