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Altered Cerebral Curvature in Preterm Infants Is Associated with the Common Genetic Variation Related to Autism Spectrum Disorder and Lipid Metabolism

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dc.contributor.authorKim, Hyuna-
dc.contributor.authorAhn, Ja-Hye-
dc.contributor.authorLee, Joo Young-
dc.contributor.authorJang, Yong Hun-
dc.contributor.authorKim, Young-Eun-
dc.contributor.authorKim, Johanna Inhyang-
dc.contributor.authorKim, Bung-Nyun-
dc.contributor.authorLee, Hyun Ju-
dc.date.accessioned2022-07-06T01:50:17Z-
dc.date.available2022-07-06T01:50:17Z-
dc.date.created2022-06-29-
dc.date.issued2022-06-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/138355-
dc.description.abstractPreterm births are often associated with neurodevelopmental impairment. In the critical developmental period of the fetal brain, preterm birth disrupts cortical maturation. Notably, preterm birth leads to alterations in the fronto-striatal and temporal lobes and the limbic region. Recent advances in MRI acquisition and analysis methods have revealed an integrated approach to the genetic influence on brain structure. Based on imaging studies, we hypothesized that the altered cortical structure observed after preterm birth is associated with common genetic variations. We found that the presence of the minor allele at rs1042778 in OXTR was associated with reduced curvature in the right medial orbitofrontal gyrus (p < 0.001). The presence of the minor allele at rs174576 in FADS2 (p < 0.001) or rs740603 in COMT (p < 0.001) was related to reduced curvature in the left posterior cingulate gyrus. This study provides biological insight into altered cortical curvature at term-equivalent age, suggesting that the common genetic variations related to autism spectrum disorder (ASD) and lipid metabolism may mediate vulnerability to early cortical dysmaturation in preterm infants.-
dc.language영어-
dc.language.isoen-
dc.publisherMDPI-
dc.titleAltered Cerebral Curvature in Preterm Infants Is Associated with the Common Genetic Variation Related to Autism Spectrum Disorder and Lipid Metabolism-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Young-Eun-
dc.contributor.affiliatedAuthorLee, Hyun Ju-
dc.identifier.doi10.3390/jcm11113135-
dc.identifier.wosid000809469100001-
dc.identifier.bibliographicCitationJOURNAL OF CLINICAL MEDICINE, v.11, no.11, pp.1 - 13-
dc.relation.isPartOfJOURNAL OF CLINICAL MEDICINE-
dc.citation.titleJOURNAL OF CLINICAL MEDICINE-
dc.citation.volume11-
dc.citation.number11-
dc.citation.startPage1-
dc.citation.endPage13-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaGeneral & Internal Medicine-
dc.relation.journalWebOfScienceCategoryMedicine, General & Internal-
dc.subject.keywordPlusCATECHOL-O-METHYLTRANSFERASE-
dc.subject.keywordPlusPOSTERIOR CINGULATE CORTEX-
dc.subject.keywordPlusRISK-
dc.subject.keywordPlusSCHIZOPHRENIA-
dc.subject.keywordPlusPOLYMORPHISM-
dc.subject.keywordPlusOXTR-
dc.subject.keywordPlusENDOPHENOTYPES-
dc.subject.keywordPlusVARIABILITY-
dc.subject.keywordPlusCOUNTRIES-
dc.subject.keywordPlusCHILDREN-
dc.subject.keywordAuthorpreterm-
dc.subject.keywordAuthorimaging genetics-
dc.subject.keywordAuthorcommon variation-
dc.subject.keywordAuthorOXTR-
dc.subject.keywordAuthorFADS2-
dc.subject.keywordAuthorCOMT-
dc.subject.keywordAuthorM-CRIB-S-
dc.identifier.urlhttps://www.mdpi.com/2077-0383/11/11/3135-
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서울 의과대학 > 서울 소아청소년과학교실 > 1. Journal Articles
서울 의과대학 > 서울 진단검사의학교실 > 1. Journal Articles

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