Dentate nuclei T2 relaxometry is a reliable neuroimaging marker in Friedreich's ataxia
Background and purpose In Friedreich's ataxia (FRDA), frataxin deficiency results in iron redistribution in the dentate nuclei (DNC). Clusters of iron cause inhomogeneities in a magnetic field and result in a reduction in T2 relaxation time (T2). Methods T2 was prospectively evaluated in DNC, p...
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Veröffentlicht in: | European journal of neurology 2014-08, Vol.21 (8), p.1131-1136 |
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creator | Bonilha da Silva, C. Bergo, F. P. G. D'Abreu, A. Cendes, F. Lopes-Cendes, I. França Jr, M. C. |
description | Background and purpose
In Friedreich's ataxia (FRDA), frataxin deficiency results in iron redistribution in the dentate nuclei (DNC). Clusters of iron cause inhomogeneities in a magnetic field and result in a reduction in T2 relaxation time (T2).
Methods
T2 was prospectively evaluated in DNC, putamen, substantia nigra (SN), cerebellar white matter (CWM) and caudate and the correlation with clinical parameters was investigated. Thirty‐five patients (range 9–51 years) and 44 controls (12–49 years) underwent T2 multi‐echo sequence in a 3T scanner. Twenty‐three patients (12–50 years) and 19 controls (14–49 years) were reassessed after 1 year. T2 was evaluated using specialized software (Aftervoxel) and severity of disease was quantified with the Friedreich Ataxia Rating Scale (FARS).
Results
T2 of both DNC was significantly shorter in the FRDA group at baseline (right, 58.6 ± 8.3 ms vs. 63.7 ± 8.1 ms, P = 0.013; left, 56.7 ± 7.7 ms vs. 62.6 ± 6.8 ms, P = 0.001). No significant difference was found between groups regarding the SN, putamen, CWM and caudate T2. DNC T2 values correlated with age, FARS total score and FARS III subscore on both sides. Prospectively, there was a significant reduction of T2 in FRDA patients in right and left DNC (P = 0.001 and 0.009) but not in other structures. Amongst controls, none of the regions significantly changed after 1 year. DNC T2 change over time correlated with GAA expansions and clinical deterioration (expressed by a change in FARS scores).
Conclusions
DNC T2 values are abnormal in FRDA, progress over time and correlate with ataxia severity. These results strongly suggest that DNC relaxometry can be a useful neuroimaging marker in FRDA. |
doi_str_mv | 10.1111/ene.12448 |
format | Article |
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In Friedreich's ataxia (FRDA), frataxin deficiency results in iron redistribution in the dentate nuclei (DNC). Clusters of iron cause inhomogeneities in a magnetic field and result in a reduction in T2 relaxation time (T2).
Methods
T2 was prospectively evaluated in DNC, putamen, substantia nigra (SN), cerebellar white matter (CWM) and caudate and the correlation with clinical parameters was investigated. Thirty‐five patients (range 9–51 years) and 44 controls (12–49 years) underwent T2 multi‐echo sequence in a 3T scanner. Twenty‐three patients (12–50 years) and 19 controls (14–49 years) were reassessed after 1 year. T2 was evaluated using specialized software (Aftervoxel) and severity of disease was quantified with the Friedreich Ataxia Rating Scale (FARS).
Results
T2 of both DNC was significantly shorter in the FRDA group at baseline (right, 58.6 ± 8.3 ms vs. 63.7 ± 8.1 ms, P = 0.013; left, 56.7 ± 7.7 ms vs. 62.6 ± 6.8 ms, P = 0.001). No significant difference was found between groups regarding the SN, putamen, CWM and caudate T2. DNC T2 values correlated with age, FARS total score and FARS III subscore on both sides. Prospectively, there was a significant reduction of T2 in FRDA patients in right and left DNC (P = 0.001 and 0.009) but not in other structures. Amongst controls, none of the regions significantly changed after 1 year. DNC T2 change over time correlated with GAA expansions and clinical deterioration (expressed by a change in FARS scores).
