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Basal Ganglia Cerebral Microbleeds and Global Cognitive Function: The Kashima Scan Study
Background We previously showed that global cognitive function was associated with deep or infratentorial (D/I) cerebral microbleeds (CMBs) in a Japanese healthy cohort. We continually recruited participates and performed further investigation to focus on the impact of different distributions of D/I...
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Published in: | Journal of stroke and cerebrovascular diseases 2015-02, Vol.24 (2), p.431-439 |
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creator | Yakushiji, Yusuke, MD, PhD Noguchi, Tomoyuki, MD, PhD Charidimou, Andreas, MD, MSc Eriguchi, Makoto, MD, PhD Nishihara, Masashi, MD Hara, Megumi, MD, PhD Nanri, Yusuke, MD, PhD Horikawa, Etsuo, PhD Nishiyama, Masanori, MD Werring, David J., MD, PhD Hara, Hideo, MD, PhD |
description | Background We previously showed that global cognitive function was associated with deep or infratentorial (D/I) cerebral microbleeds (CMBs) in a Japanese healthy cohort. We continually recruited participates and performed further investigation to focus on the impact of different distributions of D/I CMBs on gradient-echo magnetic resonance imaging on global cognitive function. Methods A total of 1392 subjects including subjects without CMBs (n = 1335), with D/I CMBs limited to the basal ganglia (BG; BG group, n = 33), thalamus (thalamus group, n = 14), and infratentorial area (infratentorial group, n = 10) were included in analyses. Subjects with strictly lobar CMBs (n = 43) were excluded, but subjects in the BG, thalamus, and infratentorial groups could also have lobar CMBs. The mini-mental state examination (MMSE) was administered to determine global cognitive function; scores less than 27 or more than 1.5 standard deviations (SDs) below the age–education-related mean were regarded as impaired. Results In the multivariable logistic regression analyses, hypertension and severe white matter hyperintensities were associated with the BG group and the thalamus group. In multivariable logistic regression analysis of the association between D/I CMBs classification and impaired MMSE score, only the BG group consistently displayed associations with both MMSE score less than 27 (odds ratio [OR], 5.96; 95% confidence interval [CI], 2.08-17.09) and MMSE score more than 1.5 SDs below the age–education-related mean (OR, 3.34; 95% CI, 1.24-8.99). In the BG group, adjusted mean scores of total MMSE and “attention and calculation” were lower compared with subjects without CMBs. Conclusions In our study of D/I CMBs, only BG CMBs have strong association with global cognitive function. This association was independent of CMBs in other location. |
doi_str_mv | 10.1016/j.jstrokecerebrovasdis.2014.09.015 |
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We continually recruited participates and performed further investigation to focus on the impact of different distributions of D/I CMBs on gradient-echo magnetic resonance imaging on global cognitive function. Methods A total of 1392 subjects including subjects without CMBs (n = 1335), with D/I CMBs limited to the basal ganglia (BG; BG group, n = 33), thalamus (thalamus group, n = 14), and infratentorial area (infratentorial group, n = 10) were included in analyses. Subjects with strictly lobar CMBs (n = 43) were excluded, but subjects in the BG, thalamus, and infratentorial groups could also have lobar CMBs. The mini-mental state examination (MMSE) was administered to determine global cognitive function; scores less than 27 or more than 1.5 standard deviations (SDs) below the age–education-related mean were regarded as impaired. Results In the multivariable logistic regression analyses, hypertension and severe white matter hyperintensities were associated with the BG group and the thalamus group. In multivariable logistic regression analysis of the association between D/I CMBs classification and impaired MMSE score, only the BG group consistently displayed associations with both MMSE score less than 27 (odds ratio [OR], 5.96; 95% confidence interval [CI], 2.08-17.09) and MMSE score more than 1.5 SDs below the age–education-related mean (OR, 3.34; 95% CI, 1.24-8.99). In the BG group, adjusted mean scores of total MMSE and “attention and calculation” were lower compared with subjects without CMBs. Conclusions In our study of D/I CMBs, only BG CMBs have strong association with global cognitive function. This association was independent of CMBs in other location.