Skip to main content
Top
Gepubliceerd in: Journal of Autism and Developmental Disorders 11/2009

01-11-2009 | Original Paper

Association of COMT (Val158Met) and BDNF (Val66Met) Gene Polymorphisms with Anxiety, ADHD and Tics in Children with Autism Spectrum Disorder

Auteurs: Kenneth D. Gadow, Jasmin Roohi, Carla J. DeVincent, Sarah Kirsch, Eli Hatchwell

Gepubliceerd in: Journal of Autism and Developmental Disorders | Uitgave 11/2009

Log in om toegang te krijgen
share
DELEN

Deel dit onderdeel of sectie (kopieer de link)

  • Optie A:
    Klik op de rechtermuisknop op de link en selecteer de optie “linkadres kopiëren”
  • Optie B:
    Deel de link per e-mail

Abstract

The aim of the study is to examine rs4680 (COMT) and rs6265 (BDNF) as genetic markers of anxiety, ADHD, and tics. Parents and teachers completed a DSM-IV-referenced rating scale for a total sample of 67 children with autism spectrum disorder (ASD). Both COMT (p = 0.06) and BDNF (p = 0.07) genotypes were marginally significant for teacher ratings of social phobia (ηp 2 = 0.06). Analyses also indicated associations of BDNF genotype with parent-rated ADHD (p = 0.01, ηp 2 = 0.10) and teacher-rated tics (p = 0.04; ηp 2 = 0.07). There was also evidence of a possible interaction (p = 0.02, ηp 2 = 0.09) of BDNF genotype with DAT1 3′ VNTR with tic severity. BDNF and COMT may be biomarkers for phenotypic variation in ASD, but these preliminary findings remain tentative pending replication with larger, independent samples.
Literatuur
go back to reference Abrahams, B. S., & Geschwind, D. H. (2008). Advances in autism genetics: On the threshold of a new neurobiology. Nature Reviews, 9, 341–355.PubMedCrossRef Abrahams, B. S., & Geschwind, D. H. (2008). Advances in autism genetics: On the threshold of a new neurobiology. Nature Reviews, 9, 341–355.PubMedCrossRef
go back to reference Baron-Cohen, S. (2006). The hyper-systemizing, assertive mating theory of autism. Progress in Neuro-Psychopharmacology and Biological Psychiatry, 30, 865–872.PubMedCrossRef Baron-Cohen, S. (2006). The hyper-systemizing, assertive mating theory of autism. Progress in Neuro-Psychopharmacology and Biological Psychiatry, 30, 865–872.PubMedCrossRef
go back to reference Belmonte, M. K., Cook, E. H., Jr., Anderson, G. M., Rubenstein, J. L. R., Greenough, W. T., Beckel-Mitchner, A., et al. (2004). Autism as a disorder of neural information processing: Directions for research and targets for therapy. Molecular Psychiatry, 9, 646–663.PubMed Belmonte, M. K., Cook, E. H., Jr., Anderson, G. M., Rubenstein, J. L. R., Greenough, W. T., Beckel-Mitchner, A., et al. (2004). Autism as a disorder of neural information processing: Directions for research and targets for therapy. Molecular Psychiatry, 9, 646–663.PubMed
go back to reference Brieber, S., Neufang, S., Bruning, N., Kamp-Becker, I., Remschmidt, H., Herpertz-Dahlmann, B., et al. (2007). Structural brain abnormalities in adolescents with autism spectrum disorder and patients with attention deficit/hyperactivity disorder. Journal of Child Psychology and Psychiatry, 48, 1251–1258.PubMedCrossRef Brieber, S., Neufang, S., Bruning, N., Kamp-Becker, I., Remschmidt, H., Herpertz-Dahlmann, B., et al. (2007). Structural brain abnormalities in adolescents with autism spectrum disorder and patients with attention deficit/hyperactivity disorder. Journal of Child Psychology and Psychiatry, 48, 1251–1258.PubMedCrossRef
go back to reference Brune, C. W., Kim, S.-J., Leventhal, B. L., Lord, C., & Cook, E. H. (2006). 5-HTTLRP genotype-specific phenotype in children and adolescents with autism. American Journal of Psychiatry, 163, 2148–2156.PubMedCrossRef Brune, C. W., Kim, S.-J., Leventhal, B. L., Lord, C., & Cook, E. H. (2006). 5-HTTLRP genotype-specific phenotype in children and adolescents with autism. American Journal of Psychiatry, 163, 2148–2156.PubMedCrossRef
go back to reference Cardon, L. R., & Palmer, L. J. (2003). Population stratification and spurious allelic association. Lancet, 361, 598–604.PubMedCrossRef Cardon, L. R., & Palmer, L. J. (2003). Population stratification and spurious allelic association. Lancet, 361, 598–604.PubMedCrossRef
go back to reference Chamberlain, B., Kasari, C., & Rotheram-Fuller, E. (2007). Involvement or isolation? The social networks of children with autism in regular classrooms. Journal of Autism and Developmental Disorders, 37, 230–242.PubMedCrossRef Chamberlain, B., Kasari, C., & Rotheram-Fuller, E. (2007). Involvement or isolation? The social networks of children with autism in regular classrooms. Journal of Autism and Developmental Disorders, 37, 230–242.PubMedCrossRef
