Transit time, trailing time, and cerebral blood flow during brain activation: Measurement using multislice, pulsed spin-labeling perfusion imaging
Transit time and trailing time in pulsed spin‐labeling perfusion imaging are likely to be modulated by local blood flow changes, such as those accompanying brain activation. The majority of transit/trailing time is due to the passage of the tagged blood bolus through the arteriole/capillary regions,...
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Veröffentlicht in: | Magnetic resonance in medicine 2000-11, Vol.44 (5), p.680-685 |
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description | Transit time and trailing time in pulsed spin‐labeling perfusion imaging are likely to be modulated by local blood flow changes, such as those accompanying brain activation. The majority of transit/trailing time is due to the passage of the tagged blood bolus through the arteriole/capillary regions, because of lower blood flow velocity in these regions. Changes of transit/trailing time during activation could affect the quantification of CBF in functional neuroimaging studies, and are therefore important to characterize. In this work, the measurement of transit and trailing times and CBF during sensorimotor activation using multislice perfusion imaging with pulsed arterial spin‐labeling is described. While CBF elevated dramatically (∼︁80.7%) during the sensorimotor activation, sizable reductions of transit time (∼︁0.11 sec) and trailing time (∼︁0.26 sec) were observed. Transit and trailing times were dependent on the distances from the leading and trailing edges of the tagged blood bolus to the location of the imaging slices. The effects of transit/trailing time changes on CBF quantification during brain activation were analyzed by simulation studies. Significant errors can be caused in the estimation of CBF if such changes of transit/trailing time are not taken into account. Magn Reson Med 44:680–685, 2000. © 2000 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/1522-2594(200011)44:5<680::AID-MRM4>3.0.CO;2-Q |
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The majority of transit/trailing time is due to the passage of the tagged blood bolus through the arteriole/capillary regions, because of lower blood flow velocity in these regions. Changes of transit/trailing time during activation could affect the quantification of CBF in functional neuroimaging studies, and are therefore important to characterize. In this work, the measurement of transit and trailing times and CBF during sensorimotor activation using multislice perfusion imaging with pulsed arterial spin‐labeling is described. While CBF elevated dramatically (∼︁80.7%) during the sensorimotor activation, sizable reductions of transit time (∼︁0.11 sec) and trailing time (∼︁0.26 sec) were observed. Transit and trailing times were dependent on the distances from the leading and trailing edges of the tagged blood bolus to the location of the imaging slices. The effects of transit/trailing time changes on CBF quantification during brain activation were analyzed by simulation studies. Significant errors can be caused in the estimation of CBF if such changes of transit/trailing time are not taken into account. Magn Reson Med 44:680–685, 2000. © 2000 Wiley‐Liss, Inc.</description><identifier>ISSN: 0740-3194</identifier><identifier>EISSN: 1522-2594</identifier><identifier>DOI: 10.1002/1522-2594(200011)44:5<680::AID-MRM4>3.0.CO;2-Q</identifier><identifier>PMID: 11064401</identifier><identifier>CODEN: MRMEEN</identifier><language>eng</language><publisher>New York: John Wiley & Sons, Inc</publisher><subject>Biological and medical sciences ; Brain - blood supply ; Brain - physiology ; brain activation ; CBF ; Cerebrovascular Circulation ; Humans ; Investigative techniques, diagnostic techniques (general aspects) ; Magnetic Resonance Imaging - methods ; Medical sciences ; Nervous system ; perfusion MRI ; Radiodiagnosis. Nmr imagery. Nmr spectrometry ; Spin Labels ; trailing time ; transit time</subject><ispartof>Magnetic resonance in medicine, 2000-11, Vol.44 (5), p.680-685</ispartof><rights>Copyright © 2000 Wiley‐Liss, Inc.