Bipolar disorder is a dynamic illness with constantly changing symptom and syndrome presentations thatconfound interpretation of neuroimaging findings, as well as treatment response. This feature of the illnessraises the need to examine patients as the condition evolves over time in order to clarify interactionsbetween neuroimaging measures, clinical response and affective state. Careful longitudinal assessmentsand subject retention are critical elements to the success of the BITREC and its proposed projects. TheLongitudinal Assessment Core (LAC) will serve this need and is a direct extension of over a decade ofexperience following young bipolar patients. Specifically, our experience with longitudinal studies isdemonstrated by the success of a number of large, long-term projects. Our previous and ongoing projectsprovide an infrastructure for the longitudinal study of bipolar disorder from which the LAC will be developed.The LAC will be fully integrated with the other BITREC cores and projects as described in the OperationalPlan. Dr. Paul Keck, Professor of Psychiatry and Pharmacology and Vice-Chair for Research in theDepartment of Psychiatry will direct the LAC. He will be responsible for overall core function and foroverseeing infrastructure development. He will be assisted by several clinicians and staff to provide excellentclinical care and ongoing assessments to subjects enrolled in the BITREC. The LAC will hold staff meetingsevery other week to ensure that recruitment benchmarks are being met and to review subjects who havedeveloped new affective episodes or symptoms in order to determine whether they qualify for additionalBITREC projects. Standard operating procedures will be developed to maximize efficiency and meetobjectives and benchmarks. Most decisions involving daily core function will be made by the personnel of thecore under the direction of Dr. Keck. These decisions will be guided by and reported to the BITREC SteeringCommittee. Additionally, Dr. Keck will be integrated within the overall administrative structure of the BITRECby serving on the Steering Committee. With this structure established the LAC will be able to meet itsprimary functions which are: 1) to provide treatment to subjects actively participating in BITREC projects;2) to provide ongoing clinical evaluations and excellent clinical care to subjects enrolled in the BITRECbetween projects; and 3) to identify subjects who meet criteria for a new BITREC project. By following andmanaging subjects across project, the LAC helps to further integrate the various components of the BITREC,assuring a cohesive and effective research center.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Specialized Center (P50)
Project #
1P50MH077138-01A1
Application #
7277388
Study Section
Special Emphasis Panel (ZMH1-ERB-S (01))
Project Start
2007-04-01
Project End
2012-03-31
Budget Start
2007-04-01
Budget End
2008-06-30
Support Year
1
Fiscal Year
2007
Total Cost
$332,898
Indirect Cost
Name
University of Cincinnati
Department
Type
DUNS #
041064767
City
Cincinnati
State
OH
Country
United States
Zip Code
45221
Nery, Fabiano G; Norris, Matthew; Eliassen, James C et al. (2017) White matter volumes in youth offspring of bipolar parents. J Affect Disord 209:246-253
Fleck, David E; Ernest, Nicholas; Adler, Caleb M et al. (2017) Prediction of lithium response in first-episode mania using the LITHium Intelligent Agent (LITHIA): Pilot data and proof-of-concept. Bipolar Disord 19:259-272
Welge, Jeffrey A; Saliba, Lawrence J; Strawn, Jeffrey R et al. (2016) Neurofunctional Differences Among Youth With and at Varying Risk for Developing Mania. J Am Acad Child Adolesc Psychiatry 55:980-989
Strakowski, Stephen M; Fleck, David E; Welge, Jeffrey et al. (2016) fMRI brain activation changes following treatment of a first bipolar manic episode. Bipolar Disord 18:490-501
McNamara, Robert K; Jandacek, Ronald; Tso, Patrick et al. (2016) Adolescents with or at ultra-high risk for bipolar disorder exhibit erythrocyte docosahexaenoic acid and eicosapentaenoic acid deficits: a candidate prodromal risk biomarker. Early Interv Psychiatry 10:203-11
McNamara, Robert K; Moser, Ann B; Jones, Richard I et al. (2016) Familial risk for bipolar disorder is not associated with impaired peroxisomal function: Dissociation from docosahexaenoic acid deficits. Psychiatry Res 246:803-807
McNamara, Robert K; Jandacek, Ronald; Tso, Patrick et al. (2015) First-episode bipolar disorder is associated with erythrocyte membrane docosahexaenoic acid deficits: Dissociation from clinical response to lithium or quetiapine. Psychiatry Res 230:447-53
Jacob, Shawna N; Shear, Paula K; Norris, Matthew et al. (2015) Impact of functional magnetic resonance imaging (fMRI) scanner noise on affective state and attentional performance. J Clin Exp Neuropsychol 37:563-70
Strawn, Jeffrey R; Adler, Caleb M; McNamara, Robert K et al. (2014) Antidepressant tolerability in anxious and depressed youth at high risk for bipolar disorder: a prospective naturalistic treatment study. Bipolar Disord 16:523-30
Cerullo, Michael A; Eliassen, James C; Smith, Christopher T et al. (2014) Bipolar I disorder and major depressive disorder show similar brain activation during depression. Bipolar Disord 16:703-12

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