Unraveling corticobasal syndrome and alien limb syndrome with structural brain imaging

Jazyk angličtina Země Itálie Médium print-electronic

Typ dokumentu časopisecké články, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/pmid30927559
Odkazy

PubMed 30927559
DOI 10.1016/j.cortex.2019.02.015
PII: S0010-9452(19)30067-X
Knihovny.cz E-zdroje

Alien limb phenomenon is a rare syndrome associated with a feeling of non-belonging and disowning toward one's limb. In contrast, anarchic limb phenomenon leads to involuntary but goal-directed movements. Alien/anarchic limb phenomena are frequent in corticobasal syndrome (CBS), an atypical parkinsonian syndrome characterized by rigidity, akinesia, dystonia, cortical sensory deficit, and apraxia. The structure-function relationship of alien/anarchic limb was investigated in multi-centric structural magnetic resonance imaging (MRI) data. Whole-group and single-subject comparisons were made in 25 CBS and eight CBS-alien/anarchic limb patients versus controls. Support vector machine was used to see if CBS with and without alien/anarchic limb could be distinguished by structural MRI patterns. Whole-group comparison of CBS versus controls revealed asymmetric frontotemporal atrophy. CBS with alien/anarchic limb syndrome versus controls showed frontoparietal atrophy including the supplementary motor area contralateral to the side of the affected limb. Exploratory analysis identified frontotemporal regions encompassing the pre-/and postcentral gyrus as compromised in CBS with alien limb syndrome. Classification of CBS patients yielded accuracies of 79%. CBS-alien/anarchic limb syndrome was differentiated from CBS patients with an accuracy of 81%. Predictive differences were found in the cingulate gyrus spreading to frontomedian cortex, postcentral gyrus, and temporoparietoocipital regions. We present the first MRI-based group analysis on CBS-alien/anarchic limb. Results pave the way for individual clinical syndrome prediction and allow understanding the underlying neurocognitive architecture.

Clinic for Neurology University of Ulm Germany

Department of Neurology and Center of Clinical Neuroscience 1st Faculty of Medicine Charles University Prague Czech Republic

FTLD Consortium Germany Germany; Clinic for Neurology Saarland University Germany

FTLD Consortium Germany Germany; Clinic for Neurology University of Ulm Germany

FTLD Consortium Germany Germany; Clinic for Psychiatry and Psychotherapy University Hospital Hamburg Eppendorf Germany

FTLD Consortium Germany Germany; Clinic for Psychiatry Psychosomatic Medicine and Psychotherapy University Würzburg Germany

FTLD Consortium Germany Germany; Clinic of Neurology Ludwig Maximilian University of Munich Germany

FTLD Consortium Germany Germany; Department of Neurodegenerative Diseases and Geriatric Psychiatry University Bonn Germany

FTLD Consortium Germany Germany; Department of Neurodegenerative Diseases Centre for Neurology and Hertie Institute for Clinical Brain Research University of Tübingen Germany; German Center for Neurodegenerative Diseases Tübingen Germany

FTLD Consortium Germany Germany; Department of Neurology Rostock University Medical Center Rostock Germany and German Center for Neurodegenerative Diseases Rostock Germany

FTLD Consortium Germany Germany; Department of Psychiatry and Psychotherapy Friedrich Alexander University Erlangen Nuremberg Germany

FTLD Consortium Germany Germany; Department of Psychiatry and Psychotherapy Technical University of Munich Germany

FTLD Consortium Germany Germany; University Medical Center Göttingen Germany and German Center for Neurodegenerative Diseases Göttingen Germany

Max Planck Institute for Human Cognitive and Brain Sciences Leipzig Germany

Max Planck Institute for Human Cognitive and Brain Sciences Leipzig Germany; Clinic of Cognitive Neurology University of Leipzig Germany

Max Planck Institute for Human Cognitive and Brain Sciences Leipzig Germany; Clinic of Cognitive Neurology University of Leipzig Germany; FTLD Consortium Germany Germany

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