Conclusions
DNC T2 values are abnormal in FRDA, progress over time and correlate with ataxia severity. These results strongly suggest that DNC relaxometry can be a useful neuroimaging marker in FRDA.</description><identifier>ISSN: 1351-5101</identifier><identifier>EISSN: 1468-1331</identifier><identifier>DOI: 10.1111/ene.12448</identifier><identifier>PMID: 24779923</identifier><identifier>CODEN: EJNEFL</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Adolescent ; Adult ; Biomarkers ; Cerebellar Nuclei ; Child ; Cross-Sectional Studies ; dentate nuclei ; Disease Progression ; Female ; Follow-Up Studies ; Friedreich Ataxia - diagnosis ; Friedreich Ataxia - genetics ; Friedreich's ataxia ; Humans ; Magnetic Resonance Imaging - methods ; Male ; Middle Aged ; MRI ; Neuroimaging - methods ; T2 relaxometry ; Young Adult</subject><ispartof>European journal of neurology, 2014-08, Vol.21 (8), p.1131-1136</ispartof><rights>2014 The Author(s) European Journal of Neurology © 2014 EAN</rights><rights>2014 The Author(s) European Journal of Neurology © 2014 EAN.</rights><rights>European Journal of Neurology © 2014 European Federation of Neurological Societies</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4598-1b8ca7d9e1f645b561ef045be84dd7abb42d26aef8409c6c4a5f0a3b59129b033</citedby><cites>FETCH-LOGICAL-c4598-1b8ca7d9e1f645b561ef045be84dd7abb42d26aef8409c6c4a5f0a3b59129b033</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fene.12448$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fene.12448$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24779923$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bonilha da Silva, C.</creatorcontrib><creatorcontrib>Bergo, F. P. G.</creatorcontrib><creatorcontrib>D'Abreu, A.</creatorcontrib><creatorcontrib>Cendes, F.</creatorcontrib><creatorcontrib>Lopes-Cendes, I.</creatorcontrib><creatorcontrib>França Jr, M. C.</creatorcontrib><title>Dentate nuclei T2 relaxometry is a reliable neuroimaging marker in Friedreich's ataxia</title><title>European journal of neurology</title><addtitle>Eur J Neurol</addtitle><description>Background and purpose
In Friedreich's ataxia (FRDA), frataxin deficiency results in iron redistribution in the dentate nuclei (DNC). Clusters of iron cause inhomogeneities in a magnetic field and result in a reduction in T2 relaxation time (T2).
Methods
T2 was prospectively evaluated in DNC, putamen, substantia nigra (SN), cerebellar white matter (CWM) and caudate and the correlation with clinical parameters was investigated. Thirty‐five patients (range 9–51 years) and 44 controls (12–49 years) underwent T2 multi‐echo sequence in a 3T scanner. Twenty‐three patients (12–50 years) and 19 controls (14–49 years) were reassessed after 1 year. T2 was evaluated using specialized software (Aftervoxel) and severity of disease was quantified with the Friedreich Ataxia Rating Scale (FARS).
Results
T2 of both DNC was significantly shorter in the FRDA group at baseline (right, 58.6 ± 8.3 ms vs. 63.7 ± 8.1 ms, P = 0.013; left, 56.7 ± 7.7 ms vs. 62.6 ± 6.8 ms, P = 0.001). No significant difference was found between groups regarding the SN, putamen, CWM and caudate T2. DNC T2 values correlated with age, FARS total score and FARS III subscore on both sides. Prospectively, there was a significant reduction of T2 in FRDA patients in right and left DNC (P = 0.001 and 0.009) but not in other structures. Amongst controls, none of the regions significantly changed after 1 year. DNC T2 change over time correlated with GAA expansions and clinical deterioration (expressed by a change in FARS scores).
Conclusions
DNC T2 values are abnormal in FRDA, progress over time and correlate with ataxia severity. These results strongly suggest that DNC relaxometry can be a useful neuroimaging marker in FRDA.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Biomarkers</subject><subject>Cerebellar Nuclei</subject><subject>Child</subject><subject>Cross-Sectional Studies</subject><subject>dentate nuclei</subject><subject>Disease Progression</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Friedreich Ataxia - diagnosis</subject><subject>Friedreich Ataxia - genetics</subject><subject>Friedreich's ataxia</subject><subject>Humans</subject><subject>Magnetic Resonance Imaging - methods</subject><subject>Male</subject><subject>Middle Aged</subject><subject>MRI</subject><subject>Neuroimaging - methods</subject><subject>T2 relaxometry</subject><subject>Young Adult</subject><issn>1351-5101</issn><issn>1468-1331</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqN0UlLxDAUB_AgivvBLyAFD-qhmrVpjzKOGzqCjDPHkLavGu2iSYsz396MsxwEwVzyCL_3SPJH6IDgM-LXOdRwRijn8RraJjyKQ8IYWfc1EyQUBJMttOPcG8aYSoo30RblUiYJZdtodAl1q1sI6i4rwQRDGlgo9aSpoLXTwLhAzw6MTktvoLONqfSLqV-CStt3sIGpgytrILdgstdjz1s9MXoPbRS6dLC_2HfR81V_2LsJ7x-vb3sX92HGReLvmcaZlnkCpIi4SEVEoMC-gJjnudRpymlOIw1FzHGSRRnXosCapSIhNEkxY7voZD73wzafHbhWVcZlUJa6hqZzigguY0EoTv5FBeeEz-jRL_rWdLb2D5kpxiMcc-nV6VxltnHOQqE-rP8cO1UEq1kuyueifnLx9nAxsUsryFdyGYQH53PwZUqY_j1J9Qf95chw3mFcC5NVh09FRZJJocaDa_XQG4zvejdPasS-ARIwpOI</recordid><startdate>201408</startdate><enddate>201408</enddate><creator>Bonilha da Silva, C.