Skip to main content

MINI REVIEW article

Front. Physiol., 10 July 2020
Sec. Respiratory Physiology and Pathophysiology
This article is part of the Research Topic Clinical Cardiopulmonary Exercise Testing View all 9 articles

Cardiopulmonary Exercise Testing in Patients With Interstitial Lung Disease

\r\nYannick Molgat-Seon,*Yannick Molgat-Seon1,2*Michele R. Schaeffer,Michele R. Schaeffer2,3Christopher J. Ryerson,Christopher J. Ryerson2,4Jordan A. Guenette,,Jordan A. Guenette2,3,4
  • 1Department of Kinesiology and Applied Health, University of Winnipeg, Winnipeg, MB, Canada
  • 2Centre for Heart Lung Innovation, St. Paul’s Hospital, The University of British Columbia, Vancouver, BC, Canada
  • 3Department of Physical Therapy, Faculty of Medicine, The University of British Columbia, Vancouver, BC, Canada
  • 4Division of Respiratory Medicine, Faculty of Medicine, The University of British Columbia, Vancouver, BC, Canada

Interstitial lung disease (ILD) is a heterogeneous group of conditions characterized by fibrosis and/or inflammation of the lung parenchyma. The pathogenesis of ILD consistently results in exertional dyspnea and exercise intolerance. Cardiopulmonary exercise testing (CPET) provides important information concerning the pathophysiology of ILD that can help inform patient management. Despite the purported benefits of CPET, its clinical utility in ILD is not well defined; however, there is a growing body of evidence that provides insight into the potential value of CPET in ILD. Characteristic responses to CPET in patients with ILD include exercise-induced arterial hypoxemia, an exaggerated ventilatory response, a rapid and shallow breathing pattern, critically low inspiratory reserve volume, and elevated sensations of dyspnea and leg discomfort. CPET is used in ILD to determine cause(s) of symptoms such as exertional dyspnea, evaluate functional capacity, inform exercise prescription, and determine the effects of pharmacological and non-pharmacological interventions on exercise capacity and exertional symptoms. However, preliminary evidence suggests that CPET in ILD may also provide valuable prognostic information and can be used to ascertain the degree of exercise-induced pulmonary hypertension. Despite these recent advances, additional research is required to confirm the utility of CPET in patients with ILD. This brief review outlines the clinical utility of CPET in patients with ILD. Typical patterns of response are described and practical issues concerning CPET interpretation in ILD are addressed. Additionally, important unanswered questions relating to the clinical utility of CPET in the assessment, prognostication, and management of patients with ILD are identified.

Introduction

The term interstitial lung disease (ILD) refers to a large, heterogenous group of conditions that involve variable degrees of fibrosis and/or inflammation of the lung parenchyma (King, 2005). Although the etiology varies across ILD subtypes, the pathogenesis of ILD leads to a host of physiological abnormalities including progressive reductions in lung volumes, pulmonary gas exchange limitations (Chetta et al., 2004; Young and Bye, 2011), decreased cardiovascular function (Panagiotou et al., 2017) as well as skeletal muscle atrophy and dysfunction (Panagiotou et al., 2016). The pathophysiological features of ILD consistently result in an increased perception of dyspnea, particularly during physical exertion, and reduced exercise tolerance (Collard and Pantilat, 2008; Holland, 2010). Cardiopulmonary exercise testing (CPET) is often considered to be the gold-standard for evaluating exertional dyspnea and exercise intolerance in patients with cardiorespiratory conditions, and provides important information that complements diagnostic investigations performed at rest (Palange et al., 2007). Despite the well-documented application of CPET in other forms of cardiorespiratory disease (American Thoracic and American College of Chest, 2003), its utility in ILD is not well characterized (Bonini and Fiorenzano, 2017); however, a growing body of evidence relating to the pathophysiological responses to exercise in patients with ILD provides new insight into the potential value of CPET in this population.

In this review, we provide a brief summary of recent findings concerning the clinical utility of CPET in patients with ILD. Typical patterns of response and how they differ from those observed in health are described and practical issues concerning the interpretation of CPET variables in ILD are addressed. Given that the focus of this review is on recent findings related to CPET in ILD, the interested reader is directed elsewhere for detailed descriptions of foundational concepts including the pathophysiology of ILD (Parker et al., 2011; Bagnato and Harari, 2015) and the physiological responses to exercise in patients with ILD (Lama and Martinez, 2004; Molgat-Seon et al., 2019).

