Publication:

Association study and a systematic meta-analysis of the VNTR polymorphism in the 3'-UTR of dopamine transporter gene and attention-deficit hyperactivity disorder

Date

Date

Date
2019
Journal Article
Published version
cris.lastimport.scopus2025-05-28T03:43:51Z
cris.lastimport.wos2025-07-20T01:32:45Z
cris.virtual.orcidhttps://orcid.org/0000-0002-8161-8683
cris.virtual.orcidhttps://orcid.org/0000-0001-8505-7265
cris.virtualsource.orciddce82cf6-f392-4a91-aa4c-42f840fc31ba
cris.virtualsource.orcid42b90188-0b80-4928-ba7f-2cc63274aefb
dc.contributor.institutionUniversity of Zurich
dc.date.accessioned2019-04-23T13:04:10Z
dc.date.available2019-04-23T13:04:10Z
dc.date.issued2019-04-01
dc.description.abstract

Attention-deficit hyperactivity disorder (ADHD) has been postulated to associate with dopaminergic dysfunction, including the dopamine transporter (DAT1). Several meta-analyses showed small but significant association between the 10-repeat allele in the DAT1 gene in 3'-untranslated region variant number tandem repeat polymorphism and child and adolescent ADHD, whereas in adult ADHD the 9-repeat allele was suggested to confer as risk allele. Interestingly, recent evidence indicated that the long-allele variants (10 repeats and longer) might confer to lower expression of the transporter in comparison to the short-allele. Therefore, we assessed here the association in samples consisting of families with child and adolescent ADHD as well as a case-control sample, using either the 10- versus 9-repeat or the long- versus short-allele approach. Following, we conducted a systematic review and meta-analysis, including family and case-control studies, using the two aforementioned approaches as well as stratifying to age and ethnicity. The first approach (10-repeat) resulted in nominal significant association in child and adolescent ADHD (OR 1.1050 p = 0.0128), that became significant stratifying to European population (OR 1.1301 p = 0.0085). The second approach (long-allele) resulted in significant association with the whole ADHD population (OR 1.1046 p = 0.0048), followed by significant association for child and adolescent ADHD (OR 1.1602 p = 0.0006) and in Caucasian and in European child and adolescent ADHD (OR 1.1310 p = 0.0114; OR 1.1661 p = 0.0061; respectively). We were not able to confirm the association reported in adults using both approaches. In conclusion, we found further indication for a possible DAT1 gene involvement; however, further studies should be conducted with stringent phenotyping to reduce heterogeneity, a limitation observed in most included studies.

dc.identifier.doi10.1007/s00702-019-01998-x
dc.identifier.issn0300-9564
dc.identifier.scopus2-s2.0-85064077543
dc.identifier.urihttps://www.zora.uzh.ch/handle/20.500.14742/157222
dc.identifier.wos000464754400013
dc.language.isoeng
dc.subject.ddc610 Medicine & health
dc.title

Association study and a systematic meta-analysis of the VNTR polymorphism in the 3'-UTR of dopamine transporter gene and attention-deficit hyperactivity disorder

dc.typearticle
dcterms.accessRightsinfo:eu-repo/semantics/openAccess
dcterms.bibliographicCitation.journaltitleJournal of Neural Transmission
dcterms.bibliographicCitation.number4
dcterms.bibliographicCitation.originalpublishernameSpringer
dcterms.bibliographicCitation.pageend529
dcterms.bibliographicCitation.pagestart517
dcterms.bibliographicCitation.pmid30923918
dcterms.bibliographicCitation.volume126
dspace.entity.typePublicationen
uzh.contributor.affiliationUniversitatsSpital Zurich, University of Zurich, University Hospital of Psychiatry Zurich
uzh.contributor.affiliationUniversitatsSpital Zurich
uzh.contributor.affiliationUniversitatsSpital Zurich
uzh.contributor.affiliationUniversitätsklinikum Würzburg
uzh.contributor.affiliationUniversitatsSpital Zurich, University of Zurich
uzh.contributor.authorGrünblatt, Edna
uzh.contributor.authorWerling, Anna Maria
uzh.contributor.authorRoth, Alexander
uzh.contributor.authorRomanos, Marcel
uzh.contributor.authorWalitza, Susanne
uzh.contributor.correspondenceYes
uzh.contributor.correspondenceNo
uzh.contributor.correspondenceNo
uzh.contributor.correspondenceNo
uzh.contributor.correspondenceNo
uzh.document.availabilitypublished_version
uzh.eprint.datestamp2019-04-23 13:04:10
uzh.eprint.lastmod2025-07-20 01:38:07
uzh.eprint.statusChange2019-04-23 13:04:10
uzh.harvester.ethYes
uzh.harvester.nbNo
uzh.identifier.doi10.5167/uzh-170441
uzh.jdb.eprintsId16264
uzh.oastatus.unpaywallhybrid
uzh.oastatus.zoraHybrid
uzh.publication.citationGrünblatt, E., Werling, A. M., Roth, A., Romanos, M., & Walitza, S. (2019). Association study and a systematic meta-analysis of the VNTR polymorphism in the 3’-UTR of dopamine transporter gene and attention-deficit hyperactivity disorder. Journal of Neural Transmission, 126, 517–529. https://doi.org/10.1007/s00702-019-01998-x
uzh.publication.freeAccessAtpubmedid
uzh.publication.originalworkoriginal
uzh.publication.publishedStatusfinal
uzh.scopus.impact28
uzh.scopus.subjectsNeurology
uzh.scopus.subjectsNeurology (clinical)
uzh.scopus.subjectsPsychiatry and Mental Health
uzh.scopus.subjectsBiological Psychiatry
uzh.workflow.doajuzh.workflow.doaj.false
uzh.workflow.eprintid170441
uzh.workflow.fulltextStatuspublic
uzh.workflow.revisions55
uzh.workflow.rightsCheckoffen
uzh.workflow.sourcePubMed:PMID:30923918
uzh.workflow.statusarchive
uzh.wos.impact23
Files

Original bundle

Name:
Grunblatt2019_Article_AssociationStudyAndASystematic.pdf
Size:
1.41 MB
Format:
Adobe Portable Document Format
Publication available in collections: