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Table of Contents - Academy of Psychosomatic Medicine

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<strong>of</strong> corticosterone responses to everyday stressors beginning<br />

in early adulthood and enduring across the lifespan.<br />

Among socially isolated rats, corticosterone recovery from<br />

an acute stressor was highly attenuated and associated with<br />

increased progression <strong>of</strong> mammary tumors.<br />

Our study <strong>of</strong>fers the first demonstration <strong>of</strong> nuclear glucocorticoid<br />

receptors in malignant and benign mammary tumors<br />

developing spontaneously, without exposure to a carcinogen<br />

or xenograph. In addition to these findings, we present an array<br />

<strong>of</strong> behavioral measures that suggest that socially isolated<br />

females are a stress and tumor-prone, anxious, neophobic,<br />

and hyper-vigilant phenotype. This animal model then demonstrates<br />

the expression <strong>of</strong> genetic risk in the absence <strong>of</strong> a<br />

social network and identifies mechanisms by which psychosocial<br />

stressors increase growth and malignancy in a wide<br />

variety <strong>of</strong> mammary tumors.<br />

16. Perceived Stress, Anxiety, and Markers <strong>of</strong><br />

Endothelial Dysfunction in Major Depression:<br />

Effects <strong>of</strong> Treatment<br />

Presenting Author: Edwin Meresh, MD, MPH<br />

Co-Authors: John Piletz, PhD, Zoe Wilson, MD, Santosh<br />

Mathapati, MD, Angelos Halaris, MD, PhD, Christopher<br />

Lowden<br />

Purpose: Cardiovascular disease (CVD) and depressive illness<br />

are two <strong>of</strong> the world’s leading health problems. There<br />

are known physiological responses to stress and depression<br />

(1). Repeated episodes <strong>of</strong> stress, anxiety, and depression<br />

can lead to chronic inflammatory processes culminating<br />

in atherosclerosis and cardiovascular diseases. We have<br />

conducted a study to determine whether otherwise healthy<br />

subjects in an acute episode <strong>of</strong> major depression, first or<br />

recurrent, display endothelial dysfunction (assessed with<br />

pulse wave analysis) (2), low heart rate variability, and/or<br />

increased inflammation (3), as reflected in specific plasma<br />

biomarkers, like Interleukin 1beta and 6 (IL1-beta & IL-6), C-<br />

Reactive Protein (CRP), Tumor Necrosis Factor alpha (TNFalpha)<br />

and Monocyte Chemoattractant Protein-1(MCP-1)<br />

before treatment and after treatment with escitalopram for 12<br />

weeks, relative to normal controls. This is an ongoing study.<br />

Methods: This open-label pilot study compared patients with<br />

Major Depressive Disorder (MDD) and matched healthy controls.<br />

The screening assessment (visit 1) included completion<br />

<strong>of</strong> Hamilton Rating Scale for Depression (HAMD), Hamilton<br />

Rating Scale for Anxiety (HAMA) and Perceived Stress<br />

Scale (PSS). Subjects underwent baseline assessment (visit<br />

2) that included blood draw for biomarkers, and pulse wave<br />

analysis (PWA). Pulse wave velocity (PWV) and heart-rate<br />

variability (HRV) were measured in conjunction with a 3-lead<br />

ECG. After completing the baseline assessment, depressed<br />

subjects received escitalopram and were reassessed at<br />

weeks 2, 4, 8, and 12. Escitalopram blood levels were measured<br />

at specified visits. Subjects completed HAMD, and<br />

HAMA at weeks 2, 4, 8 and 12, and PSS at week 12. Subjects<br />

underwent PWA at weeks 2, 4, 8 and 12 (higher the<br />

score <strong>of</strong> aortic augmentation index, higher the arterial stiffness<br />

indicating endothelial dysfunction), and HRV at weeks<br />

8 and 12. Blood draw for biomarkers after treatment was<br />

done at week 12.<br />

7<br />

Reults: In the MDD group (n=9), mean baseline PSS score<br />

was 51.1, HAMA score was 18, HAMD score was 21.66,<br />

and Aortic Augmentation Index (A-Axl) score was 11.6. In<br />

the healthy control group (n=5) mean PSS score was 29.6,<br />

HAMA score was 1.2, HAMD score was 2.8, and A-Axl<br />

score was 1.4. Statistical and regression analysis will be<br />

presented.<br />

Conclusions: This pilot study indicates that patients with<br />

MDD have increased stress perception, underlying anxiety,<br />

and increased arterial stiffness that may serve as prognostic<br />

markers <strong>of</strong> subclinical cardiovascular disease.<br />

References:<br />

1. Miller GE et al. Clinical depression and regulation <strong>of</strong> the<br />

inflammatory response during acute stress. <strong>Psychosomatic</strong><br />

<strong>Medicine</strong>, 2005 Sep-Oct; 67(5): 679-87<br />

2. Hayward CS et al. Assessment <strong>of</strong> endothelial function using<br />

peripheral waveform analysis: a clinical application, J Am<br />

Coll Cardiol 40 (2002) 521-528<br />

3. Piletz JE, Halaris A et al. Pro-inflammatory biomarkers in<br />

depression: Treatment with Venlafaxine, World J Biol Psychiatry<br />

(2008) Dec 31:1-11.<br />

17. The MMPI-2 Restructured Form in<br />

an Epilepsy Monitoring Unit Population-<br />

Preliminary Data<br />

Presenting Author: David Osborne, PhD<br />

Co-Authors: Dona Locke, PhD, Kristin Kirlin, PhD, Duane<br />

Hurst, PhD, Katherine Noe, MD, PhD, Joseph Drazkowski,<br />

MD, Joseph Sirven, MD<br />

Background: Personality assessment is a routine part <strong>of</strong><br />

evaluation <strong>of</strong> patients admitted for long-term video-EEG<br />

monitoring. The MMPI-2 has been well studied in this context.<br />

(Cragar, et al. ,2003) The MMPI-2-RF (Ben-Porath and<br />

Tellegen, 2008) includes restructured clinical scales, which<br />

were designed to remove overlap between scales, as well as<br />

new scales to assess specific problems. No research has<br />

appeared on the MMPI-2-RF in an EMU cohort.<br />

Purpose: To provide preliminary data on the MMPI-2-RF<br />

along with presentation <strong>of</strong> the original MMPI-2 clinical scales<br />

in a prospective EMU cohort with confirmed diagnosis <strong>of</strong> epilepsy<br />

or psychogenic non-epileptic events (PNES).<br />

Methods: Comparison <strong>of</strong> epilepsy (n=11) and PNES (n=11)<br />

patients on the MMPI-2-RF.<br />

Results: Groups were equivalent on age, education, and<br />

gender in this small preliminary sample. Results show significant<br />

differences (p

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