Physiological Responses to CPET

Functional Capacity

The primary pathophysiological features of ILD have a detrimental impact on the integrative physiological response to exercise. Patients with ILD have reduced functional capacity when compared to healthy individuals, as evidenced by a lower peak power output and oxygen uptake during incremental cycle exercise testing (Wehr and Johnson, 1976; Burdon et al., 1983) as well as a shorter distance achieved during 6-min walk testing (Chang et al., 1999). As is the case in other forms of cardiorespiratory disease, performing CPET in patients with ILD provides a direct assessment of their functional capacity, however, the mechanisms of exercise intolerance in ILD are complex, multifactorial, and variable across patients and ILD sub-types (Holland, 2010; Young and Bye, 2011). The restrictive ventilatory impairment and decreased pulmonary gas exchange efficiency negatively impact the ventilatory response to exercise, while pulmonary vascular destruction and arterial hypoxemia impair the cardiovascular response to exercise. Additionally, ILD may involve skeletal muscle atrophy and dysfunction, which would further decrease exercise capacity (Panagiotou et al., 2016). The abovementioned factors may act individually or synergistically to reduce exercise tolerance (Holland, 2010; Young and Bye, 2011). It is therefore challenging to determine the exact cause of exercise limitation in a given ILD patient. Nevertheless, monitoring the ventilatory, cardiovascular, skeletal muscle, and sensory responses to exercise during CPET in ILD reveals common patterns that differ from those observed in health and can enable clinicians to determine the primary cause(s) of symptom limitation (Table 1).

TABLE 1
www.frontiersin.org

Table 1. CPET responses in healthy individuals and how they differ in patients with ILD.

Ventilatory and Pulmonary Gas Exchange Responses

During incremental exercise, minute ventilation (V̇E) must increase in order to meet the demands associated with the rising oxygen uptake (V̇O2) and carbon dioxide production (V̇CO2). Similarly, the increase in V̇O2 necessitates a greater rate of oxygen diffusion into the blood in order to maintain arterial oxygen saturation (SaO2), thereby ensuring adequate oxygen delivery to exercising muscles. In health, the exercise-induced increase in V̇E is primarily achieved via an expansion of tidal volume (VT) until it reaches ∼60% of vital capacity (VC). Further increases in V̇E are then achieved by increasing breathing frequency (fB). The aforementioned breathing pattern is considered optimal as it minimizes the work of breathing and dead-space ventilation. In patients with ILD, vital capacity (VC) is reduced, which limits their ability to expand VT and by association, reduces their maximum voluntary ventilation (MVV) (Faisal et al., 2016). Moreover, their lung compliance is decreased, which correspondingly increases the mechanical and metabolic cost of breathing for a given V̇E (Faisal et al., 2016). For patients with ILD, the higher mechanical and metabolic cost of breathing during exercise may impair ventricular performance, due to the large intrathoracic pressure swings, and may increase the fraction of total cardiac output directed to the respiratory muscles at the expense of locomotor muscle blood flow (Dominelli et al., 2017); however, direct evidence supporting this notion in patients with ILD is currently lacking. Together, the reductions in VC, MVV, and lung compliance alter the ventilatory response to exercise in ILD. At rest, patients with ILD typically have a rapid breathing pattern (i.e., normal VT and high fB). During incremental exercise, patients with ILD will initially increase V̇E by expanding VT in a similar manner as observed in healthy individuals but will reach a plateau in VT at a much lower V̇E and exercise intensity due to their reduced VC. Subsequent increases in V̇E are then achieved by further increasing fB. This rapid and shallow breathing pattern implies that the ratio of dead-space volume to VT (VD/VT) is typically high during exercise in patients with ILD. At rest and during exercise at a given absolute intensity, V̇E is also increased in ILD due to ventilation-perfusion mismatch (Jernudd-Wilhelmsson et al., 1986) as well as increased ventilatory drive resulting from arterial hypoxemia and an early-onset of metabolic acidosis (Van Meerhaeghe et al., 1981), which is evidenced by an elevated V̇E/V̇CO2 throughout exercise. Thus, some patients with ILD will experience ventilatory limitation during exercise (Marciniuk et al., 1994b), which can be crudely assessed based on whether the ratio of V̇E and MVV is greater than 85%; however, it is noteworthy that in many cases, patients with ILD will terminate exercise despite having adequate ventilatory reserve (Marciniuk et al., 1994a; Faisal et al., 2016). Lastly, the pathological decrement in pulmonary gas exchange at rest is worsened during exercise, thereby resulting in a progressive decrease in SaO2, even in those who are not hypoxemic at rest (Young and Bye, 2011). Exercise-induced arterial hypoxemia is a characteristic feature of patients with ILD (Agusti et al., 1988). In fact, patients with ILD often exhibit a greater degree of arterial desaturation during exercise than patients with chronic obstructive pulmonary disease (Du Plessis et al., 2017). The importance of assessing the degree of exercise-induced arterial hypoxemia during CPET is highlighted by its association with disease severity and prognosis (Lama et al., 2003; Vainshelboim et al., 2016). Given the limitations associated with pulse oximetry, CPET involving serial assessments of arterial blood gases may be warranted if the main purpose of the test is to determine the adequacy of pulmonary gas exchange (American Thoracic and American College of Chest, 2003). Arterial blood gas sampling enables the assessment of several important parameters, including the partial pressure of arterial oxygen (PaO2) and carbon dioxide (PaCO2), the alveolar-arterial partial pressure of oxygen gradient [P(A-a)O2], as well as direct measures of SaO2 and VD/VT. The assessment of P(A-a)O2, which is characteristically widened during exercise in ILD (Agusti et al., 1991) is particularly informative given its correlation with the degree of fibrosis and cellularity obtained from a lung biopsy, as well as its potential prognostic value, at least in idiopathic pulmonary fibrosis (IPF) (Fulmer et al., 1979; Agusti et al., 1994).

