Association Study of 10 Genes Encoding Neurotrophic Factors and Their Receptors in Adult and Child Attention-Deficit/Hyperactivity Disorder

Background Attention-deficit/hyperactivity disorder (ADHD) is a common childhood-onset psychiatric disorder that often persists into adolescence and adulthood and is characterized by inappropriate levels of inattention, hyperactivity, and/or impulsivity. Genetic and environmental factors are believe...

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Published inBiological psychiatry (1969) Vol. 63; no. 10; pp. 935 - 945
Main Authors Ribasés, Marta, Hervás, Amaia, Ramos-Quiroga, Josep Antoni, Bosch, Rosa, Bielsa, Anna, Gastaminza, Xavier, Fernández-Anguiano, Mònica, Nogueira, Mariana, Gómez-Barros, Núria, Valero, Sergi, Gratacòs, Mònica, Estivill, Xavier, Casas, Miquel, Cormand, Bru, Bayés, Mònica
Format Journal Article
LanguageEnglish
Published New York, NY Elsevier Inc 15.05.2008
Elsevier Science
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Abstract Background Attention-deficit/hyperactivity disorder (ADHD) is a common childhood-onset psychiatric disorder that often persists into adolescence and adulthood and is characterized by inappropriate levels of inattention, hyperactivity, and/or impulsivity. Genetic and environmental factors are believed to be involved in the continuity of the disorder as well as in changes in ADHD symptomatology throughout life. Neurotrophic factors (NTFs), which participate in neuronal survival and synaptic efficiency, are strong candidates to contribute to the neuroplasticity changes that take place in the human central nervous system during childhood, adolescence, and early adulthood and might be involved in the genetic predisposition to ADHD. Methods We performed a population-based association study in 546 ADHD patients (216 adults and 330 children) and 546 gender-matched unrelated control subjects with 183 single nucleotide polymorphisms covering 10 candidate genes that encode four neurotrophins ( NGF, BDNF, NTF3 , and NTF4/5 ), a member of the cytokine family of NTFs ( CNTF ), and their receptors ( NTRK1, NTRK2, NTRK3, NGFR, and CNTFR ). Results The single-marker and haplotype-based analyses provided evidence of association between CNTFR and both adulthood ( p = .0077, odds ratio [OR] = 1.38) and childhood ADHD ( p = 9.1e-04, OR = 1.40) and also suggested a childhood-specific contribution of NTF3 ( p = 3.0e–04, OR = 1.48) and NTRK2 ( p = .0084, OR = 1.52) to ADHD. Conclusions Our data suggest that variations in NTFs might be involved in the genetic susceptibility to ADHD, support the contribution of the CNTFR locus as a predisposition factor for the disorder, and suggest that NTF3 and NTRK2 might be involved in the molecular basis of the age-dependent changes in ADHD symptoms throughout life span.
AbstractList Background Attention-deficit/hyperactivity disorder (ADHD) is a common childhood-onset psychiatric disorder that often persists into adolescence and adulthood and is characterized by inappropriate levels of inattention, hyperactivity, and/or impulsivity. Genetic and environmental factors are believed to be involved in the continuity of the disorder as well as in changes in ADHD symptomatology throughout life. Neurotrophic factors (NTFs), which participate in neuronal survival and synaptic efficiency, are strong candidates to contribute to the neuroplasticity changes that take place in the human central nervous system during childhood, adolescence, and early adulthood and might be involved in the genetic predisposition to ADHD. Methods We performed a population-based association study in 546 ADHD patients (216 adults and 330 children) and 546 gender-matched unrelated control subjects with 183 single nucleotide polymorphisms covering 10 candidate genes that encode four neurotrophins ( NGF, BDNF, NTF3 , and NTF4/5 ), a member of the cytokine family of NTFs ( CNTF ), and their receptors ( NTRK1, NTRK2, NTRK3, NGFR, and CNTFR ). Results The single-marker and haplotype-based analyses provided evidence of association between CNTFR and both adulthood ( p = .0077, odds ratio [OR] = 1.38) and childhood ADHD ( p = 9.1e-04, OR = 1.40) and also suggested a childhood-specific contribution of NTF3 ( p = 3.0e–04, OR = 1.48) and NTRK2 ( p = .0084, OR = 1.52) to ADHD. Conclusions Our data suggest that variations in NTFs might be involved in the genetic susceptibility to ADHD, support the contribution of the CNTFR locus as a predisposition factor for the disorder, and suggest that NTF3 and NTRK2 might be involved in the molecular basis of the age-dependent changes in ADHD symptoms throughout life span.
