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1 Serveis de Anàlisis Cliniques, 2 Pneumologia, Hospital Universitario Arnau de Vilanova Lleida, 3 Hospital Txagorritxu, Vitoria-Gasteiz, and 4 Hospital Universitari, Son Dureta, Institute Universitari de Ciencies de la Salut (IUNICS), Fundació Caubet-Cimera, Palma de Mallorca and Servicio de Neumología, Spain.
CORRESPONDENCE: A. Barceló, Servicio de Análisis Clínicos, Hospital, Universitari Son Dureta. C/ Andrea Doria 55, 07014 Palma de Mallorca, Spain. Fax: 34 971175228. E-mail: abarcelo{at}hsd.es
Keywords: Clinical trial, continuous positive airway pressure, oxidative stress
Received: June 10, 2005
Accepted November 25, 2005
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ABSTRACT |
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The plasma levels of total antioxidant status (TAS), glutathione peroxidase (GPX), 
-glutamyltransferase (GGT), vitamins A, E, B12 and folate, and homocysteine were determined in 47 patients with OSAS and 37 healthy subjects. Of these, 27 patients who used continuous positive airway pressure (CPAP) for >4 h·night–1 were re-examined 12 months later.
Patients with OSAS had lower TAS (1.4±0.16 versus 1.50±0.10 mmol·L–1), vitamin A (64±19 versus 74±17 µg·dL–1) and vitamin E levels (1,525±499 versus 1,774±503 µg·dL–1), and increased values of GGT (42±22 versus 32±16 U·L–1) than controls. There was no difference between groups in GPX, homocysteine, vitamin B12 and folate plasma levels. CPAP treatment normalised the levels of TAS (1.50±0.13 mmol·L–1) and the activity of GGT (30±14 U·L–1) without any influence on vitamins levels.
In conclusion, the results indicate that patients with obstructive sleep apnoea syndrome have a decreased antioxidant capacity that is partially reversed by continuous positive airway pressure treatment.
Obstructive sleep apnoea syndrome (OSAS) is a common disorder characterised by the occurrence of numerous episodes of absence of respiratory flow (apnoea) during sleep, which can be followed by a decrease in arterial oxygen saturation (Sa,O2) that is rapidly normalised when ventilation resumes. These episodes of hypoxia/re-oxygenation may induce the generation of oxygen free radicals 1. In fact, several studies support the existence of oxidative stress in OSAS, and several authors have suggested a possible involvement of the latter in the pathogenesis of cardiovascular disease in these patients 2–4.
Oxidative stress is characterised by an imbalance between the production and degradation of reactive oxygen species. Antioxidant enzymes and vitamins counteract reactive oxygen species and potentially reduce their cellular damage 5. The role of these protective mechanisms is poorly explored in OSAS patients. In the present study, the authors hypothesised that antioxidant defences might be altered in OSAS. To test this hypothesis, the authors compared plasma total antioxidant status (TAS), the activity of antioxidant enzymes (glutathione peroxidases (GPX) and -glutamyl transferase (GGT)), antioxidant vitamins (A, E, B12 and folate) and homocysteine levels in patients with OSAS and healthy subjects. Furthermore, to assess the reversibility of potential abnormalities once the apnoeic events had been eliminated by the use of continuous positive airway pressure (CPAP) therapy, these same variables were determined again after 12 months of treatment with CPAP.
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METHODS |
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Control subjects were healthy nonsmoker males of similar age and body mass index (BMI) than patients with OSAS. They had no personal or family history of cardiovascular disease or diabetes. Nonobese controls (n = 17) were nonsnorers recruited from nonmedical staff of the authors' hospital. In these subjects, the diagnosis of OSAS was excluded by a cardiorespiratory sleep study that recorded nasal flow, thoracic movements, heart rate, snoring, body position and transcutaneus oxyhaemoglobin saturation (Edentec, Eden Prairie, MN, USA). Obese controls (BMI >30 kg·m–2; n = 20) were recruited from obese subjects who attended the authors' sleep unit, in whom OSAS was excluded by full polysomnography. No participant (patient or control) suffered from any chronic disease (chronic obstructive pulmonary disease, diabetes mellitus, liver cirrhosis, thyroid dysfunction, rheumatoid arthritis, chronic renal failure and/or psychiatric disorders), or was taking any type of medication. The study was approved by the Ethics Committee of the authors' institution. All participants signed their consent after being fully informed of the goal and characteristics of the study.
