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Erschienen in: European Child & Adolescent Psychiatry 3/2015

01.03.2015 | Original Contribution

The role of DCDC2 genetic variants and low socioeconomic status in vulnerability to attention problems

verfasst von: Valentina Riva, Cecilia Marino, Roberto Giorda, Massimo Molteni, Maria Nobile

Erschienen in: European Child & Adolescent Psychiatry | Ausgabe 3/2015

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Abstract

Both genetic and socio-demographic factors influence the risk for behavioral problems in the developmental age. Genetic studies indicate that shared genetic factors partially contribute to behavioral and learning problems, in particular reading disabilities (RD). For the first time, we explore the conjoint role of DCDC2 gene, an identified RD candidate gene, and socioeconomic status (SES) upon behavioral phenotypes in a general population of Italian children. Two of the most replicated DCDC2 markers [i.e., regulatory element associated with dyslexia 1 (READ1), rs793862] were genotyped in 631 children (boys = 314; girls = 317) aged 11–14 years belonging to a community-based sample. Main and interactive effects were tested by MANOVA for each combination of DCDC2 genotypes and socioeconomic status upon emotional and behavioral phenotypes, assessed by Child Behavior Check-List/6–18. The two-way MANOVA (Bonferroni corrected p value = 0.01) revealed a trend toward significance of READ1(4) effect (F = 2.39; p = 0.016), a significant main effect of SES (F = 3.01; p = 0.003) and interactive effect of READ1(4) × SES (F = 2.65; p = 0.007) upon behavioral measures, showing higher attention problems scores among subjects ‘READ1(4+) and low SES’ compared to all other groups (p values range 0.00003–0.0004). ANOVAs stratified by gender confirmed main and interactive effects among girls, but not boys. Among children exposed to low socioeconomic level, READ1 genetic variant targets the worst outcome in children’s attention.
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Literatur
1.
Zurück zum Zitat van der Valk JC, van den Oord EJ, Verhulst FC, Boomsma DI (2003) Genetic and environmental contributions to stability and change in children’s internalizing and externalizing problems. J Am Acad Child Adolesc Psychiatry 42:1212–1220CrossRefPubMed van der Valk JC, van den Oord EJ, Verhulst FC, Boomsma DI (2003) Genetic and environmental contributions to stability and change in children’s internalizing and externalizing problems. J Am Acad Child Adolesc Psychiatry 42:1212–1220CrossRefPubMed
2.
Zurück zum Zitat Deater-Deckard K, Plomin R (1999) An adoption study of the etiology of teacher and parent reports of externalizing behavior problems in middle childhood. Child Dev 70:144–154CrossRefPubMed Deater-Deckard K, Plomin R (1999) An adoption study of the etiology of teacher and parent reports of externalizing behavior problems in middle childhood. Child Dev 70:144–154CrossRefPubMed
3.
Zurück zum Zitat Edelbrock C, Rende R, Plomin R, Thompson LA (1995) A twin study of competence and problem behavior in childhood and early adolescence. J Child Psychol Psychiatry 36:775–785CrossRefPubMed Edelbrock C, Rende R, Plomin R, Thompson LA (1995) A twin study of competence and problem behavior in childhood and early adolescence. J Child Psychol Psychiatry 36:775–785CrossRefPubMed
4.
Zurück zum Zitat Schmitz S, Saudino KJ, Plomin R, Fulker DW, DeFries JC (1996) Genetic and environmental influences on temperament in middle childhood: analyses of teacher and tester ratings. Child Dev 67:409–422CrossRefPubMed Schmitz S, Saudino KJ, Plomin R, Fulker DW, DeFries JC (1996) Genetic and environmental influences on temperament in middle childhood: analyses of teacher and tester ratings. Child Dev 67:409–422CrossRefPubMed
5.
Zurück zum Zitat van den Oord EJ, Boomsma DI, Verhulst FC (1994) A study of problem behaviors in 10- to 15-year-old biologically related and unrelated international adoptees. Behav Genet 24:193–205CrossRefPubMed van den Oord EJ, Boomsma DI, Verhulst FC (1994) A study of problem behaviors in 10- to 15-year-old biologically related and unrelated international adoptees. Behav Genet 24:193–205CrossRefPubMed
6.
Zurück zum Zitat Hinshaw SP (1992) Academic underachievement, attention deficits, and aggression: comorbidity and implications for intervention. J Consult Clin Psychol 60:893–903CrossRefPubMed Hinshaw SP (1992) Academic underachievement, attention deficits, and aggression: comorbidity and implications for intervention. J Consult Clin Psychol 60:893–903CrossRefPubMed
7.
