Variability in midlife systolic blood pressure is related to late-life brain white matter lesions: The Honolulu-Asia Aging Study
Although white matter lesions (WMLs) on brain MRI in older persons are common, the mechanisms are unclear. Besides the associations with advanced age and high blood pressure (BP), variability in systolic BP (SBP) and the resulting changes in blood flow to the deep arteries of the brain may be contri...
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description | Although white matter lesions (WMLs) on brain MRI in older persons are common, the mechanisms are unclear. Besides the associations with advanced age and high blood pressure (BP), variability in systolic BP (SBP) and the resulting changes in blood flow to the deep arteries of the brain may be contributing factors.
Japanese-American men in Hawaii have participated in a long-term study of cardiovascular disease, including midlife BP measurements at 3 clinical examinations in the period from 1965 to 1974. In the period from 1991 to 1993, dementia status was added to the fourth examination, and a brain MRI was completed in a fifth examination, which was from 1994 to 1996, on a subset of 575 men, who averaged 82 years. WMLs and ventricular atrophy were determined as the upper fifth in a standardized semiquantitative measure. Excess SBP variability was defined as greater than average increases in BP measurements from up to 3 examinations over 6 years. Logistic regression was used for the association of this variability with WMLs and atrophy, controlling for age, apolipoprotein E4 status, dementia diagnosis, and history of stroke.
There were significant (2-fold) increased risks for WMLs among those with moderate and high SBP variability (third and fifth quintiles compared with the lowest quintile). Those in the highest SBP variability category (the fifth quintile) also had significantly more atrophy.
These SBP variability-MRI relationships suggest that variation in SBP in midlife may be a contributing factor to the development of WMLs and ventricular atrophy in late life. |
doi_str_mv | 10.1161/hs0102.101890 |
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Japanese-American men in Hawaii have participated in a long-term study of cardiovascular disease, including midlife BP measurements at 3 clinical examinations in the period from 1965 to 1974. In the period from 1991 to 1993, dementia status was added to the fourth examination, and a brain MRI was completed in a fifth examination, which was from 1994 to 1996, on a subset of 575 men, who averaged 82 years. WMLs and ventricular atrophy were determined as the upper fifth in a standardized semiquantitative measure. Excess SBP variability was defined as greater than average increases in BP measurements from up to 3 examinations over 6 years. Logistic regression was used for the association of this variability with WMLs and atrophy, controlling for age, apolipoprotein E4 status, dementia diagnosis, and history of stroke.
There were significant (2-fold) increased risks for WMLs among those with moderate and high SBP variability (third and fifth quintiles compared with the lowest quintile). Those in the highest SBP variability category (the fifth quintile) also had significantly more atrophy.
These SBP variability-MRI relationships suggest that variation in SBP in midlife may be a contributing factor to the development of WMLs and ventricular atrophy in late life.</description><identifier>ISSN: 0039-2499</identifier><identifier>EISSN: 1524-4628</identifier><identifier>DOI: 10.1161/hs0102.101890</identifier><identifier>PMID: 11779884</identifier><identifier>CODEN: SJCCA7</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott Williams & Wilkins</publisher><subject>Age Factors ; Aged ; Asian Americans ; Atrophy - pathology ; Biological and medical sciences ; Blood Pressure ; Brain - pathology ; Brain Diseases - ethnology ; Brain Diseases - etiology ; Brain Diseases - pathology ; Cerebral Ventricles - pathology ; Cohort Studies ; Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases ; Dementia - diagnosis ; Genetic Variation ; Hawaii - epidemiology ; Humans ; Japan - ethnology ; Longitudinal Studies ; Magnetic Resonance Imaging ; Male ; Medical sciences ; Middle Aged ; Multivariate Analysis ; Neurology ; Systole</subject><ispartof>Stroke (1970), 2002, Vol.33 (1), p.26-30</ispartof><rights>2002 INIST-CNRS</rights><rights>Copyright American Heart Association, Inc. Jan 2002</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c336t-871776359cf833dfaa42461d7747db11df5e532c36c92720f3225530ceb65bad3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,3687,4024,27923,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=13449846$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11779884$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>HAVLIK, Richard J</creatorcontrib><creatorcontrib>FOLEY, Daniel J</creatorcontrib><creatorcontrib>SAYER, Bryan</creatorcontrib><creatorcontrib>MASAKI, Kamal</creatorcontrib><creatorcontrib>WHITE, Lon</creatorcontrib><creatorcontrib>LAUNER, Lenore J</creatorcontrib><title>Variability in midlife systolic blood pressure is related to late-life brain white matter lesions: The Honolulu-Asia Aging Study</title><title>Stroke (1970)</title><addtitle>Stroke</addtitle><description>Although white matter lesions (WMLs) on brain MRI in older persons are common, the mechanisms are unclear. Besides the associations with advanced age and high blood pressure (BP), variability in systolic BP (SBP) and the resulting changes in blood flow to the deep arteries of the brain may be contributing factors.