BACKGROUNDAttention-deficit/hyperactivity disorder (ADHD) is a common childhood-onset psychiatric disorder that often persists into adolescence and adulthood and is characterized by inappropriate levels of inattention, hyperactivity, and/or impulsivity. Genetic and environmental factors are believed to be involved in the continuity of the disorder as well as in changes in ADHD symptomatology throughout life. Neurotrophic factors (NTFs), which participate in neuronal survival and synaptic efficiency, are strong candidates to contribute to the neuroplasticity changes that take place in the human central nervous system during childhood, adolescence, and early adulthood and might be involved in the genetic predisposition to ADHD.METHODSWe performed a population-based association study in 546 ADHD patients (216 adults and 330 children) and 546 gender-matched unrelated control subjects with 183 single nucleotide polymorphisms covering 10 candidate genes that encode four neurotrophins (NGF, BDNF, NTF3, and NTF4/5), a member of the cytokine family of NTFs (CNTF), and their receptors (NTRK1, NTRK2, NTRK3, NGFR, and CNTFR).RESULTSThe single-marker and haplotype-based analyses provided evidence of association between CNTFR and both adulthood (p = .0077, odds ratio [OR] = 1.38) and childhood ADHD (p = 9.1e-04, OR = 1.40) and also suggested a childhood-specific contribution of NTF3 (p = 3.0e-04, OR = 1.48) and NTRK2 (p = .0084, OR = 1.52) to ADHD.CONCLUSIONSOur data suggest that variations in NTFs might be involved in the genetic susceptibility to ADHD, support the contribution of the CNTFR locus as a predisposition factor for the disorder, and suggest that NTF3 and NTRK2 might be involved in the molecular basis of the age-dependent changes in ADHD symptoms throughout life span.
Attention-deficit/hyperactivity disorder (ADHD) is a common childhood-onset psychiatric disorder that often persists into adolescence and adulthood and is characterized by inappropriate levels of inattention, hyperactivity, and/or impulsivity. Genetic and environmental factors are believed to be involved in the continuity of the disorder as well as in changes in ADHD symptomatology throughout life. Neurotrophic factors (NTFs), which participate in neuronal survival and synaptic efficiency, are strong candidates to contribute to the neuroplasticity changes that take place in the human central nervous system during childhood, adolescence, and early adulthood and might be involved in the genetic predisposition to ADHD. We performed a population-based association study in 546 ADHD patients (216 adults and 330 children) and 546 gender-matched unrelated control subjects with 183 single nucleotide polymorphisms covering 10 candidate genes that encode four neurotrophins (NGF, BDNF, NTF3, and NTF4/5), a member of the cytokine family of NTFs (CNTF), and their receptors (NTRK1, NTRK2, NTRK3, NGFR, and CNTFR). The single-marker and haplotype-based analyses provided evidence of association between CNTFR and both adulthood (p = .0077, odds ratio [OR] = 1.38) and childhood ADHD (p = 9.1e-04, OR = 1.40) and also suggested a childhood-specific contribution of NTF3 (p = 3.0e-04, OR = 1.48) and NTRK2 (p = .0084, OR = 1.52) to ADHD. Our data suggest that variations in NTFs might be involved in the genetic susceptibility to ADHD, support the contribution of the CNTFR locus as a predisposition factor for the disorder, and suggest that NTF3 and NTRK2 might be involved in the molecular basis of the age-dependent changes in ADHD symptoms throughout life span.
