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SLEEP 2011 Abstract Supplement

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B. Clinical Sleep Science I. Sleep Disorders – Breathing<br />

and sleep disorders rather than BMI in OSAS patients, suggesting that<br />

plasma vaspin level is a potential biomarker of the pathophysiology associated<br />

with OSAS.<br />

0452<br />

EFFECTS OF OBSTRUCTIVE <strong>SLEEP</strong> APNEA ON<br />

LEUKOCYTES PROFILE: A POPULATION-BASED SURVEY<br />

Ruiz FS 1 , Andersen ML 1 , Araujo P 1 , Hachul H 1,2 , Santos-Silva R 1 ,<br />

Bittencourt LA 1 , Tufik S 1<br />

1<br />

Psicobiologia, Universidade Federal de Sao Paulo, Sao Paulo, Brazil,<br />

2<br />

Ginecologia, Universidade Federal de Sao Paulo, Sao Paulo, Brazil<br />

Introduction: Accumulating evidence suggests that sleep loss can impact<br />

the immune profile in experimental conditions. However, investigations<br />

focusing whether sleep disorders are associated with host defense<br />

alterations in epidemiological studies are still limited. Aim: This study<br />

was undertaken to evaluate whether obstructive sleep apnea syndrome<br />

(OSAS), one of the most prevalent sleep disorder, was associated with<br />

hematologic changes in a sample representative of the population of Sao<br />

Paulo, Brazil.<br />

Methods: A sample of 1042 subjects was used to represent the population<br />

of Sao Paulo city according to gender, age (20-80 years), and socioeconomic<br />

status. Hematological analysis of venous blood and a full<br />

polysomnography were carried out.<br />

Results: It was found significant increased leukocytes number in OSAS<br />

subjects. Further analysis considering sex-differences demonstrated that<br />

the leukocytes number was increased only in premenopausal women.<br />

Linear regression analysis using backward method showed the following<br />

factors that independently predicted the leukocytes alterations:<br />

neutrophils, TNF-α, estradiol, age, current smoker, cortisol, body mass<br />

index and oxyhemoglobin saturation.<br />

Conclusion: The results showed that sleep apnea was associated with an<br />

exclusive increase of leukocytes in women during the young ages. The<br />

data highlighted that several outcomes induced by OSAS were determinants<br />

in the altered immune profile, indicating the influence of sleep<br />

disruption on immunity. Finally, sleep fragmentation induced by OSAS<br />

seems to be involved in the bidirectional relationship between sleep<br />

quality and immune response.<br />

Support (If Any): FAPESP (#07/55445-6 to FSR and CEPID<br />

#98/14303-3 to ST), Associação Fundo de Incentivo à Psicofarmacologia<br />

(AFIP) and CNPq<br />

0453<br />

ASSOCIATION BETWEEN URIC ACID LEVELS, HYPOXIA<br />

AND <strong>SLEEP</strong> APNEA: A POPULATION-BASED SURVEY<br />

Hirotsu C, Tufik S, Bittencourt LA, Santos-Silva R, Andersen ML<br />

Departamento de Psicobiologia, Universidade Federal de Sao Paulo,<br />

Sao Paulo, Brazil<br />

Introduction: Recurrent hypoxia associated with obstructive sleep<br />

apnea syndrome leads to an increase in the degradation of adenosine<br />

triphosphatase into xanthine, which in turn increases uric acid concentrations.<br />

The current study aimed to determine whether a correlation<br />

exists between uric acid levels in the peripheral blood and the arterial<br />

oxyhemoglobin saturation (SpO2) from a representative population of<br />

Sao Paulo.<br />

Methods: A population-based survey adopting a probabilistic threestage<br />

cluster sample of Sao Paulo was used to represent the population<br />

according to gender, age and socioeconomic class. A total of 1,021 volunteers<br />

underwent polysomnography recordings, blood pressure assessment<br />

and biochemical blood analysis.<br />

Results: The results indicated that 30.3% of women and 48.3% of<br />

men with an apnea-hypopnea index (AHI)>5 had higher uric acid levels<br />

compared with normal gender-matched individuals. Men presented<br />

higher levels of uric acid than women, independent of AHI. Uric acid<br />

levels were significantly correlated with AHI, systolic blood pressure,<br />

SpO2, arousal index, percentage of slow-wave sleep, creatinine, sodium,<br />

cholesterol, triglycerides and glucose levels. A linear regression model<br />

revealed that the predictors for uric acid concentration were gender, creatinine,<br />

