4.6 Article

The Relationship Between Common Variant Schizophrenia Liability and Number of Offspring in the UK Biobank

Journal

AMERICAN JOURNAL OF PSYCHIATRY
Volume 176, Issue 8, Pages 661-666

Publisher

AMER PSYCHIATRIC PUBLISHING, INC
DOI: 10.1176/appi.ajp.2018.18020140

Keywords

-

Categories

Funding

  1. JMAS Sim Fellowship from the Royal College of Physicians of Edinburgh
  2. Welsh Assembly Government
  3. British Heart Foundation
  4. UK Biobank
  5. Medical Research Council (MRC) Centre [MR/L010305/1]
  6. European Union's Seventh Framework Programme for research, technological development, and demonstration [279227]
  7. [G0800509]
  8. MRC [MR/L023784/2, MR/P005748/1, G0800509] Funding Source: UKRI

Ask authors/readers for more resources

Objective: Schizophrenia is associated with a marked reduction in reproductive success, yet alleles that are common contribute substantially to the liability of the disorder. Among several possible explanations for this, it has been postulated that individuals who carry risk alleles but are unaffected are at some reproductive advantage, offsetting the effects of negative selection among those who are affected. The authors sought to test this hypothesis, isolating the effects of risk alleles on fecundity from the effects that are contingent on expressing schizophrenia. Methods: The burden of schizophrenia risk alleles, as indexed by a polygenic risk score (PRS), carried by 139,679 participants in the UK Biobank study who did not have schizophrenia was compared with the number of offspring of these individuals. Results: Higher schizophrenia liability in study subjects without manifest disorder was weakly but significantly associated with having more children (B=0.006, 95% CI=0.002, 0.010). The relationship was dependent on sex, with a positive correlation between number of children and liability among females (B=0.011, 95% CI=0.006, 0.016), whereas among males, higher liability was associated with being childless (odds ratio=0.96, 95% CI=0.94, 0.98). The negative effect on number of children associated with schizophrenia itself was twofold to 15-fold greater than the positive effect associated with PRS in unaffected individuals. Conclusions: These findings suggest that a complex relationship between liability and fecundity is consistent with sexual selection. Although the overall pattern of a weak positive correlation with liability may contribute to the persistence of schizophrenia risk alleles, these results indicate that the negative selection acting on individuals affected by schizophrenia in the general population is larger than any advantage conferred by genetic loading in unaffected individuals.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

Article Psychology, Clinical

A meta-analysis comparing cognitive function across the mood/psychosis diagnostic spectrum

Amy J. Lynham, Sian L. Cleaver, Ian R. Jones, James T. R. Walters

Summary: Cognitive impairments in schizoaffective disorder are found to be between those in schizophrenia and bipolar disorder. The severity of impairments increases from bipolar disorder to schizoaffective disorder to schizophrenia. Combining the subtypes of schizoaffective disorder may hinder efforts to understand its relationship with schizophrenia or bipolar disorder.

PSYCHOLOGICAL MEDICINE (2022)

Article Health Care Sciences & Services

Web-Based Cognitive Testing in Psychiatric Research: Validation and Usability Study

Amy Joanne Lynham, Ian R. Jones, James T. R. Walters

Summary: This study developed a web-based cognitive battery for psychiatric research and validated it against the MATRICS Consensus Cognitive Battery. The results showed moderate correlations between the web-based tasks and the MATRICS tasks. The characteristics of the participants who chose to participate in the web-based assessments were different from those who did not participate. Lower performance on the battery was associated with poorer functioning.

JOURNAL OF MEDICAL INTERNET RESEARCH (2022)

Article Multidisciplinary Sciences

Transcriptional programs regulating neuronal differentiation are disrupted in DLG2 knockout human embryonic stem cells and enriched for schizophrenia and related disorders risk variants

Bret Sanders, Daniel D'Andrea, Mark O. Collins, Elliott Rees, Tom G. J. Steward, Ying Zhu, Gareth Chapman, Sophie E. Legge, Antonio F. Pardinas, Adrian J. Harwood, William P. Gray, Michael C. O'Donovan, Michael J. Owen, Adam C. Errington, Derek J. Blake, Daniel J. Whitcomb, Andrew J. Pocklington, Eunju Shin

Summary: The coordinated programs of gene expression driving brain development have been studied in relation to neuropsychiatric disorders and cognition. This research combines human genetics with transcriptomic data and analyzes genetic variants and GWAS statistics to reveal the convergence on transcriptional programs regulating excitatory cortical neurogenesis.

