Diffusion tensor imaging and tract-based spatial statistics analysis in Friedreich's ataxia patients
Abstract Introduction Friedreich's ataxia (FRDA) is the most common hereditary ataxia and thinning of the cervical spinal cord is a consistent observation in Magnetic resonance imaging (MRI), although neuropathological examination in FRDA reveals neuronal loss in gray matter (GM) nuclei and deg...
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description | Abstract Introduction Friedreich's ataxia (FRDA) is the most common hereditary ataxia and thinning of the cervical spinal cord is a consistent observation in Magnetic resonance imaging (MRI), although neuropathological examination in FRDA reveals neuronal loss in gray matter (GM) nuclei and degeneration of white matter (WM) tracts in the spinal cord, brainstem and cerebellum. Using diffusion-tensor (DTI) imaging and tract-based spatial statistics (TBSS) we tested the hypothesis that WM damage in FRDA is more extensive than previously described and probably involves normal-appearing WM. Methods This transversal study included 21 genetically confirmed FRDA patients and seventeen healthy controls that underwent structural MRI of the brain on a 1.5 T scanner. We quantify the severity of ataxia using SARA scale. DTI was performed and diffusion data were analyzed using FMRIB's Diffusion Toolbox in FSL 4.1 in order to identify Fractional anisotropy (FA) decreases in specific brain regions and also the mean, radial and axial diffusivities (MD, RD, AD). Results The greatest decreases in FA were in the left superior cerebellar peduncle, left posterior thalamic radiation, major forceps, left inferior fronto-occipital fasciculus and corpus callosum and had a significance level of p |
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Using diffusion-tensor (DTI) imaging and tract-based spatial statistics (TBSS) we tested the hypothesis that WM damage in FRDA is more extensive than previously described and probably involves normal-appearing WM. Methods This transversal study included 21 genetically confirmed FRDA patients and seventeen healthy controls that underwent structural MRI of the brain on a 1.5 T scanner. We quantify the severity of ataxia using SARA scale. DTI was performed and diffusion data were analyzed using FMRIB's Diffusion Toolbox in FSL 4.1 in order to identify Fractional anisotropy (FA) decreases in specific brain regions and also the mean, radial and axial diffusivities (MD, RD, AD). Results The greatest decreases in FA were in the left superior cerebellar peduncle, left posterior thalamic radiation, major forceps, left inferior fronto-occipital fasciculus and corpus callosum and had a significance level of p < 0.01. No significant correlation between FA, AD, MD and RD values and the clinical findings, SARA scores and genetic expansion was found. Conclusion DTI and TBSS techniques clearly demonstrate the extensive cerebral and cerebellar involvement in FRDA, partially explaining the clinical phenotype of the disease. Further studies are needed with larger samples to correlate clinical, genetic findings and ataxia scores.</description><identifier>ISSN: 1353-8020</identifier><identifier>EISSN: 1873-5126</identifier><identifier>DOI: 10.1016/j.parkreldis.2015.02.021</identifier><identifier>PMID: 25801908</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Adolescent ; Adult ; Diffusion tensor imaging ; Diffusion Tensor Imaging - methods ; Female ; Friedreich ataxia ; Friedreich Ataxia - diagnosis ; Friedreich Ataxia - metabolism ; Gait disorders ; Humans ; Magnetic Resonance Imaging - methods ; Male ; MRI ; Neurology ; Tract-based spatial statistics ; Young Adult</subject><ispartof>Parkinsonism & related disorders, 2015-05, Vol.21 (5), p.504-508</ispartof><rights>Elsevier Ltd</rights><rights>2015 Elsevier Ltd</rights><rights>Copyright © 2015 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c499t-20dfb641133df0577687be8b235e9aac0225d560c065862d1dc15d3c6954932c3</citedby><cites>FETCH-LOGICAL-c499t-20dfb641133df0577687be8b235e9aac0225d560c065862d1dc15d3c6954932c3</cites><orcidid>0000-0002-7316-5127</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1353802015000760$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25801908$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Vieira