Zurück zum Zitat Osman BB (2000) Learning disabilities and the risk of psychiatric disorders in children and adolescents. In: Greenhill LL (ed) Learning disabilities. Implications for psychiatric treatment. American Psychiatric Press Inc, Washington Osman BB (2000) Learning disabilities and the risk of psychiatric disorders in children and adolescents. In: Greenhill LL (ed) Learning disabilities. Implications for psychiatric treatment. American Psychiatric Press Inc, Washington
8.
Zurück zum Zitat Osman B (1995) No one to play with: social problems of LD and ADD children. Academic Therapy Publications, Novato Osman B (1995) No one to play with: social problems of LD and ADD children. Academic Therapy Publications, Novato
9.
Zurück zum Zitat Berger M, Yule W, Rutter M (1975) Attainment and adjustment in two geographical areas. II. The prevalence of specific reading retardation. Br J Psychiatry 126:510–519CrossRefPubMed Berger M, Yule W, Rutter M (1975) Attainment and adjustment in two geographical areas. II. The prevalence of specific reading retardation. Br J Psychiatry 126:510–519CrossRefPubMed
10.
Zurück zum Zitat Rutter M, Yule W (1970) Reading retardation and antisocial behavior—the nature of the association. In: Rutter M, Tizard J, Whitmore K (eds) Education, health and behavior. Longmans, London, pp 240–255 Rutter M, Yule W (1970) Reading retardation and antisocial behavior—the nature of the association. In: Rutter M, Tizard J, Whitmore K (eds) Education, health and behavior. Longmans, London, pp 240–255
11.
Zurück zum Zitat Svetaz MV, Ireland M, Blum R (2000) Adolescents with learning disabilities: risk and protective factors associated with emotional well-being: findings from the National Longitudinal Study of Adolescent Health. J Adolesc Health 27:340–348CrossRefPubMed Svetaz MV, Ireland M, Blum R (2000) Adolescents with learning disabilities: risk and protective factors associated with emotional well-being: findings from the National Longitudinal Study of Adolescent Health. J Adolesc Health 27:340–348CrossRefPubMed
12.
Zurück zum Zitat Halonen A, Aunola K, Ahonen T, Nurmi JE (2006) The role of learning to read in the development of problem behaviour: a cross-lagged longitudinal study. Br J Educ Psychol 76:517–534CrossRefPubMed Halonen A, Aunola K, Ahonen T, Nurmi JE (2006) The role of learning to read in the development of problem behaviour: a cross-lagged longitudinal study. Br J Educ Psychol 76:517–534CrossRefPubMed
13.
Zurück zum Zitat Maughan B, Carroll J (2006) Literacy and mental disorders. Curr Opin Psychiatry. 19:350–354CrossRefPubMed Maughan B, Carroll J (2006) Literacy and mental disorders. Curr Opin Psychiatry. 19:350–354CrossRefPubMed
14.
Zurück zum Zitat Doyle AE, Faraone SV, DuPre EP, Biederman J (2001) Separating attention deficit hyperactivity disorder and learning disabilities in girls: a familial risk analysis. Am J Psychiatry 158:1666–1672CrossRefPubMed Doyle AE, Faraone SV, DuPre EP, Biederman J (2001) Separating attention deficit hyperactivity disorder and learning disabilities in girls: a familial risk analysis. Am J Psychiatry 158:1666–1672CrossRefPubMed
15.
Zurück zum Zitat Willcutt EG, Betjemann RS, McGrath LM, Chhabildas NA, Olson RK, DeFries JC, Pennington BF (2010) Etiology and neuropsychology of comorbidity between RD and ADHD: the case for multiple-deficit models. Cortex. 46:1345–1361CrossRefPubMedCentralPubMed Willcutt EG, Betjemann RS, McGrath LM, Chhabildas NA, Olson RK, DeFries JC, Pennington BF (2010) Etiology and neuropsychology of comorbidity between RD and ADHD: the case for multiple-deficit models. Cortex. 46:1345–1361CrossRefPubMedCentralPubMed
16.
Zurück zum Zitat Gilger JW, Pennington BF, DeFries JC (1992) A twin study of the etiology of comorbidity: attention-deficit hyperactivity disorder and dyslexia. J Am Acad Child Adolesc Psychiatry 31:343–348CrossRefPubMed Gilger JW, Pennington BF, DeFries JC (1992) A twin study of the etiology of comorbidity: attention-deficit hyperactivity disorder and dyslexia. J Am Acad Child Adolesc Psychiatry 31:343–348CrossRefPubMed
17.
