Cerebral hypoperfusion and clinical onset of dementia: The Rotterdam study
Cerebral blood flow (CBF) velocity is decreased in patients with Alzheimer's disease. It is being debated whether this reflects diminished demand because of advanced neurodegeneration or that cerebral hypoperfusion contributes to dementia. We examined the relation of CBF velocity as measured wi...
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Veröffentlicht in: | Annals of neurology 2005-06, Vol.57 (6), p.789-794 |
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description | Cerebral blood flow (CBF) velocity is decreased in patients with Alzheimer's disease. It is being debated whether this reflects diminished demand because of advanced neurodegeneration or that cerebral hypoperfusion contributes to dementia. We examined the relation of CBF velocity as measured with transcranial Doppler with dementia and markers of incipient dementia (ie, cognitive decline and hippocampal and amygdalar atrophy on magnetic resonance imaging) in 1,730 participants of the Rotterdam Study aged 55 years and older. Cognitive decline in the 6.5 years preceding CBF velocity measurement was assessed with repeated Mini‐Mental State Examinations in nondemented subjects (n = 1,716). Hippocampal and amygdalar volumes were assessed in a subset of 170 nondemented subjects. Subjects with greater CBF velocity were less likely to have dementia. Furthermore, in nondemented subjects, greater CBF velocity was related to significantly less cognitive decline over the preceding period (odds ratio per standard deviation increase in mean CBF 0.74 [95% confidence interval, 0.58–0.98]) and larger hippocampal and amygdalar volumes. A low CBF is associated with dementia, but also with markers of incipient dementia. Although we cannot exclude that this is caused by preclinical neurodegeneration leading to hypoperfusion, it does suggest that cerebral hypoperfusion precedes and possibly contributes to onset of clinical dementia. Ann Neurol 2005;57:789–794 |
doi_str_mv | 10.1002/ana.20493 |
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M. ; van Swieten, John C. ; Koudstaal, Peter J. ; Hofman, Albert ; Breteler, Monique M. B.</creator><creatorcontrib>Ruitenberg, Annemieke ; den Heijer, Tom ; Bakker, Stef L. M. ; van Swieten, John C. ; Koudstaal, Peter J. ; Hofman, Albert ; Breteler, Monique M. B.</creatorcontrib><description>Cerebral blood flow (CBF) velocity is decreased in patients with Alzheimer's disease. It is being debated whether this reflects diminished demand because of advanced neurodegeneration or that cerebral hypoperfusion contributes to dementia. We examined the relation of CBF velocity as measured with transcranial Doppler with dementia and markers of incipient dementia (ie, cognitive decline and hippocampal and amygdalar atrophy on magnetic resonance imaging) in 1,730 participants of the Rotterdam Study aged 55 years and older. Cognitive decline in the 6.5 years preceding CBF velocity measurement was assessed with repeated Mini‐Mental State Examinations in nondemented subjects (n = 1,716). Hippocampal and amygdalar volumes were assessed in a subset of 170 nondemented subjects. Subjects with greater CBF velocity were less likely to have dementia. Furthermore, in nondemented subjects, greater CBF velocity was related to significantly less cognitive decline over the preceding period (odds ratio per standard deviation increase in mean CBF 0.74 [95% confidence interval, 0.58–0.98]) and larger hippocampal and amygdalar volumes. A low CBF is associated with dementia, but also with markers of incipient dementia. Although we cannot exclude that this is caused by preclinical neurodegeneration leading to hypoperfusion, it does suggest that cerebral hypoperfusion precedes and possibly contributes to onset of clinical dementia. Ann Neurol 2005;57:789–794</description><identifier>ISSN: 0364-5134</identifier><identifier>EISSN: 1531-8249</identifier><identifier>DOI: 10.1002/ana.20493</identifier><identifier>PMID: 15929050</identifier><identifier>CODEN: ANNED3</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Aged ; Alzheimer Disease - diagnostic imaging ; Alzheimer Disease - pathology ; Alzheimer Disease - physiopathology ; Amygdala - blood supply ; Amygdala - pathology ; Atrophy ; Biological and medical sciences ; Cerebrovascular Circulation ; Cognition Disorders - diagnostic imaging ; Cognition Disorders - pathology ; Cognition Disorders - physiopathology ; Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases ; Female ; Hippocampus - blood supply ; Hippocampus - pathology ; Humans ; Magnetic Resonance Imaging ; Male ; Medical sciences ; Middle Aged ; Nerve Degeneration - diagnostic imaging ; Nerve Degeneration - pathology ; Nerve Degeneration - physiopathology ; Netherlands ; Neurology ; Ultrasonography, Doppler, Transcranial ; Vascular diseases and vascular malformations of the nervous system</subject><ispartof>Annals of neurology, 2005-06, Vol.57 (6), p.789-794</ispartof><rights>Copyright © 2005 American Neurological Association</rights><rights>2005 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5283-eb68c3bd065f8d2c0428fd6f37f5358d3295285829620b3ba13d75e6c5c70f83</citedby><cites>FETCH-LOGICAL-c5283-eb68c3bd065f8d2c0428fd6f37f5358d3295285829620b3ba13d75e6c5c70f83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fana.20493$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fana.20493$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16870441$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15929050$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ruitenberg, Annemieke</creatorcontrib><creatorcontrib>den Heijer, Tom</creatorcontrib><creatorcontrib>Bakker, Stef L. M.</creatorcontrib><creatorcontrib>van Swieten, John C.</creatorcontrib><creatorcontrib>Koudstaal, Peter J.</creatorcontrib><creatorcontrib>Hofman, Albert</creatorcontrib><creatorcontrib>Breteler, Monique M. B.</creatorcontrib><title>Cerebral hypoperfusion and clinical onset of dementia: The Rotterdam study</title><title>Annals of neurology</title><addtitle>Ann Neurol</addtitle><description>Cerebral blood flow (CBF) velocity is decreased in patients with Alzheimer's disease. It is being debated whether this reflects diminished demand because of advanced neurodegeneration or that cerebral hypoperfusion contributes to dementia. We examined the relation of CBF velocity as measured with transcranial Doppler with dementia and markers of incipient dementia (ie, cognitive decline and hippocampal and amygdalar atrophy on magnetic resonance imaging) in 1,730 participants of the Rotterdam Study aged 55 years and older. Cognitive decline in the 6.5 years preceding CBF velocity measurement was assessed with repeated Mini‐Mental State Examinations in nondemented subjects (n = 1,716). Hippocampal and amygdalar volumes were assessed in a subset of 170 nondemented subjects. Subjects with greater CBF velocity were less likely to have dementia. Furthermore, in nondemented subjects, greater CBF velocity was related to significantly less cognitive decline over the preceding period (odds ratio per standard deviation increase in mean CBF 0.74 [95% confidence interval, 0.58–0.98]) and larger hippocampal and amygdalar volumes. A low CBF is associated with dementia, but also with markers of incipient dementia. Although we cannot exclude that this is caused by preclinical neurodegeneration leading to hypoperfusion, it does suggest that cerebral hypoperfusion precedes and possibly contributes to onset of clinical dementia. Ann Neurol 2005;57:789–794</description><subject>Aged</subject><subject>Alzheimer Disease - diagnostic imaging</subject><subject>Alzheimer Disease - pathology</subject><subject>Alzheimer Disease - physiopathology</subject><subject>Amygdala - blood supply</subject><subject>Amygdala - pathology</subject><subject>Atrophy</subject><subject>Biological and medical sciences</subject><subject>Cerebrovascular Circulation</subject><subject>Cognition Disorders - diagnostic imaging</subject><subject>Cognition Disorders - pathology</subject><subject>Cognition Disorders - physiopathology</subject><subject>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</subject><subject>Female</subject><subject>Hippocampus - blood supply</subject><subject>Hippocampus - pathology</subject><subject>Humans</subject><subject>Magnetic Resonance Imaging</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Nerve Degeneration - diagnostic imaging</subject><subject>Nerve Degeneration - pathology</subject><subject>Nerve Degeneration - physiopathology</subject><subject>Netherlands</subject><subject>Neurology</subject><subject>Ultrasonography, Doppler, Transcranial</subject><subject>Vascular diseases and vascular malformations of the nervous system</subject><issn>0364-5134</issn><issn>1531-8249</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0E1v1DAQBmALUdGlcOAPoFxA4pB2_BmH22rVFlBVEKwE2ovl2GPVkI_FTlT235OyS3tCnHyYZ96RX0JeUDilAOzM9vaUgaj5I7KgktNSM1E_JgvgSpSScnFMnub8HQBqReEJOaayZjVIWJAPK0zYJNsWN7vtsMUUphyHvrC9L1wb--jm0dBnHIshFB477Mdo3xbrGyw-D-OIyduuyOPkd8_IUbBtxueH94SsL87Xq3fl1cfL96vlVekk07zERmnHGw9KBu2ZA8F08CrwKkguteesnp3UrFYMGt5Yyn0lUTnpKgian5DX-9htGn5OmEfTxeywbW2Pw5SNqmpgFVf_hQxkLUR1l_hmD10ack4YzDbFzqadoWDuCjZzweZPwbN9eQidmg79gzw0OoNXB2Dz3F1ItncxPzilKxCCzu5s725ji7t_XzTL6-Xf0-V-I-YRf91v2PRj_jOvpPl6fWk2-tuniy8bZjb8N0Hnn7o</recordid><startdate>200506</startdate><enddate>200506</enddate><creator>Ruitenberg, Annemieke</creator><creator>den Heijer, Tom</creator><creator>Bakker, Stef L. M.</creator><creator>van Swieten, John C.</creator><creator>Koudstaal, Peter J.</creator><creator>Hofman, Albert</creator><creator>Breteler, Monique M. B.