</description><identifier>ISSN: 1052-3057</identifier><identifier>EISSN: 1532-8511</identifier><identifier>DOI: 10.1016/j.jstrokecerebrovasdis.2014.09.015</identifier><identifier>PMID: 25516488</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Aged ; basal ganglia ; Basal Ganglia - pathology ; Cardiovascular ; Cerebral Hemorrhage - complications ; Cerebral Hemorrhage - pathology ; Cerebral Hemorrhage - psychology ; Cerebral microbleeds ; Cognition ; Cognition Disorders - etiology ; Cognition Disorders - pathology ; Cognition Disorders - psychology ; cognitive dysfunction ; Cross-Sectional Studies ; Female ; Humans ; Magnetic Resonance Imaging ; Male ; Middle Aged ; Neurology ; Neuropsychological Tests ; Risk Factors ; small vessel disease</subject><ispartof>Journal of stroke and cerebrovascular diseases, 2015-02, Vol.24 (2), p.431-439</ispartof><rights>National Stroke Association</rights><rights>2015 National Stroke Association</rights><rights>Copyright © 2015 National Stroke Association. Published by Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c595t-b11b2c8699428265cd61bb65a17418ea620a535082d99db7a2151fe902b485c63</citedby><cites>FETCH-LOGICAL-c595t-b11b2c8699428265cd61bb65a17418ea620a535082d99db7a2151fe902b485c63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25516488$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yakushiji, Yusuke, MD, PhD</creatorcontrib><creatorcontrib>Noguchi, Tomoyuki, MD, PhD</creatorcontrib><creatorcontrib>Charidimou, Andreas, MD, MSc</creatorcontrib><creatorcontrib>Eriguchi, Makoto, MD, PhD</creatorcontrib><creatorcontrib>Nishihara, Masashi, MD</creatorcontrib><creatorcontrib>Hara, Megumi, MD, PhD</creatorcontrib><creatorcontrib>Nanri, Yusuke, MD, PhD</creatorcontrib><creatorcontrib>Horikawa, Etsuo, PhD</creatorcontrib><creatorcontrib>Nishiyama, Masanori, MD</creatorcontrib><creatorcontrib>Werring, David J., MD, PhD</creatorcontrib><creatorcontrib>Hara, Hideo, MD, PhD</creatorcontrib><title>Basal Ganglia Cerebral Microbleeds and Global Cognitive Function: The Kashima Scan Study</title><title>Journal of stroke and cerebrovascular diseases</title><addtitle>J Stroke Cerebrovasc Dis</addtitle><description>Background We previously showed that global cognitive function was associated with deep or infratentorial (D/I) cerebral microbleeds (CMBs) in a Japanese healthy cohort. We continually recruited participates and performed further investigation to focus on the impact of different distributions of D/I CMBs on gradient-echo magnetic resonance imaging on global cognitive function. Methods A total of 1392 subjects including subjects without CMBs (n = 1335), with D/I CMBs limited to the basal ganglia (BG; BG group, n = 33), thalamus (thalamus group, n = 14), and infratentorial area (infratentorial group, n = 10) were included in analyses. Subjects with strictly lobar CMBs (n = 43) were excluded, but subjects in the BG, thalamus, and infratentorial groups could also have lobar CMBs. The mini-mental state examination (MMSE) was administered to determine global cognitive function; scores less than 27 or more than 1.5 standard deviations (SDs) below the age–education-related mean were regarded as impaired. Results In the multivariable logistic regression analyses, hypertension and severe white matter hyperintensities were associated with the BG group and the thalamus group. In multivariable logistic regression analysis of the association between D/I CMBs classification and impaired MMSE score, only the BG group consistently displayed associations with both MMSE score less than 27 (odds ratio [OR], 5.96; 95% confidence interval [CI], 2.08-17.09) and MMSE score more than 1.5 SDs below the age–education-related mean (OR, 3.34; 95% CI, 1.24-8.99). In the BG group, adjusted mean scores of total MMSE and “attention and calculation” were lower compared with subjects without CMBs. Conclusions In our study of D/I CMBs, only BG CMBs have strong association with global cognitive function. This association was independent of CMBs in other location.