
Vascular Response During Mental Stress in Sedentary and Physically Active Patients With Obstructive Sleep Apnea
2018; American Academy of Sleep Medicine; Volume: 14; Issue: 09 Linguagem: Inglês
10.5664/jcsm.7314
ISSN1550-9397
AutoresRosyvaldo Ferreira-Silva, Thiago T. Goya, Eline Rozária Ferreira Barbosa, Bruno G. Durante, C.E.L. Araújo, Geraldo Lorenzi‐Filho, Linda Massako Ueno,
Tópico(s)Neuroscience of respiration and sleep
ResumoFree AccessObstructive Sleep ApneaVascular Response During Mental Stress in Sedentary and Physically Active Patients With Obstructive Sleep Apnea Rosyvaldo Ferreira-Silva, MSc, Thiago T. Goya, MSc, Eline R.F. Barbosa, MD, Bruno G. Durante, BS, Carlos E.L. Araujo, BS, Geraldo Lorenzi-Filho, MD, PhD, Linda M. Ueno-Pardi, PhD Rosyvaldo Ferreira-Silva, MSc Universidade de São Paulo, Escola de Artes Ciencias e Humanidades, São Paulo, São Paulo, Brazil Search for more papers by this author , Thiago T. Goya, MSc Faculdade de Medicina, Universidade de São Paulo, São Paulo, São Paulo, Brazil Search for more papers by this author , Eline R.F. Barbosa, MD Instituto do Coração, Divisao de Pneumologia, Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de São Paulo, São Paulo, São Paulo, Brazil Search for more papers by this author , Bruno G. Durante, BS Faculdade de Medicina, Universidade de São Paulo, São Paulo, São Paulo, Brazil Search for more papers by this author , Carlos E.L. Araujo, BS Faculdade de Medicina, Universidade de São Paulo, São Paulo, São Paulo, Brazil Search for more papers by this author , Geraldo Lorenzi-Filho, MD, PhD Instituto do Coração, Divisao de Pneumologia, Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de São Paulo, São Paulo, São Paulo, Brazil Search for more papers by this author , Linda M. Ueno-Pardi, PhD Address correspondence to: Linda Massako Ueno Pardi, Escola de Artes, Ciencias e Humanidades da Universidade de São Paulo, Rua Arlindo Bettio, 1000 Bairro: Vila Guaraciba, 03828-000, São Paulo, Brazil(55) 11 30918111(55) 11-985685530 E-mail Address: [email protected] E-mail Address: [email protected] Universidade de São Paulo, Escola de Artes Ciencias e Humanidades, São Paulo, São Paulo, Brazil Search for more papers by this author Published Online:September 15, 2018https://doi.org/10.5664/jcsm.7314Cited by:3SectionsAbstractPDF ShareShare onFacebookTwitterLinkedInRedditEmail ToolsAdd to favoritesDownload CitationsTrack Citations AboutABSTRACTStudy Objectives:To compare vascular function of sedentary (SED) versus physically active (ACTIVE) patients with obstructive sleep apnea (OSA) during rest and mental stress.Methods:Patients with untreated OSA without other comorbidities were classified into SED and ACTIVE groups according to the International Physical Activity Questionnaire. Blood pressure (BP), heart rate (HR), forearm blood flow (FBF) (plethysmography), and forearm vascular conductance (FVC = FBF / mean BP × 100) were continuously measured at rest (4 minutes) followed by 3 minutes of mental stress (Stroop Color Word Test).Results:We studied 40 patients with OSA (men = 24, age = 50 ± 1 years, body mass index = 29.3 ± 0.5 kg/m2, apnea-hypopnea index = 39.3 ± 4 events/h). Leisure time physical activity domain in SED (n = 19) and ACTIVE (n = 21) was 20 ± 8 and 239 ± 32 min/wk, (P < .05). Baseline profile and perception of stress were similar in both groups. Baseline FBF (3.5 ± 0.2 mL/min/100 mL versus 2.4 ± 0.14 mL/min/100 mL) and FVC (3.5 ± 0.2 U versus 2.3 ± 0.1 U) were significantly lower in the SED group than in the ACTIVE group, respectively (P < .05). HR and BP increased similarly during mental stress test in both groups. Changes during mental stress in FBF (0.65 ± 0.12 versus 1.04 ± 0.12) and FVC (0.58 ± 0.11 versus 0.99 ± 0.11) were significantly lower in the SED group than in the ACTIVE group, respectively (P < .05). There was a significant correlation between leisure time physical activity and FBF (r = .57, P < .05) and FVC (r = .48, P < .05) during mental stress.Conclusions:The vascular response among patients with OSA is influenced by the level of physical activity. A high level of physical activity may partially protect against the cardiovascular dysfunction associated with OSA.Citation:Ferreira-Silva R, Goya TT, Barbosa ER, Durante BG, Araujo CE, Lorenzi-Filho G, Ueno-Pardi LM. Vascular response during mental stress in sedentary and physically active patients with obstructive sleep apnea. J Clin Sleep Med. 2018;14(9):1463–1470.BRIEF SUMMARYCurrent Knowledge/Study Rationale: Leisure time physical activity is associated with vascular benefits in several diseases. However, the effect of physical activity on vascular function at rest and during stress in patients with