Symptoms of attention-deficit hyperactivity disorder, nonsyndromic orofacial cleft children, and dopamine polymorphisms: a pilot study.
Identifieur interne : 000210 ( PubMed/Checkpoint ); précédent : 000209; suivant : 000211Symptoms of attention-deficit hyperactivity disorder, nonsyndromic orofacial cleft children, and dopamine polymorphisms: a pilot study.
Auteurs : Emily E. Hopkins [États-Unis] ; Meredith L. Wallace [États-Unis] ; Yvette P. Conley [États-Unis] ; Mary L. Marazita [États-Unis]Source :
- Biological research for nursing [ 1552-4175 ] ; 2015.
Descripteurs français
- KwdFr :
- Bec-de-lièvre (génétique), Dopamine (génétique), Encéphale (malformations), Enfant, Enfant d'âge préscolaire, Femelle, Fente palatine (génétique), Génotype, Humains, Mâle, Polymorphisme génétique, Projets pilotes, Réaction de polymérisation en chaîne, Trouble déficitaire de l'attention avec hyperactivité (), Trouble déficitaire de l'attention avec hyperactivité (génétique), Études transversales.
- MESH :
- génétique : Bec-de-lièvre, Dopamine, Fente palatine, Trouble déficitaire de l'attention avec hyperactivité.
- malformations : Encéphale.
- Enfant, Enfant d'âge préscolaire, Femelle, Génotype, Humains, Mâle, Polymorphisme génétique, Projets pilotes, Réaction de polymérisation en chaîne, Trouble déficitaire de l'attention avec hyperactivité, Études transversales.
English descriptors
- KwdEn :
- Attention Deficit Disorder with Hyperactivity (complications), Attention Deficit Disorder with Hyperactivity (genetics), Brain (abnormalities), Child, Child, Preschool, Cleft Lip (genetics), Cleft Palate (genetics), Cross-Sectional Studies, Dopamine (genetics), Female, Genotype, Humans, Male, Pilot Projects, Polymerase Chain Reaction, Polymorphism, Genetic.
- MESH :
- chemical , genetics : Dopamine.
- abnormalities : Brain.
- complications : Attention Deficit Disorder with Hyperactivity.
- genetics : Attention Deficit Disorder with Hyperactivity, Cleft Lip, Cleft Palate.
- Child, Child, Preschool, Cross-Sectional Studies, Female, Genotype, Humans, Male, Pilot Projects, Polymerase Chain Reaction, Polymorphism, Genetic.
Abstract
Attention-deficit hyperactivity disorder (ADHD) is a common childhood neurobehavioral disorder characterized by inattention, poor impulse control, and motor restlessness. Risk factors include familial stressors, anxiety disorders, learning disabilities, abnormal brain development, heritability, and dopamine polymorphisms. Children with an orofacial clefting (OFC) history are at increased risk of familial stressors, anxiety disorders, learning disabilities, and abnormal brain development. Given this overlap, we present a conceptual model proposing that children with OFC may be more likely to exhibit ADHD symptoms than children without and explore this relationship using pilot data.
