메뉴 건너뛰기




Volumn 118 B, Issue 1, 2003, Pages 103-109

Family-based and case-control association studies of catechol-O-methyltransferase in attention deficit hyperactivity disorder suggest genetic sexual dimorphism

Author keywords

Association; Attention deficit hyperactivity disorder; Catechol O methyltransferase; Gender differences; Genetics

Indexed keywords

CATECHOL METHYLTRANSFERASE; METHIONINE; VALINE; DNA;

EID: 0038755196     PISSN: 15524841     EISSN: 1552485X     Source Type: Journal    
DOI: 10.1002/ajmg.b.10064     Document Type: Article
Times cited : (111)

References (38)
  • 2
    • 0033985293 scopus 로고    scopus 로고
    • Sex differences in dopamine receptors and their relevance to ADHD
    • Andersen SL, Teicher MH. 2000. Sex differences in dopamine receptors and their relevance to ADHD. Neurosci Biobehav Rev 24:137-141.
    • (2000) Neurosci Biobehav Rev , vol.24 , pp. 137-141
    • Andersen, S.L.1    Teicher, M.H.2
  • 5
    • 0002239040 scopus 로고    scopus 로고
    • Association between tridimensional personality questionnaire (TPQ) traits and three functional polymorphisms: Dopamine receptor D4 (DRD4), serotonin transporter promoter region (5-HTTLPR), and catechol-O-methyltransferase (COMT)
    • Benjamin J, Osher Y, Kotler M, Gritsenko I, Nemanov L, Belmaker RH, Ebstein RP. 2000. Association between tridimensional personality questionnaire (TPQ) traits and three functional polymorphisms: Dopamine receptor D4 (DRD4), serotonin transporter promoter region (5-HTTLPR), and catechol-O-methyltransferase (COMT). Mol Psychiatry 5:96-100.
    • (2000) Mol Psychiatry , vol.5 , pp. 96-100
    • Benjamin, J.1    Osher, Y.2    Kotler, M.3    Gritsenko, I.4    Nemanov, L.5    Belmaker, R.H.6    Ebstein, R.P.7
  • 7
    • 0026670872 scopus 로고
    • Further evidence for family-genetic risk factors in attention deficit hyperactivity disorder: Patterns of comorbidity in probands and relatives in psychiatrically and pediatrically referral samples
    • Biederman J, Faraone SV, Keenan K, Benjamin J, Krifcher B, Moore C, Sprich-Buckminster S, Ugaglia K, Jellinek MS, Steingard R, et al. 1992. Further evidence for family-genetic risk factors in attention deficit hyperactivity disorder: Patterns of comorbidity in probands and relatives in psychiatrically and pediatrically referral samples. Arch Gen Psychiatry 49:728-738.
    • (1992) Arch Gen Psychiatry , vol.49 , pp. 728-738
    • Biederman, J.1    Faraone, S.V.2    Keenan, K.3    Benjamin, J.4    Krifcher, B.5    Moore, C.6    Sprich-Buckminster, S.7    Ugaglia, K.8    Jellinek, M.S.9    Steingard, R.10
  • 8
    • 0030984889 scopus 로고    scopus 로고
    • Association study of NlaIII and MspI genetic polymorphisms of catechol-O-methyltransferase gene and susceptibility to schizophrenia
    • Chen CH, Lee YR, Wei FC, Koong FJ, Hwu HG, Hsiao KJ. 1997. Association study of NlaIII and MspI genetic polymorphisms of catechol-O-methyltransferase gene and susceptibility to schizophrenia. Biol Psychiatry 41:985-987.
    • (1997) Biol Psychiatry , vol.41 , pp. 985-987
    • Chen, C.H.1    Lee, Y.R.2    Wei, F.C.3    Koong, F.J.4    Hwu, H.G.5    Hsiao, K.J.6
  • 11
    • 0033570041 scopus 로고    scopus 로고
    • Haplotype relative risk study of catechol-O-methyltransferase (COMT) and attention deficit hyperactivity disorder (ADHD): Association of the high-enzyme activity val allele with ADHD impulsive-hyperactive phenotype