obstructive sleep apnea is unknown.Study Impact: Among patients with moderate to severe obstructive sleep apnea and no comorbidities, moderate physical activity during leisure time (approximately 4 h/wk) is associated with better vascular function at rest and during stress than in sedentary patients. Physical activity may protect vascular function in patients with obstructive sleep apnea.INTRODUCTIONObstructive sleep apnea (OSA) is characterized by recurrent episodes of partial or complete obstruction of the upper airway during sleep,1 futile efforts to breath during the obstructive events, oxygen desaturation, and arousals from sleep.2 Previous studies showed that as compared with healthy individuals, patients with OSA have compromised vascular function as observed by flow-mediated dilatation in the brachial artery.3,4 The endothelial dysfunction in OSA could be explained by intermittent hypoxemia and reoxygenation during sleep associated with enhanced generation of superoxide free radicals, sympathetic nervous system stimulation, augmented systemic inflammation, or enhanced expression of adhesion molecules.5 Impaired endothelial function is associated with development of atherosclerosis6 and increased risk of future cardiovascular events.7 Epidemiological research indicates that OSA is associated with increases in the incidence and progression of coronary heart disease, heart failure, stroke, and atrial fibrillation.7,8In addition to OSA, mental stress also represents an important risk factor for cardiovascular morbidity and mortality.9 Mental stress causes an acute increase in sympathetic nerve activity,10 heart rate, and blood pressure.11 A study including healthy subjects demonstrated that the harmful effects after 5 minutes of stress are noticeable for the next 90 minutes.12 Previous studies have shown that mild mental stress in obese subjects13 and metabolic syndrome5 are associated with impaired endothelial function, as reflected by the decrease in forearm blood flow and flow-mediated dilation.There is growing evidence that physical exercise may decrease OSA severity and improve cardiovascular function. Increases in blood flow velocity and shear rates are the main physiological stimuli for the beneficial adaptations in endothelial structure and function induced by physical exercise that provides an important stimulus for vasodilation of conduit arteries during exercise.14 Regular physical activity has also been shown to be beneficial to the vascular wall in individuals with hypertension15 and increases forearm blood flow in patients with congestive heart failure and sleep-disordered breathing when compared with baseline values.16 A previous study also demonstrated that one session of aerobic exercise prevented a reduction in the flow-mediated dilation induced by mental stress among subjects with metabolic syndrome.17 Regular physical activity was effective in increasing forearm vascular conductance during a mental stress test in obese women compared with controls.18 However, there is little information about the influence of physical activity on vascular function in patients with OSA and no comorbidities during stress conditions. The aim of this study was to compare vascular function at rest and during mental stress in sedentary and physically active patients with moderate to severe OSA and no other comorbidities. We hypothesized that the vascular response is impaired during mental stress in sedentary compared with physically active patients.METHODSPatientsMale and female individuals, 40 to 65 years of age in whom OSA was recently diagnosed as defined as apnea-hypopnea index (AHI) ≥ 15 events/h by complete nocturnal polysomnography, were considered for the study. Patients with body mass index (BMI) > 40 kg/m2, smoking or alcohol abuse (2 or more drinks/d), cardiopulmonary disease, chronic renal disease, diabetes mellitus, a history of psychiatric disorders, any OSA treatment, shift workers, resting blood pressure (BP) higher than 140/90 mmHg, use of medicines that affect sleep and the vascular system, less than 2 years of formal education, and any sleep apnea treatment were excluded from this study. Because hormonal variability during the regular menstrual cycle may affect BP and the perception of stress, all nonmenopausal women were studied between the first and the fifth day after the onset of menstruation. This study was approved by the ethics committee and research on human subjects at the University of São Paulo (CAAE: 43676515.1.0000.5390). All subjects gave written informed consent.Sleep AnalysisSleep stages, apneas, hypopneas, and arousals were defined and scored according to American Academy of Sleep Medicine