White matter involvement in sporadic Creutzfeldt-Jakob disease

Sporadic Creutzfeldt-Jakob disease is considered primarily a disease of grey matter, although the extent of white matter involvement has not been well described. We used diffusion tensor imaging to study the white matter in sporadic Creutzfeldt-Jakob disease compared to healthy control subjects and...

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Veröffentlicht in:Brain (London, England : 1878) England : 1878), 2014-12, Vol.137 (Pt 12), p.3339-3354
Hauptverfasser: CAVERZASI, Eduardo, MANDELLI, Maria Luisa, GESCHWIND, Michael D, HENRY, Roland G, DEARMOND, Stephen J, HESS, Christopher P, VITALI, Paolo, PAPINUTTO, Nico, OEHLER, Abby, MILLER, Bruce L, LOBACH, Irina V, BASTIANELLO, Stefano
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container_issue Pt 12
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container_title Brain (London, England : 1878)
container_volume 137
creator CAVERZASI, Eduardo
MANDELLI, Maria Luisa
GESCHWIND, Michael D
HENRY, Roland G
DEARMOND, Stephen J
HESS, Christopher P
VITALI, Paolo
PAPINUTTO, Nico
OEHLER, Abby
MILLER, Bruce L
LOBACH, Irina V
BASTIANELLO, Stefano
description Sporadic Creutzfeldt-Jakob disease is considered primarily a disease of grey matter, although the extent of white matter involvement has not been well described. We used diffusion tensor imaging to study the white matter in sporadic Creutzfeldt-Jakob disease compared to healthy control subjects and to correlated magnetic resonance imaging findings with histopathology. Twenty-six patients with sporadic Creutzfeldt-Jakob disease and nine age- and gender-matched healthy control subjects underwent volumetric T1-weighted and diffusion tensor imaging. Six patients had post-mortem brain analysis available for assessment of neuropathological findings associated with prion disease. Parcellation of the subcortical white matter was performed on 3D T1-weighted volumes using Freesurfer. Diffusion tensor imaging maps were calculated and transformed to the 3D-T1 space; the average value for each diffusion metric was calculated in the total white matter and in regional volumes of interest. Tract-based spatial statistics analysis was also performed to investigate the deeper white matter tracts. There was a significant reduction of mean (P=0.002), axial (P=0.0003) and radial (P=0.0134) diffusivities in the total white matter in sporadic Creutzfeldt-Jakob disease. Mean diffusivity was significantly lower in most white matter volumes of interest (P
doi_str_mv 10.1093/brain/awu298
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We used diffusion tensor imaging to study the white matter in sporadic Creutzfeldt-Jakob disease compared to healthy control subjects and to correlated magnetic resonance imaging findings with histopathology. Twenty-six patients with sporadic Creutzfeldt-Jakob disease and nine age- and gender-matched healthy control subjects underwent volumetric T1-weighted and diffusion tensor imaging. Six patients had post-mortem brain analysis available for assessment of neuropathological findings associated with prion disease. Parcellation of the subcortical white matter was performed on 3D T1-weighted volumes using Freesurfer. Diffusion tensor imaging maps were calculated and transformed to the 3D-T1 space; the average value for each diffusion metric was calculated in the total white matter and in regional volumes of interest. Tract-based spatial statistics analysis was also performed to investigate the deeper white matter tracts. There was a significant reduction of mean (P=0.002), axial (P=0.0003) and radial (P=0.0134) diffusivities in the total white matter in sporadic Creutzfeldt-Jakob disease. Mean diffusivity was significantly lower in most white matter volumes of interest (P&lt;0.05, corrected for multiple comparisons), with a generally symmetric pattern of involvement in sporadic Creutzfeldt-Jakob disease. Mean diffusivity reduction reflected concomitant decrease of both axial and radial diffusivity, without appreciable changes in white matter anisotropy. Tract-based spatial statistics analysis showed significant reductions of mean diffusivity within the white matter of patients with sporadic Creutzfeldt-Jakob disease, mainly in the left hemisphere, with a strong trend (P=0.06) towards reduced mean diffusivity in most of the white matter bilaterally. In contrast, by visual assessment there was no white matter abnormality either on T2-weighted or diffusion-weighted images. Widespread reduction in white matter mean diffusivity, however, was apparent visibly on the quantitative attenuation coefficient maps compared to healthy control subjects. Neuropathological analysis showed diffuse astrocytic gliosis and activated microglia in the white matter, rare prion deposition and subtle subcortical microvacuolization, and patchy foci of demyelination with no evident white matter axonal degeneration. Decreased mean diffusivity on attenuation coefficient maps might be associated with astrocytic gliosis. 