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Neurotrophin-3 gene, intelligence, and selective attention deficit in a Korean sample with attention-deficit/hyperactivity disorder

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dc.contributor.authorCho, Soo-Churl-
dc.contributor.authorKim, Hyo-Won-
dc.contributor.authorKim, Boong-Nyun-
dc.contributor.authorKim, Jae-Won-
dc.contributor.authorCho, Dae-Yeon-
dc.contributor.authorJung, Sun-Woo-
dc.contributor.authorChung, In-Won-
dc.contributor.authorSon, Jung-Woo-
dc.contributor.authorChung, Un-Sun-
dc.contributor.authorYoo, Hee Jeong-
dc.contributor.authorChung, Seockhoon-
dc.contributor.authorShin, Min-Sup-
dc.date.accessioned2012-07-04T08:55:17Z-
dc.date.available2012-07-04T08:55:17Z-
dc.date.issued2010-08-16-
dc.identifier.citationPROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY; Vol.34(6); 1065-1069ko_KR
dc.identifier.issn0278-5846-
dc.identifier.urihttps://hdl.handle.net/10371/78493-
dc.description.abstractObjective: Attention-deficit/hyperactivity disorder (ADHD) is a complex neurodevelopmental disorder with a strong genetic component. Neurotrophin-3 (NTF3), which participates in the differentiation and survival of dopaminergic and noradrenergic neurons, has been identified as a factor in the development of ADHD. We investigated the relationships between ADHD and NTF3 gene polymorphism. Methods: We conducted a case-control analysis of 202 ADHD subjects and 159 controls, performed a transmission disequilibrium test (TDT) on 151 trios, and compared the intelligence quotient (IQ) and a continuous performance test (CPT) according to the genotype of two single-nucleotide polymorphisms (SNPs) (rs6332 and rs6489630) in the NTF3 gene. Results: In the case-control and family-based analyses, NTF3 was not significantly associated with ADHD. However, in the ADHD probands, the subjects with AA genotype in the rs6332 SNP had significantly higher mean T-scores for commission errors on the CPT than did those with the AG genotypes (p = 0.045). The mean IQ of the ADHD probands who had the CC genotype of the rs6489630 SNP were higher compared with those who had the CT or TT genotype (p = 0.035). The mean T-score for response time on the CPT was higher in the subjects with TT genotype in the rs6489630 SNP compared to those with the CC or CT genotype, even after adjusting for the effect of IQ (p = 0.021). Conclusions: These results provide preliminary evidence of an association between NTF3 and the intelligence and selective attention deficit in the Korean population.ko_KR
dc.language.isoenko_KR
dc.publisherPERGAMON-ELSEVIER SCIENCE LTDko_KR
dc.subjectAttention-deficit/hyperactivity disorder (ADHD)ko_KR
dc.subjectGenetic polymorphismko_KR
dc.subjectContinuous performance testko_KR
dc.subjectImpulsivityko_KR
dc.subjectIntelligenceko_KR
dc.titleNeurotrophin-3 gene, intelligence, and selective attention deficit in a Korean sample with attention-deficit/hyperactivity disorderko_KR
dc.typeArticleko_KR
dc.contributor.AlternativeAuthor조수철-
dc.contributor.AlternativeAuthor김효원-
dc.contributor.AlternativeAuthor김붕년-
dc.contributor.AlternativeAuthor김재원-
dc.contributor.AlternativeAuthor신민섭-
dc.contributor.AlternativeAuthor조대연-
dc.contributor.AlternativeAuthor정석훈-
dc.contributor.AlternativeAuthor정선우-
dc.contributor.AlternativeAuthor유희정-
dc.contributor.AlternativeAuthor정인원-
dc.contributor.AlternativeAuthor정운선-
dc.contributor.AlternativeAuthor손정우-
dc.identifier.doi10.1016/j.pnpbp.2010.05.026-
