Studying the Psychophysiology of Social Dysfunction in Depression

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Studying the Psychophysiology of Social Dysfunction in Depression Cardiac Vagal Function In Depressed and

Studying the Psychophysiology of Social Dysfunction in Depression Cardiac Vagal Function In Depressed and Nondepressed Women Jill M. Cyranowski, Holly A. Swartz, Tara L. Hofkens, and Peter J. Gianaros Western Psychiatric Institute and Clinic University of Pittsburgh Medical School

Disclosures Presenter Company Product Research Other: J. M. Cyranowski NIMH X Pittsburgh Foundation X

Disclosures Presenter Company Product Research Other: J. M. Cyranowski NIMH X Pittsburgh Foundation X

Study Collaborators Tara L. Hofkens Peter J. Gianaros Kristin Salomon Holly A. Swartz Janet

Study Collaborators Tara L. Hofkens Peter J. Gianaros Kristin Salomon Holly A. Swartz Janet Amico Ellen Frank, DMDPP clinic Grant Support MH 64144, MH 30915 Clinical Neuroscience Research Center (RR 0000056), Pittsburgh Mind-Body Center (HL 076852/076858)

Cardiac Vagal Function Myocardium of the heart is dually innervated by sympathetic and parasympathetic

Cardiac Vagal Function Myocardium of the heart is dually innervated by sympathetic and parasympathetic branches of the autonomic nervous system (ANS) Parasympathetic inputs provide inhibitory control of heart rate via direct innervation of the heart by the vagus nerve The “Vagal Brake” Vagal activation: slows HR to favor energy conservation / parasympathetic dominance during times of rest or perceived safety Vagal withdrawal: rapid shift to sympathetic dominance during time of threat/stress

Cardiac Vagal Function Indirect indicators of cardiac vagal control – measured via continuous EKG,

Cardiac Vagal Function Indirect indicators of cardiac vagal control – measured via continuous EKG, spectral analyses Vagal effects on HR occur rapidly (in milliseconds) Changes in HR that occur in high frequency range of HR variability (0. 15 -0. 50 Hz) used to index vagal tone (commonly referred to as high-frequency HPV or respiratory sinus arrhythmia - RSA) Depression associated with impaired cardiac vagal function (indexed via diminished RSA) Rottenberg (2007) meta-analysis: Obtained small-to -medium (d=. 332) effect size of depression Though multiple methodological issues

 Collateral branches of the vagus also terminate on soft palate, pharynx, larynx, facial

Collateral branches of the vagus also terminate on soft palate, pharynx, larynx, facial muscles - involved in emotional expression and social communication

Depression and Vagal Dysfunction Polyvagal Theory (Porges, 2007) vagal pathways evolved in mammals to

Depression and Vagal Dysfunction Polyvagal Theory (Porges, 2007) vagal pathways evolved in mammals to allow for social engagement & affiliation via flexible (vagal) modulation of sympathetic fight-or-flight responses, and facilitation of emotional expression & social communication Diminished vagal function (⇩ RSA) associated with: (1) Cardiac-hemodynamic dysregulation - CVD risk (2) Emotional dysregulation - depression & anxiety (3) Social dysfunction – unmarried, social isolation

Methodological Issues Thus, diminished vagal function may represent a biological mechanism related to common

Methodological Issues Thus, diminished vagal function may represent a biological mechanism related to common patterns of cardiac-hemodynamic as well as emotional and social dysfunction in depression Methodological issues in extant literature Inclusion of subjects on antidepressants Lack of control for respiratory rate No control for trauma history Most designs assess resting state vagal control or vagal withdraw in response to acute stress But little on social factors expected to trigger vagal activation

Study Sample Females aged 20 -40 15 depressed, 15 age/race matched controls Medical and

Study Sample Females aged 20 -40 15 depressed, 15 age/race matched controls Medical and Psychiatric Screening Medically healthy, normal cycling Antidepressant-free for at least 4 weeks Psychiatric screening with SCID, HRSD Mean age (SD) Depressed 31. 77 (6. 65) Non-Depressed 27. 89 (4. 58) % Caucasian (n) BMI, mean (SD) 86. 6% (13) 24. 08 (2. 81) 86. 6% (13) 24. 69 (4. 34) BDI, mean (SD) * 19. 36 (7. 19) 2. 4 (2. 87) BAI, mean (SD) * 17. 07 (10. 40) 3. 07 (4. 38)

Study Design Laboratory Study Testing sessions scheduled at 2 pm Instrumented with 3 -lead