go back to reference Coffey, B. J., Biederman, J., Smoller, J. W., Geller, D. A., Sarin, P., Schwartz, S., et al. (2000). Anxiety disorders and tic severity in juveniles with Tourette’s disorder. Journal of the American Academy of Child and Adolescent Psychiatry, 39, 562–568.PubMedCrossRef Coffey, B. J., Biederman, J., Smoller, J. W., Geller, D. A., Sarin, P., Schwartz, S., et al. (2000). Anxiety disorders and tic severity in juveniles with Tourette’s disorder. Journal of the American Academy of Child and Adolescent Psychiatry, 39, 562–568.PubMedCrossRef
go back to reference Cohen, J. (1988). Statistical power analysis for the behavioral sciences (2nd ed.). Mahwah, NJ: Lawrence Erlbaum. Cohen, J. (1988). Statistical power analysis for the behavioral sciences (2nd ed.). Mahwah, NJ: Lawrence Erlbaum.
go back to reference Cohen, I. L., Liu, X., Schultz, C., White, B. N., Jenkins, E. C., Brown, W. T., et al. (2003). Association of autism severity with a monoamine oxidase A functional polymorphism. Clinical Genetics, 64, 190–197.PubMedCrossRef Cohen, I. L., Liu, X., Schultz, C., White, B. N., Jenkins, E. C., Brown, W. T., et al. (2003). Association of autism severity with a monoamine oxidase A functional polymorphism. Clinical Genetics, 64, 190–197.PubMedCrossRef
go back to reference Comings, D. E., Wu, S., Chiu, C., Ring, R. H., Gade, R., Ahn, C., et al. (1996). Polygenetic inheritance of Tourette syndrome, stuttering, attention deficit hyperactivity, conduct, and oppositional defiant disorder. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 67B, 264–288. Comings, D. E., Wu, S., Chiu, C., Ring, R. H., Gade, R., Ahn, C., et al. (1996). Polygenetic inheritance of Tourette syndrome, stuttering, attention deficit hyperactivity, conduct, and oppositional defiant disorder. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 67B, 264–288.
go back to reference Drtilkova, I., Sery, O., Theiner, P., Uhrova, A., Zackova, M., Balastikova, B., et al. (2008). Clinical and molecular-genetic markers of ADHD in children. Neuroedocrinology Letters, 29, 320–327. Drtilkova, I., Sery, O., Theiner, P., Uhrova, A., Zackova, M., Balastikova, B., et al. (2008). Clinical and molecular-genetic markers of ADHD in children. Neuroedocrinology Letters, 29, 320–327.
go back to reference Enoch, M.-A., White, K. V., Waheed, J., & Goldman, D. (2008). Neurological and genetic distinctions between pure and comorbid anxiety disorders. Depress Anxiety, 25, 383–392.PubMedCrossRef Enoch, M.-A., White, K. V., Waheed, J., & Goldman, D. (2008). Neurological and genetic distinctions between pure and comorbid anxiety disorders. Depress Anxiety, 25, 383–392.PubMedCrossRef
go back to reference Gadow, K. D., & DeVincent, C. J. (2005). Clinical significance of tics and attention-deficit hyperactivity disorder (ADHD) in children with pervasive developmental disorder. Journal of Child Neurology, 20, 481–488.PubMed Gadow, K. D., & DeVincent, C. J. (2005). Clinical significance of tics and attention-deficit hyperactivity disorder (ADHD) in children with pervasive developmental disorder. Journal of Child Neurology, 20, 481–488.PubMed
go back to reference Gadow, K. D., DeVincent, C. J., & Pomeroy, J. (2006). ADHD symptom subtypes in children with pervasive developmental disorder. Journal of Autism and Developmental Disorders, 36, 271–283.PubMedCrossRef Gadow, K. D., DeVincent, C. J., & Pomeroy, J. (2006). ADHD symptom subtypes in children with pervasive developmental disorder. Journal of Autism and Developmental Disorders, 36, 271–283.PubMedCrossRef
go back to reference Gadow, K. D., DeVincent, C. J., Pomeroy, J., & Azizian, A. (2005). Comparison of DSM-IV symptoms in elementary school-aged children with PDD versus clinic and community samples. Autism, 9, 392–415.PubMedCrossRef Gadow, K. D., DeVincent, C. J., Pomeroy, J., & Azizian, A. (2005). Comparison of DSM-IV symptoms in elementary school-aged children with PDD versus clinic and community samples. Autism, 9, 392–415.PubMedCrossRef
go back to reference Gadow, K. D., DeVincent, C., & Schneider, J. (2008a). Predictors of psychiatric symptoms in children with an autism spectrum disorder. Journal of Autism and Developmental Disorders, 38, 1710–1720.PubMedCrossRef Gadow, K. D., DeVincent, C., & Schneider, J. (2008a). Predictors of psychiatric symptoms in children with an autism spectrum disorder. Journal of Autism and Developmental Disorders, 38, 1710–1720.PubMedCrossRef