triglycerides, systolic blood pressure, SpO2 and HDL. However,<br />

when the model was controlled for body mass index, the influence of<br />

SpO2 decreased in the model.<br />

Conclusion: Uric acid levels were positively correlated with the number<br />

of obstructive respiratory episodes during sleep and present a possible<br />

marker for sleep apnea. Nevertheless, this association seems to be influenced<br />

by a confounding factor: obesity.<br />

Support (If Any): This work was supported by grants from AFIP,<br />

FAPESP and CNPq.<br />

0454<br />

QUALITY OF LIFE, DEPRESSION AND ANXIETY SCORES IN<br />

<strong>SLEEP</strong>Y AND NON-<strong>SLEEP</strong>Y OSA SUBJECTS<br />

Skomro R, Reid JK, Gjevre J, Fenton M, Stiles M, Cotton D<br />

Medicine, University of Saskatchewan, Saskatoon, SK, Canada<br />

Introduction: Excessive daytime sleepiness, a common symptom of<br />

OSA, negatively impacts QoL in these patients. It is not clear however<br />

whether non-sleepy OSA patients have similar impairments in QoL, and<br />

if mood or anxiety scores are affected independently of daytime sleepiness.<br />

The objective of this study was to compare the Quality of Life,<br />

depression and anxiety scores in sleepy and non-sleepy OSA subjects.<br />

Methods: One hundred and two consecutive patients referred to a tertiary<br />

sleep disorders clinic for evaluation of OSA completed SF-36, CES<br />

Depression Scale, State-Trait Anxiety Inventory (STAI), ESS, and underwent<br />

an in-lab PSG. Patients diagnosed with OSA (AHI > 5) were<br />

classified based on subjective sleepiness scores as sleepy (ESS ≥ 10)and<br />

non-sleepy (ESS < 10). Groups were matched for age, sex and BMI. We<br />

compared SF-36, PSQI, STAY-1 and STAY - 2 as well as CES depression<br />

scores between sleepy and non-sleepy patients prior to initiating<br />

CPAP therapy.<br />

Results: The sleepy OSA group had significantly worse depression<br />

(17.44 ± 10.16 vs. 10.86 ± 7.30, p = 0.02) and STAI anxiety scores<br />

(35.92 ± 9.95 vs 30.26 ± 6.87, p = 0.04) than the non-sleepy OSA patients.<br />

Non-sleepy and sleepy OSA patients had similar impairments in<br />

SF-36 Vitality and MCS scores. There was no significant correlation<br />

between ESS and SF-36 Vitality scores. There was a weak correlation<br />

between ESS and depression and anxiety scores.<br />

Conclusion: Sleepy OSA patients demonstrate worse depression and<br />

anxiety scores than non-sleepy subjects. Non-sleepy and sleepy OSA<br />

patients have similar decrements in general health QoL scores as measured<br />

by SF-36. Furthermore ESS scores do not correlate with SF-36<br />

QoL scores in OSA subjects.<br />

Support (If Any): The study was supported by Lung Association of<br />

Saskatchewan, Kelsey Trail Health Region and Saskatoon Health Region.<br />

0455<br />

EFFECTS OF TRAZODONE ON THE RESPIRATORY<br />

AROUSAL THRESHOLD AND UPPER AIRWAY DILATOR<br />

MUSCLE RESPONSIVENESS DURING <strong>SLEEP</strong> IN<br />

OBSTRUCTIVE <strong>SLEEP</strong> APNEA<br />

Eckert DJ, Kehlmann G, Wellman A, White D, Malhotra A<br />

Division of Sleep Medicine, Sleep Disorders Program, Brigham and<br />

Women’s Hospital and Harvard Medical School, Boston, MA, USA<br />

Introduction: Cessation of respiratory events occurs via 1) arousal from<br />

sleep or 2) sufficient recruitment of upper airway (UA) dilator muscles<br />

to restore airflow without arousal. Thus, a low respiratory arousal threshold<br />

(awaken easily to respiratory stimuli) is likely to be important in the<br />

pathogenesis of OSA for some patients. Increasing the arousal threshold<br />

with a hypnotic to enable UA muscle recruitment and restore airflow<br />

without arousal may be a therapeutic option in appropriately selected pa-<br />

<strong>SLEEP</strong>, Volume 34, <strong>Abstract</strong> <strong>Supplement</strong>, <strong>2011</strong><br />

A156

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