</description><subject>Aged</subject><subject>basal ganglia</subject><subject>Basal Ganglia - pathology</subject><subject>Cardiovascular</subject><subject>Cerebral Hemorrhage - complications</subject><subject>Cerebral Hemorrhage - pathology</subject><subject>Cerebral Hemorrhage - psychology</subject><subject>Cerebral microbleeds</subject><subject>Cognition</subject><subject>Cognition Disorders - etiology</subject><subject>Cognition Disorders - pathology</subject><subject>Cognition Disorders - psychology</subject><subject>cognitive dysfunction</subject><subject>Cross-Sectional Studies</subject><subject>Female</subject><subject>Humans</subject><subject>Magnetic Resonance Imaging</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Neurology</subject><subject>Neuropsychological Tests</subject><subject>Risk Factors</subject><subject>small vessel disease</subject><issn>1052-3057</issn><issn>1532-8511</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNqVkU1vEzEQhlcIREvhL6A9IqRdPN61Y3NAohENiCAOKRI3yx-T1tuNXezdSPn3OKRwQFw4eTR69Yznmap6DaQFAvzN0A55SvEOLSY0Ke51dj63lEDfEtkSYI-qc2AdbQQDeFxqwmjTEbY4q57lPBACwAR7Wp1RxoD3QpxX3y911mO90uFm9Lpe_iKXxhdvUzQjosu1Dq5ejdGU9jLeBD_5PdZXc7CTj-FtfX2L9Wedb_1O1xurQ72ZZnd4Xj3Z6jHji4f3ovp29eF6-bFZf119Wr5fN5ZJNjUGwFAruJQ9FZQz6zgYw5mGRQ8CNadEs44RQZ2Uziw0BQZblISaXjDLu4vq1Yl7n-KPGfOkdj5bHEcdMM5ZAWe0Z1xIUaKXp2hZLeeEW3WfyqfTQQFRR8NqUP8yrI6GFZGqGC6Qlw_zZrND9wfxW2kJrE8BLFvvPSaVrcdg0fmEdlIu-v-b9-4vnB198FaPd3jAPMQ5heJXgcpUEbU53vx4cugJ6RfAu5-uMK6i</recordid><startdate>20150201</startdate><enddate>20150201</enddate><creator>Yakushiji, Yusuke, MD, PhD</creator><creator>Noguchi, Tomoyuki, MD, PhD</creator><creator>Charidimou, Andreas, MD, MSc</creator><creator>Eriguchi, Makoto, MD, PhD</creator><creator>Nishihara, Masashi, MD</creator><creator>Hara, Megumi, MD, PhD</creator><creator>Nanri, Yusuke, MD, PhD</creator><creator>Horikawa, Etsuo, PhD</creator><creator>Nishiyama, Masanori, MD</creator><creator>Werring, David J., MD, PhD</creator><creator>Hara, Hideo, MD, PhD</creator><general>Elsevier Inc</general><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></search><sort><creationdate>20150201</creationdate><title>Basal Ganglia Cerebral Microbleeds and Global Cognitive Function: The Kashima Scan Study</title><author>Yakushiji, Yusuke, MD, PhD ; Noguchi, Tomoyuki, MD, PhD ; Charidimou, Andreas, MD, MSc ; Eriguchi, Makoto, MD, PhD ; Nishihara, Masashi, MD ; Hara, Megumi, MD, PhD ; Nanri, Yusuke, MD, PhD ; Horikawa, Etsuo, PhD ; Nishiyama, Masanori, MD ; Werring, David J., MD, PhD ; Hara, Hideo, MD, PhD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c595t-b11b2c8699428265cd61bb65a17418ea620a535082d99db7a2151fe902b485c63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Aged</topic><topic>basal ganglia</topic><topic>Basal Ganglia - pathology</topic><topic>Cardiovascular</topic><topic>Cerebral Hemorrhage - complications</topic><topic>Cerebral Hemorrhage - pathology</topic><topic>Cerebral Hemorrhage - psychology</topic><topic>Cerebral microbleeds</topic><topic>Cognition</topic><topic>Cognition Disorders - etiology</topic><topic>Cognition Disorders - pathology</topic><topic>Cognition Disorders - psychology</topic><topic>cognitive dysfunction</topic><topic>Cross-Sectional Studies</topic><topic>Female</topic><topic>Humans</topic><topic>Magnetic Resonance Imaging</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Neurology</topic><topic>Neuropsychological Tests</topic><topic>Risk Factors</topic><topic>small vessel