</creator><creator>Bergo, F. P. G.</creator><creator>D'Abreu, A.</creator><creator>Cendes, F.</creator><creator>Lopes-Cendes, I.</creator><creator>França Jr, M. C.</creator><general>Blackwell Publishing Ltd</general><general>John Wiley & Sons, Inc</general><scope>BSCLL</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>7U7</scope><scope>C1K</scope><scope>K9.</scope><scope>7X8</scope></search><sort><creationdate>201408</creationdate><title>Dentate nuclei T2 relaxometry is a reliable neuroimaging marker in Friedreich's ataxia</title><author>Bonilha da Silva, C. ; Bergo, F. P. G. ; D'Abreu, A. ; Cendes, F. ; Lopes-Cendes, I. ; França Jr, M. C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4598-1b8ca7d9e1f645b561ef045be84dd7abb42d26aef8409c6c4a5f0a3b59129b033</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Biomarkers</topic><topic>Cerebellar Nuclei</topic><topic>Child</topic><topic>Cross-Sectional Studies</topic><topic>dentate nuclei</topic><topic>Disease Progression</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Friedreich Ataxia - diagnosis</topic><topic>Friedreich Ataxia - genetics</topic><topic>Friedreich's ataxia</topic><topic>Humans</topic><topic>Magnetic Resonance Imaging - methods</topic><topic>Male</topic><topic>Middle Aged</topic><topic>MRI</topic><topic>Neuroimaging - methods</topic><topic>T2 relaxometry</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bonilha da Silva, C.</creatorcontrib><creatorcontrib>Bergo, F. P. G.</creatorcontrib><creatorcontrib>D'Abreu, A.</creatorcontrib><creatorcontrib>Cendes, F.</creatorcontrib><creatorcontrib>Lopes-Cendes, I.</creatorcontrib><creatorcontrib>França Jr, M. C.</creatorcontrib><collection>Istex</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>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>European journal of neurology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bonilha da Silva, C.</au><au>Bergo, F. P. G.</au><au>D'Abreu, A.</au><au>Cendes, F.</au><au>Lopes-Cendes, I.</au><au>França Jr, M. C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dentate nuclei T2 relaxometry is a reliable neuroimaging marker in Friedreich's ataxia</atitle><jtitle>European journal of neurology</jtitle><addtitle>Eur J Neurol</addtitle><date>2014-08</date><risdate>2014</risdate><volume>21</volume><issue>8</issue><spage>1131</spage><epage>1136</epage><pages>1131-1136</pages><issn>1351-5101</issn><eissn>1468-1331</eissn><coden>EJNEFL</coden><abstract>Background and purpose
In Friedreich's ataxia (FRDA), frataxin deficiency results in iron redistribution in the dentate nuclei (DNC). Clusters of iron cause inhomogeneities in a magnetic field and result in a reduction in T2 relaxation time (T2).
Methods
T2 was prospectively evaluated in DNC, putamen, substantia nigra (SN), cerebellar white matter (CWM) and caudate and the correlation with clinical parameters was investigated. Thirty‐five patients (range 9–51 years) and 44 controls (12–49 years) underwent T2 multi‐echo sequence in a 3T scanner. Twenty‐three patients (12–50 years) and 19 controls (14–49 years) were reassessed after 1 year. T2 was evaluated using specialized software (Aftervoxel) and severity of disease was quantified with the Friedreich Ataxia Rating Scale (FARS).
Results
T2 of both DNC was significantly shorter in the FRDA group at baseline (right, 58.6 ± 8.3 ms vs. 63.7 ± 8.1 ms, P = 0.013; left, 56.7 ± 7.7 ms vs. 62.6 ± 6.8 ms, P = 0.001). No significant difference was found between groups regarding the SN, putamen, CWM and caudate T2. DNC T2 values correlated with age, FARS total score and FARS III subscore on both sides. Prospectively, there was a significant reduction of T2 in FRDA patients in right and left DNC (P = 0.001 and 0.009) but not in other structures. Amongst controls, none of the regions significantly changed after 1 year. DNC T2 change over time correlated with GAA expansions and clinical deterioration (expressed by a change in FARS scores).
Conclusions
DNC T2 values are abnormal in FRDA, progress over time and correlate with ataxia severity. These results strongly suggest that DNC relaxometry can be a useful neuroimaging marker in FRDA.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>24779923</pmid><doi>10.1111/ene.12448</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Adult Biomarkers Cerebellar Nuclei Child Cross-Sectional Studies dentate nuclei Disease Progression Female Follow-Up Studies Friedreich Ataxia - diagnosis Friedreich Ataxia - genetics Friedreich's ataxia Humans Magnetic Resonance Imaging - methods Male Middle Aged MRI Neuroimaging - methods T2 relaxometry Young Adult |
title | Dentate nuclei T2 relaxometry is a reliable neuroimaging marker in Friedreich's ataxia |
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