DOI: 10.1177/1099800414552186
PubMed: 25271118
Affiliations:
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pubmed:25271118Le document en format XML
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Conley</name><affiliation wicri:level="4"><nlm:affiliation>Department of Health Promotion and Development, School of Nursing, University of Pittsburgh, Pittsburgh, PA, USA Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA, USA.</nlm:affiliation><country xml:lang="fr">États-Unis</country><wicri:regionArea>Department of Health Promotion and Development, School of Nursing, University of Pittsburgh, Pittsburgh, PA, USA Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA</wicri:regionArea><placeName><region type="state">Pennsylvanie</region><settlement type="city">Pittsburgh</settlement></placeName><orgName type="university">Université de Pittsburgh</orgName></affiliation></author><author><name sortKey="Marazita, Mary L" sort="Marazita, Mary L" uniqKey="Marazita M" first="Mary L" last="Marazita">Mary L. Marazita</name><affiliation wicri:level="4"><nlm:affiliation>Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA, USA Department of Oral Biology, Center for Craniofacial and Dental Genetics, University of Pittsburgh, Pittsburgh, PA, USA School of Dental Medicine, University of Pittsburgh, Pittsburgh, PA, USA School of Medicine, University of Pittsburgh, Pittsburgh, PA, USA.</nlm:affiliation><country xml:lang="fr">États-Unis</country><wicri:regionArea>Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA, USA Department of Oral Biology, Center for Craniofacial and Dental Genetics, University of Pittsburgh, Pittsburgh, PA, USA School of Dental Medicine, University of Pittsburgh, Pittsburgh, PA, USA School of Medicine, University of Pittsburgh, Pittsburgh, PA</wicri:regionArea><placeName><region type="state">Pennsylvanie</region><settlement type="city">Pittsburgh</settlement></placeName><orgName type="university">Université de Pittsburgh</orgName></affiliation></author></analytic><series><title level="j">Biological research for nursing</title><idno type="eISSN">1552-4175</idno><imprint><date when="2015" type="published">2015</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Attention Deficit Disorder with Hyperactivity (complications)</term><term>Attention Deficit Disorder with Hyperactivity (genetics)</term><term>Brain (abnormalities)</term><term>Child</term><term>Child, Preschool</term><term>Cleft Lip (genetics)</term><term>Cleft Palate (genetics)</term><term>Cross-Sectional Studies</term><term>Dopamine (genetics)</term><term>Female</term><term>Genotype</term><term>Humans</term><term>Male</term><term>Pilot Projects</term><term>Polymerase Chain Reaction</term><term>Polymorphism, Genetic</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Bec-de-lièvre (génétique)</term><term>Dopamine (génétique)</term><term>Encéphale (malformations)</term><term>Enfant</term><term>Enfant d'âge préscolaire</term><term>Femelle</term><term>Fente palatine (génétique)</term><term>Génotype</term><term>Humains</term><term>Mâle</term><term>Polymorphisme génétique</term><term>Projets pilotes</term><term>Réaction de polymérisation en chaîne</term><term>Trouble déficitaire de l'attention avec hyperactivité ()</term><term>Trouble déficitaire de l'attention avec hyperactivité (génétique)</term><term>Études transversales</term></keywords><keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Dopamine</term></keywords><keywords scheme="MESH" qualifier="abnormalities" xml:lang="en"><term>Brain</term></keywords><keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Attention Deficit Disorder with Hyperactivity</term></keywords><keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Attention Deficit Disorder with Hyperactivity</term><term>Cleft Lip</term><term>Cleft Palate</term></keywords><keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>Bec-de-lièvre</term><term>Dopamine</term><term>Fente palatine</term><term>Trouble déficitaire de l'attention avec hyperactivité</term></keywords><keywords scheme="MESH" qualifier="malformations" xml:lang="fr"><term>Encéphale</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Child</term><term>Child, Preschool</term><term>Cross-Sectional Studies</term><term>Female</term><term>Genotype</term><term>Humans</term><term>Male</term><term>Pilot