Multiple or mixed cerebral microbleeds and dementia in patients with vascular risk factors
OBJECTIVE:To investigate whether cerebral microbleeds (CMBs) are independently associated with incident dementia in patients with vascular risk factors. METHODS:Using data from a Japanese cohort of participants with vascular risk factors in an observational study from 2001, we evaluated the associat...
Gespeichert in:
Veröffentlicht in: | Neurology 2014-08, Vol.83 (7), p.646-653 |
---|---|
Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 653 |
---|---|
container_issue | 7 |
container_start_page | 646 |
container_title | Neurology |
container_volume | 83 |
creator | Miwa, Kaori Tanaka, Makiko Okazaki, Shuhei Yagita, Yoshiki Sakaguchi, Manabu Mochizuki, Hideki Kitagawa, Kazuo |
description | OBJECTIVE:To investigate whether cerebral microbleeds (CMBs) are independently associated with incident dementia in patients with vascular risk factors.
METHODS:Using data from a Japanese cohort of participants with vascular risk factors in an observational study from 2001, we evaluated the association between CMBs at baseline and incident dementia. Baseline brain MRI was used to determine small-vessel disease (CMBs, lacunar infarcts, and white matter hyperintensities) and brain atrophy. Cox proportional hazards analyses were performed for predictors of dementia adjusting for age, sex, APOE ε4 allele, educational level, baseline Mini-Mental State Examination score, cerebrovascular events, vascular risk factors, and MRI findings.
RESULTS:Of the 524 subjects (mean age 68 ± 8.3 years, 57.6% male, 12.8 ± 2.6 years of schooling, 21.6% CMBs), 44 patients with incident dementia (20 Alzheimer disease, 18 vascular dementia, 3 mixed-type, and 3 other) were diagnosed during the median 7.5-year follow-up. In multivariate analysis, the presence of overall CMBs was not associated with an increased risk of incident all-cause dementia (p = 0.15). However, multiple CMBs (≥2) or mixed (lobar and deep) CMBs were associated with the increased risk of all-cause dementia, whereas strictly lobar CMBs showed no association with any dementia.
CONCLUSIONS:Multiple CMBs or mixed CMBs independently showed higher risk of all-cause dementia. Our results reinforce the hypothesis that CMBs exert deleterious effects on dementia incidence, suggesting that this association may be mediated by vascular burden. |
doi_str_mv | 10.1212/WNL.0000000000000692 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1647025052</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1647025052</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4192-db5948ca14b29c9953865b094201982883be6dbca095d0604bf231465e95b4a83</originalsourceid><addsrcrecordid>eNqFkU2P0zAQhi0Eot3CP0DIFyQuKf6OfUTVLiCV5bIIxCWynYlq6iTFTujy7_Gq5UMc2Ll4Rn5mxn5fhJ5RsqaMslefrrdr8ncowx6gJZVMVYqzzw_RkhCmK65rvUAXOX8lpFzW5jFaMFlSrsQSfXk_xykcIuAx4T7cQos9JHDJxlL6NLoI0GZshxa30MMwBYvDgA92CqXI-BimHf5us5-jTTiFvMed9dOY8hP0qLMxw9PzuUIfry5vNm-r7Yc37zavt5UX1LCqddII7S0VjhlvjORaSUeMYIQazbTmDlTrvCVGtkQR4TrGqVASjHTCar5CL09zD2n8NkOemj5kDzHaAcY5N1SJmpQfS3Y_KiWnREglCypOaNEg5wRdc0iht-lHQ0lzZ0BTDGj-NaC0PT9vmF0P7e-mX4oX4MUZKJrZ2CU7-JD_cLrmxmhaOH3ijmOcIOV9nI-Qmh3YOO3-_4afwcmduA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1553104565</pqid></control><display><type>article</type><title>Multiple or mixed cerebral microbleeds and dementia in patients with vascular risk factors</title><source>MEDLINE</source><source>Journals@Ovid Complete</source><source>Alma/SFX Local Collection</source><creator>Miwa, Kaori ; Tanaka, Makiko ; Okazaki, Shuhei ; Yagita, Yoshiki ; Sakaguchi, Manabu ; Mochizuki, Hideki ; Kitagawa, Kazuo</creator><creatorcontrib>Miwa, Kaori ; Tanaka, Makiko ; Okazaki, Shuhei ; Yagita, Yoshiki ; Sakaguchi, Manabu ; Mochizuki, Hideki ; Kitagawa, Kazuo</creatorcontrib><description>OBJECTIVE:To investigate whether cerebral microbleeds (CMBs) are independently associated with incident dementia in patients with vascular risk factors.
