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Cerebrovascular responses to submaximal exercise in women with COPD

Abstract

Background

COPD patients have decreased physical fitness, and have an increased risk of vascular disease. In the general population, fitness is positively associated with resting cerebral blood flow velocity, however, little is known about the cerebrovascular response during exercise particularly in COPD patients. We hypothesized that COPD patients would have lower cerebral blood flow during exercise secondary to decreased physical fitness and underlying vascular disease.

Methods

Cardiopulmonary exercise testing was conducted in 11 women with GOLD stage I-II COPD, and 11 healthy controls to assess fitness. Cerebro- and cardio-vascular responses were compared between groups during two steady-state exercise tests (50% peak O2 consumption and 30 W). The main outcome variable was peak middle cerebral artery blood flow velocity ( V ¯ P ) during exercise using transcranial Doppler ultrasonography.

Results

Physical fitness was decreased in COPD patients. V ¯ P was comparable between COPD and controls (25 ± 22% versus 15 ± 13%, respectively; P > 0.05) when exercising at the same relative intensity, despite patients having higher blood pressure and greater arterial desaturation. However, V ¯ P was elevated in COPD (31 ± 26% versus 13 ± 10%; P ≤ 0.05) when exercising at the same workload as controls.

Conclusions

Our results are contradictory to our a-priori hypothesis, suggesting that during matched intensity exercise, cerebral blood flow velocity is similar between COPD and controls. However, exercise at a modestly greater workload imposes a large physical demand to COPD patients, resulting in increased CBF compared to controls. Normal activities of daily living may therefore impose a large cerebrovascular demand in COPD patients, consequently reducing their cerebrovascular reserve capacity.

Peer Review reports

Background

The regulation of cerebral blood flow (CBF) is imperative for adequate delivery of O2 and energy supply to the brain. During cerebral activation and increased metabolism, cerebral arterioles dilate, thereby increasing CBF, and ultimately O2 delivery. This process of neurovascular coupling (i.e., neural activation coupled with an adequate increase in blood flow) is challenged during dynamic exercise. Factors such as age and physical fitness have been suggested to play an important role in this regulatory process both at rest [1], and during exercise [2].

The reduction of physical activity levels and exercise capacity in COPD patients [35] may pose a risk to patients’ cerebrovascular health. Even in the early stages of COPD, patients with mild and moderate obstruction are reported to have reduced exercise capacity [6]. Evidence suggests that patients with moderate COPD are already at an increased risk of cardiovascular disease and stroke, thereby suggesting an underlying vascular pathology. We have previously reported decreased CBF responsiveness to CO2 in women with COPD, suggesting reduced cerebral dilatory function [7].

Cycle ergometry testing offers a functional and translational tool to test integrated responses during exercise. COPD patients may exhibit arterial hypercapnia [8] and hypoxemia, exaggerated vasopressor response [9], and ventilatory limitations [10] during exercise – which all have implications on the regulation of CBF. Furthermore, greater distribution of cardiac output to respiratory or peripheral muscles could impact the blood flow delivery to the brain. Presently, few studies have focused on the cerebrovascular response of COPD patients during exercise [11, 12], and of these studies, focus has been on exercise limitations. It is currently unknown if the cerebrovascular response to exercise in COPD patients differs from that of a healthy control group.

We therefore tested the hypothesis that women with mild-moderate COPD would have reduced cerebral blood flow during exercise, secondary to reduced physical fitness. Women were of particular interest in this study due to a shift in the disease burden from men to women [13], and comparatively, women report worse symptoms for a similar severity of disease to men, and for any given age, have lower aerobic capacity. Additionally, we chose to focus on patients with mild-moderate COPD because this demographic represents approximately half of all cases of COPD [14].

Methods

Study subjects

Twenty-three postmenopausal women (COPD = 11, Healthy Control = 12) between the ages of 55–79 years old were recruited for participation in this study. Control subjects were recruited from the community, and COPD patients were recruited from participating outpatient medical clinics within the Calgary Health Region. All study participants visited the Laboratory of Human Cerebrovascular Physiology at the University of Calgary (1103 m elevation) for two testing sessions. Subjects were instructed to refrain from eating or drinking 4 hours prior to each testing session. All study participants provided written, informed consent. Ethical approval was obtained by the Conjoint Health Research Ethics Board at the University of Calgary (Ethics ID: E-22138).

Since there are currently no published studies describing the CBF response in COPD during exercise, compared to healthy controls, we based our sample size using data from our previous study [7] describing changes in V ¯ P during hypercapnia. We expected a similar difference in V ¯ P between groups (Control = 37% vs. COPD = 19%). Therefore, a sample size of n = 10 in each group was needed to detect a significant difference with a power of 95%, and a two-tailed α of 0.05. It is likely that there are similar physiological mechanisms involved in the regulation of blood flow during exercise and hypercapnia, and reason that this power calculation would be an appropriate estimation of sample size.

Inclusion criteria

Patients were eligible for inclusion into the COPD cohort if they had physician-diagnosed GOLD stage I-II COPD, a smoking history >10 pack-years and, chronic airflow obstruction (FEV1/FVC <70%; FEV1 ≥ 50% predicted). To control for the immediate and lasting cardiovascular effects of nicotine, patients needed to be ex-smokers (>1 year). Additional criteria included: post-menopausal for ≥ 12 months, able to walk independently outside or on stairs, and a BMI < 35 kg m-2. Study subjects were allowed to be on long- or short-acting bronchodilators, either alone, or in combination with inhaled corticosteroids. Exclusion criteria included heart/chest pain upon physical exertion, surgery or trauma within previous 6 months, history of myocardial infarction, angina, arrhythmia, valve disease, chronic heart failure, history of stroke, cardiovascular or cerebrovascular disease, history of chronic headaches/migraines, history of blood clots/thrombosis, and patients who were on domiciliary oxygen.