NATURE COMMUNICATIONS (2022)

Article Psychiatry

Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants With Treatment Resistance in Schizophrenia

Antonio F. Pardinas, Sophie E. Smart, Isabella R. Willcocks, Peter A. Holmans, Charlotte A. Dennison, Amy J. Lynham, Sophie E. Legge, Bernhard T. Baune, Tim B. Bigdeli, Murray J. Cairns, Aiden Corvin, Ayman H. Fanous, Josef Frank, Brian Kelly, Andrew McQuillin, Ingrid Melle, Preben B. Mortensen, Bryan J. Mowry, Carlos N. Pato, Sathish Periyasamy, Marcella Rietschel, Dan Rujescu, Carmen Simonsen, David St Clair, Paul Tooney, Jing Qin Wu, Ole A. Andreassen, Kaarina Kowalec, Patrick F. Sullivan, Robin M. Murray, Michael J. Owen, James H. MacCabe, Michael C. O'Donovan, James T. R. Walters

Summary: This study examined the genetic architecture of treatment-resistant schizophrenia (TRS) by reassessing genetic data from schizophrenia studies and validating it in carefully ascertained clinical samples. The results showed that TRS is a polygenic trait with detectable heritability, and it is genetically correlated with traits related to intelligence and cognition. The study also found associations between TRS and a history of taking clozapine.

JAMA PSYCHIATRY (2022)