Cardiovascular Responses

Despite primarily affecting the lungs, many forms of ILD involve obliteration of the pulmonary capillary bed and remodeling of the pulmonary vasculature (Nathan et al., 2007; Seeger et al., 2013). Depending on the degree of pulmonary vascular involvement, some patients with ILD will have impairments in cardiovascular function that contribute to exercise limitation. In healthy individuals performing incremental exercise, there is a linear increase in cardiac output (Q̇) as a function of V̇O2. The exercise-induced increase in Q̇ is achieved via a progressive increase in heart rate (HR) and an increase in stroke volume up to approximately 50–60% of maximal oxygen uptake (V̇O2 max), at which point SV plateaus. Patients with ILD are generally capable of increasing Q̇ in proportion to V̇O2 during exercise at relatively low intensities; however, at higher exercise intensities, some patients have a diminished rate of increase in Q̇ (Bush and Busst, 1988; Degani-Costa et al., 2015), which is presumably due to a reduction in stroke volume (Degani-Costa et al., 2015). Indeed, patients with ILD typically have a lower oxygen pulse, an indirect marker of stroke volume, during exercise than healthy individuals (Faisal et al., 2016). Thus, patients with ILD often have an abnormal HR response to exercise, whereby HR is higher for a given absolute exercise intensity when compared to their healthy counterparts (Baughman et al., 1984), which may be due to constraints on stroke volume, deconditioning, or both. At peak exercise, HR values in patients with ILD are variable since some patients fail to reach their age-predicted maximum HR due to cessation of exercise prior to reaching their physiological maxima (Faisal et al., 2016), whereas others may have a critically low HR reserve (Schwaiblmair et al., 1996; Baughman et al., 2011). During standard CPET, measures of HR, electrocardiogram parameters, and non-invasive measures of arterial blood pressure are the only available direct cardiovascular measures. However, in cases where there is a high index of suspicion for exercise-induced pulmonary hypertension despite negative tests at rest, invasive CPET with right heart catherization may be warranted in order to directly evaluate the pulmonary vascular response to exercise (Maron et al., 2013). In such cases, some patients may exhibit an exaggerated pulmonary artery pressure response to exercise, whereby a given increase in Q̇ results in a greater increase in mean pulmonary artery pressure than in healthy individuals (Degani-Costa et al., 2015). Alternatively, echocardiography may be employed as a non-invasive alternative to cardiac catherization for the assessment of exercise-induced pulmonary hypertension (Himelman et al., 1989; Reichenberger et al., 2009; D’Alto et al., 2011), although echocardiographic data obtained during exercise in patients with ILD is relatively limited.

Skeletal Muscle Responses

It has been suggested that skeletal muscle atrophy and dysfunction may be an important systemic consequence of ILD (Panagiotou et al., 2016). Indeed, the strength of the quadriceps muscles is reduced in patients with ILD when compared to predicted values, and is significantly associated with functional capacity (Nishiyama et al., 2005; Watanabe et al., 2013). If present, skeletal muscle dysfunction would accelerate the onset of metabolic acidosis and skeletal muscle fatigue during exercise. Although standard CPET parameters are not directly indicative of skeletal muscle dysfunction, early termination of a test due to intolerable leg discomfort in the face of significant ventilatory and/or cardiovascular reserves may indicate locomotor muscle dysfunction (Marciniuk et al., 1994a; Nishiyama et al., 2005).

Sensory Responses

For patients with ILD, dyspnea is the most common symptom, particularly upon exertion (Collard and Pantilat, 2008). CPET is often employed to evaluate the mechanisms of unexplained dyspnea in patients with cardiorespiratory disease, including those with ILD (Bonini and Fiorenzano, 2017). During incremental exercise, patients with ILD report higher levels of dyspnea than healthy individuals for a given absolute exercise intensity or V̇E (O’Donnell et al., 1998; Faisal et al., 2016). The increased dyspnea is thought to reflect the awareness of an increased neural respiratory drive necessitated by the aforementioned pathophysiological alterations in respiratory mechanics and pulmonary gas exchange efficiency (Schaeffer et al., 2018). This notion is supported by the fact that when patients with ILD are given supplemental oxygen during constant-load exercise, the neural respiratory drive to the diaphragm decreases along with their perception of dyspnea (Schaeffer et al., 2017b). Neural respiratory drive to the diaphragm can be estimated during CPET using esophageal electromyography (Faisal et al., 2016; Schaeffer et al., 2018).