Participating control subjects were sedentary (< 3 planned exercise sessions/week), post-menopausal, and had no history of lung disease, and no significant history of smoking (< 1 pack-year lifetime smoking history). Additional exclusion criteria conformed to that as outlined above for COPD patients.

Study design

Subjects visited the laboratory on two occasions, and followed the same study protocol and procedures. On the first visit, volunteers completed a medical screening questionnaire, pulmonary function test, and cardiopulmonary exercise test (CPET) to assess physical fitness. Volunteers returned to the laboratory to complete the main experimental session involving CBF measurements during exercise. The main exercise protocol consisted of two bouts of 6-minutes each of exercise on a modified semi-supine cycle ergometer (~70 degrees upright) (Exercise 1 [EX1 = 50% V ˙ O 2 peak and Exercise 2 [EX2 = 30 Watts]), as previously described [15, 16]. The workload at 50% V ˙ O 2 peak was intended to observe the peak CBF response, while an absolute value of 30 Watts was selected to represent the intensity of common activities of daily living, comparable to household work and light gardening (~3 metabolic equivalents; METS). The exercise periods were separated by a 6-minute rest/recovery period to allow physiological variables to return to baseline (BL).

Pulmonary function testing

Spirometry, measures of lung volumes and single-breath diffusion capacity were completed according to ATS guidelines [1719].

Cardiopulmonary exercise test

Peak oxygen uptake ( V ˙ O 2 peak ) was assessed by a CPET performed on a modified semi-reclined cycle ergometer, according to ATS guidelines [20]. The test was initiated with a 3-minute warm-up period of unloaded cycling, immediately followed by an increase in workload to 20 W, with progressive increments of either 10 or 15 W·min-1 (COPD patients or controls, respectively). Ratings of perceived dyspnea and leg fatigue were scored using a modified Borg Scale every 2 minutes by the participant. Breath-by-breath metabolic and respiratory variables were collected using dedicated software (BreatheM v2.38, Oxford) and measured by mass spectrometry (AMIS 2000; Innovision, Odense, Denmark). Continuous measures of heart rate via 3-lead ECG (Micromon 7142 monitor; Kontron Medical, Milton Keynes, UK), and arterial oxygen saturation (Sao 2) (Model 3900; Datex-Ohmeda, Louisville, CO) were recorded.

Protocol to measure the cerebral blood flow response to submaximal exercise

Middle cerebral artery (MCA) blood flow velocity was continuously measured using a 2-MHz pulsed Doppler Ultrasound system (TC22, SciMed, Bristol, England) as previously described [16]. Peak middle cerebral artery velocity ( V ¯ P ) was used as a surrogate for CBF. Heart rate was collected using a 3-lead ECG (Micromon 7142B monitor; Kontron Keynes, UK), and continuous beat-beat blood pressure was measured using finger pulse photoplethysmography (Portapress; TPD Biomedical Instrumentation, Amsterdam, The Netherlands). Arterial oxygen saturation was collected using finger pulse oximetry (Model 3900; Datex-Ohmeda, Louisville, CO).

Respiratory measures

Subjects breathed through a mouthpiece with their nose occluded. Respiratory gas concentrations were sampled at the mouth at 100Hz using mass spectrometry (AMIS 2000; Innovision, Odense, Denmark). Respiratory volumes were measured with a turbine and volume transducer (VMM-400; Interface Associates, Laguna Niguel, CA), and respiratory flow direction and timing were obtained with a pneumotachograph (RSS100-HR, Hans Rudolf, Kansas City, MO, USA).

Data analysis

Analysis

Physiological data were collected on a beat-beat and breath-breath basis using dedicated software (BreatheM v2.38, University Laboratory of Physiology, Oxford, UK) and later averaged into 15-second bins. Baseline data were averaged over 2-minutes immediately preceding exercise. To achieve steady state parameters, the last 60-seconds of exercise (i.e., minute 5 to 6) were used in the stage averages. The main outcome variable in this study was V ¯ P . Secondary outcomes were V ˙ O 2 peak , mean blood pressure (MBP), and cerebrovascular conductance ( CVC = V ¯ P / MBP ).

Statistical procedures

Using statistical software (SPSS Version 20.0, SPSS Inc., Chicago, IL, USA), mean between-group differences in subject characteristics, pulmonary function data, and endpoints of the maximal cardiopulmonary exercise test were determined using independent t-tests. Paired t-tests were used to assess baseline (BL) differences within groups (i.e., COPD BL1 vs. COPD BL2). A 2×2 mixed factorial repeated measures analysis of variance was used to assess the main effect of independent variables “condition” (i.e., BL1 vs. EX1 or BL2 vs. EX2), and “grouping” (i.e., COPD or CONTROL), and the interaction between condition x grouping on physiological outcomes (i.e., V ¯ P , CVC, MBP, HR, Sao 2).

Relationships were assessed exclusively within groups using Pearson’s correlation coefficient to investigate fitness status ( V ˙ O 2 peak ), disease severity (FEV1pred, DLCO), Sao 2, Petco 2, and MBP on cerebrovascular variables at rest and during exercise. Data are presented as mean ± SD, with significance set at α-level ≤ 0.05. Two tailed tests were performed in all analyses.

Results

Two COPD patients were not able to complete the EX2 protocol; however, their data from EX1 was included in the study analysis. One control participant was excluded due to lack of a suitable CBF signal. We therefore compared the exercise responses between 11 COPD and 11 control participants in EX1, and 9 COPD and 11 control participants in EX2.

