Lesion network localization of free will

dc.contributor.authorDarby RR
dc.contributor.authorJoutsa J
dc.contributor.authorBurke MJ
dc.contributor.authorFox MD
dc.contributor.organizationfi=PET-keskus|en=Turku PET Centre|
dc.contributor.organizationfi=kliiniset neurotieteet|en=Clinical Neurosciences|
dc.contributor.organizationfi=tyks, vsshp|en=tyks, varha|
dc.contributor.organization-code1.2.246.10.2458963.20.74845969893
dc.converis.publication-id36604287
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/36604287
dc.date.accessioned2022-10-27T11:54:26Z
dc.date.available2022-10-27T11:54:26Z
dc.description.abstractOur perception of free will is composed of a desire to act (volition) and a sense of responsibility for our actions (agency). Brain damage can disrupt these processes, but which regions are most important for free will perception remains unclear. Here, we study focal brain lesions that disrupt volition, causing akinetic mutism (n = 28), or disrupt agency, causing alien limb syndrome (n = 50), to better localize these processes in the human brain. Lesion locations causing either syndrome were highly heterogeneous, occurring in a variety of different brain locations. We next used a recently validated technique termed lesion network mapping to determine whether these heterogeneous lesion locations localized to specific brain networks. Lesion locations causing akinetic mutism all fell within one network, defined by connectivity to the anterior cingulate cortex. Lesion locations causing alien limb fell within a separate network, defined by connectivity to the precuneus. Both findings were specific for these syndromes compared with brain lesions causing similar physical impairments but without disordered free will. Finally, our lesion-based localization matched network localization for brain stimulation locations that disrupt free will and neuro-imaging abnormalities in patients with psychiatric disorders of free will without overt brain lesions. Collectively, our results demonstrate that lesions in different locations causing disordered volition and agency localize to unique brain networks, lending insight into the neuroanatomical substrate of free will perception.
dc.format.pagerange10792
dc.format.pagerange10797
dc.identifier.eissn1091-6490
dc.identifier.jour-issn0027-8424
dc.identifier.olddbid172721
dc.identifier.oldhandle10024/155815
dc.identifier.urihttps://www.utupub.fi/handle/11111/54652
dc.identifier.urnURN:NBN:fi-fe2021042720147
dc.language.isoen
dc.okm.affiliatedauthorJoutsa, Juho
dc.okm.affiliatedauthorDataimport, tyks, vsshp
dc.okm.affiliatedauthorDataimport, 2609820 PET Tutkimus
dc.okm.discipline3112 Neurosciencesen_GB
dc.okm.discipline3124 Neurology and psychiatryen_GB
dc.okm.discipline3112 Neurotieteetfi_FI
dc.okm.discipline3124 Neurologia ja psykiatriafi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherNATL ACAD SCIENCES
dc.publisher.countryUnited Statesen_GB
dc.publisher.countryYhdysvallat (USA)fi_FI
dc.publisher.country-codeUS
dc.relation.doi10.1073/pnas.1814117115
dc.relation.ispartofjournalProceedings of the National Academy of Sciences of the United States of America
dc.relation.issue42
dc.relation.volume115
dc.source.identifierhttps://www.utupub.fi/handle/10024/155815
dc.titleLesion network localization of free will
dc.year.issued2018

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