go back to reference Gadow, K. D., Roohi, J., DeVincent, C. J., & Hatchwell, E. (2008b). Association of ADHD, tics, and anxiety with dopamine transporter (DAT1) genotype in autism spectrum disorder. Journal of Child Psychology and Psychiatry, 49, 1331–1338.PubMedCrossRef Gadow, K. D., Roohi, J., DeVincent, C. J., & Hatchwell, E. (2008b). Association of ADHD, tics, and anxiety with dopamine transporter (DAT1) genotype in autism spectrum disorder. Journal of Child Psychology and Psychiatry, 49, 1331–1338.PubMedCrossRef
go back to reference Gadow, K. D., Schwartz, J., DeVincent, C., Strong, G., & Cuva, S. (2008c). Clinical utility of autism spectrum disorder scoring algorithms for the child symptom inventory. Journal of Autism and Developmental Disorders, 38, 419–427.PubMedCrossRef Gadow, K. D., Schwartz, J., DeVincent, C., Strong, G., & Cuva, S. (2008c). Clinical utility of autism spectrum disorder scoring algorithms for the child symptom inventory. Journal of Autism and Developmental Disorders, 38, 419–427.PubMedCrossRef
go back to reference Gadow, K. D., & Sprafkin, J. (1986). Stony Brook child psychiatric checklist-3. Stony Brook: Department of Psychiatry, State University of New York. Gadow, K. D., & Sprafkin, J. (1986). Stony Brook child psychiatric checklist-3. Stony Brook: Department of Psychiatry, State University of New York.
go back to reference Gadow, K. D., & Sprafkin, J. (2002). Child symptom inventory-4 screening and norms manual. Stony Brook, NY: Checkmate Plus. Gadow, K. D., & Sprafkin, J. (2002). Child symptom inventory-4 screening and norms manual. Stony Brook, NY: Checkmate Plus.
go back to reference Gadow K. D., Sprafkin J. (2008). The symptom inventories: An annotated bibliography [on-line]. Checkmate plus: Stony Brook, NY. Available: www.checkmateplus.com. Gadow K. D., Sprafkin J. (2008). The symptom inventories: An annotated bibliography [on-line]. Checkmate plus: Stony Brook, NY. Available: www.​checkmateplus.​com.
go back to reference Gillott, A., Furniss, F., & Walter, A. (2001). Anxiety on high-functioning children with autism. Autism, 5, 277–286.PubMedCrossRef Gillott, A., Furniss, F., & Walter, A. (2001). Anxiety on high-functioning children with autism. Autism, 5, 277–286.PubMedCrossRef
go back to reference Goldstein, S., & Schwebach, A. J. (2004). The comorbidity of pervasive developmental disorder and attention deficit hyperactivity disorder: Results of a retrospective chart review. Journal of Autism and Developmental Disorders, 34, 329–339.PubMedCrossRef Goldstein, S., & Schwebach, A. J. (2004). The comorbidity of pervasive developmental disorder and attention deficit hyperactivity disorder: Results of a retrospective chart review. Journal of Autism and Developmental Disorders, 34, 329–339.PubMedCrossRef
go back to reference Grados, M. A., & Mathews, C. A. (2008). Latent class analysis of gilles de la tourette syndrome using comorbidities: Clinical and genetic implications. Biological Psychiatry, 64, 119–225.CrossRef Grados, M. A., & Mathews, C. A. (2008). Latent class analysis of gilles de la tourette syndrome using comorbidities: Clinical and genetic implications. Biological Psychiatry, 64, 119–225.CrossRef
go back to reference Grice, D. E., & Buxbaum, J. D. (2006). The genetic architecture of autism and related disorders. Clinical Neuroscience Research, 6, 161–168.CrossRef Grice, D. E., & Buxbaum, J. D. (2006). The genetic architecture of autism and related disorders. Clinical Neuroscience Research, 6, 161–168.CrossRef
go back to reference Hall, D., Dhilla, A., Charalambous, A., Gogos, J. A., & Karayiorgou, M. (2003). Sequence variants of the brain-derived neurotropic factor (BDNF) gene are strongly associated with obsessive-compulsive disorder. American Journal of Human Genetics, 73, 370–376.PubMedCrossRef Hall, D., Dhilla, A., Charalambous, A., Gogos, J. A., & Karayiorgou, M. (2003). Sequence variants of the brain-derived neurotropic factor (BDNF) gene are strongly associated with obsessive-compulsive disorder. American Journal of Human Genetics, 73, 370–376.PubMedCrossRef
go back to reference Happé, F., & Ronald, A. (2008). The “fractionable autism triad”: A review of evidence from behavioural, genetic, cognitive and neural research. Neuropsychology Review. doi: 10.1007/s11065-008-9076-8. Happé, F., & Ronald, A. (2008). The “fractionable autism triad”: A review of evidence from behavioural, genetic, cognitive and neural research. Neuropsychology Review. doi: 10.​1007/​s11065-008-9076-8.
