Association between lipid peroxidation and inflammation in obstructive sleep apnoea

K. Minoguchi, T. Yokoe, A. Tanaka, S. Ohta, T. Hirano, G. Yoshino, C. P. O’Donnell, M. Adachi
European Respiratory Journal 2006 28: 378-385; DOI: 10.1183/09031936.06.00084905

Abstract

In the present study, the authors examined the relationship between lipid peroxidation and inflammation in patients with obstructive sleep apnoea (OSA).

A total of 40 obese patients with OSA were studied, along with 18 obese and 12 lean subjects without OSA. Overnight excretion of 8-isoprostane in urine and serum levels of high-sensitivity C-reactive protein (hsCRP) were measured. In addition, the effects of 3 months’ treatment with nasal continuous positive airway pressure (nCPAP) were studied in 20 obese patients with moderate-to-severe OSA.

Overnight urinary excretion of 8-isoprostane and serum levels of hsCRP were significantly higher in patients with moderate-to-severe OSA compared with patients with mild OSA and obese or lean subjects without OSA. Overnight urinary excretion of 8-isoprostane significantly correlated with apnoea–hypopnoea index, duration of hypoxia during sleep, body mass index, and serum levels of hsCRP in patients with OSA. The severity of OSA was an independent factor predicting the urinary excretion of 8-isoprostane. nCPAP significantly decreased urinary excretion of 8-isoprostane and serum levels of hsCRP.

In conclusion, these results suggest that both obstructive sleep apnoea severity and obesity can independently contribute to elevations in urinary excretion of 8-isoprostane. Therefore, obstructive sleep apnoea may increase the risks of cardiovascular morbidity in obese patients.

Obstructive sleep apnoea (OSA) is associated with increased cardiovascular morbidity and mortality 1–3. Although cardiovascular morbidity in patients who have OSA is not due to atherosclerosis alone, a recent study by Marti et al. 4 showed that atherosclerosis may play an important role in cardiovascular mortality, as deaths from cardiovascular diseases in patients with untreated sleep apnoea are mainly due to acute myocardial infarction and stroke.

Ongoing inflammatory responses are involved in the pathogenesis of atherosclerosis 5, 6. Recent epidemiological studies suggest that high-sensitivity (hs) C-reactive protein (CRP) is an important risk factor for atherosclerosis and coronary artery disease 7–9. The present authors, along with others, have demonstrated that several inflammatory markers, including hsCRP, tumour necrosis factor-α and interleukin (IL)-6, are elevated in patients with OSA 10–12. In addition, levels of circulating soluble adhesion molecules, such as intercellular adhesion molecule-1, vascular cell adhesion molecule-1 and vascular endothelial growth factor, are elevated in patients with OSA 13, 14. Moreover, serum levels of matrix metalloproteinase-9 and carotid intima-media thickness are also elevated in patients with OSA 15, 16. These findings suggest that OSA may increase the risks of atherosclerosis and cardiovascular diseases.

OSA is characterised by repetitive periods of upper airway collapse and results in cyclic periods of hypoxia/reoxygeneration that cause the increased generation of oxygen species by oxidative stress 17, 18. In fact, the production of oxygen species from neutrophils and monocytes obtained from patients with OSA was increased, and treatment with nasal continuous positive airway pressure (nCPAP) significantly decreased the production of oxygen species from these cells 19, 20. Moreover, oxidative damage is involved in the pathogenesis of atherosclerosis and cardiovascular diseases 21, 22. Therefore, oxidative stress may contribute to the cardiovascular risk profile in patients with OSA.

In the cardiovascular system, lipids are in the first line of radical attack. 8-Isoprostane, 8-iso-prostaglandin F2α, is one of the lipid markers for oxidative stress 23. Due to its chemical stability, urinary excretion of 8-isoprostane is considered to be a reliable index of oxidant stress and ensuing lipid peroxidation in vivo. Although Carpagnano and co-workers 24, 25 demonstrated that 8-isoprostane was increased in both peripheral blood and exhaled breath condensates from patients with OSA, overnight urinary excretion of 8-isoprostane was not studied in these patients. Moreover, the relationship between systemic lipid peroxidation (as evaluated by overnight urinary excretion of 8-isoprostane) and systemic inflammation (reflected by serum levels of hsCRP) has not been investigated in patients with OSA.