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Cerebral palsy ; Humans ; Image Processing, Computer-Assisted ; Male ; Medical sciences ; Middle Aged ; Nerve Fibers, Myelinated - pathology ; Nervous system (semeiology, syndromes) ; Neuroimaging ; Neurology ; Original ; White Matter - pathology</subject><ispartof>Brain (London, England : 1878), 2014-12, Vol.137 (Pt 12), p.3339-3354</ispartof><rights>2015 INIST-CNRS</rights><rights>The Author (2014). Published by Oxford University Press on behalf of the Guarantors of Brain.</rights><rights>The Author (2014). 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Widespread reduction in white matter mean diffusivity, however, was apparent visibly on the quantitative attenuation coefficient maps compared to healthy control subjects. Neuropathological analysis showed diffuse astrocytic gliosis and activated microglia in the white matter, rare prion deposition and subtle subcortical microvacuolization, and patchy foci of demyelination with no evident white matter axonal degeneration. Decreased mean diffusivity on attenuation coefficient maps might be associated with astrocytic gliosis. 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Cerebral palsy</subject><subject>Humans</subject><subject>Image Processing, Computer-Assisted</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Nerve Fibers, Myelinated - pathology</subject><subject>Nervous system (semeiology, syndromes)</subject><subject>Neuroimaging</subject><subject>Neurology</subject><subject>Original</subject><subject>White Matter - pathology</subject><issn>0006-8950</issn><issn>1460-2156</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkTtPHDEURi0UBAtJRx1NE4mCCdfPsRsktOIVIdEQpbQ8nrvByTw29swi8utj2AVCR-Ur-ejou_cj5IDCVwqGH9fRhf7Y3U_M6C0yo0JByahUH8gMAFSpjYRdspfSLwAqOFM7ZJdJripgZkZOftyFEYvOjSPGIvSroV1hh_2Y5yIth-ia4It5xGn8u8C2Gctv7vdQF01I6BJ-JNsL1yb8tHn3yffzs9v5ZXl9c3E1P70uvRDVWDpBm1oZKanXktZMC65yXANNQyUXgjVGoRM199rUldKgK4WV4lqzzKHh--Rk7V1OdYeNzwGja-0yhs7FBzu4YN_-9OHO_hxWVjABHHgWHG4EcfgzYRptF5LHtnU9DlOytMrH0ZTxd6CKVVBxI2RGj9aoj0NKERcviSjYx3bsUzt23U7GP_-_xQv8XEcGvmwAl7xrF9H1PqRXzoCQJov-AWHFmMA</recordid><startdate>20141201</startdate><enddate>20141201</enddate><creator>CAVERZASI, Eduardo</creator><creator>MANDELLI, Maria Luisa</creator><creator>GESCHWIND, Michael D</creator><creator>HENRY, Roland G</creator><creator>DEARMOND, Stephen J</creator><creator>HESS, Christopher P</creator><creator>VITALI, Paolo</creator><creator>PAPINUTTO, Nico</creator><creator>OEHLER, Abby</creator><creator>MILLER, Bruce L</creator><creator>LOBACH, Irina V</creator><creator>BASTIANELLO, Stefano</creator><general>Oxford University Press</general><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><scope>7TK</scope><scope>7U9</scope><scope>H94</scope><scope>5PM</scope></search><sort><creationdate>20141201</creationdate><title>White matter involvement in sporadic Creutzfeldt-Jakob disease</title><author>CAVERZASI, Eduardo ; MANDELLI, Maria Luisa ; GESCHWIND, Michael D ; HENRY, Roland G ; DEARMOND, Stephen J ; HESS, Christopher P ; VITALI, Paolo ; PAPINUTTO, Nico ; OEHLER, Abby ; MILLER, Bruce L ; LOBACH, Irina V ; BASTIANELLO, Stefano</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c447t-a41db69551c851b2843629890dd153442d96ea4b3c89b7680876e763882629e93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Anisotropy</topic><topic>Biological and medical sciences</topic><topic>Creutzfeldt-Jakob Syndrome - pathology</topic><topic>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</topic><topic>Demyelinating Diseases - pathology</topic><topic>Diffusion Magnetic Resonance Imaging - methods</topic><topic>Female</topic><topic>Gray Matter - pathology</topic><topic>Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy</topic><topic>Humans</topic><topic>Image Processing, Computer-Assisted</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Nerve Fibers, Myelinated - pathology</topic><topic>Nervous system (semeiology, syndromes)</topic><topic>Neuroimaging</topic><topic>Neurology</topic><topic>Original</topic><topic>White Matter - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>CAVERZASI, Eduardo</creatorcontrib><creatorcontrib>MANDELLI, Maria Luisa</creatorcontrib><creatorcontrib>GESCHWIND, Michael D</creatorcontrib><creatorcontrib>HENRY, Roland G</creatorcontrib><creatorcontrib>DEARMOND, Stephen J</creatorcontrib><creatorcontrib>HESS, Christopher P</creatorcontrib><creatorcontrib>VITALI, Paolo</creatorcontrib><creatorcontrib>PAPINUTTO, Nico</creatorcontrib><creatorcontrib>OEHLER, Abby</creatorcontrib><creatorcontrib>MILLER, Bruce