The causes of bipolar disorder (BD) are unknown, but neuroimaging studies have identified abnormalities in fronto-limbic brain (FLB) regions, which parallel findings of neurocognitive impairment. There is growing evidence to support abnormalities in sub- regions of the prefrontal cortex (PFC) and medial temporal lobe. In particular, the most consistent findings implicate the dorsolateral PFC, anterior cingulate, amygdala and hippocampus. These brain regions are interlinked and abnormalities could result in emotional instability, behavioral activation and other symptoms seen in BD patients. The primary aim of our study is to determine the extent to which FLB pathology in BD is attributable to genetic effects. The relationship between FLB abnormalities and BD will be addressed in a control study of same-gender sibling pairs discordant for BD type I. We will enroll 60 male and female sibling pairs discordant for BD and 60 matched controls, in a 3 group design (BD probands, unaffected siblings and healthy controls). Each subject will undergo brain magnetic resonance imaging (MRI), spectroscopy (MRS), diffusion tensor imaging (DTI) scans and neurocognitive testing. We will examine the relationship between BD and FLB abnormalities, neurocognitive function and genetic vulnerability. We will use state-of-the art tools from brain imaging and cognitive neuroscience to study the contribution of familial factors in determining FLB impairment in sibling pairs discordant for BD. The study will further elucidate the pathophysiology of BD and the role of genetic factors in the genesis of such abnormalities. If our hypotheses are confirmed, this will indicate that FLB abnormalities in BD are heritable and could be viable endophenotypes in the search for the specific genes involved.

Public Health Relevance

Bipolar disorder is a very prevalent psychiatric illness and a major health problem worldwide. This study will examine the role of heritability on key brain abnormalities involved in causation of bipolar disorder (BD). If our hypotheses are confirmed, this will indicate that abnormalities in fronto-limbic brain regions in patients with BD are heritable and could be utilized as """"""""endophenotypes"""""""" to guide future research on the specific genes involved.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Research Project (R01)
Project #
5R01MH085667-02
Application #
8544492
Study Section
Special Emphasis Panel (ZRG1-BDCN-H (03))
Program Officer
Muehrer, Peter R
Project Start
2012-09-12
Project End
2017-06-30
Budget Start
2013-07-01
Budget End
2014-06-30
Support Year
2
Fiscal Year
2013
Total Cost
$557,539
Indirect Cost
$163,413
Name
University of Texas Health Science Center Houston
Department
Psychiatry
Type
Schools of Medicine
DUNS #
800771594
City
Houston
State
TX
Country
United States
Zip Code
77225
Scaini, G; Fries, G R; Valvassori, S S et al. (2017) Perturbations in the apoptotic pathway and mitochondrial network dynamics in peripheral blood mononuclear cells from bipolar disorder patients. Transl Psychiatry 7:e1111
Zhang, Guohao; Kochunov, Peter; Hong, Elliot et al. (2017) ENIGMA-Viewer: interactive visualization strategies for conveying effect sizes in meta-analysis. BMC Bioinformatics 18:253
Bauer, Isabelle E; Hautzinger, Martin; Meyer, Thomas D (2017) Memory performance predicts recurrence of mania in bipolar disorder following psychotherapy: A preliminary study. J Psychiatr Res 84:207-213
Wu, Mon-Ju; Mwangi, Benson; Bauer, Isabelle E et al. (2017) Identification and individualized prediction of clinical phenotypes in bipolar disorders using neurocognitive data, neuroimaging scans and machine learning. Neuroimage 145:254-264
Brouwer, Rachel M; Panizzon, Matthew S; Glahn, David C et al. (2017) Genetic influences on individual differences in longitudinal changes in global and subcortical brain volumes: Results of the ENIGMA plasticity working group. Hum Brain Mapp 38:4444-4458
Wu, Mon-Ju; Mwangi, Benson; Passos, Ives Cavalcante et al. (2017) Prediction of vulnerability to bipolar disorder using multivariate neurocognitive patterns: a pilot study. Int J Bipolar Disord 5:32
Cao, B; Passos, I C; Wu, M-J et al. (2017) Brain gyrification and neuroprogression in bipolar disorder. Acta Psychiatr Scand 135:612-613
Cao, Bo; Stanley, Jeffrey A; Passos, Ives Cavalcante et al. (2017) Elevated Choline-Containing Compound Levels in Rapid Cycling Bipolar Disorder. Neuropsychopharmacology 42:2252-2258
Cao, B; Passos, I C; Mwangi, B et al. (2017) Hippocampal subfield volumes in mood disorders. Mol Psychiatry 22:1352-1358
Passos, Ives Cavalcante; Mwangi, Benson; Cao, Bo et al. (2016) Identifying a clinical signature of suicidality among patients with mood disorders: A pilot study using a machine learning approach. J Affect Disord 193:109-16

Showing the most recent 10 out of 46 publications