Biomarkers have transformed the diagnosis and treatment of cancer, cardiovascular disease, and a host of other medical conditions. In contrast, psychiatric biomarkers remain largely elusive, due in part to the fact that there is a weak correspondence between psychiatric diagnoses and their neurobiological substrates. This is especially true for depression and anxiety disorders, clinically heterogeneous conditions associated with abnormal reactivity to rewarding and aversive stimuli?and to the cues that predict them?and varied patterns of dysfunction in neural circuits that process positive and negative valence. This project will investigate how arousal processes interact with VS circuits to influence the anticipation and experience of rewarding and aversive stimuli in patients seeking treatment for symptoms of depression and anxiety, independent of conventional diagnostic categories. It is specifically designed to advance the goals of the Research Domain Criteria (RDoC) Project, by focusing on four related RDoC constructs that are directly germane to this question?arousal, potential threat threat, approach motivation, and reward attainment?and testing whether they explain variation in symptoms of anxiety and anhedonia in clinical populations. Importantly, this project will also advance RDoC's goal of developing new ways of classifying mental disorders, which will ultimately require methods for identifying novel diagnostic classes linked to homogeneous pathophysiology. To this end, we will test a strategy for discovering novel diagnostic subtypes defined by clustered patterns of abnormal functional connectivity in valence system circuits. We will use statistical clustering and machine learning methods to develop classifiers for diagnosing these subtypes in individual patients, and we will seek to identify distinct mechanisms by which atypical valence system reactivity may contribute to anxiety, anhedonia, and abnormal approach motivation and avoidance behavior in distinct patient subgroups, indexed in the laboratory via integrated, convergent measurements across multiple units of analysis.

Public Health Relevance

Biomarkers have transformed how physicians care for patients with cancer, cardiovascular disease, and a host of other medical conditions by providing quantitative tools for diagnosing disease processes and targeting treatments to the patients most likely to benefit from them. In contrast, biomarkers for psychiatric disorders remain relatively elusive. This project will test a new strategy for developing neuroimaging (brain scan) biomarkers for diagnosing novel subtypes of depression and anxiety in individual patients and then investigate how dysfunction in specific circuits gives rise to specific clinical profiles of anxiety, reward processing, and anxious arousal within these subtypes.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
High Priority, Short Term Project Award (R56)
Project #
1R56MH114976-01A1
Application #
9733429
Study Section
Adult Psychopathology and Disorders of Aging Study Section (APDA)
Program Officer
Ferrante, Michele
Project Start
2018-08-01
Project End
2019-07-31
Budget Start
2018-08-01
Budget End
2019-07-31
Support Year
1
Fiscal Year
2018
Total Cost
Indirect Cost
Name
Weill Medical College of Cornell University
Department
Neurology
Type
Schools of Medicine
DUNS #
060217502
City
New York
State
NY
Country
United States
Zip Code
10065