Baseline characteristics

Physical characteristics and results of pulmonary function tests are listed in Table 1. Groups were well matched for age, weight and BMI (P > 0.05). By study design, COPD patients had a significantly greater smoking history than controls (P < 0.01). Based on post-spirometric FEV1 predicted values, disease severity ranged from GOLD I-II (mild to moderate) (51% to 86%) in COPD patients (n = 9, GOLD II). COPD patients had reduced diffusion capacity (DLCO), and increased hyperinflation (FRC, IC/TLC) compared to control subjects (P < 0.01), who all had normal lung function.

Table 1 Subject characteristics

Cardiopulmonary exercise test

Results of the cardiopulmonary exercise test are summarized in Table 2. Mean V ˙ O 2 peak and peak power output was lower in patients with COPD. Arterial oxygen saturation was significantly decreased in COPD patients with exercise, but not in controls (P < 0.01). At end of exercise, COPD patients achieved similar predicted heart rate values to controls, suggesting a ventilatory limitation to exercise, rather than any cardiovascular impairment (P > 0.05).

Table 2 Summary of Cardiopulmonary Exercise Test Endpoints in COPD and controls

Responses to exercise at a relative workload: 50% V ˙ O 2 peak (EX1)

The target intensity for EX1 was set at 50% V ˙ O 2 peak for 6 minutes (EX1). Accordingly, groups exercised at a similar exercise intensity ( V ˙ O 2 peak : 69% (COPD) versus 50% (controls); P > 0.05). Metabolic cost was not different between groups in EX1 ( V ˙ O 2 : 0.69 Lmin-1 (COPD) versus 0.74 Lmin-1 (controls); P > 0.05). Despite similar workrates between groups (COPD: 15 W versus Controls: 23 W; P > 0.05), COPD patients exercised at a greater capacity of their WRpeak (COPD: 25% versus Controls: 18%; P ≤ 0.05). Patients and controls had similar Petco 2 and Peto 2 at rest, and in response to EX1 (P > 0.05).

The cerebro-and cardiovascular responses to EX1 are summarized in Table 3. There were no differences between resting cerebro- or cardio-vascular variables between groups (P > 0.05). The two-factor analysis of variance revealed that there was a significant main effect of exercise in increasing V ¯ P , HR, and MBP (P ≤ 0.05). CVC was not affected by exercise (P > 0.05). There was a significant group x exercise interaction for MBP (mmHg) (P ≤ 0.05), but not V ¯ P (cm·s-1) (P = 0.17). Sao 2 decreased with exercise, and this effect was the greatest in COPD patients, as exhibited by an exercise x group interaction (P ≤ 0.05).

Table 3 Workrate, metabolic and respiratory parameters during rest and submaximal exercise

In summary, exercise increased V ¯ P similarly in COPD (42.8 to 50.2 cm·s-1) and controls (44.2 to 50.2 cm·s-1), while working at a similar exercise intensity (P > 0.05), despite COPD patients exhibiting a greater exercise-pressor response and greater arterial oxygen desaturation.

Responses to exercise at absolute workload: 30 watts (EX2)

Physiological description of the exercise protocol is summarized in Table 4. All subjects cycled at a workrate of 30 W for 6 minutes (EX2). By design, there was no difference between V ˙ O 2 between groups ( V ˙ O 2 : 0.78 Lmin-1 (COPD) versus 0.74 Lmin-1 (controls); P > 0.05). There was a trend for COPD patients to be exercising at a greater relative exercise intensity than controls ( V ˙ O 2 peak : 74% (COPD) versus 52% (controls); P = 0.08). Despite the same workrate between groups, COPD patients exercised at a greater capacity of their WRpeak (COPD: 48% versus Controls: 25%; P ≤ 0.01). Patients and controls had similar Petco 2 and Peto 2 at rest, and in response to EX2.

Table 4 Cerebro- and cardio-vascular responses to submaximal exercise in COPD and controls

The cerebro-and cardiovascular responses to EX2 are summarized in Table 3, and individual stage means are presented in Figure 1. There were no differences between resting cerebro- or cardio-vascular variables between groups (P > 0.05). The two-factor analysis of variance revealed that there was a significant main effect of exercise in increasing V ¯ P , HR, and MBP, and decreasing Sao 2 (P ≤ 0.05). There was a significant group by exercise interaction for V ¯ P (cm·s-1) (P ≤ 0.05). Exercise significantly decreased Sao 2 overall (P < 0.01), but had the greatest effect in COPD patients whom desaturated at a greater rate than controls as exhibited statistically by a grouping by exercise interaction effect (P <0.01).

Figure 1
figure 1

Continuous representation of the physiological responses to two, 6-minute exercise periods in women with moderate COPD (thick line) and healthy age-matched controls (thin line). Exercise 1 (EX1; 50% V ˙ O 2 peak ) and Exercise 2 (EX2; 30 Watts) were separated by 6-minutes of resting recovery. a) Peak cerebral blood flow velocity in the middle cerebral artery ( V ¯ P ); b) mean arterial blood pressure (MBP); c) arterial oxygen saturation (Sao 2); d) heart rate (HR); e) volume of oxygen consumption ( V ˙ O 2 ); and f) volume of carbon dioxide production ( V ˙ CO 2 ). Data represent 15-second averages. Cycling exercise periods are shaded.