Projects</term><term>Polymerase Chain Reaction</term><term>Polymorphism, Genetic</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Enfant</term><term>Enfant d'âge préscolaire</term><term>Femelle</term><term>Génotype</term><term>Humains</term><term>Mâle</term><term>Polymorphisme génétique</term><term>Projets pilotes</term><term>Réaction de polymérisation en chaîne</term><term>Trouble déficitaire de l'attention avec hyperactivité</term><term>Études transversales</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Attention-deficit hyperactivity disorder (ADHD) is a common childhood neurobehavioral disorder characterized by inattention, poor impulse control, and motor restlessness. Risk factors include familial stressors, anxiety disorders, learning disabilities, abnormal brain development, heritability, and dopamine polymorphisms. Children with an orofacial clefting (OFC) history are at increased risk of familial stressors, anxiety disorders, learning disabilities, and abnormal brain development. Given this overlap, we present a conceptual model proposing that children with OFC may be more likely to exhibit ADHD symptoms than children without and explore this relationship using pilot data.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">25271118</PMID><DateCreated><Year>2015</Year><Month>04</Month><Day>30</Day></DateCreated><DateCompleted><Year>2016</Year><Month>02</Month><Day>04</Day></DateCompleted><DateRevised><Year>2016</Year><Month>10</Month><Day>19</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1552-4175</ISSN><JournalIssue CitedMedium="Internet"><Volume>17</Volume><Issue>3</Issue><PubDate><Year>2015</Year><Month>May</Month></PubDate></JournalIssue><Title>Biological research for nursing</Title><ISOAbbreviation>Biol Res Nurs</ISOAbbreviation></Journal><ArticleTitle>Symptoms of attention-deficit hyperactivity disorder, nonsyndromic orofacial cleft children, and dopamine polymorphisms: a pilot study.</ArticleTitle><Pagination><MedlinePgn>257-62</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1177/1099800414552186</ELocationID><Abstract><AbstractText Label="PURPOSE" NlmCategory="OBJECTIVE">Attention-deficit hyperactivity disorder (ADHD) is a common childhood neurobehavioral disorder characterized by inattention, poor impulse control, and motor restlessness. Risk factors include familial stressors, anxiety disorders, learning disabilities, abnormal brain development, heritability, and dopamine polymorphisms. Children with an orofacial clefting (OFC) history are at increased risk of familial stressors, anxiety disorders, learning disabilities, and abnormal brain development. Given this overlap, we present a conceptual model proposing that children with OFC may be more likely to exhibit ADHD symptoms than children without and explore this relationship using pilot data.</AbstractText><AbstractText Label="DESIGN" NlmCategory="METHODS">This cross-sectional pilot study included 29 children with OFC or a first-degree relative with OFC recruited through a cleft research registry.</AbstractText><AbstractText Label="METHODS" NlmCategory="METHODS">The Disruptive Behavior Disorder Scale was used to collect data on children's ADHD symptoms. Saliva or whole blood samples were collected from children and parents for DNA analyses. ADHD-associated dopamine polymorphisms within the DRD4, DRD2, and DAT1 genes were genotyped. We tested for associations between presence of OFC and dopamine polymorphisms. Mixed-effects models tested whether children with OFC and dopamine polymorphisms had more ADHD symptoms.</AbstractText><AbstractText Label="RESULTS" NlmCategory="RESULTS">The DRD4 4-repeat allele was associated with increased inattentive ADHD symptoms (p = .03). Having the DRD2 Taq1A1 allele and OFC predicted fewer (p = .02) inattentive ADHD symptoms. Children with OFC were significantly less likely to have the DAT1 10-repeat allele (p = .04).</AbstractText><AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">Results indicate that further investigation among a larger sample of children with OFC is warranted, particularly for relationships with inattentive ADHD.</AbstractText><CopyrightInformation>© The Author(s) 2014.