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Association between RELN Gene Polymorphisms and Attention Deficit Hyperactivity Disorder in Korean Children

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주제분류정신과학

초록

ObjectiveaaAttention deficit hyperactivity disorder (ADHD) is common disorder of the school-age population. ADHD is familial and genetic studies estimate heritability at 80–90%. The aim of the present study was to investigate the association between the genetic type and alleles for RELN gene (rs736707, rs2229864, rs362746, rs362726, rs362691, rs1062831, rs607755, and rs2072403) in Korean children with ADHD. MethodsaaThe sample consisted of 180 ADHD children and 159 control children. We diagnosed ADHD according to DSM-IV. ADHD symptoms were evaluated with Conners’ Parent Rating Scales and Dupaul Parent ADHD Rating Scales. Blood samples were taken from the 339 subjects, DNA was extracted from blood lymphocytes, and PCR was performed for RELN Polymorphism. Alleles and genotype frequencies were compared using the chi-square test. We compared the allele and genotype frequencies of RELN gene polymorphism in the ADHD and control groups. ResultsaaThis study showed that there was a significant correlation among the frequencies of the rs736707 (OR=1.40, 95% CI=1.03– 1.90, p=0.031) of alleles of RELN, but the final conclusions are not definite. ConclusionaaFollow up studies with larger patient or pure subgroups are expected. These results suggested that RELN might be related to ADHD symptoms.

Abstract

ObjectiveaaAttention deficit hyperactivity disorder (ADHD) is common disorder of the school-age population. ADHD is familial and genetic studies estimate heritability at 80–90%. The aim of the present study was to investigate the association between the genetic type and alleles for RELN gene (rs736707, rs2229864, rs362746, rs362726, rs362691, rs1062831, rs607755, and rs2072403) in Korean children with ADHD. MethodsaaThe sample consisted of 180 ADHD children and 159 control children. We diagnosed ADHD according to DSM-IV. ADHD symptoms were evaluated with Conners’ Parent Rating Scales and Dupaul Parent ADHD Rating Scales. Blood samples were taken from the 339 subjects, DNA was extracted from blood lymphocytes, and PCR was performed for RELN Polymorphism. Alleles and genotype frequencies were compared using the chi-square test. We compared the allele and genotype frequencies of RELN gene polymorphism in the ADHD and control groups. ResultsaaThis study showed that there was a significant correlation among the frequencies of the rs736707 (OR=1.40, 95% CI=1.03– 1.90, p=0.031) of alleles of RELN, but the final conclusions are not definite. ConclusionaaFollow up studies with larger patient or pure subgroups are expected. These results suggested that RELN might be related to ADHD symptoms.

참고문헌 (30)

