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
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
| cris.lastimport.scopus | 2025-05-28T03:43:51Z | |
| cris.lastimport.wos | 2025-07-20T01:32:45Z | |
| cris.virtual.orcid | https://orcid.org/0000-0002-8161-8683 | |
| cris.virtual.orcid | https://orcid.org/0000-0001-8505-7265 | |
| cris.virtualsource.orcid | dce82cf6-f392-4a91-aa4c-42f840fc31ba | |
| cris.virtualsource.orcid | 42b90188-0b80-4928-ba7f-2cc63274aefb | |
| dc.contributor.institution | University of Zurich | |
| dc.date.accessioned | 2019-04-23T13:04:10Z | |
| dc.date.available | 2019-04-23T13:04:10Z | |
| dc.date.issued | 2019-04-01 | |
| 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.doi | 10.1007/s00702-019-01998-x | |
| dc.identifier.issn | 0300-9564 | |
| dc.identifier.scopus | 2-s2.0-85064077543 | |
| dc.identifier.uri | https://www.zora.uzh.ch/handle/20.500.14742/157222 | |
| dc.identifier.wos | 000464754400013 | |
| dc.language.iso | eng | |
| dc.subject.ddc | 610 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.type | article | |
| dcterms.accessRights | info:eu-repo/semantics/openAccess | |
| dcterms.bibliographicCitation.journaltitle | Journal of Neural Transmission | |
| dcterms.bibliographicCitation.number | 4 | |
| dcterms.bibliographicCitation.originalpublishername | Springer | |
| dcterms.bibliographicCitation.pageend | 529 | |
| dcterms.bibliographicCitation.pagestart | 517 | |
| dcterms.bibliographicCitation.pmid | 30923918 | |
| dcterms.bibliographicCitation.volume | 126 | |
| dspace.entity.type | Publication | en |
| uzh.contributor.affiliation | UniversitatsSpital Zurich, University of Zurich, University Hospital of Psychiatry Zurich | |
| uzh.contributor.affiliation | UniversitatsSpital Zurich | |
| uzh.contributor.affiliation | UniversitatsSpital Zurich | |
| uzh.contributor.affiliation | Universitätsklinikum Würzburg | |
| uzh.contributor.affiliation | UniversitatsSpital Zurich, University of Zurich | |
| uzh.contributor.author | Grünblatt, Edna | |
| uzh.contributor.author | Werling, Anna Maria | |
| uzh.contributor.author | Roth, Alexander | |
| uzh.contributor.author | Romanos, Marcel | |
| uzh.contributor.author | Walitza, Susanne | |
| uzh.contributor.correspondence | Yes | |
| uzh.contributor.correspondence | No | |
| uzh.contributor.correspondence | No | |
| uzh.contributor.correspondence | No | |
| uzh.contributor.correspondence | No | |
| uzh.document.availability | published_version | |
| uzh.eprint.datestamp | 2019-04-23 13:04:10 | |
| uzh.eprint.lastmod | 2025-07-20 01:38:07 | |
| uzh.eprint.statusChange | 2019-04-23 13:04:10 | |
| uzh.harvester.eth | Yes | |
| uzh.harvester.nb | No | |
| uzh.identifier.doi | 10.5167/uzh-170441 | |
| uzh.jdb.eprintsId | 16264 | |
| uzh.oastatus.unpaywall | hybrid | |
| uzh.oastatus.zora | Hybrid | |
| uzh.publication.citation | Grünblatt, 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.freeAccessAt | pubmedid | |
| uzh.publication.originalwork | original | |
| uzh.publication.publishedStatus | final | |
| uzh.scopus.impact | 28 | |
| uzh.scopus.subjects | Neurology | |
| uzh.scopus.subjects | Neurology (clinical) | |
| uzh.scopus.subjects | Psychiatry and Mental Health | |
| uzh.scopus.subjects | Biological Psychiatry | |
| uzh.workflow.doaj | uzh.workflow.doaj.false | |
| uzh.workflow.eprintid | 170441 | |
| uzh.workflow.fulltextStatus | public | |
| uzh.workflow.revisions | 55 | |
| uzh.workflow.rightsCheck | offen | |
| uzh.workflow.source | PubMed:PMID:30923918 | |
| uzh.workflow.status | archive | |
| uzh.wos.impact | 23 | |
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