Given that ILD primarily affects the lungs, it is logical to assume that ventilatory factors would lead to the increased perception of exertional dyspnea. Indeed, those who experience ventilatory limitation during CPET are more likely to discontinue exercise because of intolerable dyspnea; however, this may not always be the case (Marciniuk et al., 1994a). Patients with ILD who do not exhibit signs of overt ventilatory limitation typically terminate exercise due to intolerable leg discomfort (Marciniuk et al., 1994a), which may be due to attendant hypoxemia, skeletal muscle dysfunction, and/or cardiovascular limitation (Hansen and Wasserman, 1996; Panagiotou et al., 2016). Regardless of the root cause, patients with ILD experience exertional dyspnea and elevated perceptions of leg discomfort during CPET at relatively low exercise intensities. It follows that carefully assessing the perceptual responses to CPET, at rest and throughout exercise, provides important information that can be contextualized with ventilatory, cardiovascular, and metabolic measurements to gain insight regarding the cause of the aforementioned sensations. Additional assessments such as asking patients to report the reason they stopped exercising (i.e., due to dyspnea, leg discomfort, or due to another reason) and evaluating the qualitative descriptors of dyspnea using a validated questionnaire may be helpful in ascertaining the underlying cause of symptom limitation during CPET in ILD (O’Donnell et al., 1998).

Clinical Utility of CPET

It is well established that CPET is a valuable tool for the assessment of patients with several forms of cardiorespiratory disease (Arena and Sietsema, 2011; Bonini and Fiorenzano, 2017). Yet, CPET currently lacks a defined role in ILD management (Bradley et al., 2008; Raghu et al., 2011; Assayag et al., 2018). Nevertheless, recent findings highlight the potential benefits that could be derived from CPET in patients with ILD. Herein, we summarize our current understanding of the clinical utility of CPET in patients with ILD, highlight important findings that outline how the use of CPET in ILD could be expanded, and identify areas where additional research is required.

Current Use of CPET

ILD diagnosis is established by a multidisciplinary team of respirologists, chest radiologists, and lung pathologists based on a combination of clinical information derived from pulmonary function tests, chest imaging, and lung tissue histology (Richeldi et al., 2019). CPET data are not a requirement for a multidisciplinary diagnosis of ILD but may be used to inform patient management. Indeed, there are several reasons for conducting CPET in patients with ILD (Table 2; American Thoracic and American College of Chest, 2003). Its most obvious and well-established application is in assessing the cause(s) of symptoms such as exertional dyspnea, and objectively evaluating functional capacity (Mezzani, 2017). Determining the intensity at which desaturation occurs may be useful for the prescription of ambulatory oxygen therapy (Palange et al., 2007). Additionally, pulmonary rehabilitation is advocated for some patients with ILD (Assayag et al., 2018) and CPET can be used as a baseline assessment of functional capacity prior to enrollment as well as for precise exercise prescription (Bernard et al., 2014). Repeated CPET also allows clinicians to assess the change in exercise tolerance and exertional symptoms following pulmonary rehabilitation (Tonelli et al., 2017) or other pharmacological and non-pharmacological interventions (Jackson et al., 2010; Blanco et al., 2011; Schaeffer et al., 2017b). Unlike other exercise tests (e.g., 6-min walk test), CPET has the added advantage of being able to identify the physiological mechanisms of improvement. However, it is noteworthy that the minimal clinically-important difference (MCID) for CPET parameters has not yet been established in ILD, which complicates the longitudinal assessment of CPET data.

TABLE 2
www.frontiersin.org

Table 2. Primary reasons for conducting CPET in patients with ILD.

Important Considerations When Conducting CPET

As is the case with other forms of cardiorespiratory disease, the clinical utility of CPET in ILD depends on the variables measured, the exercise modality used, and how results are interpreted. CPET provides a substantial amount of data that can be used to inform patient management. Depending on the indications for CPET in patients with ILD (Table 2), several additional measures may be added to the standard, obligatory measures (i.e., V̇O2, V̇CO2, V̇E, HR, etc.) in order to achieve a particular goal. For example, if the intent is to evaluate the degree of respiratory limitation to exercise, having the patient perform inspiratory capacity maneuvers during exercise may be warranted (Guenette et al., 2013) along with flow-volume loop analyses. Similarly, comprehensively investigating decrements in pulmonary gas exchange efficiency may require arterial blood gas sampling, while determining the degree of pulmonary vascular impairment may necessitate right heart-catherization or echocardiography. In situations where repeated CPET is required, constant-load exercise, rather than incremental exercise, is most sensitive for detecting changes in key physiological and perceptual variables (Puente-Maestu et al., 2016). It is also important to compare sensory and physiological data between repeat CPETs at standardized submaximal measurement times rather than focusing exclusively on peak exercise responses (Schaeffer et al., 2017a). Regardless of the indication for CPET, it is important to define the aim of the test and tailor the method of testing accordingly.