Zurück zum Zitat Light JG, Pennington BF, Gilger JW, DeFries JC (1995) Reading disability and hyperactivity disorder: evidence for a common genetic etiology. Dev Neuropsychol 11:323–335CrossRef Light JG, Pennington BF, Gilger JW, DeFries JC (1995) Reading disability and hyperactivity disorder: evidence for a common genetic etiology. Dev Neuropsychol 11:323–335CrossRef
18.
Zurück zum Zitat Willcutt EG, Pennington BF, Olson RK, DeFries JC (2007) Understanding comorbidity: a twin study of reading disability and attention-deficit/hyperactivity disorder. Am J Med Genet B Neuropsychiatr Genet. 144B:709–714CrossRefPubMed Willcutt EG, Pennington BF, Olson RK, DeFries JC (2007) Understanding comorbidity: a twin study of reading disability and attention-deficit/hyperactivity disorder. Am J Med Genet B Neuropsychiatr Genet. 144B:709–714CrossRefPubMed
19.
Zurück zum Zitat Grigorenko EL, Wood FB, Meyer MS, Pauls DL (2000) Chromosome 6p influences on different dyslexia-related cognitive processes: further confirmation. Am J Hum Genet 66:715–723CrossRefPubMedCentralPubMed Grigorenko EL, Wood FB, Meyer MS, Pauls DL (2000) Chromosome 6p influences on different dyslexia-related cognitive processes: further confirmation. Am J Hum Genet 66:715–723CrossRefPubMedCentralPubMed
20.
Zurück zum Zitat Petryshen TL, Kaplan BJ, Fu Liu M, de French NS, Tobias R, Hughes ML, Field LL (2001) Evidence for a susceptibility locus on chromosome 6q influencing phonological coding dyslexia. Am J Med Genet 105:507–517CrossRefPubMed Petryshen TL, Kaplan BJ, Fu Liu M, de French NS, Tobias R, Hughes ML, Field LL (2001) Evidence for a susceptibility locus on chromosome 6q influencing phonological coding dyslexia. Am J Med Genet 105:507–517CrossRefPubMed
21.
Zurück zum Zitat Cardon LR, Smith SD, Fulker DW, Kimberling WJ, Pennington BF, DeFries JC (1994) Quantitative trait locus for reading disability on chromosome 6. Science 266:276–279CrossRefPubMed Cardon LR, Smith SD, Fulker DW, Kimberling WJ, Pennington BF, DeFries JC (1994) Quantitative trait locus for reading disability on chromosome 6. Science 266:276–279CrossRefPubMed
22.
Zurück zum Zitat Kaplan DE, Gayan J, Ahn J, Won TW, Pauls D, Olson RK, DeFries JC, Wood F, Pennington BF, Page GP, Smith SD, Gruen JR (2002) Evidence for linkage and association with reading disability on 6p21.3-22. Am J Hum Genet 70:1287–1298CrossRefPubMedCentralPubMed Kaplan DE, Gayan J, Ahn J, Won TW, Pauls D, Olson RK, DeFries JC, Wood F, Pennington BF, Page GP, Smith SD, Gruen JR (2002) Evidence for linkage and association with reading disability on 6p21.3-22. Am J Hum Genet 70:1287–1298CrossRefPubMedCentralPubMed
23.
Zurück zum Zitat Deffenbacher KE, Kenyon JB, Hoover DM, Olson RK, Pennington BF, DeFries JC, Smith SD (2004) Refinement of the 6p21.3 quantitative trait locus influencing dyslexia: linkage and association analyses. Hum Genet 115:128–138CrossRefPubMed Deffenbacher KE, Kenyon JB, Hoover DM, Olson RK, Pennington BF, DeFries JC, Smith SD (2004) Refinement of the 6p21.3 quantitative trait locus influencing dyslexia: linkage and association analyses. Hum Genet 115:128–138CrossRefPubMed
24.
Zurück zum Zitat Francks C, Paracchini S, Smith SD, Richardson AJ, Scerri TS, Cardon LR, Marlow AJ, MacPhie IL, Walter J, Pennington BF, Fisher SE, Olson RK, DeFries JC, Stein JF, Monaco AP (2004) A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States. Am J Hum Genet 75:1046–1058CrossRefPubMedCentralPubMed Francks C, Paracchini S, Smith SD, Richardson AJ, Scerri TS, Cardon LR, Marlow AJ, MacPhie IL, Walter J, Pennington BF, Fisher SE, Olson RK, DeFries JC, Stein JF, Monaco AP (2004) A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States. Am J Hum Genet 75:1046–1058CrossRefPubMedCentralPubMed
25.