Article Multidisciplinary Sciences

Mapping genomic loci implicates genes and synaptic biology in schizophrenia

Vassily Trubetskoy, Antonio F. Pardinas, Ting Qi, Georgia Panagiotaropoulou, Swapnil Awasthi, Tim B. Bigdeli, Julien Bryois, Chia-Yen Chen, Charlotte A. Dennison, Lynsey S. Hall, Max Lam, Kyoko Watanabe, Oleksandr Frei, Tian Ge, Janet C. Harwood, Frank Koopmans, Sigurdur Magnusson, Alexander L. Richards, Julia Sidorenko, Yang Wu, Jian Zeng, Jakob Grove, Minsoo Kim, Zhiqiang Li, Georgios Voloudakis, Wen Zhang, Mark Adams, Ingrid Agartz, Elizabeth G. Atkinson, Esben Agerbo, Mariam Al Eissa, Margot Albus, Madeline Alexander, Behrooz Z. Alizadeh, Koksal Alptekin, Thomas D. Als, Farooq Amin, Volker Arolt, Manuel Arrojo, Lavinia Athanasiu, Maria Helena Azevedo, Silviu A. Bacanu, Nicholas J. Bass, Martin Begemann, Richard A. Belliveau, Judit Bene, Beben Benyamin, Sarah E. Bergen, Giuseppe Blasi, Julio Bobes, Stefano Bonassi, Alice Braun, Rodrigo Affonseca Bressan, Evelyn J. Bromet, Richard Bruggeman, Peter F. Buckley, Randy L. Buckner, Jonas Bybjerg-Grauholm, Wiepke Cahn, Murray J. Cairns, Monica E. Calkins, Vaughan J. Carr, David Castle, Stanley Catts, Kimberley D. Chambert, Raymond C. K. Chan, Boris Chaumette, Wei Cheng, Eric F. C. Cheung, Siow Ann Chong, David Cohen, Angele Consoli, Quirino Cordeiro, Javier Costas, Charles Curtis, Michael Davidson, Kenneth L. Davis, Lieuwe de Haan, Franziska Degenhardt, Lynn E. DeLisi, Ditte Demontis, Faith Dickerson, Dimitris Dikeos, Timothy Dinan, Srdjan Djurovic, Jubao Duan, Giuseppe Ducci, Frank Dudbridge, Johan G. Eriksson, Lourdes Fananas, Stephen Faraone, Alessia Fiorentino, Andreas Forstner, Josef Frank, Nelson B. Freimer, Menachem Fromer, Alessandra Frustaci, Ary Gadelha, Giulio Genovese, Elliot S. Gershon, Marianna Giannitelli, Ina Giegling, Paola Giusti-Rodriguez, Stephanie Godard, Jacqueline Goldstein, Javier Gonzalez Penas, Ana Gonzalez-Pinto, Srihari Gopal, Jacob Gratten, Michael F. Green, Tiffany A. Greenwood, Olivier Guillin, Sinan Guloksuz, Raquel E. Gur, Ruben C. Gur, Blanca Gutierrez, Eric Hahn, Hakon Hakonarson, Vahram Haroutunian, Annette M. Hartmann, Carol Harvey, Caroline Hayward, Frans A. Henskens, Stefan Herms, Per Hoffmann, Daniel P. Howrigan, Masashi Ikeda, Conrad Iyegbe, Inge Joa, Antonio Julia, Anna K. Kahler, Tony Kam-Thong, Yoichiro Kamatani, Sena Karachanak-Yankova, Oussama Kebir, Matthew C. Keller, Brian J. Kelly, Andrey Khrunin, Sung-Wan Kim, Janis Klovins, Nikolay Kondratiev, Bettina Konte, Julia Kraft, Michiaki Kubo, Vaidutis Kucinskas, Zita Ausrele Kucinskiene, Agung Kusumawardhani, Hana Kuzelov A-Ptackova, Stefano Landi, Laura C. Lazzeroni, Phil H. Lee, Sophie E. Legge, Douglas S. Lehrer, Rebecca Lencer, Bernard Lerer, Miaoxin Li, Jeffrey Lieberman, Gregory A. Light, Svetlana Limborska, Chih-Min Liu, Jouko Lonnqvist, Carmel M. Loughland, Jan Lubinski, Jurjen J. Luykx, Amy Lynham, Milan Macek, Andrew Mackinnon, Patrik K. E. Magnusson, Brion S. Maher, Wolfgang Maier, Dolores Malaspina, Jacques Mallet, Stephen R. Marder, Sara Marsal, Alicia R. Martin, Lourdes Martorell, Manuel Mattheisen, Robert W. McCarley, Colm McDonald, John J. McGrath, Helena Medeiros, Sandra Meier, Bela Melegh, Ingrid Melle, Raquelle Mesholam-Gately, Andres Metspalu, Patricia T. Michie, Lili Milani, Vihra Milanova, Marina Mitjans, Espen Molden, Esther Molina, Maria Dolores Molto, Valeria Mondelli, Carmen Moreno, Christopher P. Morley, Gerard Muntane, Kieran C. Murphy, Inez Myin-Germeys, Igor Nenadic, Gerald Nestadt, Liene Nikitina-Zake, Cristiano Noto, Keith H. Nuechterlein, Niamh Louise O'Brien, F. Anthony O'Neill, Sang-Yun Oh, Ann Olincy, Vanessa Kiyomi Ota, Christos Pantelis, George N. Papadimitriou, Mara Parellada, Tiina