Proposed is a 5-year longitudinal, high-risk study examining the psychopathological and functional status of 800 children and adolescents (age 7-18.0 years old) of 400 parents with bipolar disorder(BPD) and compare them with 300 children of 150 non-bipolar, community control parents, with frequency matched on age, ethnicity, and neighborhood. The parents with BPD will be ascertained through the Stanley Center Community control parents will be ascertained using Cole's reverse directory. Offspring will be assessed at intake and annually, alternating between face-to-face and phone interviews, with standardized instruments to examine the differential incidence of psychopathology, dimensional measures of behavior and emotional psychiatric history. Offspring (an estimated 160 of 800) of BPD parents who at intake already have BPD (I, II, NOS and cycolthymia) will be followed through another grant Within the high-risk cohort, the investigators will examine the relationships between initial presentation and ultimate development of BPD and other mood disorders across different age groups. They hypothesize that offspring of BPD vs. offspring of control will show 1) Higher rates of incident BPD and other mood disorders and 2) Higher degree of behavior problems and mood dysregulation: 3) Within the offspring of BPD, incidence of BPD will be predicted by: early onset of parent's BPD, loaded pedigree for increased mood liability, increased exposure to familial and environmental negative events, and onset of puberty; and 4) Prepubertal onset vs. post-puberty onset BPD will show greater chronicity, frequency of mixed and rapid cycling presentations, and comorbid disruptive disorders. This unique prospective study will have important implications, and comorbid disruptive disorders. This unique prospective study will have important implications for early-detection, intervention, and prevention of childhood-onset of BPD.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Research Project (R01)
Project #
5R01MH060952-05
Application #
6898882
Study Section
Special Emphasis Panel (ZRG1-BBBP-6 (01))
Program Officer
James, Regina Smith
Project Start
2001-08-20
Project End
2006-06-30
Budget Start
2005-07-01
Budget End
2006-06-30
Support Year
5
Fiscal Year
2005
Total Cost
$655,568
Indirect Cost
Name
University of Pittsburgh
Department
Psychiatry
Type
Schools of Medicine
DUNS #
004514360
City
Pittsburgh
State
PA
Country
United States
Zip Code
15213
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Hafeman, Danella M; Chase, Henry W; Monk, Kelly et al. (2018) Intrinsic functional connectivity correlates of person-level risk for bipolar disorder in offspring of affected parents. Neuropsychopharmacology :
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Diler, Rasim Somer; Goldstein, Tina R; Hafeman, Danella et al. (2017) Characteristics of depression among offspring at high and low familial risk of bipolar disorder. Bipolar Disord 19:344-352
Angulo, Melina; Rooks, Brian T; Gill, MaryKay et al. (2017) Psychometrics of the screen for adult anxiety related disorders (SCAARED)- A new scale for the assessment of DSM-5 anxiety disorders. Psychiatry Res 253:84-90
Wise, T; Radua, J; Via, E et al. (2017) Common and distinct patterns of grey-matter volume alteration in major depression and bipolar disorder: evidence from voxel-based meta-analysis. Mol Psychiatry 22:1455-1463
Ham, Byung-Joo; Greenberg, Tsafrir; Chase, Henry W et al. (2016) Impact of the glucocorticoid receptor BclI polymorphism on reward expectancy and prediction error related ventral striatal reactivity in depressed and healthy individuals. J Psychopharmacol 30:48-55

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