go back to reference Happé, F., Ronald, A., & Plomin, R. (2006). Time to give up on a single explanation for autism. Nature Neuroscience, 9, 1218–1220.PubMedCrossRef Happé, F., Ronald, A., & Plomin, R. (2006). Time to give up on a single explanation for autism. Nature Neuroscience, 9, 1218–1220.PubMedCrossRef
go back to reference Hettema, J. M. (2008). What is the genetic relationship between anxiety and depression? American Journal of Medical Genetics: Part C Seminars in Medical Genetics, 148C, 140–146.CrossRef Hettema, J. M. (2008). What is the genetic relationship between anxiety and depression? American Journal of Medical Genetics: Part C Seminars in Medical Genetics, 148C, 140–146.CrossRef
go back to reference Hettema, J. M., An, S.-S., Bukszar, J., ven den Oord, E. J. C. G., Neale, M. C., Kendler, K. S., et al. (2008). Catechol-O-methyltransferase contributes to genetic susceptibility shared among anxiety spectrum phenotypes. Biological Psychiatry, 64, 302–310.PubMedCrossRef Hettema, J. M., An, S.-S., Bukszar, J., ven den Oord, E. J. C. G., Neale, M. C., Kendler, K. S., et al. (2008). Catechol-O-methyltransferase contributes to genetic susceptibility shared among anxiety spectrum phenotypes. Biological Psychiatry, 64, 302–310.PubMedCrossRef
go back to reference Hettema, J. M., Neale, M. C., & Kendler, K. S. (2001). A review and meta-analysis of the genetic epidemiology of anxiety disorders. American Journal of Psychiatry, 158, 1568–1578.PubMedCrossRef Hettema, J. M., Neale, M. C., & Kendler, K. S. (2001). A review and meta-analysis of the genetic epidemiology of anxiety disorders. American Journal of Psychiatry, 158, 1568–1578.PubMedCrossRef
go back to reference Hirshfeld, D. R., Micco, J. A., Simoes, N. A., & Henin, A. (2008). High risk studies and developmental antecedents of anxiety disorders. American Journal of Medical Genetics Part C: Seminars in Medical Genetics, 148C, 99–117.CrossRef Hirshfeld, D. R., Micco, J. A., Simoes, N. A., & Henin, A. (2008). High risk studies and developmental antecedents of anxiety disorders. American Journal of Medical Genetics Part C: Seminars in Medical Genetics, 148C, 99–117.CrossRef
go back to reference Hollingshead, A. B. (1975). Four factor index of social status. New Haven, CT: Department of Sociology, Yale University. Hollingshead, A. B. (1975). Four factor index of social status. New Haven, CT: Department of Sociology, Yale University.
