Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia

Archive ouverte

Witt, S | Streit, F | Jungkunz, M | Frank, J | Awasthi, S | Reinbold, C | Treutlein, J | Degenhardt, F | Forstner, A | Heilmann-Heimbach, S | Dietl, L | Schwarze, C | Schendel, D | Strohmaier, J | Abdellaoui, A | Adolfsson, R | Air, T | Akil, H | Alda, M | Alliey-Rodriguez, N | Andreassen, O | Babadjanova, G | Bass, N | Bauer, M | Baune, B | Bellivier, Frank | Bergen, S | Bethell, A | Biernacka, J | Blackwood, D | Boks, M | Boomsma, D | Børglum, A | Borrmann-Hassenbach, M | Brennan, P | Budde, M | Buttenschøn, H | Byrne, E | Cervantes, P | Clarke, T-K | Craddock, N | Cruceanu, C | Curtis, D | Czerski, P | Dannlowski, U | Davis, T | de Geus, E | Di Florio, A | Djurovic, S | Domenici, E | Edenberg, H | Etain, Bruno | Fischer, S | Forty, L | Fraser, C | Frye, M | Fullerton, J | Gade, K | Gershon, E | Giegling, I | Gordon, S | Gordon-Smith, K | Grabe, H | Green, E | Greenwood, T | Grigoroiu-Serbanescu, M | Guzman-Parra, J | Hall, L | Hamshere, M | Hauser, J | Hautzinger, M | Heilbronner, U | Herms, S | Hitturlingappa, S | Hoffmann, P | Holmans, P | Hottenga, J-J | Jamain, S | Jones, I | Jones, L | Juréus, A | Kahn, R | Kammerer-Ciernioch, J | Kirov, G | Kittel-Schneider, S | Kloiber, S | Knott, S | Kogevinas, M | Landén, M | Leber, M | Leboyer, M | Li, Q | Lissowska, J | Lucae, S | Martin, N | Mayoral-Cleries, F | Mcelroy, S | Mcintosh, A | Mckay, J | Mcquillin, A | Medland, S | Middeldorp, C | Milaneschi, Y | Mitchell, P | Montgomery, G | Morken, G | Mors, O | Mühleisen, T | Müller-Myhsok, B | Myers, R | Nievergelt, C | Nurnberger, J | O'Donovan, M | Loohuis, L | Ophoff, R | Oruc, L | Owen, M | Paciga, S | Penninx, B | Perry, A | Pfennig, A | Potash, J | Preisig, M | Reif, A | Rivas, F | Rouleau, G | Schofield, P | Schulze, T | Schwarz, M | Scott, L | Sinnamon, G | Stahl, E | Strauss, J | Turecki, G | van der Auwera, S | Vedder, H | Vincent, J | Willemsen, G | Witt, C | Wray, N | Xi, H | Tadic, A | Dahmen, N | Schott, B | Cichon, S | Nöthen, M | Ripke, S | Mobascher, A | Rujescu, D | Lieb, K | Roepke, S | Schmahl, C | Bohus, M | Rietschel, M

Edité par CCSD ; Nature Pub. Group -

International audience. Borderline personality disorder (BOR) is determined by environmental and genetic factors, and characterized by affective instability and impulsivity, diagnostic symptoms also observed in manic phases of bipolar disorder (BIP). Up to 20% of BIP patients show comorbidity with BOR. This report describes the first case-control genome-wide association study (GWAS) of BOR, performed in one of the largest BOR patient samples worldwide. The focus of our analysis was (i) to detect genes and gene sets involved in BOR and (ii) to investigate the genetic overlap with BIP. As there is considerable genetic overlap between BIP, major depression (MDD) and schizophrenia (SCZ) and a high comorbidity of BOR and MDD, we also analyzed the genetic overlap of BOR with SCZ and MDD. GWAS, gene-based tests and gene-set analyses were performed in 998 BOR patients and 1545 controls. Linkage disequilibrium score regression was used to detect the genetic overlap between BOR and these disorders. Single marker analysis revealed no significant association after correction for multiple testing. Gene-based analysis yielded two significant genes: DPYD (P=4.42 × 10-7) and PKP4 (P=8.67 × 10-7); and gene-set analysis yielded a significant finding for exocytosis (GO:0006887, PFDR=0.019; FDR, false discovery rate). Prior studies have implicated DPYD, PKP4 and exocytosis in BIP and SCZ. The most notable finding of the present study was the genetic overlap of BOR with BIP (rg=0.28 [P=2.99 × 10-3]), SCZ (rg=0.34 [P=4.37 × 10-5]) and MDD (rg=0.57 [P=1.04 × 10-3]). We believe our study is the first to demonstrate that BOR overlaps with BIP, MDD and SCZ on the genetic level. Whether this is confined to transdiagnostic clinical symptoms should be examined in future studies.

Suggestions

Du même auteur

Common variant at 16p11.2 conferring risk of psychosis

Archive ouverte | Steinberg, S | CCSD

International audience. Epidemiological and genetic data support the notion that schizophrenia and bipolar disorder share genetic risk factors. In our previous genome-wide association study, meta-analysis and follow...

Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function and bipolar disorder susceptibility

Archive ouverte | Li, M | CCSD

Bipolar disorder (BD) is a polygenic disorder that shares substantial genetic risk factors with major depressive disorder (MDD). Genetic analyses have reported numerous BD susceptibility genes, while some variants, such as single-...

A novel Alzheimer disease locus located near the gene encoding tau protein

Archive ouverte | Jun, G | CCSD

International audience. APOE ɛ4, the most significant genetic risk factor for Alzheimer disease (AD), may mask effects of other loci. We re-analyzed genome-wide association study (GWAS) data from the International G...

Chargement des enrichissements...