</rights><rights>2001 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c5534-80dd3e26d9e5bed54cbab17ad0de39fdd89bfadfe85607be083684e478b34bc03</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%2F1522-2594%28200011%2944%3A5%3C680%3A%3AAID-MRM4%3E3.0.CO%3B2-Q$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2F1522-2594%28200011%2944%3A5%3C680%3A%3AAID-MRM4%3E3.0.CO%3B2-Q$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1416,1432,27922,27923,45572,45573,46407,46831</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=821462$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11064401$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yang, Yihong</creatorcontrib><creatorcontrib>Engelien, Wolfgang</creatorcontrib><creatorcontrib>Xu, Su</creatorcontrib><creatorcontrib>Gu, Hong</creatorcontrib><creatorcontrib>Silbersweig, David A.</creatorcontrib><creatorcontrib>Stern, Emily</creatorcontrib><title>Transit time, trailing time, and cerebral blood flow during brain activation: Measurement using multislice, pulsed spin-labeling perfusion imaging</title><title>Magnetic resonance in medicine</title><addtitle>Magn. Reson. Med</addtitle><description>Transit time and trailing time in pulsed spin‐labeling perfusion imaging are likely to be modulated by local blood flow changes, such as those accompanying brain activation. The majority of transit/trailing time is due to the passage of the tagged blood bolus through the arteriole/capillary regions, because of lower blood flow velocity in these regions. Changes of transit/trailing time during activation could affect the quantification of CBF in functional neuroimaging studies, and are therefore important to characterize. In this work, the measurement of transit and trailing times and CBF during sensorimotor activation using multislice perfusion imaging with pulsed arterial spin‐labeling is described. While CBF elevated dramatically (∼︁80.7%) during the sensorimotor activation, sizable reductions of transit time (∼︁0.11 sec) and trailing time (∼︁0.26 sec) were observed. Transit and trailing times were dependent on the distances from the leading and trailing edges of the tagged blood bolus to the location of the imaging slices. The effects of transit/trailing time changes on CBF quantification during brain activation were analyzed by simulation studies. Significant errors can be caused in the estimation of CBF if such changes of transit/trailing time are not taken into account. Magn Reson Med 44:680–685, 2000. © 2000 Wiley‐Liss, Inc.</description><subject>Biological and medical sciences</subject><subject>Brain - blood supply</subject><subject>Brain - physiology</subject><subject>brain activation</subject><subject>CBF</subject><subject>Cerebrovascular Circulation</subject><subject>Humans</subject><subject>Investigative techniques, diagnostic techniques (general aspects)</subject><subject>Magnetic Resonance Imaging - methods</subject><subject>Medical sciences</subject><subject>Nervous system</subject><subject>perfusion MRI</subject><subject>Radiodiagnosis. Nmr imagery. Nmr spectrometry</subject><subject>Spin Labels</subject><subject>trailing time</subject><subject>transit time</subject><issn>0740-3194</issn><issn>1522-2594</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVkV1rE0EUhhdRbKz-BRkQxIIb52u_ohRKNLWQNERqvTzM7pwtY2d348yutX_DX-xsE-KNN14N5_DMcw7njaKU0SmjlL9jCecxTwr5hlNKGTuRcpZ8SHM6m51dfIxXX1byVEzpdL5-z-PNo2hy-PA4mtBM0liwQh5Fz7z_HgRFkcmn0RFjNJWSskn0-8qp1pue9KbBt6R3yljT3uxL1WpSocPSKUtK23Wa1La7I3pwIxTapiWq6s1P1ZuunZEVKj84bLDtyeBHphlsb7w1VdBtB-tRE781bWxViQ-TtujqgHYtMY26CZ3n0ZNaBfDF_j2Ovi4-Xc0_x8v1-cX8bBlXSSJknFOtBfJUF5iUqBNZlapkmdJUoyhqrfOirJWuMU9SmpVIc5HmEmWWl0KWFRXH0eudd-u6HwP6HhrjK7RWtdgNHjIuiiJnSQAvd2DlOu8d1rB1YVd3D4zCmBKMR4fx6LBLCaSEBEJKACElGFMCARTma-CwCcKX-8lD2aD-q9vHEoBXe0D5Stk6ZFQZf-ByzmTKA7XeUXfG4v1_LPWPnR7qYIx3RuN7_HUwKncLaSayBL5dnsNis1xcX682kIo__YfJYw</recordid><startdate>200011</startdate><enddate>200011</enddate><creator>Yang, Yihong</creator><creator>Engelien, Wolfgang</creator><creator>Xu, Su</creator><creator>Gu, Hong</creator><creator>Silbersweig, David A.