guidelines.19 Apnea was defined as a ≥ 90% drop of respiratory amplitude, lasting at least 10 seconds. Hypopnea was defined as a 50% drop of respiratory amplitude, lasting at least 10 seconds, associated with oxygen saturation drops ≥ 3% (absolute criteria) or at least 30% drop of respiratory amplitude, lasting at least 10 seconds, associated with oxygen saturation drops ≥ 4% or arousals (alternative criteria). The AHI was calculated based on the total number of respiratory events (apneas and hypopneas) per hour of sleep. Obstructive apnea was defined as a cessation of respiratory airflow for 10 seconds with thoracoabdominal effort, which was detected by using a piezo respiratory effort sensor. The average time from the diagnosis of OSA to enrollment in the research study was 1 month for all participants.Brachial Blood PressureClinical BP readings were obtained from the left arm of subjects while seated, after 5 minutes of quiet rest, with a mercury sphygmomanometer. All subjects had at least three office BP measurements obtained on separate occasions taken by one investigator. Systolic and diastolic BP was recorded at the first appearance and disappearance (phases I and V, respectively) of Korotkoff sounds. The subjects were classified as normotensive if the average systolic and diastolic BP levels were ≤ 140 or 90 mmHg.Anthropometric MeasuresBody weight (in kilograms) was measured by digital scale with 50-g precision and a 200-kg capacity. Height was measured using a Sanny stadiometer with 0.1-cm precision. Body composition was measured by bioelectrical impedance (Quantum II, RJL Systems, Clinton Township, Michigan, United States). Briefly, two signaling electrodes were placed on the dorsal surface of the right foot between the second and third toe, as well as the dorsal surface of the right hand between the second and third digits. Two sensor electrodes were placed on the right hand and right ankle. Participants were asked to remain motionless in the supine position with legs and arms slightly abducted so there was no contact between the extremities and torso. Data output included reactance, resistance, and impedance. Data were entered into the software program provided by the manufacturer (Cypress, RLJ Systems). Data output included body fat mass (%) and fat-free mass (%).Level of Physical ActivityThe physical activity level was evaluated using the International Physical Activity Questionnaire (IPAQ) that allows estimation of the weekly time spent in moderate, intense physical activity and walking in various areas of everyday life: domestic, work, transportation, leisure, and also the time that a person remains seated.20 IPAQ was previously validated in a Brazilian sample20 and showed a significant and high correlation (r = .71). In this previous study, the reliability of IPAQ was determined after 7 days, and the Spearman correlation was significant and high (rho = .69–.71, P < .01).In the current study, patients with a physical activity time < 30 min/wk were considered insufficiently active so were included in the sedentary (SED) group, and patients with physical activity time ≥ 150 min/wk including moderate or vigorous physical activity (≥ 3 d/w and ≥ 30 min/exercise session) were included in the physically active (ACTIVE) group.Experimental ProtocolThe study was performed in a quiet, temperature-controlled room (21°C to 22°C), with the subjects in the supine position in the morning at approximately the same time each day. The variables described below were continuously measured during 4 minutes at rest followed by 3 minutes of a mental stress test.Hemodynamic VariablesHeart rate (HR) was continuously measured by electrocardiography. BP was monitored noninvasively with an automatic BP cuff on the nondominant ankle with an automatic oscillometric device (DX 2022, Dixtal Biomédica e Tecnologia, Manaus, Amazonas, Brazil). The systolic, diastolic, and mean BP was recorded every minute of the mental stress test.Forearm Blood FlowVenous occlusion plethysmography (AI6, Hokanson, Bellevue, Washington, United States) was used to determine forearm blood flow, as previously described.21 Briefly, the nondominant arm was elevated above the heart level. A suitable strain gauge (Hokanson) was placed around the forearm and connected to a plethysmograph. An inflating cuff (SC12D, Hokanson) was placed around the participant's bicep to occlude venous blood flow and connected to a rapid cuff inflator (Hokanson). To exclude hand circulation, which contains a large number of arteriovenous shunts, a segmental pressure cuff (TMC7, Hokanson) was placed around the wrist and inflated to supra-arterial pressure immediately before testing commenced. At 20-second