Paunio, Renata Pellegrino, Sathish Periyasamy, Diana O. Perkins, Bruno Pfuhlmann, Olli Pietilainen, Jonathan Pimm, David Porteous, John Powell, Diego Quattrone, Digby Quested, Allen D. Radant, Antonio Rampino, Mark H. Rapaport, Anna Rautanen, Abraham Reichenberg, Cheryl Roe, Joshua L. Roffman, Julian Roth, Matthias Rothermundt, Bart P. F. Rutten, Safaa Saker-Delye, Veikko Salomaa, Julio Sanjuan, Marcos Leite Santoro, Adam Savitz, Ulrich Schall, Rodney J. Scott, Larry J. Seidman, Sally Isabel Sharp, Jianxin Shi, Larry J. Siever, Engilbert Sigurdsson, Kang Sim, Nora Skarabis, Petr Slominsky, Hon-Cheong So, Janet L. Sobell, Erik Soderman, Helen J. Stain, Nils Eiel Steen, Agnes A. Steixner-Kumar, Elisabeth Stogmann, William S. Stone, Richard E. Straub, Fabian Streit, Eric Strengman, T. Scott Stroup, Mythily Subramaniam, Catherine A. Sugar, Jaana Suvisaari, Dragan M. Svrakic, Neal R. Swerdlow, Jin P. Szatkiewicz, Thi Minh Tam Ta, Atsushi Takahashi, Chikashi Terao, Florence Thibaut, Draga Toncheva, Paul A. Tooney, Silvia Torretta, Sarah Tosato, Gian Battista Tura, Bruce Turetsky, Alp Ucok, Arne Vaaler, Therese van Amelsvoort, Ruud van Winkel, Juha Veijola, John Waddington, Henrik Walter, Anna Waterreus, Bradley T. Webb, Mark Weiser, Nigel M. Williams, Stephanie H. Witt, Brandon K. Wormley, Jing Qin Wu, Zhida Xu, Robert Yolken, Clement C. Zai, Wei Zhou, Feng Zhu, Fritz Zimprich, Muhammad Ayub, Christian Benner, Alessandro Bertolino, Donald W. Black, Nicholas J. Bray, Gerome Breen, Nancy G. Buccola, William F. Byerley, Wei J. Chen, C. Robert Cloninger, Benedicto Crespo-Facorro, Gary Donohoe, Robert Freedman, Cherrie Galletly, Michael J. Gandal, Massimo Gennarelli, David M. Hougaard, Hai-Gwo Hwu, Assen Jablensky, Steven A. McCarroll, Jennifer L. Moran, Ole Mors, Preben B. Mortensen, Bertram Muller-Myhsok, Amanda L. Neil, Merete Nordentoft, Michele T. Pato, Tracey L. Petryshen, Matti Pirinen, Ann E. Pulver, Thomas G. Schulze, Jeremy M. Silverman, Jordan W. Smoller, Eli A. Stahl, Debby W. Tsuang, Elisabet Vilella, Shi-Heng Wang, Shuhua Xu, Rolf Adolfsson, Celso Arango, Bernhard T. Baune, Sintia Iole Belangero, Anders D. Borglum, David Braff, Elvira Bramon, Joseph D. Buxbaum, Dominique Campion, Jorge A. Cervilla, Sven Cichon, David A. Collier, Aiden Corvin, David Curtis, Marta Di Forti, Enrico Domenici, Hannelore Ehrenreich, Valentina Escott-Price, Tonu Esko, Ayman H. Fanous, Anna Gareeva, Micha Gawlik, Pablo Gejman, Michael Gill, Stephen J. Glatt, Vera Golimbet, Kyung Sue Hong, Christina M. Hultman, Steven E. Hyman, Nakao Iwata, Erik G. Jonsson, Rene S. Kahn, James L. Kennedy, Elza Khusnutdinova, George Kirov, James A. Knowles, Marie-Odile Krebs, Claudine Laurent-Levinson, Jimmy Lee, Todd Lencz, Douglas F. Levinson, Qingqin S. Li, Jianjun Liu, Anil K. Malhotra, Dheeraj Malhotra, Andrew McIntosh, Andrew McQuillin, Paulo R. Menezes, Vera A. Morgan, Derek W. Morris, Bryan J. Mowry, Robin M. Murray, Vishwajit Nimgaonkar, Markus M. Nothen, Roel A. Ophoff, Sara A. Paciga, Aarno Palotie, Carlos N. Pato, Shengying Qin, Marcella Rietschel, Brien P. Riley, Margarita Rivera, Dan Rujescu, Meram C. Saka, Alan R. Sanders, Sibylle G. Schwab, Alessandro Serretti, Pak C. Sham, Yongyong Shi, David St Clair, Hreinn Stefansson, Kari Stefansson, Ming T. Tsuang, Jim van Os, Marquis P. Vawter, Daniel R. Weinberger, Thomas Werge, Dieter B. Wildenauer, Xin Yu, Weihua Yue, Peter A. Holmans, Andrew J. Pocklington, Panos Roussos, Evangelos Vassos, Matthijs Verhage, Peter M. Visscher, Jian Yang, Danielle Posthuma, Ole A. Andreassen, Kenneth S. Kendler, Michael J. Owen, Naomi R. Wray, Mark J. Daly, Hailiang Huang, Benjamin M. Neale, Patrick F. Sullivan, Stephan Ripke, James T. R. Walters, Michael C. O'Donovan

