Rationale: Evidence suggests that the pathophysiology of MOD entails alterations of glia and neurons in specific brain regions such as the striatum (i.e., caudate and putamen) and subgenual prefrontal cortex (sgPFC). This application is to initiate an investigation of adolescent MOD through the study of brain neurochemistry using proton magnetic resonance spectroscopy (1H-MRS). 1H-MRS allows the non-invasive in-vivo assessment of intra-cranial metabolite levels such as choline (Cho) and N-acetylaspartate (NAA), which reflect membrane break-down and neuronal viability respectively. Adolescent MOD is associated with serious short and long-term morbidity and mortality. Despite its public health importance, adolescent MOD has been subject to relatively little biological research. Goals: (1) To develop expertise in 1H-MRS through testing for specific neurochemical abnormalities in adolescent MOD. (2) Long-term plans are to become an independent investigator and integrate translational methods into pediatric mood disorder research. Training Plan: Includes training in: (1) MRS and analytic techniques in clinical research, (2) diagnostic and research methods relevant to mood disorders in youth, (3) biostatistics, (4) affective neuroscience, (5) ethics of clinical research, through: (1) didactic courses: MRS, neuroanatomy, biostatistics, neuroscience, and ethics;(2) mentoring;(3) consultation with multidisciplinary experts;(4) participation at scientific meetings;and (5) a research plan that complements career development activities. Research Plan:
Specific aim will test hypotheses that adolescents with MOD have significantly lower NAA levels and significantly elevated Cho levels in the caudate and putamen, compared to healthy adolescents. Exploratory aim, will examine NAA and Cho levels in the sgPFC. Methods: Based on power analyses, subjects will consist of a) 30 adolescents, ages 13 through18, with parental MOD (for a relatively homogenous group of adolescent MOD), minimum 8 weeks'duration, CDRS-R scores>40, and onset at >13;b) 30 healthy comparisons without parental MOD, matched to MOD group for gender, age, handedness, and ethnicity;all at Tanner stages 4-5, and psychotropic naive. Neuroimaging will include 3 dimensional multivoxel 1H-MRS acquired at high (3T) magnetic field with high spatial resolution, <1 cm3 voxels focusing on caudate, putamen and sgPFC. Previous spectroscopy has had the limitation of using single voxels with low resolution. Significance: The proposed research will provide knowledge of the neurobiology of MOD during a developmental stage that is particularly vulnerable to neurodevelopmental perturbations. Such knowledge would ultimately improve early identification of MOD, and the development of novel treatments. If findings are promising, larger studies will follow to assess their relevance to MOD in general (familial and non-familial), the prediction of treatment response, and the diagnostic specificity of neurochemical abnormalities.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Mentored Patient-Oriented Research Career Development Award (K23)
Project #
5K23MH077072-03
Application #
7561671
Study Section
Special Emphasis Panel (ZRG1-BBBP-H (02))
Program Officer
Avenevoli, Shelli A
Project Start
2007-02-01
Project End
2012-01-31
Budget Start
2009-02-01
Budget End
2010-01-31
Support Year
3
Fiscal Year
2009
Total Cost
$180,270
Indirect Cost
Name
New York University
Department
Psychiatry
Type
Schools of Medicine
DUNS #
121911077
City
New York
State
NY
Country
United States
Zip Code
10016
Gabbay, Vilma; Ely, Benjamin A; Li, Qingyang et al. (2013) Striatum-based circuitry of adolescent depression and anhedonia. J Am Acad Child Adolesc Psychiatry 52:628-41.e13
Gabbay, Vilma; Mao, Xiangling; Klein, Rachel G et al. (2012) Anterior cingulate cortex ?-aminobutyric acid in depressed adolescents: relationship to anhedonia. Arch Gen Psychiatry 69:139-49
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Gabbay, Vilma; Babb, James S; Klein, Rachel G et al. (2012) A double-blind, placebo-controlled trial of ?-3 fatty acids in Tourette's disorder. Pediatrics 129:e1493-500
Gabbay, Vilma; Klein, Rachel G; Katz, Yisrael et al. (2010) The possible role of the kynurenine pathway in adolescent depression with melancholic features. J Child Psychol Psychiatry 51:935-43
Gabbay, Vilma; Liebes, Leonard; Katz, Yisrael et al. (2010) The kynurenine pathway in adolescent depression: preliminary findings from a proton MR spectroscopy study. Prog Neuropsychopharmacol Biol Psychiatry 34:37-44
Gabbay, Vilma; Klein, Rachel G; Guttman, Leah E et al. (2009) A preliminary study of cytokines in suicidal and nonsuicidal adolescents with major depression. J Child Adolesc Psychopharmacol 19:423-30
Gabbay, Vilma; Klein, Rachel G; Alonso, Carmen M et al. (2009) Immune system dysregulation in adolescent major depressive disorder. J Affect Disord 115:177-82
Gabbay, Vilma; Coffey, Barbara J; Guttman, Leah E et al. (2009) A cytokine study in children and adolescents with Tourette's disorder. Prog Neuropsychopharmacol Biol Psychiatry 33:967-71
Cullen, Kathryn R; Gee, Dylan G; Klimes-Dougan, Bonnie et al. (2009) A preliminary study of functional connectivity in comorbid adolescent depression. Neurosci Lett 460:227-31

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