disease</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yakushiji, Yusuke, MD, PhD</creatorcontrib><creatorcontrib>Noguchi, Tomoyuki, MD, PhD</creatorcontrib><creatorcontrib>Charidimou, Andreas, MD, MSc</creatorcontrib><creatorcontrib>Eriguchi, Makoto, MD, PhD</creatorcontrib><creatorcontrib>Nishihara, Masashi, MD</creatorcontrib><creatorcontrib>Hara, Megumi, MD, PhD</creatorcontrib><creatorcontrib>Nanri, Yusuke, MD, PhD</creatorcontrib><creatorcontrib>Horikawa, Etsuo, PhD</creatorcontrib><creatorcontrib>Nishiyama, Masanori, MD</creatorcontrib><creatorcontrib>Werring, David J., MD, PhD</creatorcontrib><creatorcontrib>Hara, Hideo, MD, PhD</creatorcontrib><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><jtitle>Journal of stroke and cerebrovascular diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yakushiji, Yusuke, MD, PhD</au><au>Noguchi, Tomoyuki, MD, PhD</au><au>Charidimou, Andreas, MD, MSc</au><au>Eriguchi, Makoto, MD, PhD</au><au>Nishihara, Masashi, MD</au><au>Hara, Megumi, MD, PhD</au><au>Nanri, Yusuke, MD, PhD</au><au>Horikawa, Etsuo, PhD</au><au>Nishiyama, Masanori, MD</au><au>Werring, David J., MD, PhD</au><au>Hara, Hideo, MD, PhD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Basal Ganglia Cerebral Microbleeds and Global Cognitive Function: The Kashima Scan Study</atitle><jtitle>Journal of stroke and cerebrovascular diseases</jtitle><addtitle>J Stroke Cerebrovasc Dis</addtitle><date>2015-02-01</date><risdate>2015</risdate><volume>24</volume><issue>2</issue><spage>431</spage><epage>439</epage><pages>431-439</pages><issn>1052-3057</issn><eissn>1532-8511</eissn><abstract>Background We previously showed that global cognitive function was associated with deep or infratentorial (D/I) cerebral microbleeds (CMBs) in a Japanese healthy cohort. We continually recruited participates and performed further investigation to focus on the impact of different distributions of D/I CMBs on gradient-echo magnetic resonance imaging on global cognitive function. Methods A total of 1392 subjects including subjects without CMBs (n = 1335), with D/I CMBs limited to the basal ganglia (BG; BG group, n = 33), thalamus (thalamus group, n = 14), and infratentorial area (infratentorial group, n = 10) were included in analyses. Subjects with strictly lobar CMBs (n = 43) were excluded, but subjects in the BG, thalamus, and infratentorial groups could also have lobar CMBs. The mini-mental state examination (MMSE) was administered to determine global cognitive function; scores less than 27 or more than 1.5 standard deviations (SDs) below the age–education-related mean were regarded as impaired. Results In the multivariable logistic regression analyses, hypertension and severe white matter hyperintensities were associated with the BG group and the thalamus group. In multivariable logistic regression analysis of the association between D/I CMBs classification and impaired MMSE score, only the BG group consistently displayed associations with both MMSE score less than 27 (odds ratio [OR], 5.96; 95% confidence interval [CI], 2.08-17.09) and MMSE score more than 1.5 SDs below the age–education-related mean (OR, 3.34; 95% CI, 1.24-8.99). In the BG group, adjusted mean scores of total MMSE and “attention and calculation” were lower compared with subjects without CMBs. Conclusions In our study of D/I CMBs, only BG CMBs have strong association with global cognitive function. This association was independent of CMBs in other location.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>25516488</pmid><doi>10.1016/j.jstrokecerebrovasdis.2014.09.015</doi><tpages>9</tpages></addata></record> |
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subjects | Aged basal ganglia Basal Ganglia - pathology Cardiovascular Cerebral Hemorrhage - complications Cerebral Hemorrhage - pathology Cerebral Hemorrhage - psychology Cerebral microbleeds Cognition Cognition Disorders - etiology Cognition Disorders - pathology Cognition Disorders - psychology cognitive dysfunction Cross-Sectional Studies Female Humans Magnetic Resonance Imaging Male Middle Aged Neurology Neuropsychological Tests Risk Factors small vessel disease |
title | Basal Ganglia Cerebral Microbleeds and Global Cognitive Function: The Kashima Scan Study |
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