The purpose of this study was to extend the present authors’ previous work examining the relationship between OSA and inflammation 10, 11, 15, 16. Specifically, the current authors determined the following in patients with OSA: 1) whether overnight urinary excretion of 8-isoprostane is elevated; 2) if overnight urinary excretion of 8-isoprostane is associated with increases in serum levels of hsCRP; 3) what factors are independent predictors for overnight urinary excretion of 8-isoprostane; and 4) whether treatment with nCPAP decreases both overnight urinary excretion of 8-isoprostane and serum levels of hsCRP.

METHODS

Subjects

A total of 40 males with abdominal obesity and newly diagnosed OSA, 18 snoring males with abdominal obesity but no OSA, and 12 lean, nonsnoring subjects without OSA were enrolled (table 1⇓). Subjects with abdominal obesity and snoring, recruited from the outpatient clinic, were examined with polysomnography (PSG) and were classified based on their apnoea–hypopnoea index (AHI) as either OSA subjects or obese subjects without OSA. The 12 lean subjects were also examined with PSG and were classified as nonsnoring subjects without OSA. Lean and obese subjects without OSA were enrolled in order to investigate the independent effect of obesity on systemic lipid peroxidation and inflammation. Moreover, obese patients with OSA were separated into mild, moderate or severe OSA to investigate the effect of severity of OSA on systemic lipid peroxidation and inflammation. Before enrolment, all subjects were asked about their regular medications and medical history, including hypertension, cardiovascular diseases and cerebrovascular diseases, and were checked by chest radiograph, respiratory function, ECG, mouth–nose examination and systemic physical examination. Hypertension was defined by a casual blood pressure ≥140/90 mmHg or by current use of antihypertensive agents. Diabetes mellitus was defined by a fasting blood glucose level ≥126 mg·dL-1 or by use of glucose-lowering agents. Obesity was defined by a body mass index (BMI) ≥25. All subjects who were free of the above and other diseases and were taking no medications were included in the present study. Subjects who smoked or had systemic infections at the time of the study, or within 2 weeks before the study, were also excluded. The study was approved by the ethics committee of Showa University (Tokyo, Japan), and all patients gave written informed consent.

View this table:
Table 1—

Baseline characteristics in patients with obstructive sleep apnoea(OSA) and healthy and obese control subjects

Polysomnography

Full PSG monitoring was performed with the Compumedics P-series Sleep System (Compumedics Sleep, Abbotsford, Australia). Electroencephalography (EEG), electrooculography (EOG), electromyography (EMG) and electrocardiography were performed simultaneously. Surface electrodes were used to record two channels of EEG (C3/A2, C4/A1), right and left EOGs, and submental EMG. Ventilatory flow at the nose and mouth was measured with thermistors. Ventilatory movements of the chest and abdomen were monitored by inductive plethysmography bands. The arterial oxygen saturation (Sa,O2) was measured transcutaneously with fingertip pulse oximetry. Apnoea was defined as continuous cessation of airflow for >10 s, and hypopnoea was defined as a reduction in airflow for >10 s with an oxygen desaturation of ≥4% or an EEG arousal from sleep. Apnoeas were classified as obstructive, mixed or central according to standard criteria by the American Academy of Sleep Medicine 26. The AHI was calculated as the total number of episodes of apnoea and hypopnoea per hour of sleep. An AHI of ≥5·h-1 in conjunction with sleep-related symptoms was considered diagnostic of OSA. An AHI of ≥5·h-1 and <15·h-1 was classified as mild OSA, ≥15·h-1 and <30·h-1 was classified as moderate OSA, and ≥30·h-1 was classified as severe OSA. PSG was performed from 21:00–06:00 h. Of the 40 obese patients with OSA, 20 were considered to have mild OSA and 20 were considered to have moderate-to-severe OSA. The Epworth Sleepiness Scale (ESS) was used to investigate changes in subjective daytime sleepiness 27.

