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dc.contributor.authorBianciardi, Marta
dc.contributor.authorToschi, Nicola
dc.contributor.authorEdlow, Brian L.
dc.contributor.authorEichner, Cornelius
dc.contributor.authorSetsompop, Kawin
dc.contributor.authorPolimeni, Jonathan R.
dc.contributor.authorBrown, Emery Neal
dc.contributor.authorKinney, Hannah C.
dc.contributor.authorRosen, Bruce R.
dc.contributor.authorWald, Lawrence
dc.date.accessioned2020-06-04T19:45:20Z
dc.date.available2020-06-04T19:45:20Z
dc.date.issued2015-12
dc.date.submitted2015-08
dc.identifier.issn2158-0014
dc.identifier.issn2158-0022
dc.identifier.urihttps://hdl.handle.net/1721.1/125677
dc.description.abstractBrainstem nuclei (Bn) in humans play a crucial role in vital functions, such as arousal, autonomic homeostasis, sensory and motor relay, nociception, sleep, and cranial nerve function, and they have been implicated in a vast array of brain pathologies. However, an in vivo delineation of most human Bn has been elusive because of limited sensitivity and contrast for detecting these small regions using standard neuroimaging methods. To precisely identify several human Bn in vivo, we employed a 7 Tesla scanner equipped with multi-channel receive-coil array, which provided high magnetic resonance imaging sensitivity, and a multi-contrast (diffusion fractional anisotropy and T2-weighted) echo-planar-imaging approach, which provided complementary contrasts for Bn anatomy with matched geometric distortions and resolution. Through a combined examination of 1.3 mm3 multi-contrast anatomical images acquired in healthy human adults, we semi-automatically generated in vivo probabilistic Bn labels of the ascending arousal (median and dorsal raphe), autonomic (raphe magnus, periaqueductal gray), and motor (inferior olivary nuclei, two subregions of the substantia nigra compatible with pars compacta and pars reticulata, two subregions of the red nucleus, and, in the diencephalon, two subregions of the subthalamic nucleus) systems. These labels constitute a first step toward the development of an in vivo neuroimaging template of Bn in standard space to facilitate future clinical and research investigations of human brainstem function and pathology. Proof-of-concept clinical use of this template is demonstrated in a minimally conscious patient with traumatic brainstem hemorrhages precisely localized to the raphe Bn involved in arousal.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (NIH NIBIB P41-RR014075)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (NIH NIBIB R01-EB000790)en_US
dc.language.isoen
dc.publisherMary Ann Liebert Incen_US
dc.relation.isversionofhttps://dx.doi.org/10.1089/BRAIN.2015.0347en_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourcePMCen_US
dc.titleToward an In Vivo Neuroimaging Template of Human Brainstem Nuclei of the Ascending Arousal, Autonomic, and Motor Systemsen_US
dc.typeArticleen_US
dc.identifier.citationBianciardi, Marta, Nicola Toschi, Brian L. Edlow et al. "Toward an In Vivo Neuroimaging Template of Human Brainstem Nuclei of the Ascending Arousal, Autonomic, and Motor Systems." Brain Connectivity 5,10 (December 2015): p.597-607. ©2015 Mary Ann Liebert, Inc.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Institute for Medical Engineering & Scienceen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Brain and Cognitive Sciencesen_US
dc.relation.journalBrain Connectivityen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2019-09-30T14:10:02Z
dspace.orderedauthorsBianciardi, Marta; Toschi, Nicola; Edlow, Brian L.; Eichner, Cornelius; Setsompop, Kawin; Polimeni, Jonathan R.; Brown, Emery N.; Kinney, Hannah C.; Rosen, Bruce R.; Wald, Lawrence L.en_US
dspace.date.submission2019-09-30T14:10:05Z
mit.journal.volume5en_US
mit.journal.issue10en_US
mit.metadata.statusComplete


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