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In vivo quantitative whole-brain T sub(1) rho MRI of multiple sclerosis
Background To apply quantitative whole-brain T sub(1)-rho (T sub(1 rho )) and T sub(2) imaging to the detection and quantification of brain changes resulting from multiple sclerosis (MS). Methods Twenty-three MS patients with clinically isolated syndrome (10) and relapsing remitting MS (13) phenotyp...
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Published in: | Journal of magnetic resonance imaging 2015-12, Vol.42 (6), p.1623-1630 |
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creator | Gonyea, Jay V Watts, Richard Applebee, Angela Andrews, Trevor Hipko, Scott Nickerson, Joshua P Thornton, Lindsay Filippi, Christopher G |
description | Background To apply quantitative whole-brain T sub(1)-rho (T sub(1 rho )) and T sub(2) imaging to the detection and quantification of brain changes resulting from multiple sclerosis (MS). Methods Twenty-three MS patients with clinically isolated syndrome (10) and relapsing remitting MS (13) phenotypes, compared with 24 age-matched healthy controls were imaged at 3 Tesla. An axial T sub(1 rho )-weighted three-dimensional turbo spin echo sequence with a variable flip angle and fluid suppression was used. Spin-lock times of 0, 20, 40, 60, 80, and 100 ms were used. Corresponding T sub(2) maps were also acquired. Results Whole brain white matter (WM) T sub(1 rho ) maps were elevated compared with controls (P = 0.002). WM lesion T sub(1 rho ) and T sub(2) values were highly correlated (r = 0.83), but T sub(1 rho ) demonstrated 25% better contrast to noise ratio (P < 0.001). WM lesion T sub(1 rho ) correlated with disease duration. Gray matter T sub(1 rho ) was negatively correlated with the Expanded Disability Status Scale, r = -0.45, P = 0.03. Normal appearing gray matter and cortical gray matter lesions were negatively correlated on T sub(1 rho ), but not on T sub(2) (r sub(T1 rho ) = -0.63, p sub(T1 rho ) = 0.03; r sub(T2) = -0.17, p sub(T2) = 0.6). Conclusion T sub(1 rho ) MRI demonstrates enhanced lesion contrast compared with T sub(2), and in some cases may provide complementary information. T sub(1 rho ) may provide a useful measure of demyelinating processes in MS. J. MAGN. RESON. IMAGING 2015; 42:1623-1630. |
doi_str_mv | 10.1002/jmri.24954 |
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Methods Twenty-three MS patients with clinically isolated syndrome (10) and relapsing remitting MS (13) phenotypes, compared with 24 age-matched healthy controls were imaged at 3 Tesla. An axial T sub(1 rho )-weighted three-dimensional turbo spin echo sequence with a variable flip angle and fluid suppression was used. Spin-lock times of 0, 20, 40, 60, 80, and 100 ms were used. Corresponding T sub(2) maps were also acquired. Results Whole brain white matter (WM) T sub(1 rho ) maps were elevated compared with controls (P = 0.002). WM lesion T sub(1 rho ) and T sub(2) values were highly correlated (r = 0.83), but T sub(1 rho ) demonstrated 25% better contrast to noise ratio (P < 0.001). WM lesion T sub(1 rho ) correlated with disease duration. Gray matter T sub(1 rho ) was negatively correlated with the Expanded Disability Status Scale, r = -0.45, P = 0.03. Normal appearing gray matter and cortical gray matter lesions were negatively correlated on T sub(1 rho ), but not on T sub(2) (r sub(T1 rho ) = -0.63, p sub(T1 rho ) = 0.03; r sub(T2) = -0.17, p sub(T2) = 0.6). Conclusion T sub(1 rho ) MRI demonstrates enhanced lesion contrast compared with T sub(2), and in some cases may provide complementary information. T sub(1 rho ) may provide a useful measure of demyelinating processes in MS. J. MAGN. RESON. IMAGING 2015; 42:1623-1630.</description><identifier>ISSN: 1053-1807</identifier><identifier>EISSN: 1522-2586</identifier><identifier>DOI: 10.1002/jmri.24954</identifier><language>eng</language><ispartof>Journal of magnetic resonance imaging, 2015-12, Vol.42 (6), p.1623-1630</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></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></links><search><creatorcontrib>Gonyea, Jay V</creatorcontrib><creatorcontrib>Watts, Richard</creatorcontrib><creatorcontrib>Applebee, Angela</creatorcontrib><creatorcontrib>Andrews, Trevor</creatorcontrib><creatorcontrib>Hipko, Scott</creatorcontrib><creatorcontrib>Nickerson, Joshua P</creatorcontrib><creatorcontrib>Thornton, Lindsay</creatorcontrib><creatorcontrib>Filippi, Christopher G</creatorcontrib><title>In vivo quantitative whole-brain T sub(1) rho MRI of multiple sclerosis</title><title>Journal of magnetic resonance imaging</title><description>Background To apply quantitative whole-brain T sub(1)-rho (T sub(1 rho )) and T sub(2) imaging to the detection and quantification of brain changes resulting from multiple sclerosis (MS). Methods Twenty-three MS patients with clinically isolated syndrome (10) and relapsing remitting MS (13) phenotypes, compared with 24 age-matched healthy controls were imaged at 3 Tesla. An axial T sub(1 rho )-weighted three-dimensional turbo spin echo sequence