dc.citation.journaltitlePROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY-
dc.description.citedreferenceSanchez-Mora C, 2010, AM J MED GENET B, V153B, P512, DOI 10.1002/ajmg.b.31008-
dc.description.citedreferenceForero DA, 2009, J PSYCHIATR NEUROSCI, V34, P361-
dc.description.citedreferenceShaw P, 2009, AM J PSYCHIAT, V166, P58, DOI 10.1176/appi.ajp.2008.08050781-
dc.description.citedreferenceO`Connell RG, 2009, J COGNITIVE NEUROSCI, V21, P93-
dc.description.citedreferenceCHOI SJ, 2009, 56 ANN M AACAP HON H, P203-
dc.description.citedreferenceConner AC, 2008, AM J MED GENET B, V147B, P1476, DOI 10.1002/ajmg.b.30632-
dc.description.citedreferenceRommelse NNJ, 2008, AM J HUM GENET, V83, P99, DOI 10.1016/j.ajhg.2008.06.006-
dc.description.citedreferenceRibases M, 2008, BIOL PSYCHIAT, V63, P935, DOI 10.1016/j.biopsych.2007.11.004-
dc.description.citedreferenceRomanos M, 2008, MOL PSYCHIATR, V13, P522, DOI 10.1038/mp.2008.12-
dc.description.citedreferenceRapoport JL, 2008, NEUROPSYCHOPHARMACOL, V33, P181, DOI 10.1038/sj.npp.1301553-
dc.description.citedreferenceVolkow ND, 2007, ARCH GEN PSYCHIAT, V64, P932-
dc.description.citedreferenceSzatmari P, 2007, AM J MED GENET B, V144B, P581, DOI 10.1002/ajmg.b.30426-
dc.description.citedreferencePolanczyk G, 2007, AM J PSYCHIAT, V164, P942, DOI 10.1176/appi.ajp.164.6.942-
dc.description.citedreferenceSyed Z, 2007, AM J MED GENET B, V144B, P375, DOI 10.1002/ajmg.b.30459-
dc.description.citedreferenceFlint J, 2007, PSYCHOL MED, V37, P163, DOI 10.1017/S0033291706008750-
dc.description.citedreferenceShaw P, 2006, ARCH GEN PSYCHIAT, V63, P540-
dc.description.citedreferenceCHO SC, 2006, J KOREAN ACAD CHILD, V18, P138-
dc.description.citedreferencePRESSEN KJ, 2006, ARCH GEN PSYCHIAT, V63, P795-
dc.description.citedreferenceFritzsch B, 2005, HEARING RES, V206, P52, DOI 10.1016/j.heares.2004.11.025-
dc.description.citedreferenceFaraone SV, 2005, BIOL PSYCHIAT, V57, P1313, DOI 10.1016/j.biopsych.2004.11.024-
dc.description.citedreferenceKim YS, 2004, YONSEI MED J, V45, P81-
dc.description.citedreferenceLamprecht R, 2004, NAT REV NEUROSCI, V5, P45, DOI 10.1038/nrn1301-
dc.description.citedreferenceTadokoro K, 2004, NEUROPSYCHOBIOLOGY, V50, P206, DOI 10.1159/000079971-
dc.description.citedreferenceCastellanos FX, 2002, NAT REV NEUROSCI, V3, P617, DOI 10.1038/nrn896-
dc.description.citedreferenceFisher SE, 2002, AM J HUM GENET, V70, P1183-
dc.description.citedreferenceHattori M, 2002, AM J MED GENET, V114, P304, DOI 10.1002/ajmg.10248-
dc.description.citedreferenceSO YK, 2002, J KOREAN NEUROPSYCHI, V41, P283-
dc.description.citedreferencePARK KS, 2002, KOREAN ED DEV I WECH-
dc.description.citedreferenceHuang EJ, 2001, ANNU REV NEUROSCI, V24, P677-
dc.description.citedreferenceOades RD, 2000, PSYCHIAT RES, V93, P165-
dc.description.citedreferenceShaffer D, 2000, J AM ACAD CHILD PSY, V39, P28-
dc.description.citedreferenceSHIN MS, 2000, J KOR ACAD CHILD ADO, V11, P91-
dc.description.citedreferenceKaufman J, 1997, J AM ACAD CHILD PSY, V36, P980-
dc.description.citedreferenceSmalley SL, 1997, AM J HUM GENET, V60, P1276-
dc.description.citedreferenceOH KJ, 1997, DEV KOREAN VERSION C-
dc.description.citedreferenceMANESS LM, 1994, NEUROSCI BIOBEHAV R, V18, P143-
dc.description.citedreference*AM PSYCH ASS, 1994, DIAGN STAT MAN MENT-
dc.description.citedreferenceMAISONPIERRE PC, 1991, GENOMICS, V10, P558-
dc.description.citedreferenceGOTTESMAN II, 1991, SCHIZOPHRENIA GENESI-
dc.description.tc1-
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