Handedness and its genetic influences are associated with structural asymmetries of the cerebral cortex in 31,864 individuals
Roughly 10% of the human population is left-handed, and this rate is increased in some brain-related disorders. The neuroanatomical correlates of hand preference have remained equivocal. We resampled structural brain image data from 28,802 right-handers and 3,062 left-handers (UK Biobank population...
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creator | Sha, Zhiqiang Pepe, Antonietta Schijven, Dick Carrión-Castillo, Amaia Roe, James M. Westerhausen, René Joliot, Marc Fisher, Simon E. Crivello, Fabrice Francks, Clyde |
description | Roughly 10% of the human population is left-handed, and this rate is increased in some brain-related disorders. The neuroanatomical correlates of hand preference have remained equivocal. We resampled structural brain image data from 28,802 right-handers and 3,062 left-handers (UK Biobank population dataset) to a symmetrical surface template, and mapped asymmetries for each of 8,681 vertices across the cerebral cortex in each individual. Left-handers compared to right-handers showed average differences of surface area asymmetry within the fusiform cortex, the anterior insula, the anterior middle cingulate cortex, and the precentral cortex. Meta-analyzed functional imaging data implicated these regions in executive functions and language. Polygenic disposition to left-handedness was associated with two of these regional asymmetries, and 18 loci previously linked with left-handedness by genome-wide screening showed associations with one or more of these asymmetries. Implicated genes included six encoding microtubule-related proteins: TUBB, TUBA1B, TUBB3, TUBB4A, MAP2, and NME7—mutations in the latter can cause left to right reversal of the visceral organs. There were also two cortical regions where average thickness asymmetry was altered in lef-thandedness: on the postcentral gyrus and the inferior occipital cortex, functionally annotated with hand sensorimotor and visual roles. These cortical thickness asymmetries were not heritable. Heritable surface area asymmetries of language-related regions may link the etiologies of hand preference and language, whereas nonheritable asymmetries of sensorimotor cortex may manifest as consequences of hand preference. |
doi_str_mv | 10.1073/pnas.2113095118 |
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The neuroanatomical correlates of hand preference have remained equivocal. We resampled structural brain image data from 28,802 right-handers and 3,062 left-handers (UK Biobank population dataset) to a symmetrical surface template, and mapped asymmetries for each of 8,681 vertices across the cerebral cortex in each individual. Left-handers compared to right-handers showed average differences of surface area asymmetry within the fusiform cortex, the anterior insula, the anterior middle cingulate cortex, and the precentral cortex. Meta-analyzed functional imaging data implicated these regions in executive functions and language. Polygenic disposition to left-handedness was associated with two of these regional asymmetries, and 18 loci previously linked with left-handedness by genome-wide screening showed associations with one or more of these asymmetries. Implicated genes included six encoding microtubule-related proteins: TUBB, TUBA1B, TUBB3, TUBB4A, MAP2, and NME7—mutations in the latter can cause left to right reversal of the visceral organs. There were also two cortical regions where average thickness asymmetry was altered in lef-thandedness: on the postcentral gyrus and the inferior occipital cortex, functionally annotated with hand sensorimotor and visual roles. These cortical thickness asymmetries were not heritable. Heritable surface area asymmetries of language-related regions may link the etiologies of hand preference and language, whereas nonheritable asymmetries of sensorimotor cortex may manifest as consequences of hand preference.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.2113095118</identifier><identifier>PMID: 34785596</identifier><language>eng</language><publisher>United States: National Academy of Sciences</publisher><subject>Aged ; Aged, 80 and over ; Anatomy ; Apexes ; Asymmetry ; Behavior - physiology ; Biological Sciences ; Biological Specimen Banks ; Brain ; Brain - diagnostic imaging ; Brain - physiology ; Brain architecture ; Brain Mapping ; Cerebral cortex ; Cerebral Cortex - diagnostic imaging ; Cerebral Cortex - physiology ; Cortex (cingulate) ; Etiology ; Female ; Functional Laterality - genetics ; Functional Laterality - physiology ; Functionals ; Genomes ; Hand ; Hand (anatomy) ; Handedness ; Human populations ; Humans ; Language ; Magnetic Resonance Imaging ; Male ; Middle Aged ; Mutation ; Neuroimaging ; Occipital Lobe ; Organs ; Postcentral gyrus ; Sensorimotor Cortex ; Somatosensory cortex ; Surface area ; Thickness</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 2021-11, Vol.118 (47), p.1-9</ispartof><rights>Copyright © 2021 the Author(s). Published by PNAS.