go back to reference Hovatta, I., & Barlow, C. (2008). Molecular genetics of anxiety in mice and men. Annals of Medicine, 40, 92–109.PubMedCrossRef Hovatta, I., & Barlow, C. (2008). Molecular genetics of anxiety in mice and men. Annals of Medicine, 40, 92–109.PubMedCrossRef
go back to reference Huang, C. H., & Santangelo, S. L. (2008). Autism and serotonin transporter gene polymorphisms: A systematic review and meta-analysis. American Journal of Medical Genetics Part B Neuropsychiatric Genetics, 147B, 903–913.CrossRef Huang, C. H., & Santangelo, S. L. (2008). Autism and serotonin transporter gene polymorphisms: A systematic review and meta-analysis. American Journal of Medical Genetics Part B Neuropsychiatric Genetics, 147B, 903–913.CrossRef
go back to reference Hünnerkopf, R., Strobel, A., Gutknecht, L., Brocke, B., & Lesch, K. P. (2007). Interaction between BDNF Val66Met and dopamine transporter gene variation influences anxiety-related traits. Neuropsychopharmacology, 32, 2552–2560.PubMedCrossRef Hünnerkopf, R., Strobel, A., Gutknecht, L., Brocke, B., & Lesch, K. P. (2007). Interaction between BDNF Val66Met and dopamine transporter gene variation influences anxiety-related traits. Neuropsychopharmacology, 32, 2552–2560.PubMedCrossRef
go back to reference Jiang, X., Xu, K., Hoberman, J., et al. (2005). BDNF variation in mood disorders: A novel functional promoter polymorphism and Val66Met are associated with anxiety but have opposing effects. Neuropsychopharmacology, 30, 1353–1361.PubMed Jiang, X., Xu, K., Hoberman, J., et al. (2005). BDNF variation in mood disorders: A novel functional promoter polymorphism and Val66Met are associated with anxiety but have opposing effects. Neuropsychopharmacology, 30, 1353–1361.PubMed
go back to reference Kanner, L. (1943). Autistic disturbances of affective contact. Nervous Child, 2, 217–250. Kanner, L. (1943). Autistic disturbances of affective contact. Nervous Child, 2, 217–250.
go back to reference Karayiorgou, M., Altemus, M., Galke, B. L., et al. (1997). Genotype determining low catechol-O-methyltransferase activity as a risk factor for obsessive-compulsive disorder. Proceedings of the National Academy of Sciences USA, 94, 4572–4575.CrossRef Karayiorgou, M., Altemus, M., Galke, B. L., et al. (1997). Genotype determining low catechol-O-methyltransferase activity as a risk factor for obsessive-compulsive disorder. Proceedings of the National Academy of Sciences USA, 94, 4572–4575.CrossRef
go back to reference Lecavalier, L., Gadow, K. D., DeVincent, C. J., & Edwards, M. C. (2009a). Validation of DSM-IV model of psychiatric syndromes in children with autism spectrum disorder. Journal of Autism and Developmental Disorders, 39, 278–289.PubMedCrossRef Lecavalier, L., Gadow, K. D., DeVincent, C. J., & Edwards, M. C. (2009a). Validation of DSM-IV model of psychiatric syndromes in children with autism spectrum disorder. Journal of Autism and Developmental Disorders, 39, 278–289.PubMedCrossRef
go back to reference Lecavalier, L., Gadow, K. D., DeVincent, C. J., Houts, C., & Edwards, M. C. (2009). Deconstructing the PDD clinical phenotype: Internal validity of the DSM-IV. Journal of Child Psychology and Psychiatry (in press). Lecavalier, L., Gadow, K. D., DeVincent, C. J., Houts, C., & Edwards, M. C. (2009). Deconstructing the PDD clinical phenotype: Internal validity of the DSM-IV. Journal of Child Psychology and Psychiatry (in press).
go back to reference Lee, J., Laurin, N., Crosbie, J., et al. (2007). Association study of the brain-derived neurotropic factor (BDNF) gene in attention deficit hyperactivity disorder. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 114B, 976–981.CrossRef Lee, J., Laurin, N., Crosbie, J., et al. (2007). Association study of the brain-derived neurotropic factor (BDNF) gene in attention deficit hyperactivity disorder. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 114B, 976–981.CrossRef