METHODS:Using data from a Japanese cohort of participants with vascular risk factors in an observational study from 2001, we evaluated the association between CMBs at baseline and incident dementia. Baseline brain MRI was used to determine small-vessel disease (CMBs, lacunar infarcts, and white matter hyperintensities) and brain atrophy. Cox proportional hazards analyses were performed for predictors of dementia adjusting for age, sex, APOE ε4 allele, educational level, baseline Mini-Mental State Examination score, cerebrovascular events, vascular risk factors, and MRI findings.
RESULTS:Of the 524 subjects (mean age 68 ± 8.3 years, 57.6% male, 12.8 ± 2.6 years of schooling, 21.6% CMBs), 44 patients with incident dementia (20 Alzheimer disease, 18 vascular dementia, 3 mixed-type, and 3 other) were diagnosed during the median 7.5-year follow-up. In multivariate analysis, the presence of overall CMBs was not associated with an increased risk of incident all-cause dementia (p = 0.15). However, multiple CMBs (≥2) or mixed (lobar and deep) CMBs were associated with the increased risk of all-cause dementia, whereas strictly lobar CMBs showed no association with any dementia.
CONCLUSIONS:Multiple CMBs or mixed CMBs independently showed higher risk of all-cause dementia. Our results reinforce the hypothesis that CMBs exert deleterious effects on dementia incidence, suggesting that this association may be mediated by vascular burden.</description><identifier>ISSN: 0028-3878</identifier><identifier>EISSN: 1526-632X</identifier><identifier>DOI: 10.1212/WNL.0000000000000692</identifier><identifier>PMID: 25015364</identifier><identifier>CODEN: NEURAI</identifier><language>eng</language><publisher>Hagerstown, MD: American Academy of Neurology</publisher><subject>Aged ; Biological and medical sciences ; Brain - pathology ; Cerebral Hemorrhage - epidemiology ; Cerebral Hemorrhage - pathology ; Dementia - epidemiology ; Dementia - pathology ; Female ; Follow-Up Studies ; Humans ; Japan - epidemiology ; Kaplan-Meier Estimate ; Magnetic Resonance Imaging ; Male ; Medical sciences ; Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis ; Multivariate Analysis ; Neurology ; Proportional Hazards Models ; Risk Factors ; Vascular Diseases - epidemiology ; Vascular Diseases - pathology ; Vascular diseases and vascular malformations of the nervous system</subject><ispartof>Neurology, 2014-08, Vol.83 (7), p.646-653</ispartof><rights>2014 American Academy of Neurology</rights><rights>2015 INIST-CNRS</rights><rights>2014 American Academy of Neurology.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4192-db5948ca14b29c9953865b094201982883be6dbca095d0604bf231465e95b4a83</citedby><cites>FETCH-LOGICAL-c4192-db5948ca14b29c9953865b094201982883be6dbca095d0604bf231465e95b4a83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=28739981$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25015364$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Miwa, Kaori</creatorcontrib><creatorcontrib>Tanaka, Makiko</creatorcontrib><creatorcontrib>Okazaki, Shuhei</creatorcontrib><creatorcontrib>Yagita, Yoshiki</creatorcontrib><creatorcontrib>Sakaguchi, Manabu</creatorcontrib><creatorcontrib>Mochizuki, Hideki</creatorcontrib><creatorcontrib>Kitagawa, Kazuo</creatorcontrib><title>Multiple or mixed cerebral microbleeds and dementia in patients with vascular risk factors</title><title>Neurology</title><addtitle>Neurology</addtitle><description>OBJECTIVE:To investigate whether cerebral microbleeds (CMBs) are independently associated with incident dementia in patients with vascular risk factors.
METHODS:Using data from a Japanese cohort of participants with vascular risk factors in an observational study from 2001, we evaluated the association between CMBs at baseline and incident dementia. Baseline brain MRI was used to determine small-vessel disease (CMBs, lacunar infarcts, and white matter hyperintensities) and brain atrophy. Cox proportional hazards analyses were performed for predictors of dementia adjusting for age, sex, APOE ε4 allele, educational level, baseline Mini-Mental State Examination score, cerebrovascular events, vascular risk factors, and MRI findings.
