This is an application to collect a large cohort of 2,500 bipolar disorder (BP) patients from a relatively homogeneous population in The Netherlands. These patients are extensively phenotyped including a life-chart for longitudinal assessment of bipolar illness;for a selective group activity measures and brain imaging data (MRI) will be obtained. In addition to collecting blood for DNA and RNA extraction, all subjects will be consented for participation in the NIMH Human Genetics Initiative for generation of lymphoblastoid cell lines that are made available to the scientific community. We will also collect DNA of available parents and siblings of BP probands for follow-up genetic studies. Since the identification of genetic susceptibility genes for neuropsychiatric traits requires very large sample sizes, a Dutch national register of BP patients is being proposed with n>8,000 additional BP patients as a resource for phenotype information and infrastructure to collect biomaterials of even larger numbers. This application complements the ongoing NIMH-funded schizophrenia genome-wide association study (GWAS) in the same population, a collaborative effort of the same research groups at UCLA and UMC Utrecht (The Netherlands). The use of the same group of clinicians as well as the same genetically homogeneous population for the study of bipolar disorder and schizophrenia provides a unique opportunity to perform comparative analyses of both phenotypes, which will in turn facilitate the identification of overlapping as well as distinctive candidate genetic susceptibility factors. GWAS will be performed using collected probands and already available Dutch controls (n>10,000). Analysis of gene expression profiling data will compliment the genetic analyses. This study will fully integrate with the internal efforts of meta-analyses of neuropsychiatric traits and genomic data will be made available to the scientific community.

Public Health Relevance

This application is to study the genetic basis of bipolar disorder in a large group of patients from a relatively homogeneous European population. The same population is already being used for a similar schizophrenia study. Since these diseases are known to be related and yet have different characteristics, our study provides a unique opportunity to systematically study differences and overlapping features of these neuropsychiatric disorders.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Research Project (R01)
Project #
1R01MH090553-01
Application #
7879541
Study Section
Behavioral Genetics and Epidemiology Study Section (BGES)
Program Officer
Bender, Patrick
Project Start
2010-07-21
Project End
2015-03-31
Budget Start
2010-07-21
Budget End
2011-03-31
Support Year
1
Fiscal Year
2010
Total Cost
$815,159
Indirect Cost
Name
University of California Los Angeles
Department
Type
Schools of Medicine
DUNS #
092530369
City
Los Angeles
State
CA
Country
United States
Zip Code
90095
Hibar, D P; Westlye, L T; Doan, N T et al. (2018) Cortical abnormalities in bipolar disorder: an MRI analysis of 6503 individuals from the ENIGMA Bipolar Disorder Working Group. Mol Psychiatry 23:932-942
Abramovic, Lucija; Boks, Marco P M; Vreeker, Annabel et al. (2018) White matter disruptions in patients with bipolar disorder. Eur Neuropsychopharmacol 28:743-751
Olde Loohuis, Loes M; Mangul, Serghei; Ori, Anil P S et al. (2018) Transcriptome analysis in whole blood reveals increased microbial diversity in schizophrenia. Transl Psychiatry 8:96
Ori, Anil P S; Bot, Merel H M; Molenhuis, Remco T et al. (2018) A Longitudinal Model of Human Neuronal Differentiation for Functional Investigation of Schizophrenia Polygenic Risk. Biol Psychiatry :
Mangul, Serghei; Yang, Harry Taegyun; Strauli, Nicolas et al. (2018) ROP: dumpster diving in RNA-sequencing to find the source of 1 trillion reads across diverse adult human tissues. Genome Biol 19:36
Stevelink, Remi; Abramovic, Lucija; Verkooijen, Sanne et al. (2018) Childhood abuse and white matter integrity in bipolar disorder patients and healthy controls. Eur Neuropsychopharmacol 28:807-817
Snijders, Gijsje; Titulaer, Maarten J; Bergink, Veerle et al. (2018) No neuronal autoantibodies detected in plasma of patients with a bipolar I disorder. Psychiatry Res 259:460-462
Witt, S H; Streit, F; Jungkunz, M et al. (2017) Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia. Transl Psychiatry 7:e1155
Verkooijen, Sanne; Stevelink, Remi; Abramovic, Lucija et al. (2017) The association of sleep and physical activity with integrity of white matter microstructure in bipolar disorder patients and healthy controls. Psychiatry Res Neuroimaging 262:71-80
Verkooijen, Sanne; van Bergen, Annet H; Knapen, Stefan E et al. (2017) An actigraphy study investigating sleep in bipolar I patients, unaffected siblings and controls. J Affect Disord 208:248-254

Showing the most recent 10 out of 25 publications