Summary: In this study, a two-stage genome-wide association study was conducted to identify common variants associated with schizophrenia. The results revealed 287 distinct genomic loci and 120 genes likely to be involved in the development of schizophrenia. This research provides valuable insights into the pathophysiology of schizophrenia and offers a resource for further mechanistic studies.

NATURE (2022)

Article Neurosciences

Genomic Stratification of Clozapine Prescription Patterns Using Schizophrenia Polygenic Scores

Djenifer B. Kappel, Sophie E. Legge, Leon Hubbard, Isabella R. Willcocks, Kevin S. O'Connell, Robert L. Smith, Espen Molden, Ole A. Andreassen, Adrian King, John Jansen, Marinka Helthuis, Michael J. Owen, Michael C. O'Donovan, James T. R. Walters, Antonio F. Pardinas

Summary: Treatment-resistant schizophrenia requires optimization of clozapine administration and dosage titration, and factors such as genetics influence clozapine prescription and response. Linear regression models revealed a correlation between schizophrenia polygenic risk score (PRS) and the highest recorded clozapine dose.

BIOLOGICAL PSYCHIATRY (2023)

Article Neurosciences

Pathogenic Mis-splicing of CPEB4 in Schizophrenia

Ivana Olla, Antonio F. Pardinas, Alberto Parras, Ivo H. Hernandez, Maria Santos-Galindo, Sara Pico, Luis F. Callado, Ainara Elorza, Claudia Rodriguez-Lopez, Gonzalo Fernandez-Miranda, Eulalia Belloc, James T. R. Walters, Michael C. O'Donovan, Raul Mendez, Claudio Toma, J. Javier Meana, Michael J. Owen, Jose J. Lucas

Summary: Aberrant splicing of the CPEB4 gene leads to misexpression of schizophrenia risk genes, providing a novel etiological mechanism for schizophrenia.

BIOLOGICAL PSYCHIATRY (2023)

Article Neurosciences

The contribution of Neanderthal introgression and natural selection to neurodegenerative diseases

Zhongbo Chen, Regina H. Reynolds, Antonio F. Pardinas, Sarah A. Gagliano Taliun, Wouter van Rheenen, Kuang Lin, Aleksey Shatunov, Emil K. Gustavsson, Isabella Fogh, Ashley R. Jones, Wim Robberecht, Philippe Corcia, Adriano Chio, Pamela J. Shaw, Karen E. Morrison, Jan H. Veldink, Leonard H. van den Berg, Christopher E. Shaw, John F. Powell, Vincenzo Silani, John A. Hardy, Henry Houlden, Michael J. Owen, Martin R. Turner, Mina Ryten, Ammar Al-Chalabi

Summary: This study found that Neanderthal DNA introgression does not contribute to the genetic risk of neurodegenerative disorders in anatomically-modern humans. Additionally, there is no evidence to support the idea that common variants associated with these disorders are maintained by natural selection. These findings provide valuable insights into the origins of neurodegenerative diseases and address longstanding debates.

NEUROBIOLOGY OF DISEASE (2023)

Article Psychiatry

Cognitive performance at first episode of psychosis and the relationship with future treatment resistance: Evidence from an international prospective cohort study

Edward Millgate, Sophie E. Smart, Antonio F. Pardinas, Eugenia Kravariti, Olesya Ajnakina, Adrianna P. Kapinska, Ole A. Andreassen, Thomas R. E. Barnes, Domenico Berardi, Benedicto Crespo-Facorro, Giuseppe D'Andre, Arsime Demjaha, Marta Di Forti, Gillian A. Doody, Laura Kassoumeri, Aziz Ferchiou, Lorenzo Guidi, Eileen M. Joyce, Ornella Lastrina, Ingrid Melle, Baptiste Pignon, Jean-Romain Richard, Carmen Simonsen, Andrei Szoke, Ilaria Tarricone, Andrea Tortelli, Javier Vazquez-Bourgon, Robin M. Murray, James T. R. Walters, James H. MacCabe

Summary: This study aimed to determine whether cognitive impairment at first episode significantly differs between future antipsychotic responders and resistant cases. The findings showed that patients who were future classified as treatment resistant reported poorer performance across most cognitive domains at baseline. These results indicate that deficits in IQ/general cognitive functioning at first episode are associated with future treatment resistance.

