Bipolar spectrum disorder (BPD) is a severe neuropsychiatric disorder of mood disturbance. Individuals with BPD experience cyclical periods of mania or hypomania and depression, and in some cases, psychosis. With a lifetime prevalence of 3.9% in the U.S. adult population, BPD has been regarded as a common disease with a complex etiology. Various studies have categorized BPD based on age at onset. Pediatric BPD has become an established diagnosis and may be regarded as a subclass of BPD. These children have phenotypically more severe conditions than the average adult BPD patient. Although it is known that major gene effects are more likely in early-onset disorders, this subclass of BPD has remained largely uncharacterized from a genomics perspective. We employ the use of an extreme trait design in which whole genome sequencing analysis of a modest sized, carefully selected sample of a bipolar disorder population with extreme phenotypes will likely identify rare variants with modest to high effect sizes enriched for in this population. First, we determine the phenotype and genotype of our pediatric BPD cohort (Specific Aim 1). Trained experts will diagnose and clinically characterize probands (n=100), including their comorbidities, and meticulously document the phenotypes of their parents (n=175) and siblings (n=40). Blood samples will be collected from all participants. Whole genome sequencing (WGS) of probands will be performed using 10X Genomics technology, a recently introduced extension of WGS, with parents and siblings sequenced using standard short-read technology. Our laboratory will then use state-of-the-art genomic analysis tools and techniques to elucidate the genomic landscape of pediatric BPD by identifying highly penetrant and deleterious de novo, mosaic and inherited rare variants conferring risk (Specific Aim 2). Variant annotation and prioritization will be performed to determine candidate variants and Sanger sequencing will be used to validate these. Functional enrichment and pathway analyses will be used to functionally characterize candidate genes. To achieve robust and unbiased results, we propose to further validate our findings and measure recurrence rates in a replication cohort of children diagnosed with bipolar disorder. In order to determine the significance of our genomic findings in pediatric BPD to the occurrence of bipolar disorder in the adult population, we will assess their frequency within recent large-scale genomic sequencing studies of BPD (Specific Aim 3). We expect to find more rare, penetrant, deleterious genomic variants of significance to the study population, with possibly broader implications in the adult BPD population. This study employs novel and innovative approaches by the specific focus on a pediatric bipolar disorder population with severe phenotypic presentations and the use of advanced genomic tools and technologies. In conducting this research, we will contribute to the understanding of the genetic bases of a burdensome mental health condition of relevance to the mission of the National Institute of Mental Health.

Public Health Relevance

We propose the study of pediatric bipolar disorder in a population with severe phenotypic presentations. The discovery of the underlying genetic mechanism of disease by study of rare variation may elucidate potential therapeutic targets, which may be critical for decreasing the national and global disease burden of bipolar disorder, a devastating mental illness affecting young children and adolescents as well as adults.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Dissertation Award (R36)
Project #
5R36MH118005-02
Application #
9756461
Study Section
Special Emphasis Panel (ZMH1)
Program Officer
Van'T Veer, Ashlee V
Project Start
2018-08-06
Project End
2020-07-31
Budget Start
2019-08-01
Budget End
2020-07-31
Support Year
2
Fiscal Year
2019
Total Cost
Indirect Cost
Name
Hugo W. Moser Research Institute Kennedy Krieger
Department
Type
DUNS #
155342439
City
Baltimore
State
MD
Country
United States
Zip Code
21205