    • Eisenberg J, Mei-Tal G, Steinberg A, Tartakovsky E, Zohar A, Gritsenko I, Nemanov L, Ebstein RP. 1999. Haplotype relative risk study of catechol-O-methyltransferase (COMT) and attention deficit hyperactivity disorder (ADHD): Association of the high-enzyme activity val allele with ADHD impulsive-hyperactive phenotype. Am J Med Genet 88:497-502.
    • (1999) Am J Med Genet , vol.88 , pp. 497-502
    • Eisenberg, J.1    Mei-Tal, G.2    Steinberg, A.3    Tartakovsky, E.4    Zohar, A.5    Gritsenko, I.6    Nemanov, L.7    Ebstein, R.P.8
  • 13
    • 0029858544 scopus 로고    scopus 로고
    • The TDT and other family-based tests for linkage disequilibrium and association
    • Ewens WJ. 1996. The TDT and other family-based tests for linkage disequilibrium and association. Am J Hum Genet 59:983-989.
    • (1996) Am J Hum Genet , vol.59 , pp. 983-989
    • Ewens, W.J.1
  • 14
    • 0032533256 scopus 로고    scopus 로고
    • Neurobiology of attention-deficit hyperactivity disorder
    • Faraone SV, Biederman J. 1998. Neurobiology of attention-deficit hyperactivity disorder. Biol Psychiatry 44:951-958.
    • (1998) Biol Psychiatry , vol.44 , pp. 951-958
    • Faraone, S.V.1    Biederman, J.2
  • 15
    • 0035002624 scopus 로고    scopus 로고
    • The nature and heritability of attention deficit hyperactivity disorder
    • Faraone SV, Doyle A. 2001. The nature and heritability of attention deficit hyperactivity disorder. Child Adolesc Psychiatr Clinics North America 10:299-316.
    • (2001) Child Adolesc Psychiatr Clinics North America , vol.10 , pp. 299-316
    • Faraone, S.V.1    Doyle, A.2
  • 16
    • 0028278845 scopus 로고
    • An exploratory study of ADHD among second-degree relatives of ADHD children
    • Faraone SV, Biederman J, Milberger S. 1994. An exploratory study of ADHD among second-degree relatives of ADHD children. Biol Psychiatry 35:398-402.
    • (1994) Biol Psychiatry , vol.35 , pp. 398-402
    • Faraone, S.V.1    Biederman, J.2    Milberger, S.3
  • 17
    • 0032544012 scopus 로고    scopus 로고
    • Catechol-O-methyltransferase-deficient mice exhibit sexually dimorphic changes in catecholamine levels and behavior
    • Gogos JA, Morgan M, Luine V, Santha M, Ogawa S, PfaffD, Karayiorgou M. 1998. Catechol-O-methyltransferase-deficient mice exhibit sexually dimorphic changes in catecholamine levels and behavior. Proc Natl Acad Sci USA 95:9991-9996.
    • (1998) Proc Natl Acad Sci USA , vol.95 , pp. 9991-9996
    • Gogos, J.A.1    Morgan, M.2    Luine, V.3    Santha, M.4    Ogawa, S.5    Pfaff, D.6    Karayiorgou, M.7
  • 18
    • 0026518652 scopus 로고
    • Chromosomal mapping of the human catechol-O-methyltransferase gene to 22q11.1-q11.2
    • Grossman MH, Emanuel BS, Budarf ML. 1992. Chromosomal mapping of the human catechol-O-methyltransferase gene to 22q11.1-q11.2 Genomics 12(4):822-825.
    • (1992) Genomics , vol.12 , Issue.4 , pp. 822-825
    • Grossman, M.H.1    Emanuel, B.S.2    Budarf, M.L.3
  • 19
    • 0034640682 scopus 로고    scopus 로고
    • No association between catechol-O-methyltransferase (COMT) gene polymorphism and attention deficit hyperactivity disorder (ADHD) in an Irish sample
    • Hawi Z, Millar N, Daly G, Fitzgerald M, Gill M. 2000. No association between catechol-O-methyltransferase (COMT) gene polymorphism and attention deficit hyperactivity disorder (ADHD) in an Irish sample. Am J Med Genet 96:282-284.
    • (2000) Am J Med Genet , vol.96 , pp. 282-284
    • Hawi, Z.1    Millar, N.2    Daly, G.3    Fitzgerald, M.4    Gill, M.5
  • 20
    • 0034626405 scopus 로고    scopus 로고
    • Confirmation of an excess of the high enzyme activity COMT val allele in heroin addicts in a family-based haplotype relative risk study