In summary, exercise increased V ¯ P to a greater extent in COPD patients (40.2 to 51.1 cm·s-1) compared to controls (43.8 to 48.7 cm·s-1), while working at 30 Watts (and an equivalent V ˙ O 2 ). At this workload, however, there was a trend for COPD patients to be working at a higher percentage of maximum capacity than the control subjects. Blood pressure increased with exercise, but changes were similar between groups.

Relationships between fitness, disease severity, and cerebrovascular measurements during exercise

At rest, there was no relationship between fitness status, disease severity, Sao 2, Petco 2, and blood pressure on cerebrovascular measures. In both groups, and in both exercise conditions, participants with lower baseline V ¯ P were more likely to have low exercise V ¯ P , and vice versa (EX1: R 2 = 0.75, P < 0.01; EX2: R 2 = 0.78, P <0.01). Furthermore, individuals with lower baseline V ¯ P were more likely to have a greater absolute increase in exercise V ¯ P (EX1: R 2 = 0.18, P ≤ 0.05; EX2: R 2 = 0.29, P < 0.01). Percent change in MBP was positively associated with change in V ¯ P (EX1: R 2 = 0.36, P < 0.01; EX2: R 2 = 0.22, P ≤ 0.05). There was no relationship between cerebrovascular variables and Sao 2 during exercise. In EX2, the change in Petco 2 with exercise was positively related to the changes in V ¯ P and CVC ( V ¯ P : R 2 = 0.37, P < 0.01; CVC: R 2 = 0.40, respectively, P < 0.01). There was no significant correlations between V ˙ O 2 peak and V ¯ P , MBP, or CVC (P > 0.05) in either EX1 or EX2 (all subjects combined).

Discussion

Our main findings are that 1) when patients with mild to moderate COPD exercise at the same intensity to healthy controls, the CBF response is similar; and 2) when comparing CBF at a matched O2 demand (i.e., 30 Watts), CBF is elevated in this cohort of COPD patients. From these results, it is apparent that COPD does not have a detrimental effect on cerebral blood flow during moderate intensity exercise. The mechanisms underlying the increased CBF in COPD at higher workloads needs to be investigated further.

Cerebral blood flow velocity has consistently been shown to increase in healthy individuals during mild to moderate exercise intensity [16, 2123], and seems to be intensity dependent [24]. Although mechanisms are not fully elucidated [25], important regulators of the exercise-induced CBF response include: cortical activation [26], arterial blood pressure [27], cardiac output [21], and blood gases (particularly P a C O 2 ) [28]. Comparative studies are particularly lacking in the area of ageing and disease. Consequential alterations of CBF are apparent with age, however, physical fitness has been shown to offset these changes [1, 15]. Aerobic capacity appears to be an important determinant in cerebrovascular health with ageing, as it has been shown to be positively correlated with cerebrovascular CO2 reactivity [29], and better cognitive outcomes [15]. Current opinion suggests that COPD represents a case of advanced ageing [30], which may make these patients particularly susceptible to alterations in cerebrovascular responses.

We reasoned that the known vascular consequences associated with COPD, including endothelial dysfunction [31], and increased arterial stiffness [32] would play a detrimental role in the CBF response to exercise. A recent study suggests that physical fitness (i.e., 6MWD) has a favorable effect on endothelial function in COPD patients [33]. We have furthermore shown that women with moderate COPD exhibit a nearly two-fold reduction in the expected CBF response to CO2[7]. It is likely that during a more modest cerebrovascular challenge (e.g., submaximal exercise versus hypercapnia), the cerebrovascular response remains intact, despite underlying vascular pathologies that may exist.

We found patients to have decreases in Sao 2 during exercise in response to maximal and submaximal exercise. As hypoxia is known to stimulate blood flow, it is interesting that we did not find a relationship between individuals with lower Sao 2 during exercise and increased CBF. However, it is possible that increased CBF, as seen in COPD during more intense exercise (e.g., EX2), could be partially driven by decreased Sao 2, in a regulatory effort to increase cerebral oxygen delivery.

Results from a study investigating cerebral hemodynamics in severe COPD during exhaustive exercise suggest increased frontal cortex O2 delivery at the end of exhaustive normoxic exercise, in conjunction with increased CBF, despite exercise induced hypoxemia [11]. These results would suggest a regulatory difference, as it has alternatively been shown in healthy hypoxemic individuals that CBF is decreased (from rest) during exhaustive exercise [34]. The differences between these studies was explained by the lack of hyperventilation in COPD which maintained (and even increased) P a C O 2 , causing a vasodilatory response. However, caution is warranted as this study does not allow for an accurate comparison with an age-matched control group. The “normal” hyperventilation-induced hypocapnia evident during high-intensity exercise as been shown to be blunted in healthy older individuals, which in turn leads to maintenance of P a C O 2 , and CBF [35]. In patients with terminal lung disease, Jensen et al. [12] has shown continuous increases in CBF, with a slight reduction in cerebral oxygenation at end-exercise in room air, without changes in P a C O 2 . It is therefore likely, that the CBF response in COPD depends on several aspects, such as disease severity, blood gases, exercise intensity, and physical fitness. We are hesitant to draw conclusions based on P a C O 2 , as this variable was not measured in our study. However, COPD patients continue to increase V ˙ E in EX2, which would not support the hypoventilation/increased P a C O 2 theory.