intervals, the upper arm cuff was inflated above venous pressure for 10 seconds. Baseline forearm blood flow (FBF) was then recorded continuously for 4 minutes at baseline and during the 3-minute period of the Stroop Color Word Test (SCWT). Each minute of the FBF was determined based on three separate readings. Forearm vascular conductance (FVC) was calculated (FBF / mean BP × 100).Mental Stress TestThe mental stress test was performed after resting baseline using a modified version of the SCWT conducted for 3 minutes. Briefly, during the SCWT, patients were shown a series of names written with different colors of the specified word. The subjects were asked to identify the color of the ink and not read the written word. If the patient took more than 3 seconds to speak the next word, the subject received a standard verbal incentive to continue the test. At the conclusion of the protocol, each participant was asked about a perception of the stress experienced, using a scale from 0 to 5 (0: not stressful, 1: very mild stress, 2: mild stressful, 3: moderately stressful, 4: very stressful, and 5: extremely stressful).10Statistical AnalysisData are presented as mean ± standard error. An unpaired Student t test (years, BMI, left ventricular ejection fraction, cardiovascular parameters, AHI, minimum O2 saturation) of SED and ACTIVE groups was performed. The difference between sexes was tested by the χ2 test. The Kolmogorov-Smirnov and Levine tests were used to assess the normality and homogeneity of distribution of each variable studied. The FBF responses to SCWT were analyzed by relative and absolute differences (each minute of the SCWT – mean baseline) for the group. In the case of significance, post hoc comparisons were performed by Tukey honest significant difference test. The correlations between the level of physical activity and clinical variables were performed using Pearson correlation analysis. In all analyses, a value of P < .05 was considered statistically significant. All statistical analyses were performed using Statistica 12 software (StatSoft, Tulsa, Oklahoma, United States).RESULTSFrom a total of 44 subjects who were initially selected to participate in the study, 4 were excluded because of the inadequate FBF recording obtained. Thus, 40 patients with moderate to severe OSA completed the study. The patients were classified into SED (n = 21) and ACTIVE (n = 19) groups through the IPAQ. The SED and ACTIVE groups were similar regarding sex distribution, age, weight, BMI, fat mass, and years of education (Table 1). As expected, the leisure time physical activity was significantly different between groups (P < .05). Baseline HR and BP were also similar between groups. The baseline FBF and FVC were significantly lower in the SED compared to the ACTIVE subjects (P < .05). For instance, in our previous study16 the FBF and FVC were 2.50 ± 0.30 and 3.10 ± 0.40, respectively in normal healthy subjects without sleep apnea and a similar age as subjects in the current study.Table 1 Baseline characteristics and physical activity level in sedentary and physically active patients with obstructive sleep apnea.Table 1 Baseline characteristics and physical activity level in sedentary and physically active patients with obstructive sleep apnea.Regarding sleep patterns, no differences were noted in total recording time, total sleep time, percentage of sleep stages (N1, N2, and N3). Percentage rapid eye movement (REM) was greater in the ACTIVE compared with the SED group. The arousal index was higher in the SED compared with the ACTIVE group. Apnea index, hypopnea index, oxygen de-saturation index, and percentage of recording time with SaO2 of < 90% did not differ between groups (Table 2).Table 2 Sleep parameters in sedentary and physically activity patients with obstructive sleep apnea.Table 2 Sleep parameters in sedentary and physically activity patients with obstructive sleep apnea.Responses to Mental StressThe stress perception after SWCT did not differ between the SED and the ACTIVE groups (2.9 ± 0.3; 2.7 ± 0.35; P = .63), respectively. The HR response showed the greatest increase (P > .05) in the first minute of SWCT compared with baseline in both SED and ACTIVE groups (Figure 1A), with further decreases in the second and third minute. The mean BP significantly increased during the second and third minute of SWCT in both SED and ACTIVE groups compared with baseline and the first minute of SWCT (Figure 1B).Figure 1: Hemodynamic response during the Stroop Color Word Test in sedentary and physically active patients with obstructive sleep apnea.