Measurements
After fasting overnight, venous blood samples were obtained between 08:00–10:00 h. Blood was centrifuged and serum was immediately separated in aliquots and stored at –80°C until analysis. Glucose, uric acid, triglycerides and cholesterol concentrations were determined by standard enzymatic methods on a Hitachi 917 biochemical analyser (Roche Diagnostics, Indianapolis, IN, USA). High-density lipoprotein cholesterol (HDLc) was measured by a homogeneous, enzymatic colorimetric method using a commercial reagent set (Roche Diagnostics, USA). Low-density lipoprotein cholesterol was calculated using the Friedewald equation. The plasma concentration of TAS was measured by a colorimetric test (Randox laboratories Ltd, Crumlin, UK). GPX and GGT activities were determined by enzymatic methods (Randox laboratories Ltd and Roche Diagnostics, Manheim, Germany, respectively) on a Hitachi Modular Analytics system (Roche Diagnostics, Germany). The plasma levels of vitamin A and E were measured by HPLC following the manufacturers' instructions (Bio Rad laboratories GmbH, Munich, Germany). The plasma concentrations of vitamin B12, folate and homocysteine were quantified by chemiluminiscent assays on an Immulite 2000 analyzer (DPC, Los Angeles, CA, USA; vitamin B12 and folate) or Advia Centaur analyser (Bayer, Tarrytown, NY, USA).
Statistical analysis
Data are presented as mean±SD. Comparisons between patients and controls were performed with independent t-tests and Chi-squared tests for proportions. The effects of CPAP therapy were analysed using paired t-tests. The correlation between variables was explored using the Spearman test. A p-value <0.05 was considered significant.
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RESULTS |
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shows the main clinical characteristics of patients with OSAS and healthy controls. Age and BMI were similar. Patients showed significantly higher mean values of diastolic blood pressure than controls. The number of hypertensive subjects and current smokers was higher in the patient group. Patients had severe OSAS (as shown by their AHI) and reported daytime sleepiness (Epworth sleep scale).
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reports the values of the different biological markers investigated in the present study. In patients with OSAS, the levels of HDLc were significantly lower than in healthy controls. Furthermore, OSAS patients had lower TAS, vitamin A and E levels than controls. Also, increased values of GGT were detected in the OSAS group. The OSAS and control groups did not differ significantly in GPX, homocysteine, vitamin B12 and folate plasma levels.
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). Furthermore, the authors compared these variables between smoker and nonsmoker patients and found that the former had slightly higher levels of homocysteine than the latter (12.4±6.0 versus 9.8±2.1 µmol·L–1; p = 0.04). By contrast, there were no significant differences in vitamins or enzyme plasma levels. Finally, the presence of hypertension had no effect on the parameters studied because similar results were observed in hypertensive and normotensive patients (data not shown).
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between compliant and noncompliant patients. BMI did not change after CPAP therapy (30.0 versus 30.2 kg·m–2; p = 0.4). The plasma levels of HDLc and TAS were significantly higher and those of GGT significantly lower than those determined at baseline. Interestingly, values after CPAP were not different from those of the control group. In contrast, CPAP did not influence vitamins and homocysteine levels (table 4).
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DISCUSSION |
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TOPABSTRACTMETHODSRESULTSDISCUSSIONREFERENCES |
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The results of several studies, including the present study, support the presence of oxidative stress in obstructive sleep apnoea 2–4, 6, 7. In keeping with this argument, the current authors found that the patients with OSAS had lower TAS values than controls. A negative correlation between antioxidant capacity and AHI has been previously detected in patients with OSAS (AHI >20) 6. This observation could not be reproduced, probably because of the narrow range of disease severity in the study patients. The fact that TAS was normalised after CPAP therapy, known to improve other indices of oxidative stress in OSAS 3, 4, suggests that the low TAS observed in patients with OSAS at baseline is probably the consequence, not the cause, of oxidative stress in these patients.
Previous studies support the argument that serum GGT activity is a marker of oxidative stress 7. The primary function of GGT is to maintain intracellular concentrations of glutathione, a critical antioxidant molecule 8. Thus, an increased GGT activity can also be viewed as a response to oxidative stress, aimed at increasing the intracellular concentration of glutathione 8. This interpretation is further supported by the significant reduction of GGT activity after CPAP therapy. Emerging evidence shows that serum GGT might be important in the pathogenesis of oxidant-related cardiovascular disease 9. Hence, increased serum GGT activity in OSAS may identify patients with persistent oxidative stress and increased cardiovascular risk. Increased plasma levels of GGT have also been described in obese subjects 9. In the current study, the BMI of patients with OSAS was similar to that of controls (table 1), thus, excluding a significant role of obesity upon the increased GGT activity seen in OSAS. Furthermore, the decrease of GGT detected after CPAP treatment, without any change in BMI, supports the hypothesis that this increase is linked directly to OSAS.
HDLc is one of the most important protective factors for atherosclerosis 10, 11. The levels of HDLc were found to be significantly lower in OSAS than in controls, and they increased significantly after CPAP treatment. Likewise, OSAS patients were found to have lower levels of vitamin A and E than control subjects. These vitamins are considered lipid-soluble antioxidants as they can prevent oxidative damage of lipid membranes and low density lipoproteins 12, 13. Therefore, overall these findings highlight potential mechanisms for increased lipid peroxidation and enhanced atherosclerosis risk in OSAS, as well as a potentially beneficial effect of CPAP in these patients.
