Original Contribution
Am J Hypertens (1998) 11, 1284–1289; doi: S0895-7061(98)00159-9
Contributions of hypoxia and respiratory disturbance index to sympathetic activation and blood pressure in obstructive sleep apnea syndrome
Nir Peled1, Avital Greenberg2, Giora Pillar1, Oren Zinder2, Nurit Levi2 and Peretz Lavie1
- 1Sleep Laboratory, Faculty of Medicine, Technion–Israel Institute of Technology, Haifa, Israel
- 2Department of Clinical Biochemistry, Rambam Medical Center, Haifa, Israel
Correspondence: Peretz Lavie, PhD, Sleep Laboratory, Faculty of Medicine, Gutwirth Building, Technion–Israel Institute of Technology, Haifa 32000, Israel; e-mail: plavie@tx.technion.ac.il
Received 9 January 1998; Revised 0000; Accepted 12 June 1998.
Abstract
Hypertension is a common finding among obstructive sleep apnea (OSA) patients, and is thought to be caused by sympathetic hyperactivity. The present study compares the contributions of the respiratory disturbance index (RDI) as a reflection of sleep fragmentation, and the magnitude of oxygen desaturation, to sympathetic activation as indexed by urinary norepinephrine concentrations, as well as to morning and evening blood pressure in sleep apnea syndrome patients. Data (polysomnography, blood pressure [BP], and urine catecholamines) of 38 consecutive OSA patients (age, 46
14.5 years) were analyzed. Stepwise logistic regression analysis revealed that minimal oxygen saturation level (SaO2min) was a significant predictor of both morning and evening norepinephrine levels, and that 37% of morning systolic BP variance could be accounted for by a combination of age and norepinephrine, while 20% of the diastolic BP variance was accounted for by SaO2min alone. In contrast, RDI entered the prediction equation only when minimal oxygen saturation was rejected first. Our results indicate that the degree of nocturnal hypoxia is more closely associated with the level of sympathetic activation and with daytime level of blood pressure than with sleep fragmentation.
Keywords:
Blood pressure, catecholamines, obstructive sleep apnea, sympathetic system