go back to reference Lin, P.-I., Vance, J. M., Pericak-Vance, M. A., & Martin, E. R. (2007). No gene is an island: The flip-flop phenomenon. American Journal of Human Genetics, 80, 531–538.PubMedCrossRef Lin, P.-I., Vance, J. M., Pericak-Vance, M. A., & Martin, E. R. (2007). No gene is an island: The flip-flop phenomenon. American Journal of Human Genetics, 80, 531–538.PubMedCrossRef
go back to reference Lord, C., Risi, S., Lambrecht, L., Cook, E. H., Jr, Leventhal, B. L., DiLavore, P. C., et al. (2000). The autism diagnostic observation schedule-generic: A standard measure of social and communication deficits associated with the spectrum of autism. Journal of Autism and Developmental Disorders, 30, 205–223.PubMedCrossRef Lord, C., Risi, S., Lambrecht, L., Cook, E. H., Jr, Leventhal, B. L., DiLavore, P. C., et al. (2000). The autism diagnostic observation schedule-generic: A standard measure of social and communication deficits associated with the spectrum of autism. Journal of Autism and Developmental Disorders, 30, 205–223.PubMedCrossRef
go back to reference Meyer-Lindenberg, A., & Weinberger, D. R. (2006). Intermediate phenotypes and genetic mechanisms of psychiatric disorders. Nature Reviews Neuroscience, 7, 818–827.PubMedCrossRef Meyer-Lindenberg, A., & Weinberger, D. R. (2006). Intermediate phenotypes and genetic mechanisms of psychiatric disorders. Nature Reviews Neuroscience, 7, 818–827.PubMedCrossRef
go back to reference Nishimura, K., et al. (2007). Genetic analyses of the brain-derived neurotropic factor (BDNF) gene in autism. Biochemical and Biophysical Research Communications, 356, 200–206.PubMedCrossRef Nishimura, K., et al. (2007). Genetic analyses of the brain-derived neurotropic factor (BDNF) gene in autism. Biochemical and Biophysical Research Communications, 356, 200–206.PubMedCrossRef
go back to reference Perneger, T. V. (1998). What’s wrong with Bonferroni adjustments. British Medical Journal, 316, 1236–1238.PubMed Perneger, T. V. (1998). What’s wrong with Bonferroni adjustments. British Medical Journal, 316, 1236–1238.PubMed
go back to reference Ronald, A., Happé, F., & Plomin, R. (2008). A twin study investigating the genetic and environmental aetiologies of parent, teacher and child ratings of autistic-like traits and their overlap. European Child and Adolescent Psychiatry. doi: 10.1007/s00787-008-0689-5. Ronald, A., Happé, F., & Plomin, R. (2008). A twin study investigating the genetic and environmental aetiologies of parent, teacher and child ratings of autistic-like traits and their overlap. European Child and Adolescent Psychiatry. doi: 10.​1007/​s00787-008-0689-5.
go back to reference Roohi, J., DeVincent, C. J., Hatchwell, E., & Gadow, K. D. (2009). Association of a monoamine oxidase-A gene promoter polymorphism with ADHD and anxiety in boys with autism spectrum disorder. Journal of Autism and Developmental Disorders, 39, 67–74.PubMedCrossRef Roohi, J., DeVincent, C. J., Hatchwell, E., & Gadow, K. D. (2009). Association of a monoamine oxidase-A gene promoter polymorphism with ADHD and anxiety in boys with autism spectrum disorder. Journal of Autism and Developmental Disorders, 39, 67–74.PubMedCrossRef
go back to reference Rothman, K. (1990). No adjustments are needed for multiple comparisons. Epidemiology, 1, 43–46.PubMed Rothman, K. (1990). No adjustments are needed for multiple comparisons. Epidemiology, 1, 43–46.PubMed
go back to reference Rowe, D. C., Stever, C., Gard, J. M. C., Cleveland, H. H., Sanders, M. L., Abramowitz, A., et al. (1998). The relation of the dopamine transporter gene (DAT1) to symptoms of internalizing disorders in children. Behavior Genetics, 28, 215–225.PubMedCrossRef Rowe, D. C., Stever, C., Gard, J. M. C., Cleveland, H. H., Sanders, M. L., Abramowitz, A., et al. (1998). The relation of the dopamine transporter gene (DAT1) to symptoms of internalizing disorders in children. Behavior Genetics, 28, 215–225.PubMedCrossRef
go back to reference Rutter, M., Couteur, A., & Lord, C. (2003). Autism diagnostic interview-revised. Los Angeles, CA: Western Psychological Services. Rutter, M., Couteur, A., & Lord, C. (2003). Autism diagnostic interview-revised. Los Angeles, CA: Western Psychological Services.