Japanese-American men in Hawaii have participated in a long-term study of cardiovascular disease, including midlife BP measurements at 3 clinical examinations in the period from 1965 to 1974. In the period from 1991 to 1993, dementia status was added to the fourth examination, and a brain MRI was completed in a fifth examination, which was from 1994 to 1996, on a subset of 575 men, who averaged 82 years. WMLs and ventricular atrophy were determined as the upper fifth in a standardized semiquantitative measure. Excess SBP variability was defined as greater than average increases in BP measurements from up to 3 examinations over 6 years. Logistic regression was used for the association of this variability with WMLs and atrophy, controlling for age, apolipoprotein E4 status, dementia diagnosis, and history of stroke.
There were significant (2-fold) increased risks for WMLs among those with moderate and high SBP variability (third and fifth quintiles compared with the lowest quintile). Those in the highest SBP variability category (the fifth quintile) also had significantly more atrophy.
These SBP variability-MRI relationships suggest that variation in SBP in midlife may be a contributing factor to the development of WMLs and ventricular atrophy in late life.</description><subject>Age Factors</subject><subject>Aged</subject><subject>Asian Americans</subject><subject>Atrophy - pathology</subject><subject>Biological and medical sciences</subject><subject>Blood Pressure</subject><subject>Brain - pathology</subject><subject>Brain Diseases - ethnology</subject><subject>Brain Diseases - etiology</subject><subject>Brain Diseases - pathology</subject><subject>Cerebral Ventricles - pathology</subject><subject>Cohort Studies</subject><subject>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</subject><subject>Dementia - diagnosis</subject><subject>Genetic Variation</subject><subject>Hawaii - epidemiology</subject><subject>Humans</subject><subject>Japan - ethnology</subject><subject>Longitudinal Studies</subject><subject>Magnetic Resonance Imaging</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Multivariate Analysis</subject><subject>Neurology</subject><subject>Systole</subject><issn>0039-2499</issn><issn>1524-4628</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpd0c9rFDEUB_Agit1Wj14lCPY2Nb9_eFuKWqHgwep1yCSZbkpmsuZlkL35pzt1Fwqe3jt83pcHX4TeUHJFqaIfdkAoYVeUUGPJM7ShkolOKGaeow0h3HZMWHuGzgEeCCGMG_kSnVGqtTVGbNCfn64mN6Sc2gGnGU8p5DRGDAdoJSePh1xKwPsaAZYacQJcY3YtBtwKfly6f36obr3-vUst4sm1FivOEVKZ4SO-20V8U-aSl7x0W0gOb-_TfI-_tyUcXqEXo8sQX5_mBfrx-dPd9U13--3L1-vtbec5V60zen1ZcWn9aDgPo3OCCUWD1kKHgdIwyig581x5yzQjI2dMSk58HJQcXOAX6PKYu6_l1xKh9VMCH3N2cywL9JpyRRVnK3z3H3woS53X33pqtWFcS7Ki7oh8LQA1jv2-psnVQ09J_9hLf-ylP_ay-ren0GWYYnjSpyJW8P4EHHiXx-pmn-DJcSGsEYr_BY6slaA</recordid><startdate>2002</startdate><enddate>2002</enddate><creator>HAVLIK, Richard J</creator><creator>FOLEY, Daniel J</creator><creator>SAYER, Bryan</creator><creator>MASAKI, Kamal</creator><creator>WHITE, Lon</creator><creator>LAUNER, Lenore J</creator><general>Lippincott Williams & Wilkins</general><general>American Heart Association, Inc</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>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope></search><sort><creationdate>2002</creationdate><title>Variability in midlife systolic blood pressure is related to late-life brain white matter lesions: The Honolulu-Asia Aging Study</title><author>HAVLIK, Richard J ; FOLEY, Daniel J ; SAYER, Bryan ; MASAKI, Kamal ; WHITE, Lon ; LAUNER, Lenore J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c336t-871776359cf833dfaa42461d7747db11df5e532c36c92720f3225530ceb65bad3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Age Factors</topic><topic>Aged</topic><topic>Asian Americans</topic><topic>Atrophy - pathology</topic><topic>Biological and medical sciences</topic><topic>Blood Pressure</topic><topic>Brain - pathology</topic><topic>Brain Diseases - ethnology</topic><topic>Brain Diseases - etiology</topic><topic>Brain Diseases - pathology</topic><topic>Cerebral