</rights><rights>Copyright National Academy of Sciences Nov 23, 2021</rights><rights>info:eu-repo/semantics/openAccess</rights><rights>Copyright © 2021 the Author(s). Published by PNAS. 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c467t-e18ba4062c5fea6bc1473a1ae3e8c246da862b369f0b0c94fdb2ba18058ef2fe3</citedby><cites>FETCH-LOGICAL-c467t-e18ba4062c5fea6bc1473a1ae3e8c246da862b369f0b0c94fdb2ba18058ef2fe3</cites><orcidid>0000-0002-9098-890X ; 0000-0003-0226-0642 ; 0000-0001-6950-984X ; 0000-0001-7107-2712 ; 0000-0002-3407-9752 ; 0000-0001-5190-7241 ; 0000-0002-3132-1996</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/27094023$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/27094023$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,727,780,784,803,885,26567,27924,27925,53791,53793,58017,58250</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34785596$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sha, Zhiqiang</creatorcontrib><creatorcontrib>Pepe, Antonietta</creatorcontrib><creatorcontrib>Schijven, Dick</creatorcontrib><creatorcontrib>Carrión-Castillo, Amaia</creatorcontrib><creatorcontrib>Roe, James M.</creatorcontrib><creatorcontrib>Westerhausen, René</creatorcontrib><creatorcontrib>Joliot, Marc</creatorcontrib><creatorcontrib>Fisher, Simon E.</creatorcontrib><creatorcontrib>Crivello, Fabrice</creatorcontrib><creatorcontrib>Francks, Clyde</creatorcontrib><title>Handedness and its genetic influences are associated with structural asymmetries of the cerebral cortex in 31,864 individuals</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>Roughly 10% of the human population is left-handed, and this rate is increased in some brain-related disorders. The neuroanatomical correlates of hand preference have remained equivocal. We resampled structural brain image data from 28,802 right-handers and 3,062 left-handers (UK Biobank population dataset) to a symmetrical surface template, and mapped asymmetries for each of 8,681 vertices across the cerebral cortex in each individual. Left-handers compared to right-handers showed average differences of surface area asymmetry within the fusiform cortex, the anterior insula, the anterior middle cingulate cortex, and the precentral cortex. Meta-analyzed functional imaging data implicated these regions in executive functions and language. Polygenic disposition to left-handedness was associated with two of these regional asymmetries, and 18 loci previously linked with left-handedness by genome-wide screening showed associations with one or more of these asymmetries. Implicated genes included six encoding microtubule-related proteins: TUBB, TUBA1B, TUBB3, TUBB4A, MAP2, and NME7—mutations in the latter can cause left to right reversal of the visceral organs. There were also two cortical regions where average thickness asymmetry was altered in lef-thandedness: on the postcentral gyrus and the inferior occipital cortex, functionally annotated with hand sensorimotor and visual roles. These cortical thickness asymmetries were not heritable. Heritable surface area asymmetries of language-related regions may link the etiologies of hand preference and language, whereas nonheritable asymmetries of sensorimotor cortex may manifest as consequences of hand preference.</description><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Anatomy</subject><subject>Apexes</subject><subject>Asymmetry</subject><subject>Behavior - physiology</subject><subject>Biological Sciences</subject><subject>Biological Specimen Banks</subject><subject>Brain</subject><subject>Brain - diagnostic imaging</subject><subject>Brain - physiology</subject><subject>Brain architecture</subject><subject>Brain Mapping</subject><subject>Cerebral cortex</subject><subject>Cerebral Cortex - diagnostic imaging</subject><subject>Cerebral Cortex - physiology</subject><subject>Cortex (cingulate)</subject><subject>Etiology</subject><subject>Female</subject><subject>Functional Laterality - genetics</subject><subject>Functional Laterality - physiology</subject><subject>Functionals</subject><subject>Genomes</subject><subject>Hand</subject><subject>Hand (anatomy)</subject><subject>Handedness</subject><subject>Human populations</subject><subject>Humans</subject><subject>Language</subject><subject>Magnetic Resonance Imaging</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Mutation</subject><subject>Neuroimaging</subject><subject>Occipital Lobe</subject><subject>Organs</subject><subject>Postcentral gyrus</subject><subject>Sensorimotor Cortex</subject><subject>Somatosensory cortex</subject><subject>Surface