Karuta, Simone Carreiro</creatorcontrib><creatorcontrib>Raskin, Salmo</creatorcontrib><creatorcontrib>de Carvalho Neto, Arnolfo</creatorcontrib><creatorcontrib>Gasparetto, Emerson Leandro</creatorcontrib><creatorcontrib>Doring, Thomas</creatorcontrib><creatorcontrib>Teive, Helio Afonso Ghizoni</creatorcontrib><title>Diffusion tensor imaging and tract-based spatial statistics analysis in Friedreich's ataxia patients</title><title>Parkinsonism & related disorders</title><addtitle>Parkinsonism Relat Disord</addtitle><description>Abstract Introduction Friedreich's ataxia (FRDA) is the most common hereditary ataxia and thinning of the cervical spinal cord is a consistent observation in Magnetic resonance imaging (MRI), although neuropathological examination in FRDA reveals neuronal loss in gray matter (GM) nuclei and degeneration of white matter (WM) tracts in the spinal cord, brainstem and cerebellum. Using diffusion-tensor (DTI) imaging and tract-based spatial statistics (TBSS) we tested the hypothesis that WM damage in FRDA is more extensive than previously described and probably involves normal-appearing WM. Methods This transversal study included 21 genetically confirmed FRDA patients and seventeen healthy controls that underwent structural MRI of the brain on a 1.5 T scanner. We quantify the severity of ataxia using SARA scale. DTI was performed and diffusion data were analyzed using FMRIB's Diffusion Toolbox in FSL 4.1 in order to identify Fractional anisotropy (FA) decreases in specific brain regions and also the mean, radial and axial diffusivities (MD, RD, AD). Results The greatest decreases in FA were in the left superior cerebellar peduncle, left posterior thalamic radiation, major forceps, left inferior fronto-occipital fasciculus and corpus callosum and had a significance level of p < 0.01. No significant correlation between FA, AD, MD and RD values and the clinical findings, SARA scores and genetic expansion was found. Conclusion DTI and TBSS techniques clearly demonstrate the extensive cerebral and cerebellar involvement in FRDA, partially explaining the clinical phenotype of the disease. Further studies are needed with larger samples to correlate clinical, genetic findings and ataxia scores.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Diffusion tensor imaging</subject><subject>Diffusion Tensor Imaging - methods</subject><subject>Female</subject><subject>Friedreich ataxia</subject><subject>Friedreich Ataxia - diagnosis</subject><subject>Friedreich Ataxia - metabolism</subject><subject>Gait disorders</subject><subject>Humans</subject><subject>Magnetic Resonance Imaging - methods</subject><subject>Male</subject><subject>MRI</subject><subject>Neurology</subject><subject>Tract-based spatial statistics</subject><subject>Young Adult</subject><issn>1353-8020</issn><issn>1873-5126</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkUFv1DAQhSMEoqXwF5BvcMkyttdOckGCQgGpEgfgbDn2pMw2myweB3X_PY62gMQJaaSx5Pdm9L6pKiFhI0HaV7vNwafbhGMk3iiQZgOqlHxQncu20bWRyj4sb2103YKCs-oJ8w4AGgP6cXWmTAuyg_a8iu9oGBameRIZJ56ToL2_oelG-CmKnHzIde8Zo-CDz-RHwbl0zhS4SPx4ZGJBk7hKhDEhhe8vykf2d-TF6sAp89Pq0eBHxmf3_aL6dvX-6-XH-vrzh0-Xb67rsO26XCuIQ2-3UmodBzBNY9umx7ZX2mDnfQClTDQWAljTWhVlDNJEHWxntp1WQV9UL09zD2n-sSBntycOOI5-wnlhJ-0aW5vOFml7koY0Mycc3CGV5OnoJLiVsdu5v4zdytiBKiWL9fn9lqXfY_xj_A21CN6eBFiy_iRMjkPhEDBSwpBdnOl_trz-Z0gYaaLgx1s8Iu_mJRX6JZPjYnBf1luvp5ZmPbMF_QsKtqgO</recordid><startdate>20150501</startdate><enddate>20150501</enddate><creator>Vieira Karuta, Simone Carreiro</creator><creator>Raskin, Salmo</creator><creator>de Carvalho Neto, Arnolfo</creator><creator>Gasparetto, Emerson Leandro</creator><creator>Doring, Thomas</creator><creator>Teive, Helio Afonso Ghizoni</creator><general>Elsevier Ltd</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><orcidid>https://orcid.org/0000-0002-7316-5127</orcidid></search><sort><creationdate>20150501</creationdate><title>Diffusion tensor imaging and tract-based spatial statistics analysis in Friedreich's ataxia patients</title><author>Vieira Karuta, Simone Carreiro ; Raskin, Salmo ; de Carvalho Neto, Arnolfo ; Gasparetto, Emerson