Back to Search Start Over

Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder

Authors :
Arianna DiFlorio
Patrick F. Sullivan
Sebastian Zöllner
Margarita Rivera
Richard M. Myers
Stanley J. Watson
Jun Li
Anders Juréus
Sarah E. Bergen
Gonçalo R. Abecasis
Jordan W. Smoller
Michael Conlon O'Donovan
Neil Risch
Hoang T. Nguyen
Chen Jiang
Xiaoming Jia
Mehdi Pirooznia
Danielle Posthuma
Adam E. Locke
Peter P. Zandi
John B. Vincent
Niamh Mullins
Duncan Palmer
Shaun Purcell
Gerome Breen
Christina M. Hultman
Andreas Reif
Khanh K. Thai
Virginia L. Willour
Pui-Yan Kwok
Laura J. Scott
Anne U. Jackson
Michael John Owen
Fernando S. Goes
Steven A. McCarroll
James B. Potash
Mikael Landén
Jennifer L. Moran
Michele T. Pato
Hyun Min Kang
Marco P. Boks
Sinéad B. Chapman
W. Richard McCombie
Janet L. Sobell
Matthew Zawistowski
Rolf Adolfsson
Yongwen Zhuang
Michael Boehnke
René S. Kahn
Huda Akil
James T.R. Walters
Margit Burmeister
Douglas Blackwood
Cathryn M. Lewis
Eli A. Stahl
Mark N. Kvale
Melissa DelaBastide
Catherine Schaefer
Benjamin M. Neale
Giulio Genovese
Carlos N. Pato
Nicholas John Craddock
Andrew McQuillin
Shawn Levy
Aiden Corvin
Pamela Sklar
Weiqing Wang
Andrew M. McIntosh
Ling Shen
Eric T. Monson
Derek W. Morris
Douglas M. Ruderfer
Roel A. Ophoff
Peter McGuffin
Sarah Cohen-Woods
Willem H. Ouwehand
Complex Trait Genetics
Amsterdam Neuroscience - Complex Trait Genetics
Goes, Fernando S [0000-0001-6262-8264]
Locke, Adam E [0000-0001-6227-198X]
Palmer, Duncan [0000-0002-0824-0047]
Wang, Weiqing [0000-0003-1565-0148]
Genovese, Giulio [0000-0003-3066-5575]
Jackson, Anne U [0000-0002-9672-2547]
Nguyen, Hoang [0000-0001-6910-7269]
Pirooznia, Mehdi [0000-0002-4210-6458]
Zawistowski, Matthew [0000-0002-3005-083X]
Abecasis, Gonçalo [0000-0003-1509-1825]
Bergen, Sarah [0000-0002-5888-0034]
Burmeister, Margit [0000-0002-1914-2434]
Kwok, Pui-Yan [0000-0002-5087-3059]
Li, Jun Z [0000-0001-6727-0812]
Levy, Shawn E [0000-0002-1369-5740]
Watson, Stanley [0000-0003-4980-5523]
Blackwood, Douglas [0000-0002-4076-9346]
Boehnke, Michael [0000-0002-6442-7754]
Breen, Gerome [0000-0003-2053-1792]
Landen, Mikael [0000-0002-4496-6451]
Lewis, Cathryn [0000-0002-8249-8476]
McCarroll, Steven A [0000-0002-6954-8184]
McIntosh, Andrew [0000-0002-0198-4588]
McQuillin, Andrew [0000-0003-1567-2240]
Morris, Derek [0000-0002-3413-570X]
O'Donovan, Michael [0000-0001-7073-2379]
Boks, Marco [0000-0001-6163-7484]
Kahn, Rene [0000-0001-5909-8004]
Ouwehand, Willem [0000-0002-7744-1790]
Owen, Michael [0000-0003-4798-0862]
Potash, James B [0000-0002-5802-8079]
Reif, Andreas [0000-0002-0992-634X]
Vincent, John [0000-0003-0692-2519]
Neale, Benjamin [0000-0003-1513-6077]
Purcell, Shaun [0000-0002-7402-5812]
Schaefer, Catherine [0000-0003-2644-055X]
Stahl, Eli A [0000-0002-1192-0561]
Zandi, Peter P [0000-0001-8423-2623]
Scott, Laura J [0000-0002-4886-5084]
Apollo - University of Cambridge Repository
Human genetics
Amsterdam Neuroscience - Compulsivity, Impulsivity & Attention
Amsterdam Reproduction & Development (AR&D)
Psychiatry
APH - Mental Health
Amsterdam Neuroscience - Mood, Anxiety, Psychosis, Stress & Sleep
APH - Digital Health
Source :