area</subject><subject>Thickness</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>3HK</sourceid><recordid>eNpdkb1vFDEQxS0EIkegpgIs0VCwib_WazdIKAISKRIN1JbXO5vzadc-bG8gBf87Pl1yCalmpPfzmxk_hF5TckJJx0-3weYTRiknuqVUPUErSjRtpNDkKVoRwrpGCSaO0IucN4RUSpHn6IiLTrWtliv099yGAYYAOePaYV8yvoIAxTvswzgtEBxUKQG2OUfnbYEB__ZljXNJiytLslOVbuYZSvIVjSMua8AOEvQ7zcVU4E81w5x-VFLUbvDXfljslF-iZ2Mt8Oq2HqOfX7_8ODtvLr9_uzj7fNk4IbvSAFW9FUQy145gZe-o6LilFjgox4QcrJKs51KPpCdOi3HoWW-pIq2CkY3Aj9Gnve926WcYHIRSVzPb5Gebbky03vyvBL82V_HaKEk7QVU1eLc3cMnn4oMJMVlDiWqZ0UR3rBIfbkek-GuBXMzss4NpsgHikg1rtWq5klpW9P0jdBOXFOoHGCZrZERx1VXq9G5kzDnBeFiXErML3-zCN_fh1xdvH1554O_SrsCbPbDJJaaDXidqQRjn_wAhuLYq</recordid><startdate>20211123</startdate><enddate>20211123</enddate><creator>Sha, Zhiqiang</creator><creator>Pepe, Antonietta</creator><creator>Schijven, Dick</creator><creator>Carrión-Castillo, Amaia</creator><creator>Roe, James M.</creator><creator>Westerhausen, René</creator><creator>Joliot, Marc</creator><creator>Fisher, Simon E.</creator><creator>Crivello, Fabrice</creator><creator>Francks, Clyde</creator><general>National Academy of Sciences</general><general>The National Academy of Sciences</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QG</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>3HK</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-9098-890X</orcidid><orcidid>https://orcid.org/0000-0003-0226-0642</orcidid><orcidid>https://orcid.org/0000-0001-6950-984X</orcidid><orcidid>https://orcid.org/0000-0001-7107-2712</orcidid><orcidid>https://orcid.org/0000-0002-3407-9752</orcidid><orcidid>https://orcid.org/0000-0001-5190-7241</orcidid><orcidid>https://orcid.org/0000-0002-3132-1996</orcidid></search><sort><creationdate>20211123</creationdate><title>Handedness and its genetic influences are associated with structural asymmetries of the cerebral cortex in 31,864 individuals</title><author>Sha, Zhiqiang ; 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The neuroanatomical correlates of hand preference have remained equivocal. We resampled structural brain image data from 28,802 right-handers and 3,062 left-handers (UK Biobank population dataset) to a symmetrical surface template, and mapped asymmetries for each of 8,681 vertices across the cerebral cortex in each individual. Left-handers compared to right-handers showed average differences of surface area asymmetry within the fusiform cortex, the anterior insula, the anterior middle cingulate cortex, and the precentral cortex. Meta-analyzed functional imaging data implicated these regions in executive functions and language. Polygenic disposition to left-handedness was associated with two of these regional asymmetries, and 18 loci previously linked with left-handedness by genome-wide screening showed associations with one or more of these asymmetries. Implicated genes included six encoding microtubule-related proteins: TUBB, TUBA1B, TUBB3, TUBB4A, MAP2, and NME7—mutations in the latter can cause left to right reversal of the visceral organs. There were also two cortical regions where average thickness asymmetry was altered in lef-thandedness: on the postcentral gyrus and the inferior occipital cortex, functionally annotated with hand sensorimotor and visual roles. These cortical thickness asymmetries were not heritable. Heritable surface area asymmetries of language-related regions may link the etiologies of hand preference and language, whereas nonheritable asymmetries of sensorimotor cortex may manifest as consequences of hand preference.</abstract><cop>United States</cop><pub>National Academy of Sciences</pub><pmid>34785596</pmid><doi>10.1073/pnas.2113095118</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-9098-890X</orcidid><orcidid>https://orcid.org/0000-0003-0226-0642</orcidid><orcidid>https://orcid.org/0000-0001-6950-984X</orcidid><orcidid>https://orcid.org/0000-0001-7107-2712</orcidid><orcidid>https://orcid.org/0000-0002-3407-9752</orcidid><orcidid>https://orcid.org/0000-0001-5190-7241</orcidid><orcidid>https://orcid.org/0000-0002-3132-1996</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Aged Aged, 80 and over Anatomy Apexes Asymmetry Behavior - physiology Biological Sciences Biological Specimen Banks Brain Brain - diagnostic imaging Brain - physiology Brain architecture Brain Mapping Cerebral cortex Cerebral Cortex - diagnostic imaging Cerebral Cortex - physiology Cortex (cingulate) Etiology Female Functional Laterality - genetics Functional Laterality - physiology Functionals Genomes Hand Hand (anatomy) Handedness Human populations Humans Language Magnetic Resonance Imaging Male Middle Aged Mutation Neuroimaging Occipital Lobe Organs Postcentral gyrus Sensorimotor Cortex Somatosensory cortex Surface area Thickness |
title | Handedness and its genetic influences are associated with structural asymmetries of the cerebral cortex in 31,864 individuals |
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