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Analysis of genome-wide significant bipolar disorder genes in borderline personality disorder

The objective of this study was to investigate the hypothesis that borderline personality disorder (BPD) and bipolar disorder (BD) share genetic variation through analysis of known genetic risk factors for BD in a well-characterized BPD case–control cohort. Genotyping of five genome-wide significant...

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Autores principales: Witt, Stephanie H., Kleindienst, Nikolaus, Frank, Josef, Treutlein, Jens, Mühleisen, Thomas, Degenhardt, Franziska, Jungkunz, Martin, Krumm, Bertram, Cichon, Sven, Tadic, André, Dahmen, Norbert, Schwarze, Cornelia E., Schott, Björn, Dietl, Lydia, Nöthen, Markus M., Mobascher, Arian, Lieb, Klaus, Roepke, Stefan, Rujescu, Dan, Rietschel, Marcella, Schmahl, Christian, Bohus, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4219535/
https://www.ncbi.nlm.nih.gov/pubmed/25304227
http://dx.doi.org/10.1097/YPG.0000000000000060
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author Witt, Stephanie H.
Kleindienst, Nikolaus
Frank, Josef
Treutlein, Jens
Mühleisen, Thomas
Degenhardt, Franziska
Jungkunz, Martin
Krumm, Bertram
Cichon, Sven
Tadic, André
Dahmen, Norbert
Schwarze, Cornelia E.
Schott, Björn
Dietl, Lydia
Nöthen, Markus M.
Mobascher, Arian
Lieb, Klaus
Roepke, Stefan
Rujescu, Dan
Rietschel, Marcella
Schmahl, Christian
Bohus, Martin
author_facet Witt, Stephanie H.
Kleindienst, Nikolaus
Frank, Josef
Treutlein, Jens
Mühleisen, Thomas
Degenhardt, Franziska
Jungkunz, Martin
Krumm, Bertram
Cichon, Sven
Tadic, André
Dahmen, Norbert
Schwarze, Cornelia E.
Schott, Björn
Dietl, Lydia
Nöthen, Markus M.
Mobascher, Arian
Lieb, Klaus
Roepke, Stefan
Rujescu, Dan
Rietschel, Marcella
Schmahl, Christian
Bohus, Martin
author_sort Witt, Stephanie H.
collection PubMed
description The objective of this study was to investigate the hypothesis that borderline personality disorder (BPD) and bipolar disorder (BD) share genetic variation through analysis of known genetic risk factors for BD in a well-characterized BPD case–control cohort. Genotyping of five genome-wide significant variants identified for BD (in CACNA1C, ANK3, and ODZ4) was performed in 673 BPD cases and 748 controls. A nominally significant association with BPD was found for rs1006737 in CACNA1C (P=0.0498). Sex-specific analysis showed that this signal was present only in women. This is the first report of an association between a BD risk gene and BPD where selection was not based on a priori hypotheses about its function, but on an unbiased hypothesis-free screening of the genome. Genome-wide association data of large samples of BPD are warranted and will eventually identify new risk genes and the overlap between BPD and BD if it exists.
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spelling pubmed-42195352014-11-04 Analysis of genome-wide significant bipolar disorder genes in borderline personality disorder Witt, Stephanie H. Kleindienst, Nikolaus Frank, Josef Treutlein, Jens Mühleisen, Thomas Degenhardt, Franziska Jungkunz, Martin Krumm, Bertram Cichon, Sven Tadic, André Dahmen, Norbert Schwarze, Cornelia E. Schott, Björn Dietl, Lydia Nöthen, Markus M. Mobascher, Arian Lieb, Klaus Roepke, Stefan Rujescu, Dan Rietschel, Marcella Schmahl, Christian Bohus, Martin Psychiatr Genet Brief Reports The objective of this study was to investigate the hypothesis that borderline personality disorder (BPD) and bipolar disorder (BD) share genetic variation through analysis of known genetic risk factors for BD in a well-characterized BPD case–control cohort. Genotyping of five genome-wide significant variants identified for BD (in CACNA1C, ANK3, and ODZ4) was performed in 673 BPD cases and 748 controls. A nominally significant association with BPD was found for rs1006737 in CACNA1C (P=0.0498). Sex-specific analysis showed that this signal was present only in women. This is the first report of an association between a BD risk gene and BPD where selection was not based on a priori hypotheses about its function, but on an unbiased hypothesis-free screening of the genome. Genome-wide association data of large samples of BPD are warranted and will eventually identify new risk genes and the overlap between BPD and BD if it exists. Lippincott Williams & Wilkins 2014-12 2014-10-31 /pmc/articles/PMC4219535/ /pubmed/25304227 http://dx.doi.org/10.1097/YPG.0000000000000060 Text en © 2014 Wolters Kluwer Health | Lippincott Williams & Wilkins This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License, where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially. http://creativecommons.org/licenses/by-nc-nd/3.0.
spellingShingle Brief Reports
Witt, Stephanie H.
Kleindienst, Nikolaus
Frank, Josef
Treutlein, Jens
Mühleisen, Thomas
Degenhardt, Franziska
Jungkunz, Martin
Krumm, Bertram
Cichon, Sven
Tadic, André
Dahmen, Norbert
Schwarze, Cornelia E.
Schott, Björn
Dietl, Lydia
Nöthen, Markus M.
Mobascher, Arian
Lieb, Klaus
Roepke, Stefan
Rujescu, Dan
Rietschel, Marcella
Schmahl, Christian
Bohus, Martin
Analysis of genome-wide significant bipolar disorder genes in borderline personality disorder
title Analysis of genome-wide significant bipolar disorder genes in borderline personality disorder
title_full Analysis of genome-wide significant bipolar disorder genes in borderline personality disorder
title_fullStr Analysis of genome-wide significant bipolar disorder genes in borderline personality disorder
title_full_unstemmed Analysis of genome-wide significant bipolar disorder genes in borderline personality disorder
title_short Analysis of genome-wide significant bipolar disorder genes in borderline personality disorder
title_sort analysis of genome-wide significant bipolar disorder genes in borderline personality disorder
topic Brief Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4219535/
https://www.ncbi.nlm.nih.gov/pubmed/25304227
http://dx.doi.org/10.1097/YPG.0000000000000060
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