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Willey-Liss</general><scope>BSCLL</scope><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>7TK</scope><scope>7X8</scope></search><sort><creationdate>200506</creationdate><title>Cerebral hypoperfusion and clinical onset of dementia: The Rotterdam study</title><author>Ruitenberg, Annemieke ; den Heijer, Tom ; Bakker, Stef L. M. ; van Swieten, John C. ; Koudstaal, Peter J. ; Hofman, Albert ; Breteler, Monique M. 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Prion diseases</topic><topic>Female</topic><topic>Hippocampus - blood supply</topic><topic>Hippocampus - pathology</topic><topic>Humans</topic><topic>Magnetic Resonance Imaging</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Nerve Degeneration - diagnostic imaging</topic><topic>Nerve Degeneration - pathology</topic><topic>Nerve Degeneration - physiopathology</topic><topic>Netherlands</topic><topic>Neurology</topic><topic>Ultrasonography, Doppler, Transcranial</topic><topic>Vascular diseases and vascular malformations of the nervous system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ruitenberg, Annemieke</creatorcontrib><creatorcontrib>den Heijer, Tom</creatorcontrib><creatorcontrib>Bakker, Stef L. M.</creatorcontrib><creatorcontrib>van Swieten, John C.</creatorcontrib><creatorcontrib>Koudstaal, Peter J.</creatorcontrib><creatorcontrib>Hofman, Albert</creatorcontrib><creatorcontrib>Breteler, Monique M. B.</creatorcontrib><collection>Istex</collection><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>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Annals of neurology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ruitenberg, Annemieke</au><au>den Heijer, Tom</au><au>Bakker, Stef L. M.</au><au>van Swieten, John C.</au><au>Koudstaal, Peter J.</au><au>Hofman, Albert</au><au>Breteler, Monique M. B.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cerebral hypoperfusion and clinical onset of dementia: The Rotterdam study</atitle><jtitle>Annals of neurology</jtitle><addtitle>Ann Neurol</addtitle><date>2005-06</date><risdate>2005</risdate><volume>57</volume><issue>6</issue><spage>789</spage><epage>794</epage><pages>789-794</pages><issn>0364-5134</issn><eissn>1531-8249</eissn><coden>ANNED3</coden><abstract>Cerebral blood flow (CBF) velocity is decreased in patients with Alzheimer's disease. It is being debated whether this reflects diminished demand because of advanced neurodegeneration or that cerebral hypoperfusion contributes to dementia. We examined the relation of CBF velocity as measured with transcranial Doppler with dementia and markers of incipient dementia (ie, cognitive decline and hippocampal and amygdalar atrophy on magnetic resonance imaging) in 1,730 participants of the Rotterdam Study aged 55 years and older. Cognitive decline in the 6.5 years preceding CBF velocity measurement was assessed with repeated Mini‐Mental State Examinations in nondemented subjects (n = 1,716). Hippocampal and amygdalar volumes were assessed in a subset of 170 nondemented subjects. Subjects with greater CBF velocity were less likely to have dementia. Furthermore, in nondemented subjects, greater CBF velocity was related to significantly less cognitive decline over the preceding period (odds ratio per standard deviation increase in mean CBF 0.74 [95% confidence interval, 0.58–0.98]) and larger hippocampal and amygdalar volumes. A low CBF is associated with dementia, but also with markers of incipient dementia. Although we cannot exclude that this is caused by preclinical neurodegeneration leading to hypoperfusion, it does suggest that cerebral hypoperfusion precedes and possibly contributes to onset of clinical dementia. Ann Neurol 2005;57:789–794</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>15929050</pmid><doi>10.1002/ana.20493</doi><tpages>6</tpages></addata></record> |
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subjects | Aged Alzheimer Disease - diagnostic imaging Alzheimer Disease - pathology Alzheimer Disease - physiopathology Amygdala - blood supply Amygdala - pathology Atrophy Biological and medical sciences Cerebrovascular Circulation Cognition Disorders - diagnostic imaging Cognition Disorders - pathology Cognition Disorders - physiopathology Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases Female Hippocampus - blood supply Hippocampus - pathology Humans Magnetic Resonance Imaging Male Medical sciences Middle Aged Nerve Degeneration - diagnostic imaging Nerve Degeneration - pathology Nerve Degeneration - physiopathology Netherlands Neurology Ultrasonography, Doppler, Transcranial Vascular diseases and vascular malformations of the nervous system |
title | Cerebral hypoperfusion and clinical onset of dementia: The Rotterdam study |
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