    • Horowitz R, Shufman A, Aharoni S, Aharoni S, Kremer I, Cohen H, Ebstein RP. 2000. Confirmation of an excess of the high enzyme activity COMT val allele in heroin addicts in a family-based haplotype relative risk study. Am J Med Genet 96:599-603.
    • (2000) Am J Med Genet , vol.96 , pp. 599-603
    • Horowitz, R.1    Shufman, A.2    Aharoni, S.3    Aharoni, S.4    Kremer, I.5    Cohen, H.6    Ebstein, R.P.7
  • 21
  • 22
    • 0033135862 scopus 로고    scopus 로고
    • Family-based association studies support a sexually dimorphic effect of COMT and MAOA on genetic susceptibility to obsessive-compulsive disorder
    • Karayiorgou M, Sobin C, Blundell ML, Galke BL, Malinova L, Goldberg P, Ott J, Gogos JA. 1999. Family-based association studies support a sexually dimorphic effect of COMT and MAOA on genetic susceptibility to obsessive-compulsive disorder. Biol Psychiatry 45:1178-1189.
    • (1999) Biol Psychiatry , vol.45 , pp. 1178-1189
    • Karayiorgou, M.1    Sobin, C.2    Blundell, M.L.3    Galke, B.L.4    Malinova, L.5    Goldberg, P.6    Ott, J.7    Gogos, J.A.8
  • 23
    • 0033573290 scopus 로고    scopus 로고
    • Homicidal behavior in schizophrenia associated with a genetic polymorphism determining low catechol-O-methyltransferase (COMT) activity
    • Kotler M, Barak P, Cohen H, Averbuch IE, Grinshpoon A, Gritsenko I, Nemanov L, Ebstein RP. 1999. Homicidal behavior in schizophrenia associated with a genetic polymorphism determining low catechol-O-methyltransferase (COMT) activity. Am J Med Genet 88:628-633.
    • (1999) Am J Med Genet , vol.88 , pp. 628-633
    • Kotler, M.1    Barak, P.2    Cohen, H.3    Averbuch, I.E.4    Grinshpoon, A.5    Gritsenko, I.6    Nemanov, L.7    Ebstein, R.P.8
  • 26
    • 0028918413 scopus 로고
    • Kinetics of human soluble and membrane-bound catechol-O-methyltransferase: A revised mechanism and description of thermolabile variant of the enzyme
    • Lotta T, Vidgren J, Tilgmann C, Ulmanen I, Melen K, Julkunen I, Taskinen J. 1995. Kinetics of human soluble and membrane-bound catechol-O-methyltransferase: A revised mechanism and description of thermolabile variant of the enzyme. Biochemistry 34:4202-4210.
    • (1995) Biochemistry , vol.34 , pp. 4202-4210
    • Lotta, T.1    Vidgren, J.2    Tilgmann, C.3    Ulmanen, I.4    Melen, K.5    Julkunen, I.6    Taskinen, J.7
  • 27
    • 0034606270 scopus 로고    scopus 로고
    • Failure to replicate an association between the catechol-O-methyltransferase polymorphism and attention deficit hyperactivity disorder in a second, independently recruited Israeli cohort
    • Manor I, Kotler M, Sever Y, Eisenberg J, Cohen H, Ebstein RP, Tyano S. 2000. Failure to replicate an association between the catechol-O-methyltransferase polymorphism and attention deficit hyperactivity disorder in a second, independently recruited Israeli cohort. Am J Med Genet 96:858-860.
    • (2000) Am J Med Genet , vol.96 , pp. 858-860
    • Manor, I.1    Kotler, M.2    Sever, Y.3    Eisenberg, J.4    Cohen, H.5    Ebstein, R.P.6    Tyano, S.7
  • 28
    • 0030737908 scopus 로고    scopus 로고
    • Further evidence of an association between attention-deficit/hyperactivity disorder and cigarette smoking. Findings from a high-risk sample of siblings
    • Milberger S, Biederman J, Faraone SV, Chen L, Jones J. 1997. Further evidence of an association between attention-deficit/hyperactivity disorder and cigarette smoking. Findings from a high-risk sample of siblings. Am J Addiction 6:205-217.
    • (1997) Am J Addiction , vol.6 , pp. 205-217
    • Milberger, S.1    Biederman, J.2    Faraone, S.V.3    Chen, L.4    Jones, J.5
  • 31
    • 0026793049 scopus 로고
    • Sex differences in densities of dopaminergic fibers and GABAergic neurons in the prenatal rat striatum
    • Ovtscharoff W, Euaterschulte B, Zienecker R, Reisert I, Pilgrim C. 1992. Sex differences in densities of dopaminergic fibers and GABAergic neurons in the prenatal rat striatum. J Comp Neurol 323: 299-304.
    • (1992) J Comp Neurol , vol.323 , pp. 299-304
    • Ovtscharoff, W.1    Euaterschulte, B.2    Zienecker, R.3    Reisert, I.4    Pilgrim, C.5
  • 32
    • 0032777995 scopus 로고    scopus 로고
    • Global variation in the frequencies of functionally different catechol-O-methyltransferase alleles
    • Palmatier MA, Min-Kang A, Kidd KK. 1999. Global variation in the frequencies of functionally different catechol-O-methyltransferase alleles. Biol Psychiatry 46:557-567.
    • (1999) Biol Psychiatry , vol.46 , pp. 557-567
    • Palmatier, M.A.1    Min-Kang, A.2    Kidd, K.K.3
  • 33
    • 0018378334 scopus 로고
    • Catechol-O-methyltransferase thermolabile enzyme in erythrocytes of subjects for allele for low activity
    • Scalon PD, Raymond FA, Weinshilboum X. 1979. Catechol-O-methyltransferase thermolabile enzyme in erythrocytes of subjects for allele for low activity. Science 203:63-65.
    • (1979) Science , vol.203 , pp. 63-65
    • Scalon, P.D.1    Raymond, F.A.2    Weinshilboum, X.3
  • 35
    • 0027377799 scopus 로고
    • Transmission test for linkage disequilibrium: The insulin gene region and insulin-dependent diabetes mellitus (IDDM)
    • Spielman RS, McGinnis RE, Ewens WJ. 1993. Transmission test for linkage disequilibrium: The insulin gene region and insulin-dependent diabetes mellitus (IDDM). Am J Hum Genet 52:506-516.
    • (1993) Am J Hum Genet , vol.52 , pp. 506-516
    • Spielman, R.S.1    McGinnis, R.E.2    Ewens, W.J.3
  • 36
    • 0034640691 scopus 로고    scopus 로고
    • No association between low- and high-activity catechol-O-methyltransferase (COMT) and attention deficit hyperactivity disorder (ADHD) in a sample of Turkish children
    • Tahir E, Curran S, Yazgan Y, Ozbay F, Cirakoglu B, Asherson PJ. 2000. No association between low- and high-activity catechol-O-methyltransferase (COMT) and attention deficit hyperactivity disorder (ADHD) in a sample of Turkish children. Am J Med Genet 96:285-288.
    • (2000) Am J Med Genet , vol.96 , pp. 285-288
    • Tahir, E.1    Curran, S.2    Yazgan, Y.3    Ozbay, F.4    Cirakoglu, B.5    Asherson, P.J.6
  • 37
    • 0030836682 scopus 로고    scopus 로고
    • High-activity catechol-O-methyltransferase allele is more prevalent in polysubstance abusers
    • Vandenbergh DJ, Rodriguez LA, Miller IT, Uhl GR, Lachman HM. 1997. High-activity catechol-O-methyltransferase allele is more prevalent in polysubstance abusers. Am J Med Genet 74:439-442.
    • (1997) Am J Med Genet , vol.74 , pp. 439-442
    • Vandenbergh, D.J.1    Rodriguez, L.A.2    Miller, I.T.3    Uhl, G.R.4    Lachman, H.M.5
  • 38
    • 0019566947 scopus 로고
    • Thermal stability and biochemical genetics of erythrocyte catechol-O-methyltransferase and plasma dopamine-beta-hydroxylase
    • Weinshilboum R, Dunnette J. 1981. Thermal stability and biochemical genetics of erythrocyte catechol-O-methyltransferase and plasma dopamine-beta-hydroxylase. Clin Genet 19:426-437.
    • (1981) Clin Genet , vol.19 , pp. 426-437
    • Weinshilboum, R.1    Dunnette, J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.