</CopyrightInformation></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Hopkins</LastName><ForeName>Emily E</ForeName><Initials>EE</Initials><AffiliationInfo><Affiliation>College of Continuing and Professional Studies, Chatham University, Pittsburgh, PA, USA ehopkins@chatham.edu.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Wallace</LastName><ForeName>Meredith L</ForeName><Initials>ML</Initials><AffiliationInfo><Affiliation>Department of Psychiatry, School of Medicine, University of Pittsburgh, Pittsburgh, PA, USA.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Conley</LastName><ForeName>Yvette P</ForeName><Initials>YP</Initials><AffiliationInfo><Affiliation>Department of Health Promotion and Development, School of Nursing, University of Pittsburgh, Pittsburgh, PA, USA Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA, USA.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Marazita</LastName><ForeName>Mary L</ForeName><Initials>ML</Initials><AffiliationInfo><Affiliation>Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA, USA Department of Oral Biology, Center for Craniofacial and Dental Genetics, University of Pittsburgh, Pittsburgh, PA, USA School of Dental Medicine, University of Pittsburgh, Pittsburgh, PA, USA School of Medicine, University of Pittsburgh, Pittsburgh, PA, USA.</Affiliation></AffiliationInfo></Author></AuthorList><Language>eng</Language><GrantList CompleteYN="Y"><Grant><GrantID>K01 MH096944</GrantID><Acronym>MH</Acronym><Agency>NIMH NIH HHS</Agency><Country>United States</Country></Grant><Grant><GrantID>R01 DE016148</GrantID><Acronym>DE</Acronym><Agency>NIDCR NIH HHS</Agency><Country>United States</Country></Grant><Grant><GrantID>T32 NR009759</GrantID><Acronym>NR</Acronym><Agency>NINR NIH HHS</Agency><Country>United States</Country></Grant><Grant><GrantID>R01DE016148</GrantID><Acronym>DE</Acronym><Agency>NIDCR NIH HHS</Agency><Country>United States</Country></Grant></GrantList><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D052061">Research Support, N.I.H., Extramural</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2014</Year><Month>09</Month><Day>29</Day></ArticleDate></Article><MedlineJournalInfo><Country>United States</Country><MedlineTA>Biol Res Nurs</MedlineTA><NlmUniqueID>9815758</NlmUniqueID><ISSNLinking>1099-8004</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>VTD58H1Z2X</RegistryNumber><NameOfSubstance UI="D004298">Dopamine</NameOfSubstance></Chemical></ChemicalList><SupplMeshList><SupplMeshName Type="Disease" UI="C566121">Orofacial Cleft 1</SupplMeshName></SupplMeshList><CitationSubset>IM</CitationSubset><CitationSubset>N</CitationSubset><CommentsCorrectionsList><CommentsCorrections RefType="Cites"><RefSource>Acta Psychiatr Scand. 2002 May;105(5):396-9</RefSource><PMID Version="1">11942948</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>J Psychiatr Res. 2011 May;45(5):626-9</RefSource><PMID Version="1">21035130</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Am J Med Genet B Neuropsychiatr Genet. 2003 May 15;119B(1):77-85</RefSource><PMID Version="1">12707943</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Hum Mol Genet. 1993 Dec;2(12):2197</RefSource><PMID Version="1">7906592</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>JAMA. 1991 Oct 2;266(13):1793-800</RefSource><PMID Version="1">1832466</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Cleft Palate Craniofac J. 2004 Jul;41(4):351-4</RefSource><PMID Version="1">15222786</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Am J Hum Genet. 1995 Apr;56(4):993-8</RefSource><PMID Version="1">7717410</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Am J Hum Genet. 1998 Dec;63(6):1767-76</RefSource><PMID Version="1">9837830</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Neuropsychologia. 2005;43(13):1847-57</RefSource><PMID Version="1">16168728</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Clin Psychol Rev. 2006 Aug;26(4):396-432</RefSource><PMID Version="1">16513236</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Am J Med Genet B Neuropsychiatr Genet. 