Zurück zum Zitat Willcutt EG, Pennington BF, Smith SD, Cardon LR, Gayan J, Knopik VS, Olson RK, DeFries JC (2002) Quantitative trait locus for reading disability on chromosome 6p is pleiotropic for attention-deficit/hyperactivity disorder. Am J Med Genet 114:260–268CrossRefPubMed Willcutt EG, Pennington BF, Smith SD, Cardon LR, Gayan J, Knopik VS, Olson RK, DeFries JC (2002) Quantitative trait locus for reading disability on chromosome 6p is pleiotropic for attention-deficit/hyperactivity disorder. Am J Med Genet 114:260–268CrossRefPubMed
26.
Zurück zum Zitat Brkanac Z, Chapman NH, Matsushita MM, Chun L, Nielsen K, Cochrane E, Berninger VW, Wijsman EM, Raskind WH (2007) Evaluation of candidate genes for DYX1 and DYX2 in families with dyslexia. Am J Med Genet B Neuropsychiatr Genet. 144B:556–560CrossRefPubMed Brkanac Z, Chapman NH, Matsushita MM, Chun L, Nielsen K, Cochrane E, Berninger VW, Wijsman EM, Raskind WH (2007) Evaluation of candidate genes for DYX1 and DYX2 in families with dyslexia. Am J Med Genet B Neuropsychiatr Genet. 144B:556–560CrossRefPubMed
27.
Zurück zum Zitat Meng H, Smith SD, Hager K, Held M, Liu J, Olson RK, Pennington BF, DeFries JC, Gelernter J, O’Reilly-Pol T, Somlo S, Skudlarski P, Shaywitz SE, Shaywitz BA, Marchione K, Wang Y, Paramasivam M, LoTurco JJ, Page GP, Gruen JR (2005) DCDC2 is associated with reading disability and modulates neuronal development in the brain. Proc Natl Acad Sci USA 102:17053–17058CrossRefPubMedCentralPubMed Meng H, Smith SD, Hager K, Held M, Liu J, Olson RK, Pennington BF, DeFries JC, Gelernter J, O’Reilly-Pol T, Somlo S, Skudlarski P, Shaywitz SE, Shaywitz BA, Marchione K, Wang Y, Paramasivam M, LoTurco JJ, Page GP, Gruen JR (2005) DCDC2 is associated with reading disability and modulates neuronal development in the brain. Proc Natl Acad Sci USA 102:17053–17058CrossRefPubMedCentralPubMed
28.
Zurück zum Zitat Schumacher J, Anthoni H, Dahdouh F, Konig IR, Hillmer AM, Kluck N, Manthey M, Plume E, Warnke A, Remschmidt H, Hulsmann J, Cichon S, Lindgren CM, Propping P, Zucchelli M, Ziegler A, Peyrard-Janvid M, Schulte-Korne G, Nothen MM, Kere J (2006) Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia. Am J Hum Genet 78:52–62CrossRefPubMedCentralPubMed Schumacher J, Anthoni H, Dahdouh F, Konig IR, Hillmer AM, Kluck N, Manthey M, Plume E, Warnke A, Remschmidt H, Hulsmann J, Cichon S, Lindgren CM, Propping P, Zucchelli M, Ziegler A, Peyrard-Janvid M, Schulte-Korne G, Nothen MM, Kere J (2006) Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia. Am J Hum Genet 78:52–62CrossRefPubMedCentralPubMed
29.
Zurück zum Zitat Powers NR, Eicher JD, Butter F, Kong Y, Miller LL, Ring SM, Mann M, Gruen JR (2013) Alleles of a polymorphic ETV6 binding site in DCDC2 confer risk of reading and language impairment. Am J Hum Genet 93:19–28CrossRefPubMedCentralPubMed Powers NR, Eicher JD, Butter F, Kong Y, Miller LL, Ring SM, Mann M, Gruen JR (2013) Alleles of a polymorphic ETV6 binding site in DCDC2 confer risk of reading and language impairment. Am J Hum Genet 93:19–28CrossRefPubMedCentralPubMed
30.
Zurück zum Zitat Wilcke A, Weissfuss J, Kirsten H, Wolfram G, Boltze J, Ahnert P (2009) The role of gene DCDC2 in German dyslexics. Ann Dyslexia. 59:1–11CrossRefPubMed Wilcke A, Weissfuss J, Kirsten H, Wolfram G, Boltze J, Ahnert P (2009) The role of gene DCDC2 in German dyslexics. Ann Dyslexia. 59:1–11CrossRefPubMed
31.