RESULTS:Of the 524 subjects (mean age 68 ± 8.3 years, 57.6% male, 12.8 ± 2.6 years of schooling, 21.6% CMBs), 44 patients with incident dementia (20 Alzheimer disease, 18 vascular dementia, 3 mixed-type, and 3 other) were diagnosed during the median 7.5-year follow-up. In multivariate analysis, the presence of overall CMBs was not associated with an increased risk of incident all-cause dementia (p = 0.15). However, multiple CMBs (≥2) or mixed (lobar and deep) CMBs were associated with the increased risk of all-cause dementia, whereas strictly lobar CMBs showed no association with any dementia.
CONCLUSIONS:Multiple CMBs or mixed CMBs independently showed higher risk of all-cause dementia. Our results reinforce the hypothesis that CMBs exert deleterious effects on dementia incidence, suggesting that this association may be mediated by vascular burden.</description><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>Brain - pathology</subject><subject>Cerebral Hemorrhage - epidemiology</subject><subject>Cerebral Hemorrhage - pathology</subject><subject>Dementia - epidemiology</subject><subject>Dementia - pathology</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Humans</subject><subject>Japan - epidemiology</subject><subject>Kaplan-Meier Estimate</subject><subject>Magnetic Resonance Imaging</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis</subject><subject>Multivariate Analysis</subject><subject>Neurology</subject><subject>Proportional Hazards Models</subject><subject>Risk Factors</subject><subject>Vascular Diseases - epidemiology</subject><subject>Vascular Diseases - pathology</subject><subject>Vascular diseases and vascular malformations of the nervous system</subject><issn>0028-3878</issn><issn>1526-632X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU2P0zAQhi0Eot3CP0DIFyQuKf6OfUTVLiCV5bIIxCWynYlq6iTFTujy7_Gq5UMc2Ll4Rn5mxn5fhJ5RsqaMslefrrdr8ncowx6gJZVMVYqzzw_RkhCmK65rvUAXOX8lpFzW5jFaMFlSrsQSfXk_xykcIuAx4T7cQos9JHDJxlL6NLoI0GZshxa30MMwBYvDgA92CqXI-BimHf5us5-jTTiFvMed9dOY8hP0qLMxw9PzuUIfry5vNm-r7Yc37zavt5UX1LCqddII7S0VjhlvjORaSUeMYIQazbTmDlTrvCVGtkQR4TrGqVASjHTCar5CL09zD2n8NkOemj5kDzHaAcY5N1SJmpQfS3Y_KiWnREglCypOaNEg5wRdc0iht-lHQ0lzZ0BTDGj-NaC0PT9vmF0P7e-mX4oX4MUZKJrZ2CU7-JD_cLrmxmhaOH3ijmOcIOV9nI-Qmh3YOO3-_4afwcmduA</recordid><startdate>20140812</startdate><enddate>20140812</enddate><creator>Miwa, Kaori</creator><creator>Tanaka, Makiko</creator><creator>Okazaki, Shuhei</creator><creator>Yagita, Yoshiki</creator><creator>Sakaguchi, Manabu</creator><creator>Mochizuki, Hideki</creator><creator>Kitagawa, Kazuo</creator><general>American Academy of Neurology</general><general>Lippincott Williams & Wilkins</general><scope>IQODW</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>7X8</scope><scope>7TK</scope></search><sort><creationdate>20140812</creationdate><title>Multiple or mixed cerebral microbleeds and dementia in patients with vascular risk factors</title><author>Miwa, Kaori ; Tanaka, Makiko ; Okazaki, Shuhei ; Yagita, Yoshiki ; Sakaguchi, Manabu ; Mochizuki, Hideki ; Kitagawa, Kazuo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4192-db5948ca14b29c9953865b094201982883be6dbca095d0604bf231465e95b4a83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Aged</topic><topic>Biological and medical sciences</topic><topic>Brain - pathology</topic><topic>Cerebral Hemorrhage - epidemiology</topic><topic>Cerebral Hemorrhage - pathology</topic><topic>Dementia - epidemiology</topic><topic>Dementia - pathology</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Humans</topic><topic>Japan - epidemiology</topic><topic>Kaplan-Meier Estimate</topic><topic>Magnetic Resonance Imaging</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis</topic><topic>Multivariate Analysis</topic><topic>Neurology</topic><topic>Proportional Hazards Models</topic><topic>Risk Factors</topic><topic>Vascular Diseases - epidemiology</topic><topic>Vascular Diseases - pathology</topic><topic>Vascular diseases and vascular malformations of the nervous system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Miwa, Kaori</creatorcontrib><creatorcontrib>Tanaka, Makiko</creatorcontrib><creatorcontrib>Okazaki, Shuhei</creatorcontrib><creatorcontrib>Yagita, Yoshiki</creatorcontrib><creatorcontrib>Sakaguchi, Manabu</creatorcontrib><creatorcontrib>Mochizuki, Hideki</creatorcontrib><creatorcontrib>Kitagawa, Kazuo</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Neurosciences Abstracts</collection><jtitle>Neurology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Miwa, Kaori</au><au>Tanaka, Makiko</au><au>Okazaki, Shuhei</au><au>Yagita, Yoshiki</au><au>Sakaguchi, Manabu</au><au>Mochizuki, Hideki</au><au>Kitagawa, Kazuo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Multiple or mixed cerebral microbleeds and dementia in patients with vascular risk factors</atitle><jtitle>Neurology</jtitle><addtitle>Neurology</addtitle><date>2014-08-12</date><risdate>2014</risdate><volume>83</volume><issue>7</issue><spage>646</spage><epage>653</epage><pages>646-653</pages><issn>0028-3878</issn><eissn>1526-632X</eissn><coden>NEURAI</coden><abstract>OBJECTIVE:To investigate whether cerebral microbleeds (CMBs) are independently associated with incident dementia in patients with vascular risk factors.