Measurement of 8-isoprostane and hsCRP

All subjects went to bed at 21:00 h and were woken at 06:00 h. Samples of peripheral venous blood were collected at 06:00 h after PSG was performed. In addition, urine was stored from 21:00–06:00 h and overnight urinary excretion of 8-isoprostane was measured with an enzyme immunoassay (Cayman Chemical Co., Ann Arbor, MI, USA) and corrected by urinary creatinine levels. Samples were stored at -80°C until assay. hsCRP was measured with a latex particle-enhanced immunoturbidimetric assay as described previously 28.

nCPAP treatment

A total of 20 patients with moderate-to-severe OSA slept while using the automatic titration device (AutoSet Portable II Plus; ResMed, North Ryde, Australia). The following night, these patients slept with an autoCPAP machine using the AutoSet-S (ResMed). Afterwards, the patients were sent home. The duration of nCPAP treatment was 3 months. The mean daily duration of nCPAP use was 4.8±1.3 h in patients with moderate-to-severe OSA. Patients with moderate-to-severe OSA were admitted after 3 months of treatment and PSG was performed while patients received nCPAP. Urine was stored from 21:00–06:00 h and overnight urinary excretion of 8-isoprostane was measured. Samples of venous blood were obtained at 06:00 h, and serum levels of hsCRP were measured again.

Statistical analysis

When comparing four groups, data were analysed by ANOVA with Bonferroni correction. Correlations were determined using Spearman’s rank correlation coefficient. To assess the relative strength of association of overnight urinary excretion of 8-isoprostane with possible contributing factors, a stepwise multiple regression analysis was employed for patients with OSA. In the analysis, the present authors used overnight urinary excretion of 8-isoprostane as a dependent variable and evaluated the order of inclusion in the model of the following independent variables: age, BMI, ESS, waist/hip ratio, PSG variables, metabolic variables, and levels of hsCRP. Data are presented as mean±sem, and a p-value <0.05 was considered statistically significant.

RESULTS

Subject characteristics

Characteristics of the 12 lean and 18 obese subjects without OSA, 20 obese patients with mild OSA, and 20 obese patients with moderate-to-severe OSA, including age, BMI, blood pressure, metabolic variables, PSG variables, respiratory function and ESS, are shown in table 1⇑. AHI, percentage of time with Sa,O2 <90%, arousal index and ESS were significantly higher in patients with moderate-to-severe OSA than in lean subjects without OSA, obese subjects without OSA, or patients with mild OSA. Lowest Sa,O2and total sleep time were significantly lower in patients with moderate-to-severe OSA than in lean subjects without OSA, obese subjects without OSA or patients with mild OSA. Moreover, presence of snoring and OSA did not alter respiratory function.

Overnight urinary excretion of 8-isoprostane and serum levels of hsCRP

Overnight urinary excretion of 8-isoprostane in patients with moderate-to-severe OSA was significantly higher (412.6±50.5 pg·mL-1) than in lean subjects without OSA (111.3±7.9 pg·mL-1; p<0.0001; fig. 1a⇓), obese subjects without OSA (211.9±11.6 pg·mL-1; p<0.001) or patients with mild OSA (257.4±16.7 pg·mL-1; p<0.01; fig. 1a⇓). In addition, serum levels of hsCRP in patients with moderate-to-severe OSA (0.23±0.05 mg·dL-1) were significantly higher than in lean subjects without OSA (0.05±0.001 mg·dL-1; p<0.01), obese subjects without OSA (0.07±0.03 mg·dL-1; p<0.01) or patients with mild OSA (0.09±0.02 mg·dL-1; p<0.01; fig. 1b⇓).

Fig. 1—
Fig. 1—

a) Overnight urinary excretion of 8-isoprostane and b) serum levels of high-sensitivity C-reactive protein (hsCRP) in lean subjects without obstructive sleep apnoea (OSA; n = 12), obese subjects without OSA (n = 18), obese patients with mild OSA (n = 20) and obese patients with moderate-to-severe OSA (n = 20). The boundaries of each box represents the interquartile range (25th–75th centiles), the horizontal line inside the box represents the median, and the error bars outside the box represent the 95% confidence intervals of the mean. *: p<0.05; **: p<0.01; ***: p<0.001; #: p<0.0001; ns: nonsignificant.