(A) Heart rate and (B) ankle mean blood pressure. Dagger indicates versus baseline, P < .05 (within groups). Double daggers indicate versus first minute, P < .05 (within groups). ACTIVE = physically active group, SED = sedentary group.Download FigureThe absolute values of FBF and FVC increased significantly during 3 minutes of SWCT in both groups (Figure 2A, 2B). The FBF and FVC responses (each minute of SWCT – baseline) increased in both SED and ACTIVE groups during 3 minutes of SWCT compared to baseline (Figure 2C, 2D). However, there was a significant difference between groups in the first, second, and third minute of SWCT. Exploratory analysis including sex as a covariate did not alter the results. In addition, a significant correlation was found between FBF during SWCT (r = .57; P < .05; Figure 3A) and FVC during SWCT (r = .48; P < .05; Figure 3B) with the time spent in leisure physical activity.Figure 2 (A) Forearm blood flow and (C) forearm blood flow response during the Stroop Color Word Test in patients with obstructive sleep apnea. (B) Forearm vascular conductance and (D) forearm vascular conductance response during the Stroop Color Word Test in patients with obstructive sleep apnea. Asterisk indicates ACTIVE versus SED, P < .05. Dagger indicates versus baseline, P < .05 (within groups). Double daggers indicate versus first minute, P < .05 (within groups). ACTIVE = physically active group, SED = sedentary group.Download FigureFigure 3 Group data correlations between forearm blood flow and leisure time physical activity (A) and forearm vascular conductance and leisure time physical activity (B). Open circles indicate sedentary (SED) and dark circles indicate physically active (ACTIVE) patients with obstructive sleep apnea.Download FigureDISCUSSIONIn this study we found that among a homogeneous group of patients with OSA with no other comorbidities, ACTIVE patients had better vascular function at rest and during mental stress compared with the SED patients. The main findings that support this observation are as follows: ACTIVE compared with SED patients had 37% higher FBF and 33% higher FVC at rest. The ACTIVE group compared with SED group had a better vascular response to mental stress, as observed by a significantly higher change in FBF (32%) and FVC (35%). In addition, there was a positive correlation between mean FBF and FVC during mental stress and leisure time physical activity.There is consistent evidence indicating that OSA may affect endothelial function.22 OSA has been independently associated with lower nitric oxide bioavailability23 and increased vasoconstrictor tone.24 Consistent with the literature, the baseline mean values of FBF and FVC in our SED group were similar to those of a previous study that evaluated patients with OSA and congestive heart failure. The baseline mean values of FBF and FVC in our ACTIVE group were similar to those in healthy control subjects with similar mean age but without OSA.16 Therefore, our finding of better baseline vascular function in ACTIVE than SED patients with OSA is consistent with previous studies in other populations.17,18Our study extends these previous findings by investigating the possible effect of physical activity level on vascular function in patients with OSA without other comorbidities. Aerobic exercise improves endothelial function in healthy adults,25 obese subjects,26 patients with hypertension,27 and patients with heart failure.28 In addition, cross-sectional studies that evaluate the level of physical activity in real-world conditions have shown that compared with sedentary subjects, regular physical activity is associated with better vascular function.29 In our study, the mean leisure physical activity level in the ACTIVE group was moderate and corresponded to approximately 4 h/week of moderate to vigorous activities. This amount of physical activity is similar to that reported in a recent study that showed that moderate physical activity levels (≥ 4 h/wk) is sufficient to obtain health benefits, reduction in mortality, and development of cardiovascular diseases in older adults independently of associated risk factors.30In the current study we also evaluated vascular functional response to mental stress tests that have been extensively used to evaluate endothelial function in distinct groups with cardiovascular risk.13,18 Studies have shown that vascular functional response to stress is a marker of endothelial dysfunction or atherosclerosis as reflected by increased carotid intima media thickness14 and decreased flow-mediated dilation.17,31The HR and BP response to mental stress was similar in SED and ACTIVE groups. HR peak at the first minute of mental stress is caused by a β-adrenergic receptor stimulation32 and probably represents a defensive reaction of