METHODS:Using data from a Japanese cohort of participants with vascular risk factors in an observational study from 2001, we evaluated the association between CMBs at baseline and incident dementia. Baseline brain MRI was used to determine small-vessel disease (CMBs, lacunar infarcts, and white matter hyperintensities) and brain atrophy. Cox proportional hazards analyses were performed for predictors of dementia adjusting for age, sex, APOE ε4 allele, educational level, baseline Mini-Mental State Examination score, cerebrovascular events, vascular risk factors, and MRI findings.
RESULTS:Of the 524 subjects (mean age 68 ± 8.3 years, 57.6% male, 12.8 ± 2.6 years of schooling, 21.6% CMBs), 44 patients with incident dementia (20 Alzheimer disease, 18 vascular dementia, 3 mixed-type, and 3 other) were diagnosed during the median 7.5-year follow-up. In multivariate analysis, the presence of overall CMBs was not associated with an increased risk of incident all-cause dementia (p = 0.15). However, multiple CMBs (≥2) or mixed (lobar and deep) CMBs were associated with the increased risk of all-cause dementia, whereas strictly lobar CMBs showed no association with any dementia.
CONCLUSIONS:Multiple CMBs or mixed CMBs independently showed higher risk of all-cause dementia. Our results reinforce the hypothesis that CMBs exert deleterious effects on dementia incidence, suggesting that this association may be mediated by vascular burden.</abstract><cop>Hagerstown, MD</cop><pub>American Academy of Neurology</pub><pmid>25015364</pmid><doi>10.1212/WNL.0000000000000692</doi><tpages>8</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0028-3878 |
ispartof | Neurology, 2014-08, Vol.83 (7), p.646-653 |
issn | 0028-3878 1526-632X |
language | eng |
recordid | cdi_proquest_miscellaneous_1647025052 |
source | MEDLINE; Journals@Ovid Complete; Alma/SFX Local Collection |
subjects | Aged Biological and medical sciences Brain - pathology Cerebral Hemorrhage - epidemiology Cerebral Hemorrhage - pathology Dementia - epidemiology Dementia - pathology Female Follow-Up Studies Humans Japan - epidemiology Kaplan-Meier Estimate Magnetic Resonance Imaging Male Medical sciences Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis Multivariate Analysis Neurology Proportional Hazards Models Risk Factors Vascular Diseases - epidemiology Vascular Diseases - pathology Vascular diseases and vascular malformations of the nervous system |
title | Multiple or mixed cerebral microbleeds and dementia in patients with vascular risk factors |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-25T18%3A22%3A59IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Multiple%20or%20mixed%20cerebral%20microbleeds%20and%20dementia%20in%20patients%20with%20vascular%20risk%20factors&rft.jtitle=Neurology&rft.au=Miwa,%20Kaori&rft.date=2014-08-12&rft.volume=83&rft.issue=7&rft.spage=646&rft.epage=653&rft.pages=646-653&rft.issn=0028-3878&rft.eissn=1526-632X&rft.coden=NEURAI&rft_id=info:doi/10.1212/WNL.0000000000000692&rft_dat=%3Cproquest_cross%3E1647025052%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1553104565&rft_id=info:pmid/25015364&rfr_iscdi=true |