</creator><creator>Stern, Emily</creator><general>John Wiley & Sons, Inc</general><general>Williams & Wilkins</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>7X8</scope></search><sort><creationdate>200011</creationdate><title>Transit time, trailing time, and cerebral blood flow during brain activation: Measurement using multislice, pulsed spin-labeling perfusion imaging</title><author>Yang, Yihong ; Engelien, Wolfgang ; Xu, Su ; Gu, Hong ; Silbersweig, David A. ; Stern, Emily</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5534-80dd3e26d9e5bed54cbab17ad0de39fdd89bfadfe85607be083684e478b34bc03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Biological and medical sciences</topic><topic>Brain - blood supply</topic><topic>Brain - physiology</topic><topic>brain activation</topic><topic>CBF</topic><topic>Cerebrovascular Circulation</topic><topic>Humans</topic><topic>Investigative techniques, diagnostic techniques (general aspects)</topic><topic>Magnetic Resonance Imaging - methods</topic><topic>Medical sciences</topic><topic>Nervous system</topic><topic>perfusion MRI</topic><topic>Radiodiagnosis. Nmr imagery. Nmr spectrometry</topic><topic>Spin Labels</topic><topic>trailing time</topic><topic>transit time</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yang, Yihong</creatorcontrib><creatorcontrib>Engelien, Wolfgang</creatorcontrib><creatorcontrib>Xu, Su</creatorcontrib><creatorcontrib>Gu, Hong</creatorcontrib><creatorcontrib>Silbersweig, David A.</creatorcontrib><creatorcontrib>Stern, Emily</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>MEDLINE - Academic</collection><jtitle>Magnetic resonance in medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yang, Yihong</au><au>Engelien, Wolfgang</au><au>Xu, Su</au><au>Gu, Hong</au><au>Silbersweig, David A.</au><au>Stern, Emily</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Transit time, trailing time, and cerebral blood flow during brain activation: Measurement using multislice, pulsed spin-labeling perfusion imaging</atitle><jtitle>Magnetic resonance in medicine</jtitle><addtitle>Magn. Reson. Med</addtitle><date>2000-11</date><risdate>2000</risdate><volume>44</volume><issue>5</issue><spage>680</spage><epage>685</epage><pages>680-685</pages><issn>0740-3194</issn><eissn>1522-2594</eissn><coden>MRMEEN</coden><abstract>Transit time and trailing time in pulsed spin‐labeling perfusion imaging are likely to be modulated by local blood flow changes, such as those accompanying brain activation. The majority of transit/trailing time is due to the passage of the tagged blood bolus through the arteriole/capillary regions, because of lower blood flow velocity in these regions. Changes of transit/trailing time during activation could affect the quantification of CBF in functional neuroimaging studies, and are therefore important to characterize. In this work, the measurement of transit and trailing times and CBF during sensorimotor activation using multislice perfusion imaging with pulsed arterial spin‐labeling is described. While CBF elevated dramatically (∼︁80.7%) during the sensorimotor activation, sizable reductions of transit time (∼︁0.11 sec) and trailing time (∼︁0.26 sec) were observed. Transit and trailing times were dependent on the distances from the leading and trailing edges of the tagged blood bolus to the location of the imaging slices. The effects of transit/trailing time changes on CBF quantification during brain activation were analyzed by simulation studies. Significant errors can be caused in the estimation of CBF if such changes of transit/trailing time are not taken into account. Magn Reson Med 44:680–685, 2000. © 2000 Wiley‐Liss, Inc.</abstract><cop>New York</cop><pub>John Wiley & Sons, Inc</pub><pmid>11064401</pmid><doi>10.1002/1522-2594(200011)44:5<680::AID-MRM4>3.0.CO;2-Q</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Biological and medical sciences Brain - blood supply Brain - physiology brain activation CBF Cerebrovascular Circulation Humans Investigative techniques, diagnostic techniques (general aspects) Magnetic Resonance Imaging - methods Medical sciences Nervous system perfusion MRI Radiodiagnosis. Nmr imagery. Nmr spectrometry Spin Labels trailing time transit time |
title | Transit time, trailing time, and cerebral blood flow during brain activation: Measurement using multislice, pulsed spin-labeling perfusion imaging |
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