Leandro ; Doring, Thomas ; Teive, Helio Afonso Ghizoni</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c499t-20dfb641133df0577687be8b235e9aac0225d560c065862d1dc15d3c6954932c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Diffusion tensor imaging</topic><topic>Diffusion Tensor Imaging - methods</topic><topic>Female</topic><topic>Friedreich ataxia</topic><topic>Friedreich Ataxia - diagnosis</topic><topic>Friedreich Ataxia - metabolism</topic><topic>Gait disorders</topic><topic>Humans</topic><topic>Magnetic Resonance Imaging - methods</topic><topic>Male</topic><topic>MRI</topic><topic>Neurology</topic><topic>Tract-based spatial statistics</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Vieira Karuta, Simone Carreiro</creatorcontrib><creatorcontrib>Raskin, Salmo</creatorcontrib><creatorcontrib>de Carvalho Neto, Arnolfo</creatorcontrib><creatorcontrib>Gasparetto, Emerson Leandro</creatorcontrib><creatorcontrib>Doring, Thomas</creatorcontrib><creatorcontrib>Teive, Helio Afonso Ghizoni</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>Parkinsonism & related disorders</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Vieira Karuta, Simone Carreiro</au><au>Raskin, Salmo</au><au>de Carvalho Neto, Arnolfo</au><au>Gasparetto, Emerson Leandro</au><au>Doring, Thomas</au><au>Teive, Helio Afonso Ghizoni</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Diffusion tensor imaging and tract-based spatial statistics analysis in Friedreich's ataxia patients</atitle><jtitle>Parkinsonism & related disorders</jtitle><addtitle>Parkinsonism Relat Disord</addtitle><date>2015-05-01</date><risdate>2015</risdate><volume>21</volume><issue>5</issue><spage>504</spage><epage>508</epage><pages>504-508</pages><issn>1353-8020</issn><eissn>1873-5126</eissn><abstract>Abstract Introduction Friedreich's ataxia (FRDA) is the most common hereditary ataxia and thinning of the cervical spinal cord is a consistent observation in Magnetic resonance imaging (MRI), although neuropathological examination in FRDA reveals neuronal loss in gray matter (GM) nuclei and degeneration of white matter (WM) tracts in the spinal cord, brainstem and cerebellum. Using diffusion-tensor (DTI) imaging and tract-based spatial statistics (TBSS) we tested the hypothesis that WM damage in FRDA is more extensive than previously described and probably involves normal-appearing WM. Methods This transversal study included 21 genetically confirmed FRDA patients and seventeen healthy controls that underwent structural MRI of the brain on a 1.5 T scanner. We quantify the severity of ataxia using SARA scale. DTI was performed and diffusion data were analyzed using FMRIB's Diffusion Toolbox in FSL 4.1 in order to identify Fractional anisotropy (FA) decreases in specific brain regions and also the mean, radial and axial diffusivities (MD, RD, AD). Results The greatest decreases in FA were in the left superior cerebellar peduncle, left posterior thalamic radiation, major forceps, left inferior fronto-occipital fasciculus and corpus callosum and had a significance level of p < 0.01. No significant correlation between FA, AD, MD and RD values and the clinical findings, SARA scores and genetic expansion was found. Conclusion DTI and TBSS techniques clearly demonstrate the extensive cerebral and cerebellar involvement in FRDA, partially explaining the clinical phenotype of the disease. Further studies are needed with larger samples to correlate clinical, genetic findings and ataxia scores.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>25801908</pmid><doi>10.1016/j.parkreldis.2015.02.021</doi><tpages>5</tpages><orcidid>https://orcid.org/0000-0002-7316-5127</orcidid></addata></record> |
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subjects | Adolescent Adult Diffusion tensor imaging Diffusion Tensor Imaging - methods Female Friedreich ataxia Friedreich Ataxia - diagnosis Friedreich Ataxia - metabolism Gait disorders Humans Magnetic Resonance Imaging - methods Male MRI Neurology Tract-based spatial statistics Young Adult |
title | Diffusion tensor imaging and tract-based spatial statistics analysis in Friedreich's ataxia patients |
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