the body preparing the body for a fight or flight response33 to the mental stress. Elevation in BP may occur mainly because of an increase in cardiac output and increased sympathetic activity.10In the current study, ACTIVE and SED groups significantly increased FBF and FVC during mental stress. However, the level of vasodilation was significantly higher in the ACTIVE than in the SED group. Our results are in line with the observation that regular physical activity is effective in preventing endothelial dysfunction during mental stress in subjects with metabolic syndrome17 and obesity.18 Thus, it might be speculated that the increased forearm vasodilation during mental stress in our ACTIVE group may be related to a protective factor of some of the vascular pathophysiology observed in patients with moderate to severe OSA. Physical exercise improves nitric oxide-mediated endothelial function,34 promotes metabolic vasodilation that is partly dependent on the release of nitric oxide35 and its greatest importance is in autonomic control during mental stress.36,37The observation of the increased percentage of REM and reduced arousals in the ACTIVE compared with the SED group demonstrate that regular physical activity improves sleep pattern in patients with OSA. These findings are in line with a previous study in which regular exercise improved sleep parameters in OSA patients with heart failure.15 Cooper et al.38 also indicate an association between impaired vasodilatory capacity and decreased percentage of REM, suggesting that diminished vascular function in OSA could be a mechanism also linking poor sleep parameters.This study has limitations that should be noted. We only studied patients with OSA; no healthy control patients were included. However, a previous study has shown that patients with OSA have impaired vascular function compared with healthy control patients.39 Our study design allowed us to isolate one single variable (level of physical activity) in an otherwise homogenous group of patients with OSA with no other comorbidities. This was a cross-sectional study and therefore the association found between FBF and FVC with leisure time physical activity level does not necessarily imply a causal relationship. The evaluation of FBF by venous occlusion plethysmography calculates the total amount of blood in the forearm muscle. Further studies using pharmacological blockade of adrenergic and cholinergic receptors are needed to explain the endothelial dependent and neuronal mechanisms associated with the level of physical activity among patients with OSA.In summary, active patients with OSA have increased resting and vasodilator response during mental stress than do sedentary patients. Our results reinforce the importance of regular physical activity, especially in leisure time, as a potential nonpharmacologic preventive measure for vascular dysfunction in patients with moderate to severe OSA. Our study also indicates that the level of physical activity must be clearly determined in future studies that evaluate cardiovascular function in patients with OSA.DISCLOSURE STATEMENTThis study was supported in part by Pro-Reitoria de Pesquisa da Universidade de São Paulo (FAPESP # 2010/15064-6) to Dra. Linda M. Ueno Pardi. Rosyvaldo F. Silva was supported by Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP # 2015/14795-0). Thiago T. Goya was supported by Coordenação de Aperfeiçoamento de Pessoal de Nível Superior. The authors report no conflicts of interest.ABREVIATIONSACTIVEactive groupAHIapnea-hypopnea indexBMIbody mass indexBPblood pressureFBFforearm blood flowFVCforearm vascular conductanceHRheart rateIPAQInternational Physical Activity QuestionnaireOSAobstructive sleep apneaSCWTStroop Color Word TestSEDsedentary groupREFERENCES1 Phillips CL, O'Driscoll DMHypertension and obstructive sleep apnea. Nat Sci Sleep; 2013;5:43-52, 23750107. CrossrefGoogle Scholar2 Somers VK, White WP, Amin Ret al.Sleep Apnea and Cardiovascular Disease An American Heart Association/American College of Cardiology Foundation Scientific Statement From the American Heart Association Council for High Blood Pressure Research Professional Education Committee, Council on Clinical Cardiology, Stroke Council, and Council on Cardiovascular Nursing In Collaboration With the National Heart, Lung, and Blood Institute National Center on Sleep Disorders Research (National Institutes of Health). Circulation; 2008;11810:1080-1111, 18725495. Google Scholar3 Oflaz H, Cuhadaroglu C, Pamukcu Bet al.Endothelial function in patients with obstructive sleep apnea syndrome but without hypertension. Respiration; 2006;736:751-756, 16804287. CrossrefGoogle Scholar4 Namtvedt SK, Hisdal