Abstract

Two emotional/motivational constructs that have been posited to underlie anxiety and depressive disorders are heightened sensitivity to threat and reduced sensitivity to reward, respectively. It is unclear, though, whether these constructs are only epiphenomena or also connote risk for these disorders (and relatedly, whether they connote risk for separate disorders). Using family history of psychopathology as an indicator of risk, the present study examined whether biomarkers of sensitivity to threat (startle potentiation) and reward (frontal EEG asymmetry) were associated with similar or different familial liabilities. In addition, the present study examined whether these biomarkers were associated with risk independent of proband DSM-IV diagnosis. One-hundred and seventy-three individuals diagnosed with panic disorder (PD), early onset major depressive disorder (MDD), both (comorbids), or controls completed two laboratory paradigms assessing sensitivity to predictable/unpredictable threat (measured via startle response) and reward (measured via frontal EEG asymmetry during a gambling task). Results indicated that across all participants: (a) startle potentiation to unpredictable threat was associated with family history of PD (but not MDD); and (b) frontal EEG asymmetry while anticipating reward was associated with family history of MDD (but not PD). Additionally, both measures continued to be associated with family history of psychopathology after controlling for proband DSM-IV diagnosis. Results suggest that the proposed biomarkers of sensitivity to unpredictable threat and reward exhibit discriminant validity and may add to the predictive validity of the DSM-IV defined constructs of PD and MDD, respectively.

Highlights

  • IntroductionResearch has sought to identify biomarkers (i.e., objective biological indicators of normal or disease processes) of depressive and anxiety disorders to aid in diagnosis, prevention, and treatment efforts (Biomarkers Definitions Working Group, 2001; Hyman, 2007)

  • In the past decade, research has sought to identify biomarkers of depressive and anxiety disorders to aid in diagnosis, prevention, and treatment efforts (Biomarkers Definitions Working Group, 2001; Hyman, 2007)

  • The present study examined whether individual differences on biomarkers of sensitivity to threat and reward were associated with an indicator of risk - family history of psychopathology - in a sample of individuals with panic disorder (PD) and/or early-onset major depressive disorder (MDD) and healthy controls

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Summary

Introduction

Research has sought to identify biomarkers (i.e., objective biological indicators of normal or disease processes) of depressive and anxiety disorders to aid in diagnosis, prevention, and treatment efforts (Biomarkers Definitions Working Group, 2001; Hyman, 2007). Numerous studies have found reduced left relative to right frontal EEG asymmetries in individuals who are at risk for depression (Tomarken, Dichter, Garber, & Simien, 2004), currently experiencing depression (Thibodeau, Jorgensen, & Kim, 2006), and in remission from depression (Gotlib, Ranganath, & Rosenfeld, 1998; Stewart, Bismark, Towers, Coan, & Allen, 2010). Most of these investigations examined EEG asymmetry during an uncontrolled ‘resting’ state and not during an actual reward manipulation. Coan, Allen, and McKnight (2006) compared EEG asymmetry during both ‘resting’ and ‘emotional challenge’ conditions, and found that the ‘emotional challenge’ condition was associated with more pronounced individual differences, resistance to undesirable variance from reference scheme, and reliable relationships with criterion measures

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