Zurück zum Zitat Marino C, Meng H, Mascheretti S, Rusconi M, Cope N, Giorda R, Molteni M, Gruen JR (2012) DCDC2 genetic variants and susceptibility to developmental dyslexia. Psychiatr Genet 22:25–30CrossRefPubMedCentralPubMed Marino C, Meng H, Mascheretti S, Rusconi M, Cope N, Giorda R, Molteni M, Gruen JR (2012) DCDC2 genetic variants and susceptibility to developmental dyslexia. Psychiatr Genet 22:25–30CrossRefPubMedCentralPubMed
32.
Zurück zum Zitat Newbury DF, Paracchini S, Scerri TS, Winchester L, Addis L, Richardson AJ, Walter J, Stein JF, Talcott JB, Monaco AP (2011) Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects. Behav Genet 41:90–104CrossRefPubMedCentralPubMed Newbury DF, Paracchini S, Scerri TS, Winchester L, Addis L, Richardson AJ, Walter J, Stein JF, Talcott JB, Monaco AP (2011) Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects. Behav Genet 41:90–104CrossRefPubMedCentralPubMed
33.
Zurück zum Zitat Cope N, Eicher JD, Meng H, Gibson CJ, Hager K, Lacadie C, Fulbright RK, Constable RT, Page GP, Gruen JR (2012) Variants in the DYX2 locus are associated with altered brain activation in reading-related brain regions in subjects with reading disability. Neuroimage. 63:148–156CrossRefPubMedCentralPubMed Cope N, Eicher JD, Meng H, Gibson CJ, Hager K, Lacadie C, Fulbright RK, Constable RT, Page GP, Gruen JR (2012) Variants in the DYX2 locus are associated with altered brain activation in reading-related brain regions in subjects with reading disability. Neuroimage. 63:148–156CrossRefPubMedCentralPubMed
34.
Zurück zum Zitat Harold D, Paracchini S, Scerri T, Dennis M, Cope N, Hill G, Moskvina V, Walter J, Richardson AJ, Owen MJ, Stein JF, Green ED, O’Donovan MC, Williams J, Monaco AP (2006) Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia. Mol Psychiatry. 11:1085–1091 (1061)CrossRefPubMed Harold D, Paracchini S, Scerri T, Dennis M, Cope N, Hill G, Moskvina V, Walter J, Richardson AJ, Owen MJ, Stein JF, Green ED, O’Donovan MC, Williams J, Monaco AP (2006) Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia. Mol Psychiatry. 11:1085–1091 (1061)CrossRefPubMed
35.
Zurück zum Zitat Zhong R, Yang B, Tang H, Zou L, Song R, Zhu LQ, Miao X (2013) Meta-analysis of the association between DCDC2 polymorphisms and risk of dyslexia. Mol Neurobiol 47:435–442CrossRefPubMed Zhong R, Yang B, Tang H, Zou L, Song R, Zhu LQ, Miao X (2013) Meta-analysis of the association between DCDC2 polymorphisms and risk of dyslexia. Mol Neurobiol 47:435–442CrossRefPubMed
36.
Zurück zum Zitat Ludwig KU, Roeske D, Schumacher J, Schulte-Korne G, Konig IR, Warnke A, Plume E, Ziegler A, Remschmidt H, Muller-Myhsok B, Nothen MM, Hoffmann P (2008) Investigation of interaction between DCDC2 and KIAA0319 in a large German dyslexia sample. J Neural Transm. 115:1587–1589CrossRefPubMed Ludwig KU, Roeske D, Schumacher J, Schulte-Korne G, Konig IR, Warnke A, Plume E, Ziegler A, Remschmidt H, Muller-Myhsok B, Nothen MM, Hoffmann P (2008) Investigation of interaction between DCDC2 and KIAA0319 in a large German dyslexia sample. J Neural Transm. 115:1587–1589CrossRefPubMed
37.
Zurück zum Zitat Paracchini S, Ang QW, Stanley FJ, Monaco AP, Pennell CE, Whitehouse AJ (2011) Analysis of dyslexia candidate genes in the Raine cohort representing the general Australian population. Genes Brain Behav. 10:158–165CrossRefPubMedCentralPubMed Paracchini S, Ang QW, Stanley FJ, Monaco AP, Pennell CE, Whitehouse AJ (2011) Analysis of dyslexia candidate genes in the Raine cohort representing the general Australian population. Genes Brain Behav. 10:158–165CrossRefPubMedCentralPubMed
38.