J, Randby Aet al.Impaired endothelial function in persons with obstructive sleep apnoea: impact of obesity. Heart; 2013;991:30-34, 23048165. CrossrefGoogle Scholar5 Nieto FJ, Herrington DM, Redline S, Benjamin EJ, Robbins JASleep apnea and markers of vascular endothelial function in a large community sample of older adults. Am J Respir Crit Care Med; 2004;1693:354-360, 14551166. CrossrefGoogle Scholar6 Celermajer DS, Sorensen KE, Gooch VMet al.Non-invasive detection of endothelial dysfunction in children and adults at risk of atherosclerosis. Lancet; 1992;3408828:1111-1115, 1359209. CrossrefGoogle Scholar7 Marin JM, Carrizo SJ, Vicente E, Agusti AGLong-term cardiovascular outcomes in men with obstructive sleep apnoea hypopnoea with or without treatment with continuous positive airway pressure: an observational study. Lancet; 2005;3659464:1046-1053, 15781100. CrossrefGoogle Scholar8 Yaggi HK, Concato J, Kernan WN, Lichtman JH, Brass LM, Mohsenin VObstructive sleep apnea as a risk factor for stroke and death. N Engl J Med; 2005;35319:2034-2041, 16282178. CrossrefGoogle Scholar9 Esler MMental stress and human cardiovascular disease. Neurosci Biobehav Rev; 2017;74Pt B:269-276, 27751732. CrossrefGoogle Scholar10 Goya TT, Silva RF, Guerra RSet al.Increased muscle sympathetic nerve activity and impaired executive performance capacity in obstructive sleep apnea. Sleep; 2016;391:25-33, 26237773. CrossrefGoogle Scholar11 Mausbach BT, Chattillion E, Roepke SKet al.A longitudinal analysis of the relations among stress, depressive symptoms, leisure satisfaction, and endothelial function in caregivers. Health Psychol; 2012;314:433-440, 22486550. CrossrefGoogle Scholar12 Poitras VJ, Pyke KEThe impact of acute mental stress on vascular endothelial function: evidence, mechanisms and importance. Int J Psychophysiol; 2013;882:124-135, 23562766. CrossrefGoogle Scholar13 Kuniyoshi FH, Trombetta IC, Batalha LTet al.Abnormal neurovascular control during sympathoexcitation in obesity. Obes Res; 2003;1111:1411-1419, 14627763. CrossrefGoogle Scholar14 Padilla J, Simmons GH, Vianna LC, Davis MJ, Laughlin MH, Fadel PJBrachial artery vasodilatation during prolonged lower limb exercise: role of shear rate. Exp Physiol; 2011;9610:1019-1027, 21784788. CrossrefGoogle Scholar15 Roque FR, Briones AM, Garcia-Redondo ABet al.Aerobic exercise reduces oxidative stress and improves vascular changes of small mesenteric and coronary arteries in hypertension. Br J Pharmacol; 2013;1683:686-703, 22994554. CrossrefGoogle Scholar16 Ueno LM, Drager LF, Rodrigues ACet al.Effects of exercise training in patients with chronic heart failure and sleep apnea. Sleep; 2009;325:637-647, 19480231. CrossrefGoogle Scholar17 Sales AR, Fernandes IA, Rocha NGet al.Aerobic exercise acutely prevents the endothelial dysfunction induced by mental stress among subjects with metabolic syndrome: the role of shear rate. Am J Physiol Heart Circ Physiol; 2014;3067:H963-H971, 24531810. CrossrefGoogle Scholar18 Tonacio AC, Trombetta IC, Rondon MUet al.Effects of diet and exercise training on neurovascular control during mental stress in obese women. Braz J Med Biol Res; 2006;391:53-62, 16400464. CrossrefGoogle Scholar19 Iber C, Ancoli-Israel S, Chesson AL, Quan SFfor the American Academy of Sleep MedicineThe AASM Manual for the Scoring of Sleep and Associated Events: Rules. Terminology and Technical Specifications1st edWestchester, IL: American. Academy of Sleep Medicine; 2007. Google Scholar20 Matsudo S, Araujo T, Matsudo Vet al.Questionário Internacional de Atividade Física (IPAQ): estudo de validade e reprodutibilidade no Brasil. Rev Bras Ativ Saúde; 2001;10:5-18. Google Scholar21 Antunes-Correa LM, Nobre TS, Groehs RVet al.Molecular basis for the Improvement in muscle metaboreflex and mechanoreflex Control in 2 exercise-trained humans with chronic heart failure. Am J Physiol Heart Circ Physiol; 2014;30711:H1655-H666, 25305179. CrossrefGoogle Scholar22 Jelic S, Padeletti M, Kawut SMet al.Inflammation, oxidative stress, and repair capacity of the vascular endothelium in obstructive sleep apnea. Circulation; 2008;29;11717:2270-2278. CrossrefGoogle Scholar23 Badran M, Golbidi S, Ayas N, Laher INitric oxide bioavailability in obstructive sleep apnea: interplay of asymmetric dimethylarginine and free radicals. Sleep Disord; 2015;2015:e387801. CrossrefGoogle Scholar24 Moradkhan R, Spitnale B, McQuillan P, Hogeman C, Gray KS, Leuenberger UAHypoxia-induced vasodilation and effects of regional phentolamine in awake patients with sleep apnea. J Appl Physiol; 2010;1085:1234-1240, 20223993. CrossrefGoogle Scholar25 DeSouza CA, Shapiro LF, Clevenger CMet al.Regular aerobic exercise prevents and restores age-related