Cardio-pulmonary interactions during exercise in COPD have the potential to have an adverse influence on CBF. Increased expiratory loading and dynamic hyperinflation (DH) during exercise may impair venous return, and consequently lead to a reduction in right heart preload, and ultimately stroke volume. O2 pulse is commonly used as a surrogate measure of stroke volume (and cardiac efficiency). Studies have shown DH to be negatively correlated with O2 Pulse during incremental exercise in COPD [36, 37]. Furthermore, resting hyperinflation (IC/TLC) was associated with a reduction of O2 pulse at peak exercise. We did not find a difference in O2 pulse at peak exercise between COPD patients and controls (Table 2), and take this to indicate that cardiac function was not impaired in our patients. Despite COPD patients in this study having significantly lower IC/TLC ratio at rest (37% versus 49%), this level of hyperinflation is noticeably less when compared to results of the aforementioned studies which reported DH during exercise. Furthermore, the role of DH in mild-moderate COPD remains to be clearly defined. Lastly, although cardiac output remains an important determinant in cerebrovascular regulation, reductions in cardiac output (by lower body negative pressure) reduce CBF, but seem to be less important during exercise compared to the resting state, which has been explained as a counter-regulatory activation of the sympathetic nervous system [38]. Overall, we speculate, that DH is not a major contributor to the determinants of CBF in our sample population. As this remains beyond the scope of this study, it should be considered in future studies.

One strength of our study is that it includes data comparing the physiological response during both as exercise challenge that is a fixed percentage of each person’s maximal workload, and an absolute workload - which represents a value that may be a more realistic occurrence in activities of daily living. Although we found that patients with mild and moderate COPD have a normal CBF response at 50% V ˙ O 2 peak , it is important to highlight that this workload is equivalent to ~2.9 METS, which would equate to light housework such as self care, washing dishes, and walking to a parking lot [39]. When physical demands are slightly increased to 30 Watts (~3.2 METS), these COPD patients further increase CBF. The importance of absolute requirements are highlighted by Paterson et al. [40] who report that a relative V ˙ O 2 of ~15 mL O2·kg-1·min-1 is required for independent living in the aging population. During moderate activities (e.g., vigorous cleaning, sweeping, etc.), COPD patients would be exposed to increased aerobic demand, which may have cerebrovascular implications, including a reduced cerebrovascular reserve capacity compared to healthy controls. This remains highly speculative, and the implications of this are unclear at this time. Although we do not have measures of habitual activity, we have previously shown a significant, positive agreement between self-reported physical and V ˙ O 2 max in healthy, older women [41]. In this same study, fitness was correlated with better vascular outcomes during exercise [15]. We therefore suspect that individuals in the present study who have a higher V ˙ O 2 max are also more physically active, although this needs to be confirmed in future research. Conversely, it is possible that frequent increases in CBF may pose a vascular benefit to COPD patients, whereby increases in CBF result in shear stress on the vascular endothelium, thus providing beneficial adaptations through the up-regulation of nitric oxide synthase [42]. In contrast, modest activities increase CBF in COPD and may limit the supply of blood flow available for additional challenges, such as cognitive tasks.

Our selection of mild – moderate COPD patients includes 9 of 11 patients with GOLD II, moderate COPD. Of these 11 patients, 2 could not complete a 6-minute workload of 30 Watts. We believe that more severe patients would have further difficulty completing 2×6-min bouts of cycling exercise. Further, our selected cohort of COPD patients represents the patients that are most likely either still physically active, or still have the potential to become more active, and we would therefore gain the greatest insight into studying this population. Women in particular have lower V ˙ O 2 max , smaller lung volumes, and exhibit greater dyspnea at a similar V ˙ O 2 compared to men [43]. Finally, a homogeneous sample of women reduces additional heterogeneity between subjects, and is particularly important in this smaller sample size.

Limitations

Transcranial Doppler ultrasound is a commonly used, non-invasive tool to measure the velocity of blood in the MCA. The MCA provides ~ 80% of the blood flow to the brain, and perfuses the frontal and temporal lobe, including the motor-sensory cortex, which is activated during exercise. This technique offers several advantages over other methodologies because of its non-invasive properties, and high temporal resolution [44, 45]. One drawback of using this method, however, is the assumption that the MCA diameter remains constant, allowing us to infer that velocity represents flow. The regulation of CBF is thought to occur in the small arterioles, such that the large basal cerebral arteries maintain a constant diameter thus, providing an accurate representation of CBF [16, 45].

We firstly chose to compare the steady-state CBF response at a relative exercise intensity. Secondarily, we studied the physiological response between COPD and controls at an absolute workload. We acknowledge that at an absolute workload participants are working at a different relative exercise capacity, which introduces confounding variables. It is therefore difficult to interpret the specific mechanisms involved in the observed differences in CBF during this stage. However, we believe this exercise workload to be of significant importance and these findings notable.

Lastly, a limitation of our study was the absence of arterial blood gases as part of our methodology. We therefore are precluded from making a conclusion regarding the influence of P a C O 2 on the regulation of CBF during exercise in COPD.

Conclusion

Cerebral blood flow responsiveness appears to be normal in patients with mild to moderate COPD compared to healthy controls when exercising at a moderate intensity (50% V ˙ O 2 max ), but not when exercising at a slightly greater, matched workload (i.e., 30 Watts). It is likely that decreased physical fitness contribute to this. These results have implications for normal activities of daily living such as household activities in which COPD patients would likely experience greater increases in CBF, thereby decreasing the cerebral vascular reserve.

Abbreviations

BL:

baseline stage

CBF:

cerebral blood flow velocity

CPET:

Cardio-pulmonary exercise test

COPD:

Chronic obstructive pulmonary disease

DLCO :

Diffusion capacity of the lung for carbon monoxide

EX:

Exercise stage

FEV1 :

Forced expiratory volume in 1 second

MBP:

Mean blood pressure

MCA:

Middle cerebral artery

METS:

Metabolic equivalents

P a C O 2 :

Arterial CO2 pressure

Petco 2 :

End-tidal CO2 pressure

Sao 2 :

Arterial oxygen saturation

V ¯ P :

Peak cerebral blood flow velocity

V ˙ O 2 :

Oxygen uptake.