Potential Application of CPET

In comparison to other forms of cardiorespiratory disease, the application of CPET in ILD has been relatively limited (American Thoracic and American College of Chest, 2003; Bonini and Fiorenzano, 2017). However, recent evidence highlights promising areas where pulmonary gas exchange parameters obtained during CPET could improve the management of patients with ILD (Bonini and Fiorenzano, 2017). Pulmonary gas exchange measures during CPET have been used to non-invasively determine whether patients with ILD have pulmonary hypertension. Specifically, patients with ILD who had resting pulmonary hypertension that was confirmed by right heart catheterization had significantly lower partial pressure of end-tidal carbon dioxide and mixed expired carbon dioxide during incremental exercise than those who had no evidence of resting pulmonary hypertension (Armstrong et al., 2013). Thus, CPET may be helpful in revealing possible co-morbidities such as pulmonary hypertension. Another area that has garnered interest is the utility of CPET data to inform ILD prognosis. Pulmonary gas exchange parameters obtained during CPET appear to be superior to resting pulmonary function tests for the prognostication of ILD (Keogh and Crystal, 1980; Miller et al., 1995) and PaO2 at peak exercise is a significant predictor of survival in IPF (King et al., 2001). The utility of CPET for ILD prognostication may have important implications for the referral of patients for lung transplants (Layton et al., 2017) given that the allocation of lungs is primarily based on 1-year mortality risk (McCurry et al., 2009). However, the notion that CPET parameters have value in the prognostication of ILD remains controversial and requires additional research (American Thoracic and American College of Chest, 2003).

Challenges Associated With CPET Interpretation

The interpretation of CPET data in patients with ILD is challenging for several reasons. First, similar pathological responses may occur in several other forms of disease (e.g., chronic obstructive pulmonary disease, pulmonary hypertension, and chronic heart failure) (Marciniuk and Gallagher, 1994) with these conditions also frequently occurring in patients with ILD. Second, CPET responses can differ substantially across patients given the variable etiology, symptoms, and prognosis of the various ILD subtypes. Finally, in certain cases, patients with ILD may terminate exercise due to factors that are unrelated to their underlying lung disease, such as physical deconditioning or malingering (Marciniuk and Gallagher, 1994). Therefore, it is critical that CPET responses be interpreted in the context of all available information, including whether or not physiological maxima was reached during testing (Younes, 1984).

Considerations for Future Research

The widespread use of 6 min walk tests in ILD highlights the value of using exercise to gain information that can be used to inform the management of patients with ILD (du Bois et al., 2011). Given the host of additional data obtained, it stands to reason that CPET may be even more valuable from a clinical perspective despite its resource intensive nature. Indeed, the potential uses of CPET in ILD are numerous, but additional research is required to promote its widespread use. Most notably, establishing the MCID for CPET parameters in ILD is critical. Future studies should also consider the variability in exercise responses between ILD subtypes and how these differences might provide information to improve patient management. Particular focus should be placed on pulmonary gas exchange responses as they appear to be the most sensitive to the pathophysiological changes associated with ILD.

Summary and Conclusion

The pathophysiology of ILD has a negative impact on the ventilatory, cardiovascular, and skeletal muscle responses to exercise, thereby leading to exertional dyspnea and reduced exercise capacity. CPET is an excellent tool for assessing the severity of exertional dyspnea and mechanisms of exercise limitation in patients with various forms of cardiorespiratory disease; however, its application in ILD has remained limited. A growing body of evidence supports the use of CPET in patients with ILD. CPET is currently used to assess functional capacity, to inform exercise prescription, and to evaluate the effects of various interventions. Recent findings highlight that, in addition to its current uses, CPET-derived measures may help improve the management of patients with ILD. Despite these recent advances, additional research is required in order to confirm the utility of CPET in this population.

Author Contributions

All authors contributed to drafting and critically revising the manuscript, approved the final version of the manuscript, and take responsibility for the integrity of its content.

Funding

YM-S was supported by the fellowships from the Canadian Institutes of Health Research (CIHR), the Michael Smith Foundation for Health Research (MSFHR), and the British Columbia Lung Association (BCLA). MS was supported by the fellowships from the MSFHR and the BCLA. CR was supported by a Scholar Award from the MSFHR. JG was supported by a Clinical Rehabilitation New Investigator Award from the CIHR and a Scholar Award from the MSFHR.

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

References

Agusti, A. G., Roca, J., Gea, J., Wagner, P. D., Xaubet, A., and Rodriguez-Roisin, R. (1991). Mechanisms of gas-exchange impairment in idiopathic pulmonary fibrosis. Am. Rev. Respir. Dis. 143, 219–225. doi: 10.1164/ajrccm/143.2.219

PubMed Abstract | CrossRef Full Text | Google Scholar

Agusti, A. G., Roca, J., Rodriguez-Roisin, R., Xaubet, A., and Agusti-Vidal, A. (1988). Different patterns of gas exchange response to exercise in asbestosis and idiopathic pulmonary fibrosis. Eur. Respir. J. 1, 510–516.