declines in endothelium-dependent vasodilation in healthy men. Circulation; 2000;10212:1351-1357, 10993851. CrossrefGoogle Scholar26 Cotie LM, Josse AR, Phillips SM, MacDonald MJEndothelial function increases after a 16-week diet and exercise intervention in overweight and obese young women. Biomed Res Int; 2014;2014:327-395. CrossrefGoogle Scholar27 Higashi Y, Sasaki S, Kurisu Set al.Regular aerobic exercise augments endothelium-dependent vascular relaxation in normotensive as well as hypertensive subjects: role of endothelium-derived nitric oxide. Circulation; 1999;10011:1194-1202, 10484540. CrossrefGoogle Scholar28 Hambrecht R, Fiehn E, Weigl Cet al.Regular physical exercise corrects endothelial dysfunction and improves exercise capacity in patients with chronic heart failure. Circulation; 1998;9824:2709-2715, 9851957. CrossrefGoogle Scholar29 Rinder MR, Spina RJ, Ehsani AAEnhanced endothelium-dependent vasodilation in older endurance-trained men. J Appl Physiol; 2000;882:761-766, 10658048. CrossrefGoogle Scholar30 Barengo NC, Antikainen R, Borodulin K, Harald K, Jousilahti PLeisure-time physical activity reduces total and cardiovascular mortality and cardiovascular disease incidence in older adults. J Am Geriatr Soc; 2017;653:504-510, 28024086. CrossrefGoogle Scholar31 Rocha NG, Sales AR, Miranda RLet al.Aerobic exercise modulation of mental stress-induced responses in cultured endothelial progenitor cells from healthy and metabolic syndrome subjects. Life Sci; 2015;15;123:93-99. CrossrefGoogle Scholar32 Silva AS, Zanesco AExercício físico, receptores ß-adrenérgicos e resposta vascular. J Vasc Bras; 2010;92:47-56. CrossrefGoogle Scholar33 Rimmele U, Zelweger BC, Bernad Marti Bet al.Trained men show lower cortisol, heart rate and psychological responses to psychosocial stress compared with untrained men. Psychoneuroendocrinology; 2007;326:627-635, 17560731. CrossrefGoogle Scholar34 Green DJ, Maiorana A, O'Driscoll G, Taylor REffect of exercise training on endothelium-derived nitric oxide function in humans. J Physiol; 2004;561Pt 1:1-25, 15375191. CrossrefGoogle Scholar35 Duffy SJ, New G, Harper RW, Meredith ITMetabolic vasodilation in the human forearm is preserved in hypercholesterolemia despite impairment of endothelium-dependent and independent vasodilation. Cardiovasc Res; 1999;433:721-730, 10690343. CrossrefGoogle Scholar36 Dietz NM, Rivera JM, Eggener SE, Fix RT, Warner DO, Joyner MJNitric oxide contributes to the rise in forearm blood flow during mental stress in humans. J Physiol; 1994;480Pt 2:361-368, 7869251. CrossrefGoogle Scholar37 Cardillo C, Kilcoyne CM, Quyyumi AA, Cannon RO, Panza JARole of nitric oxide in the vasodilator response to mental stress in normal subjects. Am J Cardiol; 1997;808:1070-1074, 9352980. CrossrefGoogle Scholar38 Cooper DC, Ziegler MG, Milic MSet al.Endothelial function and sleep: associations of flow-mediated dilation with perceived sleep quality and rapid eye movement (REM) sleep. J Sleep Res; 2014;231:84-93, 24033699. CrossrefGoogle Scholar39 Ip MS, Tse HF, Lam B, Tsang KW, Lam WKEndothelial function in obstructive sleep apnea and response to treatment. Am J Respir Crit Care Med; 2004;1693:348-353, 14551167. CrossrefGoogle Scholar Previous article Next article FiguresReferencesRelatedDetailsCited by Effects of exercise training on brain metabolism and cognitive functioning in sleep apneaUeno-Pardi L, Souza-Duran F, Matheus L, Rodrigues A, Barbosa E, Cunha P, Carneiro C, Costa N, Ono C, Buchpiguel C, Negrão C, Lorenzi-Filho G and Busatto-Filho G Scientific Reports, 10.1038/s41598-022-13115-2, Vol. 12, No. 1, Online publication date: 1-Dec-2022. Sedentary behaviour is associated with heightened cardiovascular, inflammatory and cortisol reactivity to acute psychological stressChauntry A, Bishop N, Hamer M, Kingsnorth A, Chen Y and Paine N Psychoneuroendocrinology, 10.1016/j.psyneuen.2022.105756, Vol. 141, , (105756), Online publication date: 1-Jul-2022. Sedentary behaviour, physical activity and psychobiological stress reactivity: A systematic reviewChauntry A, Bishop N, Hamer M and Paine N Biological Psychology, 10.1016/j.biopsycho.2022.108374, Vol. 172, , (108374), Online publication date: 1-Jul-2022. Volume 14 • Issue 09 • September 15, 2018ISSN (print): 1550-9389ISSN (online): 1550-9397Frequency: Monthly Metrics History Submitted for publicationJanuary 8, 2018Submitted in final revised formMarch 29, 2018Accepted for publicationMay 3, 2018Published onlineSeptember 15, 2018 Information© 2018 American Academy of Sleep MedicineKeywordsobstructive sleep apneaforearm vascular conductanceforearm blood flowphysical activitymental stressPDF download
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