Molecular Psychiatry, 26(9), 5239-5250. Nature Publishing Group, Molecular psychiatry, vol 26, iss 9, Jia, X, Goes, F S, Locke, A E, Palmer, D, Wang, W, Cohen-Woods, S, Genovese, G, Jackson, A U, Jiang, C, Kvale, M, Mullins, N, Nguyen, H, Pirooznia, M, Rivera, M, Ruderfer, D M, Shen, L, Thai, K, Zawistowski, M, Zhuang, Y, Abecasis, G, Akil, H, Bergen, S, Burmeister, M, Chapman, S, DelaBastide, M, Juréus, A, Kang, H M, Kwok, P Y, Li, J Z, Levy, S E, Monson, E T, Moran, J, Sobell, J, Watson, S, Willour, V, Zöllner, S, Adolfsson, R, Blackwood, D, Boehnke, M, Breen, G, Corvin, A, Craddock, N, DiFlorio, A, Hultman, C M, Landen, M, Lewis, C, McCarroll, S A, Richard McCombie, W, McGuffin, P, McIntosh, A, McQuillin, A, Morris, D, Myers, R M, O’Donovan, M, Ophoff, R, Boks, M, Kahn, R, Ouwehand, W, Owen, M, Pato, C, Pato, M, Posthuma, D, Potash, J B, Reif, A, Sklar, P, Smoller, J, Sullivan, P F, Vincent, J, Walters, J, Neale, B, Purcell, S, Risch, N, Schaefer, C, Stahl, E A, Zandi, P P & Scott, L J 2021, ' Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder ', Molecular Psychiatry, vol. 26, no. 9, pp. 5239-5250 . https://doi.org/10.1038/s41380-020-01006-9, Molecular Psychiatry, Jia, X, Goes, F S, Locke, A E, Palmer, D, Wang, W, Cohen-Woods, S, Genovese, G, Jackson, A U, Jiang, C, Kvale, M, Mullins, N, Nguyen, H, Pirooznia, M, Rivera, M, Ruderfer, D M, Shen, L, Thai, K, Zawistowski, M, Zhuang, Y, Abecasis, G, Akil, H, Bergen, S, Burmeister, M, Champion, S, DelaBastide, M, Juréus, A, Kang, H M, Kwok, P-Y, Li, J Z, Levy, S E, Monson, E T, Moran, J, Sobell, J, Watson, S, Willour, V, Zöllner, S, Adolfsson, R, Blackwood, D, Boehnke, M, Breen, G, Corvin, A, Craddock, N, DiFlorio, A, Hultman, C M, Landen, M, Lewis, C, McCarroll, S A, Richard McCombie, W, McGuffin, P, McIntosh, A, McQuillin, A, Morris, D, Myers, R M, O’Donovan, M, Ophoff, R, Boks, M, Kahn, R, Ouwehand, W, Owen, M, Pato, C, Pato, M, Posthuma, D, Potash, J B, Reif, A, Sklar, P, Smoller, J, Sullivan, P F, Vincent, J, Walters, J, Neale, B, Purcell, S, Risch, N, Schaefer, C, Stahl, E A, Zandi, P P & Scott, L J 2021, ' Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder ', Molecular Psychiatry, vol. 26, no. 9, pp. 5239-5250 . https://doi.org/10.1038/s41380-020-01006-9, Jia, X, Goes, F S, Locke, A E, Palmer, D, Wang, W, Cohen-woods, S, Genovese, G, Jackson, A U, Jiang, C, Kvale, M, Mullins, N, Nguyen, H, Pirooznia, M, Rivera, M, Ruderfer, D M, Shen, L, Thai, K, Zawistowski, M, Zhuang, Y, Abecasis, G, Akil, H, Bergen, S, Burmeister, M, Chapman, S, Delabastide, M, Juréus, A, Kang, H M, Kwok, P, Li, J Z, Levy, S E, Monson, E T, Moran, J, Sobell, J, Watson, S, Willour, V, Zöllner, S, Adolfsson, R, Blackwood, D, Boehnke, M, Breen, G, Corvin, A, Craddock, N, Diflorio, A, Hultman, C M, Landen, M, Lewis, C, Mccarroll, S A, Richard Mccombie, W, Mcguffin, P, Mcintosh, A, Mcquillin, A, Morris, D, Myers, R M, O’donovan, M, Ophoff, R, Boks, M, Kahn, R, Ouwehand, W, Owen, M, Pato, C, Pato, M, Posthuma, D, Potash, J B, Reif, A, Sklar, P, Smoller, J, Sullivan, P F, Vincent, J, Walters, J, Neale, B, Purcell, S, Risch, N, Schaefer, C, Stahl, E A, Zandi, P P & Scott, L J 2021, ' Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder ', Molecular Psychiatry . https://doi.org/10.1038/s41380-020-01006-9, Digibug. Repositorio Institucional de la Universidad de Granada, instname, Digibug: Repositorio Institucional de la Universidad de Granada, Universidad de Granada (UGR)