L</creatorcontrib><creatorcontrib>LOBACH, Irina V</creatorcontrib><creatorcontrib>BASTIANELLO, Stefano</creatorcontrib><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><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Brain (London, England : 1878)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>CAVERZASI, Eduardo</au><au>MANDELLI, Maria Luisa</au><au>GESCHWIND, Michael D</au><au>HENRY, Roland G</au><au>DEARMOND, Stephen J</au><au>HESS, Christopher P</au><au>VITALI, Paolo</au><au>PAPINUTTO, Nico</au><au>OEHLER, Abby</au><au>MILLER, Bruce L</au><au>LOBACH, Irina V</au><au>BASTIANELLO, Stefano</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>White matter involvement in sporadic Creutzfeldt-Jakob disease</atitle><jtitle>Brain (London, England : 1878)</jtitle><addtitle>Brain</addtitle><date>2014-12-01</date><risdate>2014</risdate><volume>137</volume><issue>Pt 12</issue><spage>3339</spage><epage>3354</epage><pages>3339-3354</pages><issn>0006-8950</issn><eissn>1460-2156</eissn><abstract>Sporadic Creutzfeldt-Jakob disease is considered primarily a disease of grey matter, although the extent of white matter involvement has not been well described. We used diffusion tensor imaging to study the white matter in sporadic Creutzfeldt-Jakob disease compared to healthy control subjects and to correlated magnetic resonance imaging findings with histopathology. Twenty-six patients with sporadic Creutzfeldt-Jakob disease and nine age- and gender-matched healthy control subjects underwent volumetric T1-weighted and diffusion tensor imaging. Six patients had post-mortem brain analysis available for assessment of neuropathological findings associated with prion disease. Parcellation of the subcortical white matter was performed on 3D T1-weighted volumes using Freesurfer. Diffusion tensor imaging maps were calculated and transformed to the 3D-T1 space; the average value for each diffusion metric was calculated in the total white matter and in regional volumes of interest. Tract-based spatial statistics analysis was also performed to investigate the deeper white matter tracts. There was a significant reduction of mean (P=0.002), axial (P=0.0003) and radial (P=0.0134) diffusivities in the total white matter in sporadic Creutzfeldt-Jakob disease. Mean diffusivity was significantly lower in most white matter volumes of interest (P&lt;0.05, corrected for multiple comparisons), with a generally symmetric pattern of involvement in sporadic Creutzfeldt-Jakob disease. Mean diffusivity reduction reflected concomitant decrease of both axial and radial diffusivity, without appreciable changes in white matter anisotropy. Tract-based spatial statistics analysis showed significant reductions of mean diffusivity within the white matter of patients with sporadic Creutzfeldt-Jakob disease, mainly in the left hemisphere, with a strong trend (P=0.06) towards reduced mean diffusivity in most of the white matter bilaterally. In contrast, by visual assessment there was no white matter abnormality either on T2-weighted or diffusion-weighted images. Widespread reduction in white matter mean diffusivity, however, was apparent visibly on the quantitative attenuation coefficient maps compared to healthy control subjects. Neuropathological analysis showed diffuse astrocytic gliosis and activated microglia in the white matter, rare prion deposition and subtle subcortical microvacuolization, and patchy foci of demyelination with no evident white matter axonal degeneration. Decreased mean diffusivity on attenuation coefficient maps might be associated with astrocytic gliosis. We show for the first time significant global reduced mean diffusivity within the white matter in sporadic Creutzfeldt-Jakob disease, suggesting possible primary involvement of the white matter, rather than changes secondary to neuronal degeneration/loss.</abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>25367029</pmid><doi>10.1093/brain/awu298</doi><tpages>16</tpages><oa>free_for_read</oa></addata></record>
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subjects Aged
Aged, 80 and over
Anisotropy
Biological and medical sciences
Creutzfeldt-Jakob Syndrome - pathology
Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases
Demyelinating Diseases - pathology
Diffusion Magnetic Resonance Imaging - methods
Female
Gray Matter - pathology
Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy
Humans
Image Processing, Computer-Assisted
Male
Medical sciences
Middle Aged
Nerve Fibers, Myelinated - pathology
Nervous system (semeiology, syndromes)
Neuroimaging
Neurology
Original
White Matter - pathology
title White matter involvement in sporadic Creutzfeldt-Jakob disease
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