References

  1. Ainslie PN, Cotter JD, George KP, Lucas S, Murrell C, Shave R, Thomas KN, Williams MJ, Atkinson G: Elevation in cerebral blood flow velocity with aerobic fitness throughout healthy human ageing. J Physiol. 2008, 586: 4005-4010. 10.1113/jphysiol.2008.158279.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  2. Heckmann J, Brown C, Cheregi M, Hilz M, Neundorfer B: Delayed cerebrovascular autoregulatory response to ergometer exercise in normotensive elderly humans. Cerebrovasc Dis. 2003, 16: 423-429. 10.1159/000072567.

    Article  PubMed  Google Scholar 

  3. Hirayama F, Lee A, Binns C, Leong C, Hiramatsu T: Physical activity of patients with chronic obstructive pulmonary disease. Implications for pulmonary rehabilitation. J Cardiopulm Rehabil Rev. 2008, 28: 330-334. 10.1097/01.HCR.0000336145.79192.17.

    Article  Google Scholar 

  4. Troosters T, Sciurba F, Battaglia S, Langer D, Valluri SR, Martino L, Benzo R, Andre D, Weisman I, Decramer M: Physical inactivity in patients with COPD, a controlled multi-center pilot-study. Respir Med. 2010, 104: 1005-1011. 10.1016/j.rmed.2010.01.012.

    Article  PubMed  PubMed Central  Google Scholar 

  5. Watz H, Waschki B, Meyer T, Magnussen H: Physical activity in patients with COPD. Eur Respir J. 2009, 33: 262-272.

    Article  CAS  PubMed  Google Scholar 

  6. Babb TG, Viggiano R, Hurley B, Staats B, Rodarte JR: Effect of mild-to-moderate airflow limitation on exercise capacity. J Appl Physiol. 1991, 70: 223-230.

    CAS  PubMed  Google Scholar 

  7. Hartmann SE, Pialoux V, Leigh R, Poulin MJ: Decreased cerebrovascular response to CO2 in post-menopausal females with COPD: role of oxidative stress. Eur Respir J. 2012, 40 (6): 1354-1361. 10.1183/09031936.00197211.

    Article  CAS  PubMed  Google Scholar 

  8. O'Donnell DE: Exercise Hypercapnia in Advanced Chronic Obstructive Pulmonary Disease: The Role of Lung Hyperinflation. Am J Respir Crit Care Med. 2002, 166: 663-668. 10.1164/rccm.2201003.

    Article  PubMed  Google Scholar 

  9. Bond V, Millis RM, Campbell A, Harrell J, Goring KL, Reeves I, Johnson SM, Adams RG: Exaggerated vasopressor response to exercise and cerebral blood flow velocity. Clin Exp Hypertens. 2012, 34: 370-376. 10.3109/10641963.2012.665537.

    Article  PubMed  Google Scholar 

  10. O'Donnell DE, Webb K: The major limitation to exercise performance in COPD is dynamic hyperinflation. J Appl Physiol. 2008, 105: 753-755. 10.1152/japplphysiol.90336.2008b.

    Article  PubMed  Google Scholar 

  11. Vogiatzis I, Louvaris Z, Habazettl H, Andrianopoulos V, Wagner H, Roussos C, Wagner PD, Zakynthinos S: Cerebral cortex oxygen delivery and exercise limitation in patients with COPD. Eur Respir J. 2013, 41: 295-301. 10.1183/09031936.00016312.

    Article  PubMed  Google Scholar 

  12. Jensen G, Nielsen H, Ide K, Madsen P, Svendsen L, Svendsen U, Secher N: Cerebral oxygenation during exercise in patients with terminal lung disease. Chest. 2002, 122: 445-450. 10.1378/chest.122.2.445.

    Article  PubMed  Google Scholar 

  13. Gershon AS, Wang C, Wilton AS, Raut R, To T: Trends in chronic obstructive pulmonary disease prevalence, incidence, and mortality in ontario, Canada, 1996 to 2007: a population-based study. Arch Intern Med. 2010, 170: 560-565. 10.1001/archinternmed.2010.17.

    Article  PubMed  Google Scholar 

  14. Hurst J, Vestbo J, Anzueto A, Locantore N, Müllerova H, Tal-singer R, Miller B, Lomas DA, Agusti A, Macnee W, Calverley P, Rennard S, Wouters EFM, Wedzicha J: Susceptibility to exacerbation in chronic obstructive pulmonary disease. N Engl J Med. 2010, 363 (12): 1128-1138. 10.1056/NEJMoa0909883.

    Article  CAS  PubMed  Google Scholar 

  15. Brown AD, McMorris CA, Longman RS, Leigh R, Hill MD, Friedenreich CM, Poulin MJ: Effects of cardiorespiratory fitness and cerebral blood flow on cognitive outcomes in older women. Neurobiol Aging. 2010, 31: 2047-2057. 10.1016/j.neurobiolaging.2008.11.002.

    Article  PubMed  Google Scholar 

  16. Poulin MJ, Syed RJ, Robbins P: Assessments of flow by transcranial Doppler ultrasound in the middle cerebral artery during exercise in humans. J Appl Physiol. 1999, 86: 1632-1637.

    CAS  PubMed  Google Scholar 

  17. Miller MR, Hankinson J, Brusasco V, Burgos F, Casaburi R, Coates A, Crapo R, Enright P, van der Grinten CPM, Gustafsson P, Jensen R, Johnson DC, MacIntyre N, McKay R, Navajas D, Pedersen OF, Pellegrino R, Viegi G, Wanger J: Standardisation of spirometry. Eur Respir J. 2005, 26: 319-338. 10.1183/09031936.05.00034805.

