<HashMap><database>biostudies-literature</database><scores><citationCount>0</citationCount><reanalysisCount>0</reanalysisCount><viewCount>49</viewCount><searchCount>0</searchCount></scores><additional><omics_type>Unknown</omics_type><volume>9(12)</volume><submitter>Jao CW</submitter><funding>Ministry of Science and Technology, Taiwan</funding><funding>National Health Research Institute Taiwan</funding><funding>National Yang-Ming University and Shin-Kong Wu-Ho Su Memorial Hospital Research Program</funding><pubmed_abstract>Multiple system atrophy cerebellar type (MSA-C) and spinocerebellar ataxia type 3 (SCA3) demonstrate similar manifestations, including ataxia, pyramidal and extrapyramidal signs, as well as atrophy and signal intensity changes in the cerebellum and brainstem. MSA-C and SCA3 cannot be clinically differentiated through T1-weighted magnetic resonance imaging (MRI) alone; therefore, clinical consensus criteria and genetic testing are also required. Here, we used diffusion tensor imaging (DTI) to measure water molecular diffusion of white matter and investigate the difference between MSA-C and SCA3. Four measurements were calculated from DTI images, including fractional anisotropy (FA), axial diffusivity (AD), radial diffusivity (RD), and mean diffusivity (MD). Fifteen patients with MSA-C, 15 patients with SCA3, and 30 healthy individuals participated in this study. Both patient groups demonstrated a significantly decreased FA but a significantly increased AD, RD, and MD in the cerebello-ponto-cerebral tracts. Moreover, patients with SCA3 demonstrated a significant decrease in FA but more significant increases in AD, RD, and MD in the cerebello-cerebral tracts than patients with MSAC. Our results may suggest that FA and MD can be effectively used for differentiating SCA3 and MSA-C, both of which are cerebellar ataxias and have many common atrophied regions in the cerebral and cerebellar cortex.</pubmed_abstract><journal>Brain sciences</journal><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6956111</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Diffusion Tensor Magnetic Resonance Imaging for Differentiating Multiple System Atrophy Cerebellar Type and Spinocerebellar Ataxia Type 3.</pubmed_title><pmcid>PMC6956111</pmcid><funding_grant_id>NHRI-EX106-10526EI</funding_grant_id><funding_grant_id>107GB006</funding_grant_id><funding_grant_id>MOST 106-2221-E-010-010-MY2</funding_grant_id><pubmed_authors>Wang PS</pubmed_authors><pubmed_authors>Wu YT</pubmed_authors><pubmed_authors>Soong BW</pubmed_authors><pubmed_authors>Huang CW</pubmed_authors><pubmed_authors>Duan CA</pubmed_authors><pubmed_authors>Jao CW</pubmed_authors><pubmed_authors>Wu CC</pubmed_authors><view_count>49</view_count></additional><is_claimable>false</is_claimable><name>Diffusion Tensor Magnetic Resonance Imaging for Differentiating Multiple System Atrophy Cerebellar Type and Spinocerebellar Ataxia Type 3.</name><description>Multiple system atrophy cerebellar type (MSA-C) and spinocerebellar ataxia type 3 (SCA3) demonstrate similar manifestations, including ataxia, pyramidal and extrapyramidal signs, as well as atrophy and signal intensity changes in the cerebellum and brainstem. MSA-C and SCA3 cannot be clinically differentiated through T1-weighted magnetic resonance imaging (MRI) alone; therefore, clinical consensus criteria and genetic testing are also required. Here, we used diffusion tensor imaging (DTI) to measure water molecular diffusion of white matter and investigate the difference between MSA-C and SCA3. Four measurements were calculated from DTI images, including fractional anisotropy (FA), axial diffusivity (AD), radial diffusivity (RD), and mean diffusivity (MD). Fifteen patients with MSA-C, 15 patients with SCA3, and 30 healthy individuals participated in this study. Both patient groups demonstrated a significantly decreased FA but a significantly increased AD, RD, and MD in the cerebello-ponto-cerebral tracts. Moreover, patients with SCA3 demonstrated a significant decrease in FA but more significant increases in AD, RD, and MD in the cerebello-cerebral tracts than patients with MSAC. Our results may suggest that FA and MD can be effectively used for differentiating SCA3 and MSA-C, both of which are cerebellar ataxias and have many common atrophied regions in the cerebral and cerebellar cortex.</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Dec</publication><modification>2021-02-20T11:38:51Z</modification><creation>2020-05-22T08:16:37Z</creation></dates><accession>S-EPMC6956111</accession><cross_references><pubmed>31817016</pubmed><doi>10.3390/brainsci9120354</doi></cross_references></HashMap>