Zurück zum Zitat Becker J, Czamara D, Scerri TS, Ramus F, Csepe V, Talcott JB, Stein J, Morris A, Ludwig KU, Hoffmann P, Honbolygo F, Toth D, Fauchereau F, Bogliotti C, Iannuzzi S, Chaix Y, Valdois S, Billard C, George F, Soares-Boucaud I, Gerard CL, van der Mark S, Schulz E, Vaessen A, Maurer U, Lohvansuu K, Lyytinen H, Zucchelli M, Brandeis D, Blomert L, Leppanen PH, Bruder J, Monaco AP, Muller-Myhsok B, Kere J, Landerl K, Nothen MM, Schulte-Korne G, Paracchini S, Peyrard-Janvid M, Schumacher J (2014) Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort. Eur J Hum Genet 22:675–680CrossRefPubMed Becker J, Czamara D, Scerri TS, Ramus F, Csepe V, Talcott JB, Stein J, Morris A, Ludwig KU, Hoffmann P, Honbolygo F, Toth D, Fauchereau F, Bogliotti C, Iannuzzi S, Chaix Y, Valdois S, Billard C, George F, Soares-Boucaud I, Gerard CL, van der Mark S, Schulz E, Vaessen A, Maurer U, Lohvansuu K, Lyytinen H, Zucchelli M, Brandeis D, Blomert L, Leppanen PH, Bruder J, Monaco AP, Muller-Myhsok B, Kere J, Landerl K, Nothen MM, Schulte-Korne G, Paracchini S, Peyrard-Janvid M, Schumacher J (2014) Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort. Eur J Hum Genet 22:675–680CrossRefPubMed
39.
Zurück zum Zitat Couto JM, Gomez L, Wigg K, Ickowicz A, Pathare T, Malone M, Kennedy JL, Schachar R, Barr CL (2009) Association of attention-deficit/hyperactivity disorder with a candidate region for reading disabilities on chromosome 6p. Biol Psychiatry 66:368–375CrossRefPubMed Couto JM, Gomez L, Wigg K, Ickowicz A, Pathare T, Malone M, Kennedy JL, Schachar R, Barr CL (2009) Association of attention-deficit/hyperactivity disorder with a candidate region for reading disabilities on chromosome 6p. Biol Psychiatry 66:368–375CrossRefPubMed
40.
Zurück zum Zitat Burbridge TJ, Wang Y, Volz AJ, Peschansky VJ, Lisann L, Galaburda AM, Lo Turco JJ, Rosen GD (2008) Postnatal analysis of the effect of embryonic knockdown and overexpression of candidate dyslexia susceptibility gene homolog DCDC2 in the rat. Neuroscience 152:723–733CrossRefPubMedCentralPubMed Burbridge TJ, Wang Y, Volz AJ, Peschansky VJ, Lisann L, Galaburda AM, Lo Turco JJ, Rosen GD (2008) Postnatal analysis of the effect of embryonic knockdown and overexpression of candidate dyslexia susceptibility gene homolog DCDC2 in the rat. Neuroscience 152:723–733CrossRefPubMedCentralPubMed
41.
Zurück zum Zitat Meng H, Powers NR, Tang L, Cope NA, Zhang PX, Fuleihan R, Gibson C, Page GP, Gruen JR (2011) A dyslexia-associated variant in DCDC2 changes gene expression. Behav Genet 41:58–66CrossRefPubMedCentralPubMed Meng H, Powers NR, Tang L, Cope NA, Zhang PX, Fuleihan R, Gibson C, Page GP, Gruen JR (2011) A dyslexia-associated variant in DCDC2 changes gene expression. Behav Genet 41:58–66CrossRefPubMedCentralPubMed
42.
Zurück zum Zitat DuBois DL, Felner RD, Meares H, Krier M (1994) Prospective investigation of the effects of socioeconomic disadvantage, life stress, and social support on early adolescent adjustment. J Abnorm Psychol 103:511–522CrossRefPubMed DuBois DL, Felner RD, Meares H, Krier M (1994) Prospective investigation of the effects of socioeconomic disadvantage, life stress, and social support on early adolescent adjustment. J Abnorm Psychol 103:511–522CrossRefPubMed
43.
Zurück zum Zitat Lorant V, Deliege D, Eaton W, Robert A, Philippot P, Ansseau M (2003) Socioeconomic inequalities in depression: a meta-analysis. Am J Epidemiol 157:98–112CrossRefPubMed Lorant V, Deliege D, Eaton W, Robert A, Philippot P, Ansseau M (2003) Socioeconomic inequalities in depression: a meta-analysis. Am J Epidemiol 157:98–112CrossRefPubMed
44.