Ventricles - pathology</topic><topic>Cohort Studies</topic><topic>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</topic><topic>Dementia - diagnosis</topic><topic>Genetic Variation</topic><topic>Hawaii - epidemiology</topic><topic>Humans</topic><topic>Japan - ethnology</topic><topic>Longitudinal Studies</topic><topic>Magnetic Resonance Imaging</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Multivariate Analysis</topic><topic>Neurology</topic><topic>Systole</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>HAVLIK, Richard J</creatorcontrib><creatorcontrib>FOLEY, Daniel J</creatorcontrib><creatorcontrib>SAYER, Bryan</creatorcontrib><creatorcontrib>MASAKI, Kamal</creatorcontrib><creatorcontrib>WHITE, Lon</creatorcontrib><creatorcontrib>LAUNER, Lenore J</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>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>Stroke (1970)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>HAVLIK, Richard J</au><au>FOLEY, Daniel J</au><au>SAYER, Bryan</au><au>MASAKI, Kamal</au><au>WHITE, Lon</au><au>LAUNER, Lenore J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Variability in midlife systolic blood pressure is related to late-life brain white matter lesions: The Honolulu-Asia Aging Study</atitle><jtitle>Stroke (1970)</jtitle><addtitle>Stroke</addtitle><date>2002</date><risdate>2002</risdate><volume>33</volume><issue>1</issue><spage>26</spage><epage>30</epage><pages>26-30</pages><issn>0039-2499</issn><eissn>1524-4628</eissn><coden>SJCCA7</coden><abstract>Although white matter lesions (WMLs) on brain MRI in older persons are common, the mechanisms are unclear. Besides the associations with advanced age and high blood pressure (BP), variability in systolic BP (SBP) and the resulting changes in blood flow to the deep arteries of the brain may be contributing factors.
Japanese-American men in Hawaii have participated in a long-term study of cardiovascular disease, including midlife BP measurements at 3 clinical examinations in the period from 1965 to 1974. In the period from 1991 to 1993, dementia status was added to the fourth examination, and a brain MRI was completed in a fifth examination, which was from 1994 to 1996, on a subset of 575 men, who averaged 82 years. WMLs and ventricular atrophy were determined as the upper fifth in a standardized semiquantitative measure. Excess SBP variability was defined as greater than average increases in BP measurements from up to 3 examinations over 6 years. Logistic regression was used for the association of this variability with WMLs and atrophy, controlling for age, apolipoprotein E4 status, dementia diagnosis, and history of stroke.
There were significant (2-fold) increased risks for WMLs among those with moderate and high SBP variability (third and fifth quintiles compared with the lowest quintile). Those in the highest SBP variability category (the fifth quintile) also had significantly more atrophy.
These SBP variability-MRI relationships suggest that variation in SBP in midlife may be a contributing factor to the development of WMLs and ventricular atrophy in late life.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott Williams & Wilkins</pub><pmid>11779884</pmid><doi>10.1161/hs0102.101890</doi><tpages>5</tpages></addata></record> |
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subjects | Age Factors Aged Asian Americans Atrophy - pathology Biological and medical sciences Blood Pressure Brain - pathology Brain Diseases - ethnology Brain Diseases - etiology Brain Diseases - pathology Cerebral Ventricles - pathology Cohort Studies Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases Dementia - diagnosis Genetic Variation Hawaii - epidemiology Humans Japan - ethnology Longitudinal Studies Magnetic Resonance Imaging Male Medical sciences Middle Aged Multivariate Analysis Neurology Systole |
title | Variability in midlife systolic blood pressure is related to late-life brain white matter lesions: The Honolulu-Asia Aging Study |
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