go back to reference Rzhetsky, A., Wajngurt, D., Park, N., & Zheng, T. (2007). Probing genetic overlap among complex human phenotypes. PNAS, 104, 11694–11699.PubMedCrossRef Rzhetsky, A., Wajngurt, D., Park, N., & Zheng, T. (2007). Probing genetic overlap among complex human phenotypes. PNAS, 104, 11694–11699.PubMedCrossRef
go back to reference Singer, H. S., Szymanski, S., Guiliano, J., Yokoi, F., Dogan, A. S., Brasic, J. R., et al. (2002). Elevated intrasynaptic dopamine release in Tourette syndrome measured by PET. American Journal of Psychiatry, 159, 1329–1336.PubMedCrossRef Singer, H. S., Szymanski, S., Guiliano, J., Yokoi, F., Dogan, A. S., Brasic, J. R., et al. (2002). Elevated intrasynaptic dopamine release in Tourette syndrome measured by PET. American Journal of Psychiatry, 159, 1329–1336.PubMedCrossRef
go back to reference Sinzig, J., Morsch, D., Bruning, N., Schmidt, M. H., & Lehmkuhl, G. (2008). Inhibition, flexibility, working memory and planning in autism spectrum disorders with and without comorbid ADHD-symptoms. Child and Adolescent Psychiatry and Mental Health, 2(1), 4.PubMedCrossRef Sinzig, J., Morsch, D., Bruning, N., Schmidt, M. H., & Lehmkuhl, G. (2008). Inhibition, flexibility, working memory and planning in autism spectrum disorders with and without comorbid ADHD-symptoms. Child and Adolescent Psychiatry and Mental Health, 2(1), 4.PubMedCrossRef
go back to reference Smalley, S. L., Kustanovich, V., Minassian, S. L., Stone, J. L., Ogdie, M. N., McGough, J. J., et al. (2002). Genetic linkage of attention-deficit/hyperactivity disorder on chromosome 16p13, in a region implicated in autism. American Journal of Human Genetics, 71, 959–963.PubMedCrossRef Smalley, S. L., Kustanovich, V., Minassian, S. L., Stone, J. L., Ogdie, M. N., McGough, J. J., et al. (2002). Genetic linkage of attention-deficit/hyperactivity disorder on chromosome 16p13, in a region implicated in autism. American Journal of Human Genetics, 71, 959–963.PubMedCrossRef
go back to reference Smalley, S. L., McCracken, J., & Tanguay, P. (1995). Autism, affective disorders, and social phobia. American Journal of Medical Genetics, 60, 19–26.PubMedCrossRef Smalley, S. L., McCracken, J., & Tanguay, P. (1995). Autism, affective disorders, and social phobia. American Journal of Medical Genetics, 60, 19–26.PubMedCrossRef
go back to reference Smoller, J. W., Gardner-Schuster, E., & Misiaszek, M. (2008). Genetics of anxiety: Would the genome recognize the DSM? Depression and Anxiety, 25, 368–377.PubMedCrossRef Smoller, J. W., Gardner-Schuster, E., & Misiaszek, M. (2008). Genetics of anxiety: Would the genome recognize the DSM? Depression and Anxiety, 25, 368–377.PubMedCrossRef
go back to reference Snow, A. V., Lecavalier, L., & Houts, C. (2009). Structure of the autism diagnostic interview-revised: Diagnostic and phenotypic implications. Journal of Child Psychology and Psychiatry, 50, 734–742.PubMedCrossRef Snow, A. V., Lecavalier, L., & Houts, C. (2009). Structure of the autism diagnostic interview-revised: Diagnostic and phenotypic implications. Journal of Child Psychology and Psychiatry, 50, 734–742.PubMedCrossRef
go back to reference Sukhodolsky, D. G., Scahill, L., Gadow, K. D., Eugene, A. L., Aman, M. G., McDougle, C. J., et al. (2008). Parent-rated anxiety symptoms in children with pervasive developmental disorders: Frequency and association with core autism symptoms and cognitive functioning. Journal of Abnormal Child Psychology, 36, 117–128.PubMedCrossRef Sukhodolsky, D. G., Scahill, L., Gadow, K. D., Eugene, A. L., Aman, M. G., McDougle, C. J., et al. (2008). Parent-rated anxiety symptoms in children with pervasive developmental disorders: Frequency and association with core autism symptoms and cognitive functioning. Journal of Abnormal Child Psychology, 36, 117–128.PubMedCrossRef
go back to reference Sverd, J. (2003). Psychiatric disorders in individuals with pervasive developmental disorder. Journal of Psychiatric Practice, 9, 111–127.PubMedCrossRef Sverd, J. (2003). Psychiatric disorders in individuals with pervasive developmental disorder. Journal of Psychiatric Practice, 9, 111–127.PubMedCrossRef
go back to reference Szatmari, P., Maziade, M., Zwaigenbaum, L., Merette, C., Roy, M.-A., Joober, R., et al. (2007). Informative phenotypes for genetic studies of psychiatric disorders. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 144B, 581–588.CrossRef Szatmari, P., Maziade, M., Zwaigenbaum, L., Merette, C., Roy, M.-A., Joober, R., et al. (2007). Informative phenotypes for genetic studies of psychiatric disorders. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 144B, 581–588.CrossRef