2006 Dec 5;141B(8):907-11</RefSource><PMID Version="1">16917940</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Neuro Endocrinol Lett. 2006 Feb-Apr;27(1-2):236-40</RefSource><PMID Version="1">16648784</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Arch Pediatr Adolesc Med. 2007 Aug;161(8):753-8</RefSource><PMID Version="1">17679656</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Neuro Endocrinol Lett. 2008 Apr;29(2):246-51</RefSource><PMID Version="1">18404133</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Neuro Endocrinol Lett. 2008 Jun;29(3):320-7</RefSource><PMID Version="1">18580852</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Psychiatr Clin North Am. 2010 Mar;33(1):159-80</RefSource><PMID Version="1">20159345</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Behav Genet. 2011 Jan;41(1):165-74</RefSource><PMID Version="1">21207241</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>BMC Neurosci. 2002 Oct 4;3:14</RefSource><PMID Version="1">12366871</PMID></CommentsCorrections></CommentsCorrectionsList><MeshHeadingList><MeshHeading><DescriptorName UI="D001289" MajorTopicYN="N">Attention Deficit Disorder with Hyperactivity</DescriptorName><QualifierName UI="Q000150" MajorTopicYN="N">complications</QualifierName><QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D001921" MajorTopicYN="N">Brain</DescriptorName><QualifierName UI="Q000002" MajorTopicYN="Y">abnormalities</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D002648" MajorTopicYN="N">Child</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D002675" MajorTopicYN="N">Child, Preschool</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D002971" MajorTopicYN="N">Cleft Lip</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D002972" MajorTopicYN="N">Cleft Palate</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D003430" MajorTopicYN="N">Cross-Sectional Studies</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D004298" MajorTopicYN="N">Dopamine</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D005260" MajorTopicYN="N">Female</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D005838" MajorTopicYN="N">Genotype</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D008297" MajorTopicYN="N">Male</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D010865" MajorTopicYN="N">Pilot Projects</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D016133" MajorTopicYN="N">Polymerase Chain Reaction</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D011110" MajorTopicYN="Y">Polymorphism, Genetic</DescriptorName></MeshHeading></MeshHeadingList><OtherID Source="NLM">NIHMS611082</OtherID><OtherID Source="NLM">PMC4377310</OtherID><KeywordList Owner="NOTNLM"><Keyword MajorTopicYN="N">attention deficit hyperactivity disorder</Keyword><Keyword MajorTopicYN="N">dopamine polymorphism</Keyword><Keyword MajorTopicYN="N">nonsyndromic orofacial cleft</Keyword></KeywordList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="entrez"><Year>2014</Year><Month>10</Month><Day>2</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>2014</Year><Month>10</Month><Day>2</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2016</Year><Month>2</Month><Day>5</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">25271118</ArticleId><ArticleId IdType="pii">1099800414552186</ArticleId><ArticleId IdType="doi">10.1177/1099800414552186</ArticleId><ArticleId IdType="pmc">PMC4377310</ArticleId><ArticleId IdType="mid">NIHMS611082</ArticleId></ArticleIdList></PubmedData></pubmed><affiliations><list><country><li>États-Unis</li></country><region><li>Pennsylvanie</li></region><settlement><li>Pittsburgh</li></settlement><orgName><li>Université de Pittsburgh</li></orgName></list><tree><country name="États-Unis"><region name="Pennsylvanie"><name sortKey="Hopkins, Emily E" sort="Hopkins, Emily E" uniqKey="Hopkins E" first="Emily E" last="Hopkins">Emily E. Hopkins</name></region><name sortKey="Conley, Yvette P" sort="Conley, Yvette P" uniqKey="Conley Y" first="Yvette P" last="Conley">Yvette P. Conley</name><name sortKey="Marazita, Mary L" sort="Marazita, Mary L" uniqKey="Marazita M" first="Mary L" last="Marazita">Mary L. Marazita</name><name sortKey="Wallace, Meredith L" sort="Wallace, Meredith L" uniqKey="Wallace M" first="Meredith L" last="Wallace">Meredith L. Wallace</name></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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HfdIndexSelect -h $EXPLOR_AREA/Data/PubMed/Checkpoint/RBID.i -Sk "pubmed:25271118" \
| HfdSelect -Kh $EXPLOR_AREA/Data/PubMed/Checkpoint/biblio.hfd \
| NlmPubMed2Wicri -a PittsburghV1
| This area was generated with Dilib version V0.6.38. |  |