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SLEEP 2011 Abstract Supplement

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B. Clinical Sleep Science IX. Psychiatric and Behavioral Disorders and Sleep<br />

0713<br />

INSOMNIA SYMPTOMS AND CARDIOVASCULAR RISK<br />

AMONG RESPONDENTS WITH BIPOLAR DISORDER IN<br />

THE NATIONAL COMORBIDITY SURVEY-REPLICATION<br />

Soehner A, Harvey AG<br />

Psychology, University of California, Berkeley, Berkeley, CA, USA<br />

Introduction: In the past decade, there has been increasing concern<br />

about the elevated prevalence of cardiovascular risk factors in bipolar<br />

disorder. Parallel to these findings, epidemiologic evidence suggests that<br />

insomnia symptoms (e.g. difficulty falling or staying asleep, or waking<br />

up too early) are independently associated with higher rates of cardiovascular<br />

risk factors in the general population. Given that sleep is pervasively<br />

disturbed in bipolar populations, the aim of the study was to<br />

examine the association between insomnia symptoms and cardiovascular<br />

risk factors in patients with bipolar disorder in the National Comorbidity<br />

Survey - Replication (NCS-R).<br />

Methods: The NCS-R is a nationally representative survey of the U.S.<br />

population (ages 18+) conducted between 2001 and 2003. From this<br />

sample, 176 respondents with a lifetime bipolar disorder diagnosis were<br />

identified for the present study. The prevalence of self-reported cardiovascular<br />

risk factors (obesity, hypertension, and diabetes/high blood<br />

sugar) was compared across three subgroups of respondents with bipolar<br />

diagnoses, based on the presence of (a) chronic insomnia symptoms,<br />

(b) acute insomnia symptoms, or (c) no sleep problems in the past year.<br />

Prevalence estimates, as well as odds ratios adjusted for demographic<br />

and clinical variables (AORs) in logistic regression analyses, were corrected<br />

for the complex survey design.<br />

Results: Rates of obesity and hypertension were statistically greater in<br />

bipolar patients with chronic (41.8%; 28.8%) and acute (43.7%; 24.1%)<br />

insomnia symptoms compared to bipolar patients with good sleep<br />

(19.7%; 5.9%). Diabetes/high blood sugar prevalence did not significantly<br />

differ between groups. Insomnia symptom duration remained a<br />

significant predictor of obesity (AOR=1.5) and hypertension (AOR=2.2)<br />

after controlling for clinical and demographic factors.<br />

Conclusion: Insomnia symptoms, particularly those that are chronic in<br />

nature, may confer risk for obesity and hypertension in bipolar disorder.<br />

Thus, sleep disturbance may represent one pathway contributing to the<br />

high rates of CVD observed in bipolar disorder.<br />

Support (If Any): R34MH080958<br />

0714<br />

DIURNAL VARIATION IN RELATIVE BRAIN GLUCOSE<br />

METABOLISM WITHIN THE REWARD CIRCUIT IN ADULTS<br />

WITH PRIMARY INSOMNIA<br />

Hasler BP 1 , Nofzinger E 1 , Germain A 1 , James JA 2 , Buysse DJ 1<br />

1<br />

Psychiatry, University of Pittsburgh School of Medicine, Pittsburgh,<br />

PA, USA, 2 Radiology, University of Pittsburgh, Pittsburgh, PA, USA<br />

Introduction: Converging evidence indicates that reward motivation<br />

shows circadian modulation. Self-reported positive affect, as well as<br />

reward-related behaviors and physiology, show circadian rhythms, with<br />

lowest levels in the morning and peaks in the evening. These rhythms<br />

may be particularly salient for insomnia patients, who have altered diurnal<br />

variation in mood and arousal. However, no prior studies have<br />

examined the neural underpinnings of circadian-reward interactions in<br />

insomnia patients. The aim of these analyses was to characterize diurnal<br />

variation in relative brain glucose metabolism of regions within the reward<br />

circuit in adults with insomnia.<br />

Methods: [18F]-fluorodeoxyglucose positron emission tomography<br />

scans were conducted during quiet wakefulness in the morning and evening<br />

in 23 adults with primary insomnia. Statistical parametric mapping<br />

was used to compare relative glucose metabolism during the two scans.<br />

Region-of-interest (ROI) analyses focused on reward-related regions,<br />

including the medial prefrontal cortex (mPFC) and striatum (caudate,<br />

putamen, and nucleus accumbens), using a threshold of p

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