Zurück zum Zitat van Oort FV, van der Ende J, Wadsworth ME, Verhulst FC, Achenbach TM (2011) Cross-national comparison of the link between socioeconomic status and emotional and behavioral problems in youths. Soc Psychiatry Psychiatr Epidemiol 46:167–172CrossRefPubMedCentralPubMed van Oort FV, van der Ende J, Wadsworth ME, Verhulst FC, Achenbach TM (2011) Cross-national comparison of the link between socioeconomic status and emotional and behavioral problems in youths. Soc Psychiatry Psychiatr Epidemiol 46:167–172CrossRefPubMedCentralPubMed
45.
Zurück zum Zitat Wadsworth ME, Achenbach TM (2005) Explaining the link between low socioeconomic status and psychopathology: testing two mechanisms of the social causation hypothesis. J Consult Clin Psychol 73:1146–1153CrossRefPubMed Wadsworth ME, Achenbach TM (2005) Explaining the link between low socioeconomic status and psychopathology: testing two mechanisms of the social causation hypothesis. J Consult Clin Psychol 73:1146–1153CrossRefPubMed
46.
Zurück zum Zitat Achenbach TM, Rescorla LA (2001) Manual for the ASEBA school forms and profiles. ASEBA, Burlington Achenbach TM, Rescorla LA (2001) Manual for the ASEBA school forms and profiles. ASEBA, Burlington
47.
Zurück zum Zitat Frigerio A, Vanzin L, Pastore V, Nobile M, Giorda R, Marino C, Molteni M, Rucci P, Ammaniti M, Lucarelli L, Lenti C, Walder M, Martinuzzi A, Carlet O, Muratori F, Milone A, Zuddas A, Cavolina P, Nardocci F, Tullini A, Morosini P, Polidori G, De Girolamo G (2006) The Italian preadolescent mental health project (PrISMA): rationale and methods. Int J Methods Psychiatr Res. 15:22–35CrossRefPubMed Frigerio A, Vanzin L, Pastore V, Nobile M, Giorda R, Marino C, Molteni M, Rucci P, Ammaniti M, Lucarelli L, Lenti C, Walder M, Martinuzzi A, Carlet O, Muratori F, Milone A, Zuddas A, Cavolina P, Nardocci F, Tullini A, Morosini P, Polidori G, De Girolamo G (2006) The Italian preadolescent mental health project (PrISMA): rationale and methods. Int J Methods Psychiatr Res. 15:22–35CrossRefPubMed
48.
Zurück zum Zitat Achenbach TM, Becker A, Dopfner M, Heiervang E, Roessner V, Steinhausen HC, Rothenberger A (2008) Multicultural assessment of child and adolescent psychopathology with ASEBA and SDQ instruments: research findings, applications, and future directions. J Child Psychol Psychiatry 49:251–275CrossRefPubMed Achenbach TM, Becker A, Dopfner M, Heiervang E, Roessner V, Steinhausen HC, Rothenberger A (2008) Multicultural assessment of child and adolescent psychopathology with ASEBA and SDQ instruments: research findings, applications, and future directions. J Child Psychol Psychiatry 49:251–275CrossRefPubMed
49.
Zurück zum Zitat Hollingshead AB (1975) Four factor index of social status (unpublished manuscript). Yale University, New Haven Hollingshead AB (1975) Four factor index of social status (unpublished manuscript). Yale University, New Haven
50.
Zurück zum Zitat DeCoster J, Iselin AM, Gallucci M (2009) A conceptual and empirical examination of justifications for dichotomization. Psychol Methods 14:349–366CrossRefPubMed DeCoster J, Iselin AM, Gallucci M (2009) A conceptual and empirical examination of justifications for dichotomization. Psychol Methods 14:349–366CrossRefPubMed
51.
Zurück zum Zitat Nobile M, Giorda R, Marino C, Carlet O, Pastore V, Vanzin L, Bellina M, Molteni M, Battaglia M (2007) Socioeconomic status mediates the genetic contribution of the dopamine receptor D4 and serotonin transporter linked promoter region repeat polymorphisms to externalization in preadolescence. Dev Psychopathol 19:1147–1160CrossRefPubMed Nobile M, Giorda R, Marino C, Carlet O, Pastore V, Vanzin L, Bellina M, Molteni M, Battaglia M (2007) Socioeconomic status mediates the genetic contribution of the dopamine receptor D4 and serotonin transporter linked promoter region repeat polymorphisms to externalization in preadolescence. Dev Psychopathol 19:1147–1160CrossRefPubMed
52.