Correlations between overnight urinary excretion of 8-isoprostane and different variables in patients with OSA

Overnight urinary excretion of 8-isoprostane was positively correlated with AHI (r = 0.55; p = 0.0004; fig. 2a⇓), percentage of time with Sa,O2 <90% (r = 0.40; p = 0.02; fig. 2b⇓), serum levels of hsCRP (r = 0.50; p = 0.002; fig. 2c⇓) and BMI (r = 0.40; p = 0.02; fig. 2d⇓) but was not significantly correlated with age, ESS or metabolic variables (table 2⇓). Thus, in males with OSA, an increase in overnight urinary excretion of 8-isoprostane was related to the severity of OSA with longer duration of hypoxaemia and to higher serum levels of hsCRP and BMI.

Fig. 2—
Fig. 2—

Correlations between overnight urinary excretion of 8-isoprostane and a) apnoea–hypopnoea index (AHI; r = 0.55; p = 0.0004), b) percentage of time with arterial oxygen saturation (Sa,O2) <90% (r = 0.40; p = 0.02), c) serum levels of high-sensitivity C-reactive protein (hsCRP; r = 0.5; p = 0.002), and d) body mass index (BMI; r = 0.4; p = 0.02) in patients with obstructive sleep apnoea (n = 40).

View this table:
Table 2—

Correlation coefficients between overnight urinary excretion of 8-isoprostane and different variables in patients with obstructive sleep apnoea

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Table 3—

Multiple regression analysis to predict 8-isoprostane levels

Stepwise multiple regression analysis in patients with OSA

To examine independent predictors of overnight urinary excretion of 8-isoprostane in patients with OSA, a stepwise multiple regression analysis was performed. After adjusting for age, ESS, PSG variables and metabolic variables, including BMI and triglyceride levels, AHI (p = 0.02) was the only significant independent predictor of overnight urinary excretion of 8-isoprostane (table 3⇑).

Effect of nCPAP on overnight urinary excretion of 8-isoprostane and serum levels of hsCRP in patients with moderate-to-severe OSA

In 20 patients with moderate-to-severe OSA who successfully completed 3 months of treatment, BMI did not change significantly and no new cardiovascular diseases were detected during the 3-month treatment with nCPAP. Treatment with nCPAP significantly decreased the AHI (46.5±9.8 to 2.8±0.9 events·h-1; p<0.001), increased the lowest nocturnal Sa,O2(70.9±7.9 to 92.0±3.9%; p<0.001) and total sleep time (328.0±68.1 to 418.3±49.6 min; p<0.01), and decreased the percentage of time with Sa,O2<90% (38.9±12.9 to 0.12±0.3%; p<0.001) and the arousal index (42.3±6.8 to 16.2±3.4·h-1; p<0.01). Treatment with nCPAP also significantly decreased overnight urinary excretion of 8-isoprostane (412.6±50.5 to 246.2±11.9 pg·mL-1; p<0.03; fig. 3a⇓). In addition, serum levels of hsCRP were significantly decreased by the treatment with nCPAP (0.23±0.05 to 0.11±0.02 pg·mL-1; p<0.03; fig. 3b⇓).

Fig. 3—
Fig. 3—

Effect of nasal continuous positive airway pressure (nCPAP) on a) overnight urinary excretion of 8-isoprostane and b) serum levels of high-sensitivity C-reactive protein (hsCRP) in patients with moderate-to-severe obstructive sleep apnoea (OSA; n = 20). Patients with moderate-to-severe OSA were treated with nCPAP for 3 months. The boundaries of each box represent the interquartile range (25th–75th centiles), the horizontal line inside the box represents the median, and the error bars outside the box represent the 95% confidence intervals of the mean. #: p<0.03.

