dc.contributor.author |
Rónai, Zsolt |
|
dc.contributor.author |
Kovács-Nagy, Réka |
|
dc.contributor.author |
Szantai, Eszter |
|
dc.contributor.author |
Elek, Zsuzsanna |
|
dc.contributor.author |
Sasvári-Székely, Mária |
|
dc.contributor.author |
Faludi, Gábor |
|
dc.contributor.author |
Benkovits, Judit |
|
dc.contributor.author |
Réthelyi, János |
|
dc.contributor.author |
Székely, Anna |
|
dc.date.accessioned |
2022-06-15T12:24:52Z |
|
dc.date.available |
2022-06-15T12:24:52Z |
|
dc.date.issued |
2014 |
|
dc.identifier |
84897480864 |
|
dc.identifier.citation |
journalVolume=165;journalIssueNumber=3;journalTitle=AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS;pagerange=217-222;journalAbbreviatedTitle=AM J MED GENET B; |
|
dc.identifier.uri |
http://repo.lib.semmelweis.hu//handle/123456789/9194 |
|
dc.identifier.uri |
doi:10.1002/ajmg.b.32223 |
|
dc.description.abstract |
The glycogen synthase kinase 3B (GSK3B) is an important target protein of several antidepressants, such as lithium, a mood stabilizer. Recent studies associated structural variations of the GSK3B gene to bipolar disorder (BP), although replications were not conclusive. Here we present data on copy number variations (CNVs) of the GSK3B gene probing the 9th exon region in 846 individuals (414 controls, 172 patients with major depressive disorder (MDD) and 260 with BP). A significant accumulation (odds ratio: 5.5, P=0.00051) of the amplified exon 9 region was found in patients (22 out of 432) compared to controls (4 of 414). Analyzing patient subgroups, GSK3B structural variants were found to be risk factors of BP particularly (P=0.00001) with an odds ratio of 8.1 while no such effect was shown in the MDD group. The highest odds (19.7 ratio) for bipolar disorder was observed in females with the amplified exon 9 region. A more detailed analysis of the identified GSK3B CNV by a set of probes covering the GSK3B gene and the adjacent NR1I2 and C3orf15 genes showed that the amplified sequences contained 3' (downstream) segments of the GSK3B and NR1I2 genes but none of them involved the C3orf15 gene. Therefore, the copy number variation of the GSK3B gene could be described as a complex set of structural variants involving partial duplications and deletions, simultaneously. In summary, here we confirmed significant association of the GSK3B CNV and bipolar disorder pointing out that the copy number and extension of the CNV varies among individuals. © 2014 Wiley Periodicals, Inc. |
|
dc.format.extent |
217-222 |
|
dc.relation.ispartof |
urn:issn:1552-4841 |
|
dc.title |
Glycogen synthase kinase 3 beta gene structural variants as possible risk factors of bipolar depression |
|
dc.type |
Journal Article |
|
dc.date.updated |
2022-06-14T12:02:23Z |
|
dc.language.rfc3066 |
en |
|
dc.rights.holder |
NULL |
|
dc.identifier.mtmt |
2552266 |
|
dc.identifier.wos |
000333835100002 |
|
dc.identifier.pubmed |
24677591 |
|
dc.contributor.institution |
MTA-SE-NAP B Molekuláris pszichiátriai és in vitro betegségmodellezési kutatócsoport |
|
dc.contributor.institution |
Magatartástudományi Intézet |
|
dc.contributor.institution |
MTA-SE-NAP B Molekuláris pszichiátriai és in vitro betegségmodellezési kutatócsoport |
|
dc.contributor.institution |
Doktori Iskola |
|
dc.contributor.institution |
Orvosi Vegytani, Molekuláris Biológiai és Patobiokémiai Intézet |
|
dc.contributor.institution |
Semmelweis Egyetem |
|
dc.contributor.institution |
Kútvölgyi Klinikai Tömb Klinikai és Kutatási Mentálhigiénés Osztály |
|
dc.contributor.institution |
Pszichiátriai és Pszichoterápiás Klinika |
|
dc.contributor.institution |
Affektív Pszichológia Tanszék |
|
dc.contributor.institution |
Kútvölgyi Klinikai Tömb Klinikai és Kutatási Mentálhigiénés Osztály |
|
dc.mtmt.swordnote |
Megjegyzés-23843767
N1 Funding Details: R03 TW007656, NIH, National Institutes of Health
Megjegyzés-23843815
N1 Funding Details: R03 TW007656, NIH, National Institutes of Health
Megjegyzés-23843827
N1 Funding Details: R03 TW007656, NIH, National Institutes of Health
Megjegyzés-24057544
N1 Funding Details: R03 TW007656, NIH, National Institutes of Health
Institute of Medical Chemistry, Molecular Biology and Pathobiochemistry, Semmelweis University, Budapest, Hungary
Department of Clinical and Theoretical Mental Health, Kutvolgyi Clinical Center, Semmelweis University, Budapest, Hungary
Department of Psychiatry and Psychotherapy, Semmelweis University, Budapest, Hungary
Institute of Psychology, Eotvos Lorand University, Budapest, Hungary
Cited By :19
Export Date: 25 January 2020
CODEN: AJMGE
Correspondence Address: Szekely, A.; Institute of Psychology, Eotvos Lorand University, Izabella u. 46, Budapest 1064, Hungary; email: szekely.anna@ppk.elte.hu |
|