go back to reference Thapar, A., Langley, K., O’Donovan, M., & Owen, M. (2006). Refining the attention deficit hyperactivity disorder phenotype for molecular genetic studies. Molecular Psychiatry, 11, 714–720.PubMedCrossRef Thapar, A., Langley, K., O’Donovan, M., & Owen, M. (2006). Refining the attention deficit hyperactivity disorder phenotype for molecular genetic studies. Molecular Psychiatry, 11, 714–720.PubMedCrossRef
go back to reference Tordjman, S., Gutknecht, L., Carlier, M., Spitz, E., Antoine, C., Slama, F., et al. (2001). Role of the serotonin transporter gene in the behavioral expression of autism. Molecular Psychiatry, 6, 434–439.PubMedCrossRef Tordjman, S., Gutknecht, L., Carlier, M., Spitz, E., Antoine, C., Slama, F., et al. (2001). Role of the serotonin transporter gene in the behavioral expression of autism. Molecular Psychiatry, 6, 434–439.PubMedCrossRef
go back to reference Turri, M. G., Datta, S. R., DeFries, J., Henderson, N. D., & Flint, J. (2001). QTL analysis identifies multiple behavioral dimensions in etiological tests of anxiety in laboratory mice. Current Biology, 11, 725–734.PubMedCrossRef Turri, M. G., Datta, S. R., DeFries, J., Henderson, N. D., & Flint, J. (2001). QTL analysis identifies multiple behavioral dimensions in etiological tests of anxiety in laboratory mice. Current Biology, 11, 725–734.PubMedCrossRef
go back to reference Weisbrot, D. M., Gadow, K. D., DeVincent, C. J., & Pomeroy, J. (2005). The presentation of anxiety in children with pervasive developmental disorders. Journal of Child and Adolescent Psychopharmacology, 15, 477–496.PubMedCrossRef Weisbrot, D. M., Gadow, K. D., DeVincent, C. J., & Pomeroy, J. (2005). The presentation of anxiety in children with pervasive developmental disorders. Journal of Child and Adolescent Psychopharmacology, 15, 477–496.PubMedCrossRef
go back to reference Yang, M. S., & Gill, M. (2007). A review of gene linkage, association and expression studies in autism and an assessment of convergent evidence. International Journal of Developmental Neuroscience, 25, 69–85.PubMedCrossRef Yang, M. S., & Gill, M. (2007). A review of gene linkage, association and expression studies in autism and an assessment of convergent evidence. International Journal of Developmental Neuroscience, 25, 69–85.PubMedCrossRef
go back to reference Yonan, A. L., Palmer, A. A., & Gilliam, T. C. (2006). Hardy–Weinberg disequilibrium identified genotyping error of the serotonin transporter (SLC6A4) promoter polymorphism. Psychiatric Genetics, 16, 31–34.PubMedCrossRef Yonan, A. L., Palmer, A. A., & Gilliam, T. C. (2006). Hardy–Weinberg disequilibrium identified genotyping error of the serotonin transporter (SLC6A4) promoter polymorphism. Psychiatric Genetics, 16, 31–34.PubMedCrossRef
go back to reference Yoon, D. Y., Rippel, C. A., Kobets, A. J., Morris, C. M., Lee, J. E., Williams, P. N., et al. (2007). Dopaminergic polymorphisms in Tourette syndrome: Association with DAT gene (SLC6A3). American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 114B, 605–610.CrossRef Yoon, D. Y., Rippel, C. A., Kobets, A. J., Morris, C. M., Lee, J. E., Williams, P. N., et al. (2007). Dopaminergic polymorphisms in Tourette syndrome: Association with DAT gene (SLC6A3). American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 114B, 605–610.CrossRef
go back to reference Zhou, L., Myers, A. N., Vandersteen, J. G., Wang, L., & Wittwer, C. T. (2004). Closed-tube genotyping with unlabeled oligonucleotide probes and a saturating DNA dye. Clinical Chemistry, 50, 328–335. Epub 27 May 2004.CrossRef Zhou, L., Myers, A. N., Vandersteen, J. G., Wang, L., & Wittwer, C. T. (2004). Closed-tube genotyping with unlabeled oligonucleotide probes and a saturating DNA dye. Clinical Chemistry, 50, 328–335. Epub 27 May 2004.CrossRef
Metagegevens
Titel
Association of COMT (Val158Met) and BDNF (Val66Met) Gene Polymorphisms with Anxiety, ADHD and Tics in Children with Autism Spectrum Disorder
Auteurs
Kenneth D. Gadow
Jasmin Roohi
Carla J. DeVincent
Sarah Kirsch
Eli Hatchwell
Publicatiedatum
01-11-2009
Uitgeverij
Springer US
Gepubliceerd in
Journal of Autism and Developmental Disorders / Uitgave 11/2009
Print ISSN: 0162-3257
Elektronisch ISSN: 1573-3432
DOI
https://doi.org/10.1007/s10803-009-0794-4

Andere artikelen Uitgave 11/2009

Journal of Autism and Developmental Disorders 11/2009 Naar de uitgave