Google Scholar

Agusti, C., Xaubet, A., Agusti, A. G., Roca, J., Ramirez, J., and Rodriguez-Roisin, R. (1994). Clinical and functional assessment of patients with idiopathic pulmonary fibrosis: results of a 3 year follow-up. Eur. Respir. J. 7, 643–650. doi: 10.1183/09031936.94.07040643

PubMed Abstract | CrossRef Full Text | Google Scholar

American Thoracic, S., and American College of Chest, P. (2003). ATS/ACCP Statement on cardiopulmonary exercise testing. Am. J. Respir. Crit. Care Med. 167, 211–277. doi: 10.1164/rccm.167.2.211

PubMed Abstract | CrossRef Full Text | Google Scholar

Arena, R., and Sietsema, K. E. (2011). Cardiopulmonary exercise testing in the clinical evaluation of patients with heart and lung disease. Circulation 123, 668–680. doi: 10.1161/CIRCULATIONAHA.109.914788

PubMed Abstract | CrossRef Full Text | Google Scholar

Armstrong, H. F., Thirapatarapong, W., Dussault, N. E., and Bartels, M. N. (2013). Distinguishing pulmonary hypertension in interstitial lung disease by ventilation and perfusion defects measured by cardiopulmonary exercise testing. Respiration 86, 407–413. doi: 10.1159/000350445

PubMed Abstract | CrossRef Full Text | Google Scholar

Assayag, D., Camp, P. G., Fisher, J. H., Johannson, K. A., Kolb, M., Lohmann, T., et al. (2018). Comprehensive management of fibrotic interstitial lung diseases: a Canadian Thoracic Society position statement. Can. J. Respir. Crit. Care Sleep Med. 2, 234–243. doi: 10.1080/24745332.2018.1503456

CrossRef Full Text | Google Scholar

Bagnato, G., and Harari, S. (2015). Cellular interactions in the pathogenesis of interstitial lung diseases. Eur. Respir. Rev. 24, 102–114. doi: 10.1183/09059180.00003214

PubMed Abstract | CrossRef Full Text | Google Scholar

Baughman, R. P., Culver, D. A., and Judson, M. A. (2011). A concise review of pulmonary sarcoidosis. Am. J. Respir. Crit. Care Med. 183, 573–581. doi: 10.1164/rccm.201006-0865CI

PubMed Abstract | CrossRef Full Text | Google Scholar

Baughman, R. P., Gerson, M., and Bosken, C. H. (1984). Right and left ventricular function at rest and with exercise in patients with sarcoidosis. Chest 85, 301–306. doi: 10.1378/chest.85.3.301

PubMed Abstract | CrossRef Full Text | Google Scholar

Bernard, S., Ribeiro, F., Maltais, F., and Saey, D. (2014). Prescribing exercise training in pulmonary rehabilitation: a clinical experience. Rev. Port. Pneumol. 20, 92–100. doi: 10.1016/j.rppneu.2013.10.005

PubMed Abstract | CrossRef Full Text | Google Scholar

Blanco, I., Ribas, J., Xaubet, A., Gomez, F. P., Roca, J., Rodriguez-Roisin, R., et al. (2011). Effects of inhaled nitric oxide at rest and during exercise in idiopathic pulmonary fibrosis. J. Appl. Physiol. 110, 638–645. doi: 10.1152/japplphysiol.01104.2010

PubMed Abstract | CrossRef Full Text | Google Scholar

Bonini, M., and Fiorenzano, G. (2017). Exertional dyspnoea in interstitial lung diseases: the clinical utility of cardiopulmonary exercise testing. Eur. Respir. Rev. 26:160099. doi: 10.1183/16000617.0099-2016

PubMed Abstract | CrossRef Full Text | Google Scholar

Bradley, B., Branley, H. M., Egan, J. J., Greaves, M. S., Hansell, D. M., Harrison, N. K., et al. (2008). Interstitial lung disease guideline: the British Thoracic Society in collaboration with the Thoracic Society of Australia and New Zealand and the Irish Thoracic Society. Thorax 63(Suppl. 5), v1–v58. doi: 10.1136/thx.2008.101691

PubMed Abstract | CrossRef Full Text | Google Scholar

Burdon, J. G., Killian, K. J., and Jones, N. L. (1983). Pattern of breathing during exercise in patients with interstitial lung disease. Thorax 38, 778–784. doi: 10.1136/thx.38.10.778

PubMed Abstract | CrossRef Full Text | Google Scholar

Bush, A., and Busst, C. M. (1988). Cardiovascular function at rest and on exercise in patients with cryptogenic fibrosing alveolitis. Thorax 43, 276–283. doi: 10.1136/thx.43.4.276

PubMed Abstract | CrossRef Full Text | Google Scholar

Chang, J. A., Curtis, J. R., Patrick, D. L., and Raghu, G. (1999). Assessment of health-related quality of life in patients with interstitial lung disease. Chest 116, 1175–1182. doi: 10.1378/chest.116.5.1175

PubMed Abstract | CrossRef Full Text | Google Scholar

Chetta, A., Marangio, E., and Olivieri, D. (2004). Pulmonary function testing in interstitial lung diseases. Respiration 71, 209–213. doi: 10.1159/000077416

PubMed Abstract | CrossRef Full Text | Google Scholar

Collard, H. R., and Pantilat, S. Z. (2008). Dyspnea in interstitial lung disease. Curr. Opin. Support Palliat. Care 2, 100–104. doi: 10.1097/SPC.0b013e3282ff6336