A recent prospective study has reported that low erythrocyte glutathione peroxidase-1 activity identifies patients with coronary artery disease with the highest risk of acute cardiovascular events 14. The authors suggested that this can be a useful marker to identify patients who would benefit most from preventive antioxidant treatment 14. In the present study, significant differences in GPX activity between OSAS and controls were not detected. However, the intracellular activity of GPX was not measured, which may limit the interpretation of the present results.
Homocysteine is emerging as an independent risk factor for cardiovascular disease 15, 16, but it is not clear if homocysteine is associated with sleep apnoea. Lavie et al. 2 showed that patients with a combination of OSAS and ischaemic heart disease have elevated homocysteine levels. By contrast, the results of another study suggest that OSAS is not associated with raised homocysteine levels 17. There were no significant differences in vitamin B12, folate and homocysteine levels between OSAS and controls. Cigarette smoking is known to influence homocysteine levels and it is a possible confounder in the relationship between homocysteine and cardiovascular disease 18. In fact, in the present study, OSAS patients who smoked showed higher homocysteine levels than nonsmokers. Yet, a potential influence of smoking on other variables can be excluded because differences between smoker versus nonsmoker patients, and between control subjects and nonsmoker patients, were not significant.
Previous studies have demonstrated a beneficial effect of CPAP on several markers of oxidative stress in patients with OSAS 3, 19. As oxidative stress is likely to play an important role in the increased cardiovascular risk that characterises this disease, these observations support a potential effect of CPAP in the prevention of cardiovascular complications in OSAS. In keeping with this view, it was found that chronic treatment with CPAP improves TAS, further supporting a potential beneficial effect of CPAP on oxidative stress in these patients. However, these effects must be taken with caution because the current study was not a randomised, controlled trial.
In conclusion, the present results indicate that antioxidant capacity is decreased in patients with obstructive sleep apnoea syndrome and that it is partially restored by continuous positive airway pressure treatment. These observations may be relevant for a better understanding of the pathogenesis of cardiovascular disorders in these patients.
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REFERENCES |
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-glutamyltransferase: the cardiovascular risk development in young adults (CARDIA) study. Clin Chem 2004;50:582–588.This article has been cited by other articles:
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  M D Cross, N L Mills, M Al-Abri, R Riha, M Vennelle, T W Mackay, D E Newby, and N J Douglas Continuous positive airway pressure improves vascular function in obstructive sleep apnoea/hypopnoea syndrome: a randomised controlled trial Thorax, July 1, 2008; 63(7): 578 - 583. [Abstract] [Full Text] [PDF]
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 P. Faure, R. Tamisier, J-P. Baguet, A. Favier, S. Halimi, P. Levy, and J-L. Pepin Impairment of serum albumin antioxidant properties in obstructive sleep apnoea syndrome Eur. Respir. J., May 1, 2008; 31(5): 1046 - 1053. [Abstract] [Full Text] [PDF]
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 M. H. Sanders, J. M. Montserrat, R. Farre, and R. J. Givelber Positive Pressure Therapy: A Perspective on Evidence-based Outcomes and Methods of Application Proceedings of the ATS, February 15, 2008; 5(2): 161 - 172. [Abstract] [Full Text] [PDF]
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 D. Gozal and L. Kheirandish-Gozal Cardiovascular Morbidity in Obstructive Sleep Apnea: Oxidative Stress, Inflammation, and Much More Am. J. Respir. Crit. Care Med., February 15, 2008; 177(4): 369 - 375. [Abstract] [Full Text] [PDF]
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 |
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 A. I. Sergueeva, G. Y. Miasnikova, D. J. Okhotin, A. A. Levina, Z. Debebe, T. Ammosova, X. Niu, E. A. Romanova, S. Nekhai, P. M. DiBello, et al. Elevated homocysteine, glutathione and cysteinylglycine concentrations in patients homozygous for the Chuvash polycythemia VHL mutation Haematologica, February 1, 2008; 93(2): 279 - 282. [Abstract] [Full Text] [PDF]
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 L. Kheirandish-Gozal, O. Sans Capdevila, E. Kheirandish, and D. Gozal Elevated Serum Aminotransferase Levels in Children at Risk for Obstructive Sleep Apnea Chest, January 1, 2008; 133(1): 92 - 99. [Abstract] [Full Text] [PDF]
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 T. H. Le Jemtel and S. Jelic Seek and Treat Obstructive Sleep Apnea in Heart Failure J. Am. Coll. Cardiol., April 17, 2007; 49(15): 1632 - 1633. [Full Text] [PDF]
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C. L. Phillips and R. R. Grunstein Obstructive sleep apnoea: time for a radical change? Eur. Respir. J., April 1, 2006; 27(4): 671 - 673. [Full Text] [PDF]
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