Publication Year :
2021

Abstract

Bipolar disorder (BD) is a serious mental illness with substantial common variant heritability. However, the role of rare coding variation in BD is not well established. We examined the protein-coding (exonic) sequences of 3,987 unrelated individuals with BD and 5,322 controls of predominantly European ancestry across four cohorts from the Bipolar Sequencing Consortium (BSC). We assessed the burden of rare, protein-altering, single nucleotide variants classified as pathogenic or likely pathogenic (P-LP) both exome-wide and within several groups of genes with phenotypic or biologic plausibility in BD. While we observed an increased burden of rare coding P-LP variants within 165 genes identified as BD GWAS regions in 3,987 BD cases (meta-analysis OR = 1.9, 95% CI = 1.3–2.8, one-sided p = 6.0 × 10−4), this enrichment did not replicate in an additional 9,929 BD cases and 14,018 controls (OR = 0.9, one-side p = 0.70). Although BD shares common variant heritability with schizophrenia, in the BSC sample we did not observe a significant enrichment of P-LP variants in SCZ GWAS genes, in two classes of neuronal synaptic genes (RBFOX2 and FMRP) associated with SCZ or in loss-of-function intolerant genes. In this study, the largest analysis of exonic variation in BD, individuals with BD do not carry a replicable enrichment of rare P-LP variants across the exome or in any of several groups of genes with biologic plausibility. Moreover, despite a strong shared susceptibility between BD and SCZ through common genetic variation, we do not observe an association between BD risk and rare P-LP coding variants in genes known to modulate risk for SCZ.<br />International Bipolar Sequencing Consortium (NIMH) R01 MH 110437<br />Whole Genome Sequencing for Schizophrenia and Biopolar Disorder in the GPS (NIMH) UO1 MH105653<br />Whole Genome and Exome Sequencing for Bipolar Disorder (NIMH) R01 MH 094145<br />Multi-ethnic GWAS of Bipolar I Disorder (NIH) R01 MH 085543<br />Genetic Epidemiology Research in Adult Health and Aging (GERA) RC2 AG036607<br />Kaiser Permanente Research Program on Genes, Environment, and Health<br />Rare Bipolar Loci Identification Through Synaptome Sequencing (NIMH) R01 MH 087979 MH 087992<br />2/2 Large Scale Genetic Studies of Schizophrenia in Sweden R01MH095034<br />1/3 Genetic Analysis of the International Cohort Collection for Bipolar Disorder R01MH106531<br />1/2 Large Scale Genetic Studies of Schizophrenia in Sweden R01MH077139<br />2/3 Genetic Analysis of the International Cohort Collection for Bipolar Disorder R01MH106527<br />Dalio Foundation

Details

Language :
English
ISSN :
13594184
Database :
OpenAIRE
Journal :