SCHIZOPHRENIA RESEARCH (2023)

Article Psychiatry

DRAGON-Data: a platform and protocol for integrating genomic and phenotypic data across large psychiatric cohorts

Amy J. Lynham, Sarah Knott, Jack F. G. Underwood, Leon Hubbard, Sharifah S. Agha, Jonathan I. Bisson, Marianne B. M. van den Bree, Samuel J. R. A. Chawner, Nicholas Craddock, Michael O'Donovan, Ian R. Jones, George Kirov, Kate Langley, Joanna Martin, Frances Rice, Neil P. Roberts, Anita Thapar, Richard Anney, Michael J. Owen, Jeremy Hall, Antonio F. F. Pardinas, James T. R. Walters

Summary: The aim of this study is to develop procedures for curating and aggregating genotypic and phenotypic data in psychiatric research to investigate the relationship between shared symptoms and shared genetic liability. DRAGON-Data is a resource that combines genetic and non-genetic information and can be used for research across traditional psychiatric diagnostic categories.

BJPSYCH OPEN (2023)

Article Health Care Sciences & Services

Cardiff Online Cognitive Assessment in a National Sample: Cross-Sectional Web-Based Study

Amy Joanne Lynham, Ian R. Jones, James T. R. Walters

Summary: This study developed a web-based cognitive assessment tool (CONCA) to measure the core cognitive domains affected in people with psychiatric disorders. The results showed that CONCA can provide a valid measure of cognitive ability (g) within 15 minutes and demonstrated associations with demographic characteristics and current depression and anxiety symptoms.

JOURNAL OF MEDICAL INTERNET RESEARCH (2023)

Article Biochemistry & Molecular Biology

An empirical test of the estimation of historical effective population size using Drosophila melanogaster

Irene Novo, Noelia Perez-Pereira, Enrique Santiago, Humberto Quesada, Armando Caballero

Summary: The availability of high-density markers allows the estimation of historical effective population size. Recent refinement methods have been shown to be accurate with simulation data and have been applied to real data of various species. An experimental design with Drosophila melanogaster was carried out to test the method, which showed generally good performance. The limitations of the method and its application were discussed.

MOLECULAR ECOLOGY RESOURCES (2023)

Article Psychiatry

Pharmacokinetics and pharmacogenomics of clozapine in an ancestrally diverse sample: a longitudinal analysis and genome-wide association study using UK clinical monitoring data

Antonio F. Pardinas, Djenifer B. Kappel, Milly Roberts, Francesca Tipple, Lisa M. Shitomi-Jones, Adrian King, John Jansen, Marinka Helthuis, Michael J. Owen, Michael C. O'Donovan, James T. R. Walters

Summary: This study used a cross-ancestry GWAS design to investigate variations in clozapine metabolism across different ancestral backgrounds. The study identified genomic associations with clozapine plasma concentrations and assessed the effects of pharmacogenomic predictors across different ancestries. The findings suggest that ancestral differences in clozapine metabolism can be considered for optimizing individualized clozapine prescriptions.

LANCET PSYCHIATRY (2023)

Article Biochemistry & Molecular Biology

Estimation of the contemporary effective population size from SNP data while accounting for mating structure

Enrique Santiago, Armando Caballero, Carlos Kopke, Irene Novo

Summary: A new method is developed to estimate the contemporary effective population size (Ne) based on linkage disequilibrium (LD) in non-model species. It can be applied to different mating systems and variations in family size distribution. The method uses an artificial neural network to predict confidence intervals, providing more consistent estimates.

MOLECULAR ECOLOGY RESOURCES (2023)

Article Anthropology

Sex differences in the distribution of entheseal changes: Meta-analysis of published evidence and its use in Bayesian paleopathological modeling

Carmen Alonso-Llamazares, Belen Lopez, Antonio Pardinas

Summary: This study investigated the sex differences in the distribution of entheseal changes in an archaeological population using a Bayesian approach and meta-analysis. The results showed that males usually had higher frequencies of EC, with bone formation more commonly present in male lower limbs and erosion more frequent in male upper limbs.

AMERICAN JOURNAL OF BIOLOGICAL ANTHROPOLOGY (2022)

No Data Available