Brain lesions disrupting addiction map to a common human brain circuit

dc.contributor.authorJoutsa Juho
dc.contributor.authorMoussawi Khaled
dc.contributor.authorSiddiqi Shan H.
dc.contributor.authorAbdolahi Amir
dc.contributor.authorDrew William
dc.contributor.authorCohen Alexander L.
dc.contributor.authorRoss Thomas J.
dc.contributor.authorDeshpande Harshawardhan U.
dc.contributor.authorWang Henry Z.
dc.contributor.authorBruss Joel
dc.contributor.authorStein Elliot A.
dc.contributor.authorVolkow Nora D.
dc.contributor.authorGrafman Jordan H.
dc.contributor.authorvan Wijngaarden Edwin
dc.contributor.authorBoes Aaron D.
dc.contributor.authorFox Michael D.
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.contributor.organization-code2609810
dc.converis.publication-id175766914
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/175766914
dc.date.accessioned2026-01-21T15:05:22Z
dc.date.available2026-01-21T15:05:22Z
dc.description.abstract<p>Drug addiction is a public health crisis for which new treatments are urgently needed. In rare cases, regional brain damage can lead to addiction remission. These cases may be used to identify therapeutic targets for neuromodulation. We analyzed two cohorts of patients addicted to smoking at the time of focal brain damage (cohort 1 n = 67; cohort 2 n = 62). Lesion locations were mapped to a brain atlas and the brain network functionally connected to each lesion location was computed using human connectome data (n = 1,000). Associations with addiction remission were identified. Generalizability was assessed using an independent cohort of patients with focal brain damage and alcohol addiction risk scores (n = 186). Specificity was assessed through comparison to 37 other neuropsychological variables. Lesions disrupting smoking addiction occurred in many different brain locations but were characterized by a specific pattern of brain connectivity. This pattern involved positive connectivity to the dorsal cingulate, lateral prefrontal cortex, and insula and negative connectivity to the medial prefrontal and temporal cortex. This circuit was reproducible across independent lesion cohorts, associated with reduced alcohol addiction risk, and specific to addiction metrics. Hubs that best matched the connectivity profile for addiction remission were the paracingulate gyrus, left frontal operculum, and medial fronto-polar cortex. We conclude that brain lesions disrupting addiction map to a specific human brain circuit and that hubs in this circuit provide testable targets for therapeutic neuromodulation.Lesions resulting in addiction remission occur in multiple different brain locations but map to a specific brain circuit and that hubs in this circuit provide testable targets for therapeutic neuromodulation.</p>
dc.format.pagerange1249
dc.format.pagerange1255
dc.identifier.eissn1546-170X
dc.identifier.jour-issn1078-8956
dc.identifier.olddbid214081
dc.identifier.oldhandle10024/197099
dc.identifier.urihttps://www.utupub.fi/handle/11111/56344
dc.identifier.urlhttps://www.nature.com/articles/s41591-022-01834-y
dc.identifier.urnURN:NBN:fi-fe2022081155093
dc.language.isoen
dc.okm.affiliatedauthorJoutsa, Juho
dc.okm.affiliatedauthorDataimport, tyks, vsshp
dc.okm.discipline3112 Neurosciencesen_GB
dc.okm.discipline3112 Neurotieteetfi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherNATURE PORTFOLIO
dc.publisher.countryUnited Statesen_GB
dc.publisher.countryYhdysvallat (USA)fi_FI
dc.publisher.country-codeUS
dc.relation.doi10.1038/s41591-022-01834-y
dc.relation.ispartofjournalNature Medicine
dc.relation.issue6
dc.relation.volume28
dc.source.identifierhttps://www.utupub.fi/handle/10024/197099
dc.titleBrain lesions disrupting addiction map to a common human brain circuit
dc.year.issued2022

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