  1. American Psychiatric Association Committee on Nomenclature and Statistics, "Diagnostic and Statistical Manual of Mental Disorders" (1994), American Psychiatric Association Press
  2. Cho SC, "Prevalence of disruptive behavior disorders", Korean J Child Adolesc Psychiatry, 5, pp.141~149 (1994)
  3. Kim JY, "An epidemiological study of attention deficit hyperactivity disorder and learning disabilities in a rural area", J Korean Neuropsychiatr Assoc, 38, pp.788~793 (1999)
  4. Faraone SV, "The nature and heritability of attention-deficit", hyperactivity disorder, 2001, pp.10, 299~316
  5. de Bergeyck V, "A panel of monoclonal antibodies against reelin, the extracellular matrix protein defective in reeler mutant mice", J Neurosci Methods, 82, pp.17~24 (1998)
  6. DeSilva U, "The human reelin gene: isolation, sequencing, and mapping on chromosome 7", Genome Res, 7, pp.157~164 (1997)
  7. Tueting P, "Reelin down-regulation in mice and psychosis endophenotypes", Neurosci Biobehav Rev, 30, pp.1065~1077 (2006)
  8. Qiu S, "Cognitive disruption and altered hippocampus synaptic function in reelin haploinsufficient mice", Neurobiol Learn Mem, 85, pp.228~242 (2006)
  9. Weeber EJ, "Reelin and ApoE receptors cooperate to enhance hippocampal synaptic plasticity and learning", J Biol Chem, 277, pp.39944~39952 (2002)
  10. Ventruti A, "Reelin deficiency causes specific defects in the molecular composition of the synapses in the adult brain", Neuroscience, 189, pp.32~42 (2011)
  11. Beffert U, "Reelin-mediated signaling locally regulates protein kinase B", Akt and glycogen synthase kinase 3beta, 2002, pp.277, 49958~49964
  12. Sinagra M, "Reelin, very-low-density lipoprotein receptor, and apolipoprotein E receptor 2 control somatic NMDA receptor composition during hippocampal maturation in vitro", J Neurosci, 25, pp.6127~6136 (2005)
  13. Folsom TD, "The involvement of Reelin in neurodevelopmental disorders", Neuropharmacology, 68, pp.122~135 (2013)
  14. Serajee FJ, "Association of Reelin gene polymorphisms with autism", Genomics, 87, pp.75~83 (2006)
  15. Li H, "The association analysis of RELN and GRM8 genes with autistic spectrum disorder in Chinese Han population", Am J Med Genet B Neuropsychiatr Genet, 147B, pp.194~200 (2008)
  16. Ashley-Koch AE, "Investigation of potential gene-gene interactions between APOE and RELN contributing to autism risk", Psychiatr Genet, 17, pp.221~226 (2007)
  17. Goes FS, "Sex-specific association of the reelin gene with bipolar disorder", Am J Med Genet B Neuropsychiatr Genet, 153B, pp.549~553 (2010)
  18. Falconer DS, "Two new mutants, trembler and ‘reeler’, with neurological actions in the house mouse (Mus musculus L.)", J Genet, 50, pp.192~201 (1951)
  19. Curran T, "Role of reelin in the control of brain development", Brain Res Brain Res Rev, 26, pp.285~294 (1998)
  20. Tissir F, "Reelin and brain development", Nat Rev Neurosci, 4, pp.496~505 (2003)
  21. Hamburgh M, "Analysis of the postnatal developmental effects of “reeler” a neurological mutation in mice. A study in developmental genetics", Dev Biol, 8, pp.165~185 (1963)
  22. Boyle MP, "Cell-type-specific consequences of Reelin deficiency in the mouse neocortex, hippocampus, and amygdala", J Comp Neurol, 519, pp.2061~2089 (2011)
  23. 소유경, "한국어판 부모, 교사 ADHD 평가 척도의 신뢰도와 타당도 연구", 신경정신의학, 41(2) (2002), 대한신경정신의학회
  24. Kovacs M, "The Children’s Depression Inventory: A Self-Rated Depression Scale for School-Aged Youngsters" (1983), University of Pittsburgh
  25. Cho SC, "Development of the Korean form of the Kovacs’ Childhood Depression Inventory", J Korean Neuropsychiatr Assoc, 29, pp.943~956 (1990)
  26. Cho SC, "Development of Korean form of the state-trait anxiety inventory for children", J Seoul Psychiatry, 14, pp.150~157 (1989)
  27. Shin MS, "A study of the development and standardization of ADHD diagnostic system", Korean J Child Adolesc Psychiatry, 11, pp.91~99 (2000)
  28. Plessen KJ, "Hippocampus and amygdale morphology in attention-deficit", hyperactivity disorder, 2006, pp.63, 795~807
  29. Bedard AC, "Methylphenidate improves visual-spatial memory in children with attention-deficit", hyperactivity disorder, 2004, pp.43, 260~268
  30. Sergeant JA, "How specific is a deficit of executive functioning for attention-deficit", hyperactivity disorder?, 2002, pp.130, 3~28

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