PubMed Abstract | CrossRef Full Text | Google Scholar

D’Alto, M., Ghio, S., D’Andrea, A., Pazzano, A. S., Argiento, P., Camporotondo, R., et al. (2011). Inappropriate exercise-induced increase in pulmonary artery pressure in patients with systemic sclerosis. Heart 97, 112–117. doi: 10.1136/hrt.2010.203471

PubMed Abstract | CrossRef Full Text | Google Scholar

Degani-Costa, L. H., Levarge, B., Digumarthy, S. R., Eisman, A. S., Harris, R. S., and Lewis, G. D. (2015). Pulmonary vascular response patterns during exercise in interstitial lung disease. Eur. Respir. J. 46, 738–749. doi: 10.1183/09031936.00191014

PubMed Abstract | CrossRef Full Text | Google Scholar

Dominelli, P. B., Archiza, B., Ramsook, A. H., Mitchell, R. A., Peters, C. M., Molgat-Seon, Y., et al. (2017). Effects of respiratory muscle work on respiratory and locomotor blood flow during exercise. Exp. Physiol. 102, 1535–1547. doi: 10.1113/EP086566

PubMed Abstract | CrossRef Full Text | Google Scholar

du Bois, R. M., Weycker, D., Albera, C., Bradford, W. Z., Costabel, U., Kartashov, A., et al. (2011). Six-minute-walk test in idiopathic pulmonary fibrosis: test validation and minimal clinically important difference. Am. J. Respir. Crit. Care Med. 183, 1231–1237. doi: 10.1164/rccm.201007-1179OC

PubMed Abstract | CrossRef Full Text | Google Scholar

Du Plessis, J. P., Fernandes, S., Jamal, R., Camp, P., Johannson, K., Schaeffer, M., et al. (2017). Exertional hypoxemia is more severe in fibrotic interstitial lung disease than in COPD. Respirology 23, 392–398. doi: 10.1111/resp.13226

PubMed Abstract | CrossRef Full Text | Google Scholar

Faisal, A., Alghamdi, B. J., Ciavaglia, C. E., Elbehairy, A. F., Webb, K. A., Ora, J., et al. (2016). Common mechanisms of dyspnea in chronic interstitial and obstructive lung disorders. Am. J. Respir. Crit. Care Med. 193, 299–309. doi: 10.1164/rccm.201504-0841OC

PubMed Abstract | CrossRef Full Text | Google Scholar

Fulmer, J. D., Roberts, W. C., von Gal, E. R., and Crystal, R. G. (1979). Morphologic-physiologic correlates of the severity of fibrosis and degree of cellularity in idiopathic pulmonary fibrosis. J. Clin. Invest. 63, 665–676. doi: 10.1172/JCI109349

PubMed Abstract | CrossRef Full Text | Google Scholar

Guenette, J. A., Chin, R. C., Cory, J. M., Webb, K. A., and O’Donnell, D. E. (2013). Inspiratory capacity during exercise: measurement, analysis, and interpretation. Pulm. Med. 2013:956081. doi: 10.1155/2013/956081

PubMed Abstract | CrossRef Full Text | Google Scholar

Hansen, J. E., and Wasserman, K. (1996). Pathophysiology of activity limitation in patients with interstitial lung disease. Chest 109, 1566–1576. doi: 10.1378/chest.109.6.1566

PubMed Abstract | CrossRef Full Text | Google Scholar

Himelman, R. B., Stulbarg, M., Kircher, B., Lee, E., Kee, L., Dean, N. C., et al. (1989). Noninvasive evaluation of pulmonary artery pressure during exercise by saline-enhanced Doppler echocardiography in chronic pulmonary disease. Circulation 79, 863–871. doi: 10.1161/01.cir.79.4.863

CrossRef Full Text | Google Scholar

Holland, A. E. (2010). Exercise limitation in interstitial lung disease - mechanisms, significance and therapeutic options. Chron. Respir. Dis. 7, 101–111. doi: 10.1177/1479972309354689

PubMed Abstract | CrossRef Full Text | Google Scholar

Jackson, R. M., Glassberg, M. K., Ramos, C. F., Bejarano, P. A., Butrous, G., and Gomez-Marin, O. (2010). Sildenafil therapy and exercise tolerance in idiopathic pulmonary fibrosis. Lung 188, 115–123. doi: 10.1007/s00408-009-9209-8

PubMed Abstract | CrossRef Full Text | Google Scholar

Jernudd-Wilhelmsson, Y., Hornblad, Y., and Hedenstierna, G. (1986). Ventilation-perfusion relationships in interstitial lung disease. Eur. J. Respir. Dis. 68, 39–49.