    Article  CAS  PubMed  Google Scholar 

  18. Wanger J, Clausen JL, Coates A, Pedersen OF, Brusasco V, Burgos F, Casaburi R, Crapo R, Enright P, van der Grinten CPM, Gustafsson P, Hankinson J, Jensen R, Johnson D, Macintyre N, McKay R, Miller MR, Navajas D, Pellegrino R, Viegi G: Standardisation of the measurement of lung volumes. Eur Respir J. 2005, 26: 511-522. 10.1183/09031936.05.00035005.

    Article  CAS  PubMed  Google Scholar 

  19. Macintyre N, Crapo RO, Viegi G, Johnson DC, van der Grinten CPM, Brusasco V, Burgos F, Casaburi R, Coates A, Enright P, Gustafsson P, Hankinson J, Jensen R, McKay R, Miller MR, Navajas D, Pedersen OF, Pellegrino R, Wanger J: Standardisation of the single-breath determination of carbon monoxide uptake in the lung. Eur Respir J. 2005, 26: 720-735. 10.1183/09031936.05.00034905.

    Article  CAS  PubMed  Google Scholar 

  20. Weisman IM, Marciniuk D, Martinez FJ, Sciurba F, Sue D, Myers J, Casaburi R, Beck K, Zeballos J, Swanson G, Johnson B, Whipp B, Mahler D, Cotes J, Sietsema K: ATS/ACCP Statement on cardiopulmonary exercise testing. Am J Respir Crit Care Med. 2003, 167: 211-277.

    Article  Google Scholar 

  21. Ide K, Pott F, Van Lieshout JJ, Secher NH: Middle cerebral artery blood velocity depends on cardiac output during exercise with a large muscle mass. Acta Physiol Scand. 1998, 162: 13-20. 10.1046/j.1365-201X.1998.0280f.x.

    Article  CAS  PubMed  Google Scholar 

  22. Madsen PL, Sperling BK, Warming T, Schmidt JF, Secher NH, Wildschiodtz G, Holm S, Lassen NA: Middle cerebral artery blood velocity and cerebral blood flow and O2 uptake during dynamic exercise. J Appl Physiol. 1993, 74: 245-250.

    CAS  PubMed  Google Scholar 

  23. Ide K, Horn A, Secher NH: Cerebral metabolic response to submaximal exercise. J Appl Physiol. 1999, 87: 1604-1608.

    CAS  PubMed  Google Scholar 

  24. Moraine JJ, Lamotte M, Berr J, Niset G, Leduc A, Naeije R: Relationship of middle cerebral artery blood flow velocity to intensity during dynamic exercise in normal subjects. Eur J Appl Physiol Occup Physiol. 1993, 67: 35-38. 10.1007/BF00377701.

    Article  CAS  PubMed  Google Scholar 

  25. Ogoh S, Ainslie PN: Cerebral blood flow during exercise: mechanisms of regulation. J Appl Physiol. 2009, 107: 1370-1380. 10.1152/japplphysiol.00573.2009.

    Article  CAS  PubMed  Google Scholar 

  26. Linkis P, Jorgensen LG, Olesen HL, Madsen PL, Lassen NA, Secher NH: Dynamic exercise enhances regional cerebral artery mean flow velocity. J Appl Physiol. 1995, 78: 12-16.

    CAS  PubMed  Google Scholar 

  27. Pott F, Knudsen L, Nowak M, Nielsen HB, Hanel B, Secher NH: Middle cerebral artery blood velocity during rowing. Acta Physiol Scand. 1997, 160: 251-255. 10.1046/j.1365-201X.1997.00144.x.

    Article  CAS  PubMed  Google Scholar 

  28. Rasmussen P, Stie H, Nielsen B, Nybo L: Enhanced cerebral CO2 reactivity during strenuous exercise in man. Eur J Appl Physiol. 2006, 96 (3): 299-304. 10.1007/s00421-005-0079-3.

    Article  CAS  PubMed  Google Scholar 

  29. Barnes JN, Taylor JL, Kluck BN, Johnson CP, Joyner MJ: Cerebrovascular reactivity is associated with maximal aerobic capacity in healthy older adults. J Appl Physiol. 2013, 114 (10): 1383-1387. 10.1152/japplphysiol.01258.2012.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  30. Lee J, Sandford A, Man P, Sin DD: Is the aging process accelerated in chronic obstructive pulmonary disease?. Curr Opin Pulm Med. 2011, 17: 90-97. 10.1097/MCP.0b013e328341cead.

    Article  CAS  PubMed  Google Scholar 

  31. Barr RG, Mesia-Vela S, Austin JH, Basner RC, Keller BM, Reeves AP, Shimbo D, Stevenson L: Impaired flow-mediated dilation is associated with low pulmonary function and emphysema in ex-smokers: the Emphysema and Cancer Action Project (EMCAP) Study. Am J Respir Crit Care Med. 2007, 176: 1200-1207. 10.1164/rccm.200707-980OC.

    Article  PubMed  PubMed Central  Google Scholar 

  32. McAllister DA, Maclay JD, Mills NL, Mair G, Miller J, Anderson D, Newby DE, Murchison JT, Macnee W: Arterial stiffness is independently associated with emphysema severity in patients with chronic obstructive pulmonary disease. Am J Respir Crit Care Med. 2007, 176: 1208-1214. 10.1164/rccm.200707-1080OC.