Changes in AHI after 3 months’ treatment with nCPAP were correlated with changes in overnight urinary excretion of 8-isoprostane (r = 0.72; p = 0.01) and serum levels of hsCRP (r = 0.62; p = 0.01). In addition, changes in the percentage of time with Sa,O2<90% after 3 months’ treatment with nCPAP were correlated with changes in overnight urinary excretion of 8-isoprostane (r = 0.63; p = 0.03) and serum levels of hsCRP (r = 0.51; p = 0.04). Moreover, changes in overnight urinary excretion of 8-isoprostane after treatment with nCPAP correlated with changes in serum levels of hsCRP (r = 0.68; p = 0.02) in patients with moderate-to-severe OSA.

DISCUSSION

In the present study, it was found that overnight urinary excretion of 8-isoprostane and serum levels of hsCRP in patients with moderate-to-severe OSA were significantly higher than in lean or obese subjects without OSA, or patients with mild OSA. Overnight urinary excretion of 8-isoprostane was correlated with the severity of OSA, duration of hypoxia during sleep period, BMI and serum levels of hsCRP in patients with OSA. In addition, the severity of OSA was an independent predictor of overnight urinary excretion of 8-isoprostane. Moreover, nCPAP significantly decreased both overnight urinary excretion of 8-isoprostane and serum levels of hsCRP in patients with moderate-to-severe OSA. Therefore, these findings are the first to show the significant association between systemic lipid peroxidation and inflammation in patients with OSA.

Isoprostanes are reliable biomarkers of lipid peroxidation and oxidative stress because of their stability and specificity. 8-isoprostane is widely studied as a marker of oxidative stress in various respiratory diseases, including bronchial asthma, chronic obstructive pulmonary disease, cystic fibrosis and interstitial lung diseases 29–32. Increased lipid peroxidation has also been reported in patients with OSA. Carpagnano and co-workers 24, 25 have reported increased production of 8-isoprostane in the blood and exhaled breath condensates of patients with OSA. In addition, levels of other biomarkers of lipid peroxidation, oxidised low density lipoprotein cholesterol and thiobarbituric reactive substances are significantly higher in patients with OSA than in controls 33, 34. Moreover, urinary 8-isoprostane is a risk marker for coronary artery disease 35. In the present study, the overnight urinary excretion of 8-isoprostane was measured as a marker for oxidative stress during the sleep period in patients with OSA and it was found to be significantly elevated in these patients. These results suggest that lipid peroxidation is increased during sleep in patients with OSA.

Intermittent hypoxia observed in patients with OSA seems to resemble ischaemia–reperfusion. Several studies suggest that ischaemia–reperfusion represents oxidative stress and increases the generation of reactive oxygen species (ROS). On the basis of these findings, intermittent hypoxia is believed to increase the generation of ROS in patients with OSA 36. In fact, production of superoxide by neutrophils and monocytes from patients with OSA is increased 19, 20, 33. In the present study, the duration of hypoxia during sleep was found to be significantly correlated with overnight urinary excretion of 8-isoprostane in patients with OSA. Moreover, changes in the duration of hypoxia during sleep after treatment with nCPAP were significantly correlated with changes in overnight urinary excretion of 8-isoprostane. Therefore, repeated apnoea-related hypoxia is an important factor in the overnight production of 8-isoprostane in patients with OSA.

Basic research studies have found that oxidative stress is critical for activation of nuclear factor (NF)-κB 37. Activation of NF-κB induces expression of pro-inflammatory cytokines, including IL-6, which stimulate the production of CRP by the liver 38. Several clinical studies have suggested that oxidative stress markers are associated with CRP levels in healthy subjects without coronary artery disease 39–41. In addition, a previous study has shown that oxidative stress is related to airway inflammation in patients with OSA because levels of exhaled 8-isoprostane were correlated with levels of IL-6 in exhaled breath condensates 24. The present authors have confirmed and extended the close relationship between systemic oxidative stress and inflammation in patients with OSA by demonstrating that overnight urinary excretion of 8-isoprostane was significantly correlated with serum levels of hsCRP.

Inflammation is associated with increased vascular production of ROS 42. Specimens obtained at directional coronary atherectomy from patients with higher serum hsCRP levels showed greater immunoreactivity for CRP 42. In addition, CRP directly enhances the expression of the reduced forms of nicotinamide adenine dinucleotide/nicotinamide adenine dinucleotide phosphate oxidase p22phox protein, as well as the generation of ROS in cultured human coronary artery smooth muscle cells 43. Moreover, expression of 8-isoprostane is increased in atheroma 44. These results suggest that CRP may directly promote oxidative stress.