Zurück zum Zitat Nobile M, Rusconi M, Bellina M, Marino C, Giorda R, Carlet O, Vanzin L, Molteni M, Battaglia M (2010) COMT Val158Met polymorphism and socioeconomic status interact to predict attention deficit/hyperactivity problems in children aged 10–14. Eur Child Adolesc Psychiatry 19:549–557CrossRefPubMed Nobile M, Rusconi M, Bellina M, Marino C, Giorda R, Carlet O, Vanzin L, Molteni M, Battaglia M (2010) COMT Val158Met polymorphism and socioeconomic status interact to predict attention deficit/hyperactivity problems in children aged 10–14. Eur Child Adolesc Psychiatry 19:549–557CrossRefPubMed
53.
Zurück zum Zitat Ward R, Carroll RJ (2014) Testing Hardy–Weinberg equilibrium with a simple root-mean-square statistic. Biostatistics. 15:74–86CrossRefPubMed Ward R, Carroll RJ (2014) Testing Hardy–Weinberg equilibrium with a simple root-mean-square statistic. Biostatistics. 15:74–86CrossRefPubMed
54.
Zurück zum Zitat Marino C, Mascheretti S, Riva V, Cattaneo F, Rigoletto C, Rusconi M, Gruen JR, Giorda R, Lazazzera C, Molteni M (2011) Pleiotropic effects of DCDC2 and DYX1C1 genes on language and mathematics traits in nuclear families of developmental dyslexia. Behav Genet 41:67–76CrossRefPubMedCentralPubMed Marino C, Mascheretti S, Riva V, Cattaneo F, Rigoletto C, Rusconi M, Gruen JR, Giorda R, Lazazzera C, Molteni M (2011) Pleiotropic effects of DCDC2 and DYX1C1 genes on language and mathematics traits in nuclear families of developmental dyslexia. Behav Genet 41:67–76CrossRefPubMedCentralPubMed
55.
Zurück zum Zitat Cohen P, Cohen J, Kasen S, Velez CN, Hartmark C, Johnson J, Rojas M, Brook J, Streuning EL (1993) An epidemiological study of disorders in late childhood and adolescence. I. Age- and gender-specific prevalence. J Child Psychol Psychiatry 34:851–867CrossRefPubMed Cohen P, Cohen J, Kasen S, Velez CN, Hartmark C, Johnson J, Rojas M, Brook J, Streuning EL (1993) An epidemiological study of disorders in late childhood and adolescence. I. Age- and gender-specific prevalence. J Child Psychol Psychiatry 34:851–867CrossRefPubMed
56.
Zurück zum Zitat Leadbeater BJ, Kuperminc GP, Blatt SJ, Hertzog C (1999) A multivariate model of gender differences in adolescents’ internalizing and externalizing problems. Dev Psychol 35:1268–1282CrossRefPubMed Leadbeater BJ, Kuperminc GP, Blatt SJ, Hertzog C (1999) A multivariate model of gender differences in adolescents’ internalizing and externalizing problems. Dev Psychol 35:1268–1282CrossRefPubMed
57.
Zurück zum Zitat Nopoulos P, Berg S, Castellenos FX, Delgado A, Andreasen NC, Rapoport JL (2000) Developmental brain anomalies in children with attention-deficit hyperactivity disorder. J Child Neurol 15:102–108CrossRefPubMed Nopoulos P, Berg S, Castellenos FX, Delgado A, Andreasen NC, Rapoport JL (2000) Developmental brain anomalies in children with attention-deficit hyperactivity disorder. J Child Neurol 15:102–108CrossRefPubMed
58.
Zurück zum Zitat Conger RD, Wallace LE, Sun Y, Simons RL, McLoyd VC, Brody GH (2002) Economic pressure in African American families: a replication and extension of the family stress model. Dev Psychol 38:179–193CrossRefPubMed Conger RD, Wallace LE, Sun Y, Simons RL, McLoyd VC, Brody GH (2002) Economic pressure in African American families: a replication and extension of the family stress model. Dev Psychol 38:179–193CrossRefPubMed
59.
Zurück zum Zitat Nathanielsz PW (2006) Animal models that elucidate basic principles of the developmental origins of adult diseases. ILAR J 47:73–82CrossRefPubMed Nathanielsz PW (2006) Animal models that elucidate basic principles of the developmental origins of adult diseases. ILAR J 47:73–82CrossRefPubMed
60.
Metadaten
Titel
The role of DCDC2 genetic variants and low socioeconomic status in vulnerability to attention problems
verfasst von
Valentina Riva
Cecilia Marino
Roberto Giorda
Massimo Molteni
Maria Nobile
Publikationsdatum
01.03.2015
Verlag
Springer Berlin Heidelberg
Erschienen in
European Child & Adolescent Psychiatry / Ausgabe 3/2015
Print ISSN: 1018-8827
Elektronische ISSN: 1435-165X
DOI
https://doi.org/10.1007/s00787-014-0580-5

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