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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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 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7184053</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2350902224</sourcerecordid><originalsourceid>FETCH-LOGICAL-c474t-7b49fbb2d59c0ecf564e8ec6a98271cc512ef4764b100b7810dafa74f6eff8da3</originalsourceid><addsrcrecordid>eNp9kUtPwzAQhC0EoqXwBzigSFx6CaxfcXJBQoiXVMQFzpbjrFtXaVLiFtR_j6GlPA6cfJhvxzs7hBxTOKMA6jwACCpTYJBCoXiWwg7pU8FZSoUsdkkfuIBUcil65CCEKQDkUdgnPc6AZhkTfTJ88LZryxqxColvkgpn2Cy8Sd78YpKM8G2VlG3lMRySPWfqgEebd0Ceb66fru7S0ePt_dXlKLVCiUWqSlG4smSVLCygdTITmKPNTJEzRa2VlKETKhNljFCqnEJlnFHCZehcXhk-IBdr3_mynGFl4zadqfW88zPTrXRrvP6tNH6ix-2rVjQXIHk0GG4MuvZliWGhZz5YrGvTYLsMmnEJBTDGRERP_6DTdtk1MV6kCqGkYlxFiq2peKgQOnTbZSjojyL0uggdi9CfRWiIQyc_Y2xHvi4fAb4GQpSaMXbff_9j-w558ZMW</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2394757237</pqid></control><display><type>article</type><title>Microbleeds in dementia with Lewy bodies</title><source>MEDLINE</source><source>SpringerLink_现刊</source><creator>Donaghy, Paul C. ; Firbank, Michael ; Mitra, Dipayan ; Petrides, George ; Lloyd, Jim ; Barnett, Nicola ; Olsen, Kirsty ; Thomas, Alan J. ; O’Brien, John T.</creator><creatorcontrib>Donaghy, Paul C. ; Firbank, Michael ; Mitra, Dipayan ; Petrides, George ; Lloyd, Jim ; Barnett, Nicola ; Olsen, Kirsty ; Thomas, Alan J. ; O’Brien, John T.</creatorcontrib><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.</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 & 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. The relationship between microbleeds and clinical presentation remains unclear.</description><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Alzheimer Disease - diagnostic imaging</subject><subject>Alzheimer Disease - metabolism</subject><subject>Alzheimer Disease - pathology</subject><subject>Alzheimer Disease - physiopathology</subject><subject>Alzheimer's disease</subject><subject>Amyloid beta-Peptides - metabolism</subject><subject>Blood pressure</subject><subject>Blood Pressure - physiology</subject><subject>Cerebral Hemorrhage - diagnostic imaging</subject><subject>Cerebral Hemorrhage - metabolism</subject><subject>Cerebral Hemorrhage - pathology</subject><subject>Cerebral Hemorrhage - physiopathology</subject><subject>Dementia</subject><subject>Dementia disorders</subject><subject>Female</subject><subject>Humans</subject><subject>Lewy bodies</subject><subject>Lewy Body Disease - diagnostic imaging</subject><subject>Lewy Body Disease - metabolism</subject><subject>Lewy Body Disease - pathology</subject><subject>Lewy Body Disease - physiopathology</subject><subject>Longitudinal Studies</subject><subject>Magnetic Resonance Imaging</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Neurodegenerative diseases</subject><subject>Neurology</subject><subject>Neuroradiology</subject><subject>Neurosciences</subject><subject>Older people</subject><subject>Original Communication</subject><subject>Positron-Emission Tomography</subject><subject>Vascular diseases</subject><issn>0340-5354</issn><issn>1432-1459</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp9kUtPwzAQhC0EoqXwBzigSFx6CaxfcXJBQoiXVMQFzpbjrFtXaVLiFtR_j6GlPA6cfJhvxzs7hBxTOKMA6jwACCpTYJBCoXiWwg7pU8FZSoUsdkkfuIBUcil65CCEKQDkUdgnPc6AZhkTfTJ88LZryxqxColvkgpn2Cy8Sd78YpKM8G2VlG3lMRySPWfqgEebd0Ceb66fru7S0ePt_dXlKLVCiUWqSlG4smSVLCygdTITmKPNTJEzRa2VlKETKhNljFCqnEJlnFHCZehcXhk-IBdr3_mynGFl4zadqfW88zPTrXRrvP6tNH6ix-2rVjQXIHk0GG4MuvZliWGhZz5YrGvTYLsMmnEJBTDGRERP_6DTdtk1MV6kCqGkYlxFiq2peKgQOnTbZSjojyL0uggdi9CfRWiIQyc_Y2xHvi4fAb4GQpSaMXbff_9j-w558ZMW</recordid><startdate>20200501</startdate><enddate>20200501</enddate><creator>Donaghy, Paul C.</creator><creator>Firbank, Michael</creator><creator>Mitra, Dipayan</creator><creator>Petrides, George</creator><creator>Lloyd, Jim</creator><creator>Barnett, Nicola</creator><creator>Olsen, Kirsty</creator><creator>Thomas, Alan J.</creator><creator>O’Brien, John T.</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>C6C</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-7195-4846</orcidid></search><sort><creationdate>20200501</creationdate><title>Microbleeds in dementia with Lewy bodies</title><author>Donaghy, Paul C. ; Firbank, Michael ; Mitra, Dipayan ; Petrides, George ; Lloyd, Jim ; Barnett, Nicola ; Olsen, Kirsty ; Thomas, Alan J. ; O’Brien, John T.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c474t-7b49fbb2d59c0ecf564e8ec6a98271cc512ef4764b100b7810dafa74f6eff8da3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Alzheimer Disease - diagnostic imaging</topic><topic>Alzheimer Disease - metabolism</topic><topic>Alzheimer Disease - pathology</topic><topic>Alzheimer Disease - physiopathology</topic><topic>Alzheimer's disease</topic><topic>Amyloid beta-Peptides - metabolism</topic><topic>Blood pressure</topic><topic>Blood Pressure - physiology</topic><topic>Cerebral Hemorrhage - diagnostic imaging</topic><topic>Cerebral Hemorrhage - metabolism</topic><topic>Cerebral Hemorrhage - pathology</topic><topic>Cerebral Hemorrhage - physiopathology</topic><topic>Dementia</topic><topic>Dementia disorders</topic><topic>Female</topic><topic>Humans</topic><topic>Lewy bodies</topic><topic>Lewy Body Disease - diagnostic imaging</topic><topic>Lewy Body Disease - metabolism</topic><topic>Lewy Body Disease - pathology</topic><topic>Lewy Body Disease - physiopathology</topic><topic>Longitudinal Studies</topic><topic>Magnetic Resonance Imaging</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine & 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 & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of neurology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Donaghy, Paul C.</au><au>Firbank, Michael</au><au>Mitra, Dipayan</au><au>Petrides, George</au><au>Lloyd, Jim</au><au>Barnett, Nicola</au><au>Olsen, Kirsty</au><au>Thomas, Alan J.</au><au>O’Brien, John T.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Microbleeds in dementia with Lewy bodies</atitle><jtitle>Journal of neurology</jtitle><stitle>J Neurol</stitle><addtitle>J Neurol</addtitle><date>2020-05-01</date><risdate>2020</risdate><volume>267</volume><issue>5</issue><spage>1491</spage><epage>1498</epage><pages>1491-1498</pages><issn>0340-5354</issn><eissn>1432-1459</eissn><abstract>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.</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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