Once increased systemic inflammation and oxidative stress are established, a vicious circle may develop in which oxidative stress can induce CRP production and increased CRP levels can in turn enhance oxidative stress. In addition, a recent study has suggested that visceral obesity is an important factor for enhanced oxidative stress in males 45. Since repeated apnoea-related hypoxia and visceral obesity are present in patients with OSA, oxidative stress may promote both systemic lipid peroxidation and inflammation. Thus, the combination of visceral obesity and OSA may exacerbate oxidative stress and fuel a vicious circle between lipid peroxidation and inflammation.

Previous studies have shown that elevated levels of both systemic and airway oxidative stress are reduced by nCPAP therapy 19, 20, 25. In the present study, it was also confirmed that nCPAP significantly decreases both overnight urinary excretion of 8-isoprostane and serum levels of hsCRP in patients with moderate-to-severe OSA. Moreover, changes in overnight urinary excretion of 8-isoprostane after treatment with nCPAP were correlated with changes in serum levels of hsCRP in these patients. Therefore, these results imply that nCPAP might be useful for decreasing systemic lipid peroxidation and inflammation in patients with OSA.

In the present study, no significant differences were found in the serum levels of hsCRP between lean subjects without OSA, obese subjects without OSA, and patients with mild OSA. The small number of subjects may explain the lack of significant differences between these groups. Moreover, the degree of adiposity in the presented subjects may not be sufficient to establish an independent effect of obesity on hsCRP levels. However, there was a significant difference in urinary levels of 8-isoprostane between lean subjects without OSA, obese subjects without OSA and patients with mild OSA. The excretion of higher levels of urinary 8-isoprostane in obese patients with mild OSA compared with obese subjects without OSA is consistent with both OSA and obesity impacting on oxidative stress and lipid peroxidation. In addition, AHI was an independent factor predicting the levels of urinary excretion of 8-isoprostane. Therefore, the current authors speculate that 8-isoprostane may be a more sensitive marker for the presence of obesity and OSA than serum levels of hsCRP.

Limitations of the present study include the recruitment of only male subjects and the relatively small numbers of patients with OSA and control subjects. In addition, the effects of nCPAP on overnight urinary excretion of 8-isoprostane and serum levels of hsCRP in patients with OSA were not examined using a randomised, placebo-controlled design. However, significant correlations were found between changes in AHI and changes in overnight urinary excretion of 8-isoprostane and serum levels of hsCRP after treatment with nCPAP in patients with moderate-to-severe OSA. Therefore, nCPAP might decrease both overnight urinary excretion of 8-isoprostane and serum levels of hsCRP in patients with moderate-to-severe OSA. The effects of nCPAP on these variables should be examined in a large, placebo-controlled study.

In conclusion, the present authors first demonstrated that overnight urinary excretion of 8-isoprostane and serum levels of high sensitivity C-reactive protein are elevated and correlated in patients with obstructive sleep apnoea. Moreover, obstructive sleep apnoea severity and obesity acted independently to elevate overnight urinary excretion of 8-isoprostane. As systemic lipid peroxidation by oxidative stress and inflammation are increased, obstructive sleep apnoea may increase the risks of cardiovascular morbidity in obese individuals. In addition, nasal continuous positive airway pressure might be useful for decreasing these risks by, in part, reducing systemic lipid peroxidation and inflammation in patients with obstructive sleep apnoea.

Acknowledgments

The authors would like to thank H. Takeuchi for skilful technical assistance.

  • Received July 21, 2005.
  • Accepted March 22, 2006.

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Association between lipid peroxidation and inflammation in obstructive sleep apnoea
K. Minoguchi, T. Yokoe, A. Tanaka, S. Ohta, T. Hirano, G. Yoshino, C. P. O’Donnell, M. Adachi
European Respiratory Journal Aug 2006, 28 (2) 378-385; DOI: 10.1183/09031936.06.00084905
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