Previous efforts to identify biological correlates of anti-depressant response in bipolar disorder have yielded only modest success. The degree to which depression arises from serotonergic or other neurotransmitter abnormalities remains an unsolved question. Moreover, standard anti-depressants may be less effective for bipolar than unipolar depression and pose unique risks for inducing mania or cycle acceleration. Therefore, a compelling need exists to develop new methodologies to better anticipate treatment outcomes. The focus of this Career Development Award is to provide a translational research and training experience for the P.I. in applications of psychiatric genetics to clinically-based studies of psychopathology and treatment outcome in bipolar illness. As a model for this type of research, pharmacogenetic correlates of anti-depressant response, focusing on serotonin system candidate gene polymorphisms, will be examined in a family-based cohort. While preliminary studies have identified candidate genes with polymorphisms of significance to psychopathology, or psychotropic drug action, pharmacogenetic applications ti bipolar disorder remain largely unexplored. The proposed core research project will be an ancillary study to the Systematic Treatment Enhancement Program for Bipolar Disorder (STEP-BD), an NIMH-sponsored multi-clinical trial. DNA samples will initially be obtained from a minimum of 100 depressed probands and family members; probands already optimized on valproate or lithium will undergo a 6-week trial of a serotonin reuptake inhibitor. In later years of the Award period, family-based genotype and SSRI antidepressant response data will be added from several hundred additional bipolar probands at collaborative research sites. Antidepressant responsivity will be analyzed relative to allele frequencies of 4 serotonin-related polymorphic candidate genes of known functional significance. Multivariate models will be developed to assess the relative statistical contribution of pharmacogenetic polymorphisms added to clinical factors potentially associated with treatment response. The primary aim of the career development plan is for the P.I. to acquire expertise in human genetics and candidate gene polymorphism analyses in order to inform future clinical studies of psychotropic drug response and other aspects of psychopathology that may represent phenotypes of bipolar disorder.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Mentored Patient-Oriented Research Career Development Award (K23)
Project #
1K23MH001936-01A1
Application #
6333854
Study Section
Special Emphasis Panel (ZMH1-CRB-J (02))
Program Officer
Desmond, Nancy L
Project Start
2002-04-20
Project End
2003-03-31
Budget Start
2002-04-20
Budget End
2003-03-31
Support Year
1
Fiscal Year
2002
Total Cost
$170,745
Indirect Cost
Name
Weill Medical College of Cornell University
Department
Psychiatry
Type
Schools of Medicine
DUNS #
060217502
City
New York
State
NY
Country
United States
Zip Code
10065
Brooks 3rd, John O; Goldberg, Joseph F; Ketter, Terence A et al. (2011) Safety and tolerability associated with second-generation antipsychotic polytherapy in bipolar disorder: findings from the Systematic Treatment Enhancement Program for Bipolar Disorder. J Clin Psychiatry 72:240-7
Goldberg, Joseph F; Brooks 3rd, John O; Kurita, Keiko et al. (2009) Depressive illness burden associated with complex polypharmacy in patients with bipolar disorder: findings from the STEP-BD. J Clin Psychiatry 70:155-62
Goldberg, Joseph F; Garno, Jessica L (2009) Age at onset of bipolar disorder and risk for comorbid borderline personality disorder. Bipolar Disord 11:205-8
Goldberg, Joseph F; Perlis, Roy H; Bowden, Charles L et al. (2009) Manic symptoms during depressive episodes in 1,380 patients with bipolar disorder: findings from the STEP-BD. Am J Psychiatry 166:173-81
Goldberg, Joseph F; Gerstein, Rachel K; Wenze, Susan J et al. (2008) Dysfunctional attitudes and cognitive schemas in bipolar manic and unipolar depressed outpatients: implications for cognitively based psychotherapeutics. J Nerv Ment Dis 196:207-10
Goldberg, Joseph F; Perlis, Roy H; Ghaemi, S Nassir et al. (2007) Adjunctive antidepressant use and symptomatic recovery among bipolar depressed patients with concomitant manic symptoms: findings from the STEP-BD. Am J Psychiatry 164:1348-55
Goldberg, Joseph F; Allen, Michael H; Miklowitz, David A et al. (2005) Suicidal ideation and pharmacotherapy among STEP-BD patients. Psychiatr Serv 56:1534-40
Garno, Jessica L; Goldberg, Joseph F; Ramirez, Paul Michael et al. (2005) Impact of childhood abuse on the clinical course of bipolar disorder. Br J Psychiatry 186:121-5
Goldberg, Joseph F; Harrow, Martin (2005) Subjective life satisfaction and objective functional outcome in bipolar and unipolar mood disorders: a longitudinal analysis. J Affect Disord 89:79-89
Goldberg, Joseph F; Wenze, Susan J; Welker, Tara M et al. (2005) Content-specificity of dysfunctional cognitions for patients with bipolar mania versus unipolar depression: a preliminary study. Bipolar Disord 7:49-56

Showing the most recent 10 out of 21 publications