Attention-deficit/hyperactivity disorder (ADHD) is a common childhood-onset psychiatric disorder that often persists into adolescence and adulthood and is characterized by inappropriate levels of inattention, hyperactivity, and/or impulsivity. Genetic and environmental factors are believed to be involved in the continuity of the disorder as well as in changes in ADHD symptomatology throughout life. Neurotrophic factors (NTFs), which participate in neuronal survival and synaptic efficiency, are strong candidates to contribute to the neuroplasticity changes that take place in the human central nervous system during childhood, adolescence, and early adulthood and might be involved in the genetic predisposition to ADHD. We performed a population-based association study in 546 ADHD patients (216 adults and 330 children) and 546 gender-matched unrelated control subjects with 183 single nucleotide polymorphisms covering 10 candidate genes that encode four neurotrophins ( NGF, BDNF, NTF3, and NTF4/5), a member of the cytokine family of NTFs ( CNTF), and their receptors ( NTRK1, NTRK2, NTRK3, NGFR, and CNTFR). The single-marker and haplotype-based analyses provided evidence of association between CNTFR and both adulthood ( p = .0077, odds ratio [OR] = 1.38) and childhood ADHD ( p = 9.1e-04, OR = 1.40) and also suggested a childhood-specific contribution of NTF3 ( p = 3.0e–04, OR = 1.48) and NTRK2 ( p = .0084, OR = 1.52) to ADHD. Our data suggest that variations in NTFs might be involved in the genetic susceptibility to ADHD, support the contribution of the CNTFR locus as a predisposition factor for the disorder, and suggest that NTF3 and NTRK2 might be involved in the molecular basis of the age-dependent changes in ADHD symptoms throughout life span.
Author Hervás, Amaia
Ribasés, Marta
Fernández-Anguiano, Mònica
Casas, Miquel
Gastaminza, Xavier
Ramos-Quiroga, Josep Antoni
Bosch, Rosa
Estivill, Xavier
Gratacòs, Mònica
Nogueira, Mariana
Gómez-Barros, Núria
Bielsa, Anna
Bayés, Mònica
Valero, Sergi
Cormand, Bru
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Issue 10
Keywords ADHD
attention-deficit hyperactivity disorder
CNTFR
NTRK2
neurotrophic factors
association study
NTF3
neurotrophins
Human
Neurotrophin
Hyperactivity
Genetic determinism
Neurotrophic factor
Attentional disorder
Gene
Coding
Genetics
Adult
Attention disorder with hyperactivity
Child
Biological receptor
Language English
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SSID ssj0007221
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Snippet Background Attention-deficit/hyperactivity disorder (ADHD) is a common childhood-onset psychiatric disorder that often persists into adolescence and adulthood...
Attention-deficit/hyperactivity disorder (ADHD) is a common childhood-onset psychiatric disorder that often persists into adolescence and adulthood and is...
BACKGROUNDAttention-deficit/hyperactivity disorder (ADHD) is a common childhood-onset psychiatric disorder that often persists into adolescence and adulthood...
SourceID proquest
crossref
pubmed
pascalfrancis
elsevier
SourceType Aggregation Database
Index Database
Publisher
StartPage 935
SubjectTerms ADHD
Adult
Age Factors
association study
Attention Deficit Disorder with Hyperactivity - genetics
Attention deficit disorders. Hyperactivity
attention-deficit hyperactivity disorder
Biological and medical sciences
Child
Child clinical studies
CNTFR
Confidence Intervals
Female
Gene Frequency
Genetic Predisposition to Disease
Haplotypes
Humans
Male
Medical sciences
Nerve Growth Factors - genetics
neurotrophic factors
neurotrophins
NTF3
NTRK2
Odds Ratio
Polymorphism, Single Nucleotide
Psychiatry
Psychology. Psychoanalysis. Psychiatry
Psychopathology. Psychiatry
Receptors, Nerve Growth Factor - genetics
Retrospective Studies
Title Association Study of 10 Genes Encoding Neurotrophic Factors and Their Receptors in Adult and Child Attention-Deficit/Hyperactivity Disorder
URI https://www.clinicalkey.es/playcontent/1-s2.0-S0006322307010980
https://dx.doi.org/10.1016/j.biopsych.2007.11.004
https://www.ncbi.nlm.nih.gov/pubmed/18179783
https://search.proquest.com/docview/69165066
Volume 63
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