Study Design Laboratory Study Testing sessions scheduled at 2 pm Instrumented with 3 -lead EKG and upper abdominal strain gauge to assess respiratory rate 2 Laboratory Tasks (order counterbalanced) Stress task ⇨ vagal withdrawal Relationship-focused imagery ⇨ vagal activation 20 minute 25 m Habituation Resting Baseline 10 min TASK #1 30 minute 20 minute 30 minute Resting Recovery Resting Baseline Resting Recovery 20 min Rest

Measures Respiratory Sinus Arrhythmia (RSA) EKG signal sampled continuously at 1000 Hz Spectral-power values

Measures Respiratory Sinus Arrhythmia (RSA) EKG signal sampled continuously at 1000 Hz Spectral-power values in the 0. 15 -0. 50 Hz bandwidth integrated for each 1 -min epoch Respiration Rate Breaths per minute via strain gauge Trauma History Questionnaire (Green, 1995) Lifetime history of crime, general disaster or trauma, sexual/physical assault experiences Low (0 -1 event) High (>2 events) Depressed 7 (46. 7%) 8 (53. 3%) Non-Depressed 9 (60%) 6 (40%)

Analyses Repeated measures ANOVAs for RSA outcomes over the course of each study task

Analyses Repeated measures ANOVAs for RSA outcomes over the course of each study task 2 (Group) x 2 (Trauma History) x 2 (Task Order) Period (Baseline, Task, Recovery 1, Recovery 2) Models controlling for respiratory rate Methods advocated by Grossman et al (2007) Within-subject linear regression models – calculated standardized residual scores representing the variance in RSA for each 1 min epoch that could not be attributed to withinsubject fluctuations in respiration rate for the same 1 -min epoch

Results: Impact of Lab Tasks on RSA Speech Stress Task F(3, 66) = 4.

Results: Impact of Lab Tasks on RSA Speech Stress Task F(3, 66) = 4. 36, p=. 02 Relationship Imagery Task F(3, 66) = 3. 79, p=. 02

Relationship Imagery Results Non-adjusted RSA: Period [F(3, 66)=3. 79, p=. 02]; Group [F(1, 22)=5.

Relationship Imagery Results Non-adjusted RSA: Period [F(3, 66)=3. 79, p=. 02]; Group [F(1, 22)=5. 54, p=. 028]

Relationship Imagery Results Non-adjusted RSA: Period [F(3, 66)=3. 79, p=. 02]; Group [F(1, 22)=5.

Relationship Imagery Results Non-adjusted RSA: Period [F(3, 66)=3. 79, p=. 02]; Group [F(1, 22)=5. 54, p=. 028]

Stress Task Results Models with non-adjusted RSA. Period [F(3, 66)=4. 36, p=. 02], Group

Stress Task Results Models with non-adjusted RSA. Period [F(3, 66)=4. 36, p=. 02], Group x Trauma History [F(1, 22)=9. 61, p=. 05]

Stress Task Results Models with non-adjusted RSA. Period [F(3, 66)=4. 36, p=. 02], Group

Stress Task Results Models with non-adjusted RSA. Period [F(3, 66)=4. 36, p=. 02], Group x Trauma History [F(1, 22)=9. 61, p=. 05]

Stress Task Results Models with adjusted RSA. Period [F(3, 60)=3. 79, p =. 04],

Stress Task Results Models with adjusted RSA. Period [F(3, 60)=3. 79, p =. 04], Trauma History [F(1, 20)=4. 05, p=. 058], Trauma History X Task Order [F(1, 20)=6. 46, p=. 02]

Study Limitations Small, selected sample of depressed women Generalizability of study findings High level

Study Limitations Small, selected sample of depressed women Generalizability of study findings High level of anxiety comorbidity in the depressed group (no anxiety among controls) Particularly comorbid GAD (73%) However, findings held after removing 2 subjects with PTSD Trauma history assessment - simple event count Did not assess timing or severity of trauma

Study Strengths / Future Directions Select, well-characterized study group Medically healthy, antidepressant free Well-controlled

Study Strengths / Future Directions Select, well-characterized study group Medically healthy, antidepressant free Well-controlled study design Assessment of respiratory rate Large effect sizes (partial eta squared >. 14) Inclusion of tasks designed to elicit vagal activation and vagal withdrawal Conclusions – Directions for future research Importance of social context in RSA assessment Potential impact of trauma history in evaluating of stress-induced vagal withdrawal among depressed samples

Vagal Function, Depression and IPT treatment targets relevant to vagal function Depression, anxiety and

Vagal Function, Depression and IPT treatment targets relevant to vagal function Depression, anxiety and social function Prospective research designs needed IPT could be used as nonpharmacologic probe Will within-subject, IPT-related improvements in depression / anxiety, ⇩ in social distress, or ⇧ in perceived social support impact vagal function? Improvement in vagal function - potential biological mechanism of change in effective IPT treatment?