with a variable flip angle and fluid suppression was used. Spin-lock times of 0, 20, 40, 60, 80, and 100 ms were used. Corresponding T sub(2) maps were also acquired. Results Whole brain white matter (WM) T sub(1 rho ) maps were elevated compared with controls (P = 0.002). WM lesion T sub(1 rho ) and T sub(2) values were highly correlated (r = 0.83), but T sub(1 rho ) demonstrated 25% better contrast to noise ratio (P < 0.001). WM lesion T sub(1 rho ) correlated with disease duration. Gray matter T sub(1 rho ) was negatively correlated with the Expanded Disability Status Scale, r = -0.45, P = 0.03. Normal appearing gray matter and cortical gray matter lesions were negatively correlated on T sub(1 rho ), but not on T sub(2) (r sub(T1 rho ) = -0.63, p sub(T1 rho ) = 0.03; r sub(T2) = -0.17, p sub(T2) = 0.6). Conclusion T sub(1 rho ) MRI demonstrates enhanced lesion contrast compared with T sub(2), and in some cases may provide complementary information. T sub(1 rho ) may provide a useful measure of demyelinating processes in MS. J. MAGN. RESON. IMAGING 2015; 42:1623-1630.</description><issn>1053-1807</issn><issn>1522-2586</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNqVyrsOwiAUgGFiNPG6-ARn1KF6oEXb2XgbXIy7oQ1GDC3Kgfr6OvgCTv83_IxNOS44olg-am8WIitk1mEDLoVIhMxX3a9RpgnPcd1nQ6IHIhZFJgdsf2ygNa2DV1RNMEEF02p4353VSemVaeACFMsZn4O_Ozidj-BuUEcbzNNqoMpq78jQmPVuypKe_Dpis932sjkkT-9eUVO41oYqba1qtIt05escJV-lqUz_WD8B9ESJ</recordid><startdate>20151201</startdate><enddate>20151201</enddate><creator>Gonyea, Jay V</creator><creator>Watts, Richard</creator><creator>Applebee, Angela</creator><creator>Andrews, Trevor</creator><creator>Hipko, Scott</creator><creator>Nickerson, Joshua P</creator><creator>Thornton, Lindsay</creator><creator>Filippi, Christopher G</creator><scope>7TK</scope></search><sort><creationdate>20151201</creationdate><title>In vivo quantitative whole-brain T sub(1) rho MRI of multiple sclerosis</title><author>Gonyea, Jay V ; Watts, Richard ; Applebee, Angela ; Andrews, Trevor ; Hipko, Scott ; Nickerson, Joshua P ; Thornton, Lindsay ; Filippi, Christopher G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-proquest_miscellaneous_17805163353</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gonyea, Jay V</creatorcontrib><creatorcontrib>Watts, Richard</creatorcontrib><creatorcontrib>Applebee, Angela</creatorcontrib><creatorcontrib>Andrews, Trevor</creatorcontrib><creatorcontrib>Hipko, Scott</creatorcontrib><creatorcontrib>Nickerson, Joshua P</creatorcontrib><creatorcontrib>Thornton, Lindsay</creatorcontrib><creatorcontrib>Filippi, Christopher G</creatorcontrib><collection>Neurosciences Abstracts</collection><jtitle>Journal of magnetic resonance imaging</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gonyea, Jay V</au><au>Watts, Richard</au><au>Applebee, Angela</au><au>Andrews, Trevor</au><au>Hipko, Scott</au><au>Nickerson, Joshua P</au><au>Thornton, Lindsay</au><au>Filippi, Christopher G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>In vivo quantitative whole-brain T sub(1) rho MRI of multiple sclerosis</atitle><jtitle>Journal of magnetic resonance imaging</jtitle><date>2015-12-01</date><risdate>2015</risdate><volume>42</volume><issue>6</issue><spage>1623</spage><epage>1630</epage><pages>1623-1630</pages><issn>1053-1807</issn><eissn>1522-2586</eissn><abstract>Background To apply quantitative whole-brain T sub(1)-rho (T sub(1 rho )) and T sub(2) imaging to the detection and quantification of brain changes resulting from multiple sclerosis (MS). Methods Twenty-three MS patients with clinically isolated syndrome (10) and relapsing remitting MS (13) phenotypes, compared with 24 age-matched healthy controls were imaged at 3 Tesla. An axial T sub(1 rho )-weighted three-dimensional turbo spin echo sequence with a variable flip angle and fluid suppression was used. Spin-lock times of 0, 20, 40, 60, 80, and 100 ms were used. Corresponding T sub(2) maps were also acquired. Results Whole brain white matter (WM) T sub(1 rho ) maps were elevated compared with controls (P = 0.002). WM lesion T sub(1 rho ) and T sub(2) values were highly correlated (r = 0.83), but T sub(1 rho ) demonstrated 25% better contrast to noise ratio (P < 0.001). WM lesion T sub(1 rho ) correlated with disease duration. Gray matter T sub(1 rho ) was negatively correlated with the Expanded Disability Status Scale, r = -0.45, P = 0.03. Normal appearing gray matter and cortical gray matter lesions were negatively correlated on T sub(1 rho ), but not on T sub(2) (r sub(T1 rho ) = -0.63, p sub(T1 rho ) = 0.03; r sub(T2) = -0.17, p sub(T2) = 0.6). Conclusion T sub(1 rho ) MRI demonstrates enhanced lesion contrast compared with T sub(2), and in some cases may provide complementary information. T sub(1 rho ) may provide a useful measure of demyelinating processes in MS. J. MAGN. RESON. IMAGING 2015; 42:1623-1630.</abstract><doi>10.1002/jmri.24954</doi></addata></record> |
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title | In vivo quantitative whole-brain T sub(1) rho MRI of multiple sclerosis |
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