Molecular Psychiatry, 26(9), 5239-5250. Nature Publishing Group, Molecular psychiatry, vol 26, iss 9, Jia, X, Goes, F S, Locke, A E, Palmer, D, Wang, W, Cohen-Woods, S, Genovese, G, Jackson, A U, Jiang, C, Kvale, M, Mullins, N, Nguyen, H, Pirooznia, M, Rivera, M, Ruderfer, D M, Shen, L, Thai, K, Zawistowski, M, Zhuang, Y, Abecasis, G, Akil, H, Bergen, S, Burmeister, M, Chapman, S, DelaBastide, M, Juréus, A, Kang, H M, Kwok, P Y, Li, J Z, Levy, S E, Monson, E T, Moran, J, Sobell, J, Watson, S, Willour, V, Zöllner, S, Adolfsson, R, Blackwood, D, Boehnke, M, Breen, G, Corvin, A, Craddock, N, DiFlorio, A, Hultman, C M, Landen, M, Lewis, C, McCarroll, S A, Richard McCombie, W, McGuffin, P, McIntosh, A, McQuillin, A, Morris, D, Myers, R M, O’Donovan, M, Ophoff, R, Boks, M, Kahn, R, Ouwehand, W, Owen, M, Pato, C, Pato, M, Posthuma, D, Potash, J B, Reif, A, Sklar, P, Smoller, J, Sullivan, P F, Vincent, J, Walters, J, Neale, B, Purcell, S, Risch, N, Schaefer, C, Stahl, E A, Zandi, P P & Scott, L J 2021, ' Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder ', Molecular Psychiatry, vol. 26, no. 9, pp. 5239-5250 . https://doi.org/10.1038/s41380-020-01006-9, Molecular Psychiatry, Jia, X, Goes, F S, Locke, A E, Palmer, D, Wang, W, Cohen-Woods, S, Genovese, G, Jackson, A U, Jiang, C, Kvale, M, Mullins, N, Nguyen, H, Pirooznia, M, Rivera, M, Ruderfer, D M, Shen, L, Thai, K, Zawistowski, M, Zhuang, Y, Abecasis, G, Akil, H, Bergen, S, Burmeister, M, Champion, S, DelaBastide, M, Juréus, A, Kang, H M, Kwok, P-Y, Li, J Z, Levy, S E, Monson, E T, Moran, J, Sobell, J, Watson, S, Willour, V, Zöllner, S, Adolfsson, R, Blackwood, D, Boehnke, M, Breen, G, Corvin, A, Craddock, N, DiFlorio, A, Hultman, C M, Landen, M, Lewis, C, McCarroll, S A, Richard McCombie, W, McGuffin, P, McIntosh, A, McQuillin, A, Morris, D, Myers, R M, O’Donovan, M, Ophoff, R, Boks, M, Kahn, R, Ouwehand, W, Owen, M, Pato, C, Pato, M, Posthuma, D, Potash, J B, Reif, A, Sklar, P, Smoller, J, Sullivan, P F, Vincent, J, Walters, J, Neale, B, Purcell, S, Risch, N, Schaefer, C, Stahl, E A, Zandi, P P & Scott, L J 2021, ' Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder ', Molecular Psychiatry, vol. 26, no. 9, pp. 5239-5250 . https://doi.org/10.1038/s41380-020-01006-9, Jia, X, Goes, F S, Locke, A E, Palmer, D, Wang, W, Cohen-woods, S, Genovese, G, Jackson, A U, Jiang, C, Kvale, M, Mullins, N, Nguyen, H, Pirooznia, M, Rivera, M, Ruderfer, D M, Shen, L, Thai, K, Zawistowski, M, Zhuang, Y, Abecasis, G, Akil, H, Bergen, S, Burmeister, M, Chapman, S, Delabastide, M, Juréus, A, Kang, H M, Kwok, P, Li, J Z, Levy, S E, Monson, E T, Moran, J, Sobell, J, Watson, S, Willour, V, Zöllner, S, Adolfsson, R, Blackwood, D, Boehnke, M, Breen, G, Corvin, A, Craddock, N, Diflorio, A, Hultman, C M, Landen, M, Lewis, C, Mccarroll, S A, Richard Mccombie, W, Mcguffin, P, Mcintosh, A, Mcquillin, A, Morris, D, Myers, R M, O’donovan, M, Ophoff, R, Boks, M, Kahn, R, Ouwehand, W, Owen, M, Pato, C, Pato, M, Posthuma, D, Potash, J B, Reif, A, Sklar, P, Smoller, J, Sullivan, P F, Vincent, J, Walters, J, Neale, B, Purcell, S, Risch, N, Schaefer, C, Stahl, E A, Zandi, P P & Scott, L J 2021, ' Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder ', Molecular Psychiatry . https://doi.org/10.1038/s41380-020-01006-9, Digibug. Repositorio Institucional de la Universidad de Granada, instname, Digibug: Repositorio Institucional de la Universidad de Granada, Universidad de Granada (UGR)
Accession number :
edsair.doi.dedup.....d2b28270dff0616afd7d691245b0f9b8
Full Text :
https://doi.org/10.1038/s41380-020-01006-9