    Article  PubMed  PubMed Central  Google Scholar 

  33. Clarenbach CF, Senn O, Sievi Na, Camen G, van Gestel AJ, Rossi Va, Puhan Ma, Thurnheer R, Russi EW, Kohler M: Determinants of endothelial function in patients with COPD. Eur Respir J. 2013, 42: 1194-1204. 10.1183/09031936.00144612.

    Article  CAS  PubMed  Google Scholar 

  34. Vogiatzis I, Louvaris Z, Habazettl H, Athanasopoulos D, Andrianopoulos V, Cherouveim E, Wagner H, Roussos C, Wagner PD, Zakynthinos S: Frontal cerebral cortex blood flow, oxygen delivery and oxygenation during normoxic and hypoxic exercise in athletes. J Physiol. 2011, 589: 4027-4039.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  35. Marsden KR, Haykowsky MJ, Smirl JD, Jones H, Nelson MD, Altamirano-Diaz La, Gelinas JC, Tzeng YC, Smith KJ, Willie CK, Bailey DM, Ainslie PN: Aging blunts hyperventilation-induced hypocapnia and reduction in cerebral blood flow velocity during maximal exercise. Age. 2012, 34: 725-735. 10.1007/s11357-011-9258-9.

    Article  CAS  PubMed  Google Scholar 

  36. Vassaux C, Torre-Bouscoulet L, Zeineldine S, Cortopassi F, Paz-Díaz H, Celli BR, Pinto-Plata VM: Effects of hyperinflation on the oxygen pulse as a marker of cardiac performance in COPD. Eur Respir J. 2008, 32: 1275-1282. 10.1183/09031936.00151707.

    Article  CAS  PubMed  Google Scholar 

  37. Tzani P, Aiello M, Elia D, Boracchia L, Marangio E, Olivieri D, Clini E, Chetta A: Dynamic hyperinflation is associated with a poor cardiovascular response to exercise in COPD patients. Respir Res. 2011, 12: 150-10.1186/1465-9921-12-150.

    Article  PubMed  PubMed Central  Google Scholar 

  38. Ogoh S, Brothers RM, Barnes Q, Eubank WL, Hawkins MN, Purkayastha S, O-Yurvati A, Raven PB: The effect of changes in cardiac output on middle cerebral artery mean blood velocity at rest and during exercise. J Physiol. 2005, 569: 697-704. 10.1113/jphysiol.2005.095836.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  39. Haskell WL, Lee I-M, Pate RR, Powell KE, Blair SN, Franklin BA, Macera CA, Heath GW, Thompson PD, Bauman A: Physical activity and public health: updated recommendation for adults from the American College of Sports Medicine and the American Heart Association. Med Sci Sports Exerc. 2007, 39: 1423-1434. 10.1249/mss.0b013e3180616b27.

    Article  PubMed  Google Scholar 

  40. Paterson D, Cunningham D, Koval J, St. Croix C: Aerobic fitness in a population of independently living men and women aged 55–86. Med Sci Sports Exerc. 1999, 31 (12): 1813-1820. 10.1097/00005768-199912000-00018.

    Article  CAS  PubMed  Google Scholar 

  41. Brown A: M.Sc. Thesis. Effects of Aging and Aerobic Fitness on Cerebrovascular Regulation and Cognition in Postmenopausal Women. 2008, Calgary, Alberta: University of Calgary, Faculty of Medicine

    Google Scholar 

  42. Endres M, Gertz K, Lindauer U, Katchanov J, Schultze J, Schröck H, Nickenig G, Kuschinsky W, Dirnagl U, Laufs U: Mechanisms of stroke protection by physical activity. Ann Neurol. 2003, 54: 582-590. 10.1002/ana.10722.

    Article  PubMed  Google Scholar 

  43. Laviolette L, O'Donnell DE, Webb KA, Hamilton AL, Kesten S, Maltais F: Performance during constant workrate cycling exercise in women with COPD and hyperinflation. COPD. 2009, 6: 340-351. 10.1080/15412550903140873.

    Article  PubMed  Google Scholar 

  44. Poulin MJ, Liang PJ, Robbins PA: Dynamics of the cerebral blood flow response to step changes in end-tidal PCO2 and PO2 in humans. J Appl Physiol. 1996, 81: 1084-1095.

    CAS  PubMed  Google Scholar 

  45. Poulin MJ, Robbins PA: Indexes of flow and cross-sectional area of the middle cerebral artery using Doppler ultrasound during hypoxia and hypercapnia in humans. Stroke. 1996, 12: 2244-2250.

    Article  Google Scholar 

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Acknowledgements

The authors are especially grateful to the subjects for their participation in this study.

Financial support was provided by the Hotchkiss Brain Institute (HBI) (S.E.H., M.J.P); Alberta Lung Association (S.E.H), University of Calgary (S.E.H), Alberta Heritage for Medical Research (R.L. and M.J.P), Canadian Institutes of Health Research (M.J.P), The Calgary Foundation (S.E.H). M.J.P. holds the Brenda Strafford Foundation Chair in Alzheimer Research.

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SEH contributed to study design, data collection, data analysis, and interpretation, and wrote the first draft of the manuscript. RL contributed to study design, medical coverage and patient referral, data interpretation, and critically reviewed the manuscript; MJP contributed to study design, fundraising, study supervision, data interpretation, and critically reviewed the manuscript. All authors read and approved the final manuscript.

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Hartmann, S.E., Leigh, R. & Poulin, M.J. Cerebrovascular responses to submaximal exercise in women with COPD. BMC Pulm Med 14, 99 (2014). https://doi.org/10.1186/1471-2466-14-99

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