<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>34</volume><submitter>van der Horn HJ</submitter><pubmed_abstract>Spinocerebellar ataxia type 3 (SCA3) is a rare genetic neurodegenerative disease. The neurobiological basis of SCA3 is still poorly understood, and up until now resting-state fMRI (rs-fMRI) has not been used to study this disease. In the current study we investigated (multi-echo) rs-fMRI data from patients with genetically confirmed SCA3 (n = 17) and matched healthy subjects (n = 16). Using independent component analysis (ICA) and subsequent regression with bootstrap resampling, we identified a pattern of differences between patients and healthy subjects, which we coined the fMRI SCA3 related pattern (fSCA3-RP) comprising cerebellum, anterior striatum and various cortical regions. Individual fSCA3-RP scores were highly correlated with a previously published &lt;sup>18&lt;/sup>F-FDG PET pattern f</pubmed_abstract><journal>NeuroImage. Clinical</journal><pagination>103023</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9062756</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>A resting-state fMRI pattern of spinocerebellar ataxia type 3 and comparison with &lt;sup>18&lt;/sup>F-FDG PET.</pubmed_title><pmcid>PMC9062756</pmcid><pubmed_authors>Vergara VM</pubmed_authors><pubmed_authors>Spikman JM</pubmed_authors><pubmed_authors>Meles SK</pubmed_authors><pubmed_authors>van der Horn HJ</pubmed_authors><pubmed_authors>Qi S</pubmed_authors><pubmed_authors>De Jong BM</pubmed_authors><pubmed_authors>Renken RJ</pubmed_authors><pubmed_authors>Kremer HPH</pubmed_authors><pubmed_authors>Calhoun VD</pubmed_authors><pubmed_authors>de Vries JJ</pubmed_authors><pubmed_authors>Kok JG</pubmed_authors><pubmed_authors>Dalenberg JR</pubmed_authors><pubmed_authors>Siero JCW</pubmed_authors></additional><is_claimable>false</is_claimable><name>A resting-state fMRI pattern of spinocerebellar ataxia type 3 and comparison with &lt;sup>18&lt;/sup>F-FDG PET.</name><description>Spinocerebellar ataxia type 3 (SCA3) is a rare genetic neurodegenerative disease. The neurobiological basis of SCA3 is still poorly understood, and up until now resting-state fMRI (rs-fMRI) has not been used to study this disease. In the current study we investigated (multi-echo) rs-fMRI data from patients with genetically confirmed SCA3 (n = 17) and matched healthy subjects (n = 16). Using independent component analysis (ICA) and subsequent regression with bootstrap resampling, we identified a pattern of differences between patients and healthy subjects, which we coined the fMRI SCA3 related pattern (fSCA3-RP) comprising cerebellum, anterior striatum and various cortical regions. Individual fSCA3-RP scores were highly correlated with a previously published &lt;sup>18&lt;/sup>F-FDG PET pattern f</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2025-04-25T18:06:16.217Z</modification><creation>2025-04-25T18:06:16.217Z</creation></dates><accession>S-EPMC9062756</accession><cross_references><pubmed>35489193</pubmed><doi>10.1016/j.nicl.2022.103023</doi></cross_references></HashMap>