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The G allele in IL-10-1082 G/A may have a role in lowering the susceptibility to panic disorder in female patients

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dc.contributor.authorKim, Han-Joon-
dc.contributor.authorKim, Yong-Ku-
dc.date.accessioned2021-09-03T16:01:04Z-
dc.date.available2021-09-03T16:01:04Z-
dc.date.created2021-06-16-
dc.date.issued2016-12-
dc.identifier.issn0924-2708-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/86584-
dc.description.abstractBackground: Immune system activation is involved in the pathophysiology of panic disorder (PD). We investigated INF-gamma+ 874 A/T, TNF-alpha-308 G/A, and IL-10-1082 G/A single nucleotide polymorphisms (SNPs) to determine their association with PD. Method: This study enroled 135 PD patients and 135 healthy controls. INF-gamma+874 A/T (rs2430561), TNF-alpha-308 G/A (rs1800629), and IL-10-1082 G/A (rs1800896) were genotyped. Results: There were no differences in genotypes or allele frequencies between the patient and control groups, regardless of accompanying agoraphobia. However, for female patients, the G allele frequency in IL-10 SNP was higher in the control group than in the patient group. Additionally, the female control group had a higher frequency of the A/G and G/G genotype in the IL-10 SNP than the female patient group. Conclusion: We suggest that the G allele in IL-10-1082 G/A might have a role in reducing the manifestations of PD in female patients. Further studies are needed to extend and confirm our findings.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherCAMBRIDGE UNIV PRESS-
dc.subjectMAJOR DEPRESSIVE DISORDER-
dc.subjectNEURODEGENERATION HYPOTHESIS-
dc.subjectRHEUMATOID-ARTHRITIS-
dc.subjectGENETIC-POLYMORPHISM-
dc.subjectINTERFERON-GAMMA-
dc.subjectIFN-GAMMA-
dc.subjectASSOCIATION-
dc.subjectPROMOTER-
dc.subjectSPECTRUM-
dc.subjectCHINESE-
dc.titleThe G allele in IL-10-1082 G/A may have a role in lowering the susceptibility to panic disorder in female patients-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Yong-Ku-
dc.identifier.doi10.1017/neu.2016.25-
dc.identifier.scopusid2-s2.0-84976329003-
dc.identifier.wosid000387823800008-
dc.identifier.bibliographicCitationACTA NEUROPSYCHIATRICA, v.28, no.6, pp.357 - 361-
dc.relation.isPartOfACTA NEUROPSYCHIATRICA-
dc.citation.titleACTA NEUROPSYCHIATRICA-
dc.citation.volume28-
dc.citation.number6-
dc.citation.startPage357-
dc.citation.endPage361-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaNeurosciences & Neurology-
dc.relation.journalResearchAreaPsychiatry-
dc.relation.journalWebOfScienceCategoryNeurosciences-
dc.relation.journalWebOfScienceCategoryPsychiatry-
dc.subject.keywordPlusMAJOR DEPRESSIVE DISORDER-
dc.subject.keywordPlusNEURODEGENERATION HYPOTHESIS-
dc.subject.keywordPlusRHEUMATOID-ARTHRITIS-
dc.subject.keywordPlusGENETIC-POLYMORPHISM-
dc.subject.keywordPlusINTERFERON-GAMMA-
dc.subject.keywordPlusIFN-GAMMA-
dc.subject.keywordPlusASSOCIATION-
dc.subject.keywordPlusPROMOTER-
dc.subject.keywordPlusSPECTRUM-
dc.subject.keywordPlusCHINESE-
dc.subject.keywordAuthorcytokine-
dc.subject.keywordAuthorIFN-r-
dc.subject.keywordAuthorIL-10-
dc.subject.keywordAuthorpanic disorder-
dc.subject.keywordAuthorTNF-alpha-
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