Google Scholar

Keogh, B. A., and Crystal, R. G. (1980). Clinical significance of pulmonary function tests. Pulmonary function testing in interstitial pulmonary disease. What does it tell us? Chest 78, 856–865. doi: 10.1378/chest.78.6.856

PubMed Abstract | CrossRef Full Text | Google Scholar

King, T. E. (2005). Clinical advances in the diagnosis and therapy of the interstitial lung diseases. Am. J. Respir. Crit. Care Med. 172, 268–279. doi: 10.1164/rccm.200503-483OE

PubMed Abstract | CrossRef Full Text | Google Scholar

King, T. E., Tooze, J. A., Schwarz, M. I., Brown, K. R., and Cherniack, R. M. (2001). Predicting survival in idiopathic pulmonary fibrosis: scoring system and survival model. Am. J. Respir. Crit. Care Med. 164, 1171–1181. doi: 10.1164/ajrccm.164.7.2003140

PubMed Abstract | CrossRef Full Text | Google Scholar

Lama, V. N., Flaherty, K. R., Toews, G. B., Colby, T. V., Travis, W. D., Long, Q., et al. (2003). Prognostic value of desaturation during a 6-minute walk test in idiopathic interstitial pneumonia. Am. J. Respir. Crit. Care Med. 168, 1084–1090. doi: 10.1164/rccm.200302-219OC

PubMed Abstract | CrossRef Full Text | Google Scholar

Lama, V. N., and Martinez, F. J. (2004). Resting and exercise physiology in interstitial lung diseases. Clin. Chest Med. 25, 435–453. doi: 10.1016/j.ccm.2004.05.005

PubMed Abstract | CrossRef Full Text | Google Scholar

Layton, A. M., Armstrong, H. F., Kim, H. P., Meza, K. S., D’Ovidio, F., and Arcasoy, S. M. (2017). Cardiopulmonary exercise factors predict survival in patients with advanced interstitial lung disease referred for lung transplantation. Respir. Med. 126, 59–67. doi: 10.1016/j.rmed.2017.03.022

PubMed Abstract | CrossRef Full Text | Google Scholar

Marciniuk, D. D., and Gallagher, C. G. (1994). Clinical exercise testing in interstitial lung disease. Clin. Chest Med. 15, 287–303.

Google Scholar

Marciniuk, D. D., Sridhar, G., Clemens, R. E., Zintel, T. A., and Gallagher, C. G. (1994a). Lung volumes and expiratory flow limitation during exercise in interstitial lung disease. J. Appl. Physiol. 77, 963–973. doi: 10.1152/jappl.1994.77.2.963

PubMed Abstract | CrossRef Full Text | Google Scholar

Marciniuk, D. D., Watts, R. E., and Gallagher, C. G. (1994b). Dead space loading and exercise limitation in patients with interstitial lung disease. Chest 105, 183–189. doi: 10.1378/chest.105.1.183

PubMed Abstract | CrossRef Full Text | Google Scholar

Maron, B. A., Cockrill, B. A., Waxman, A. B., and Systrom, D. M. (2013). The invasive cardiopulmonary exercise test. Circulation 127, 1157–1164. doi: 10.1161/CIRCULATIONAHA.112.104463

PubMed Abstract | CrossRef Full Text | Google Scholar

McCurry, K. R., Shearon, T. H., Edwards, L. B., Chan, K. M., Sweet, S. C., Valapour, M., et al. (2009). Lung transplantation in the United States, 1998-2007. Am. J. Transplant. 9(4 Pt 2), 942–958. doi: 10.1111/j.1600-6143.2009.02569.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Mezzani, A. (2017). Cardiopulmonary exercise testing: basics of methodology and measurements. Ann. Am. Thorac. Soc. 14, S3–S11. doi: 10.1513/AnnalsATS.201612-997FR

PubMed Abstract | CrossRef Full Text | Google Scholar

Miller, A., Brown, L. K., Sloane, M. F., Bhuptani, A., and Teirstein, A. S. (1995). Cardiorespiratory responses to incremental exercise in sarcoidosis patients with normal spirometry. Chest 107, 323–329. doi: 10.1378/chest.107.2.323

PubMed Abstract | CrossRef Full Text | Google Scholar

Molgat-Seon, Y., Schaeffer, M. R., Ryerson, C. J., and Guenette, J. A. (2019). Exercise pathophysiology in interstitial lung disease. Clin. Chest Med. 40, 405–420. doi: 10.1016/j.ccm.2019.02.011

PubMed Abstract | CrossRef Full Text | Google Scholar

Nathan, S. D., Noble, P. W., and Tuder, R. M. (2007). Idiopathic pulmonary fibrosis and pulmonary hypertension: connecting the dots. Am. J. Respir. Crit. Care Med. 175, 875–880. doi: 10.1164/rccm.200608-1153CC

PubMed Abstract | CrossRef Full Text | Google Scholar

Nishiyama, O., Taniguchi, H., Kondoh, Y., Kimura, T., Ogawa, T., Watanabe, F., et al. (2005). Quadriceps weakness is related to exercise capacity in idiopathic pulmonary fibrosis. Chest 127, 2028–2033. doi: 10.1378/chest.127.6.2028

PubMed Abstract | CrossRef Full Text | Google Scholar

O’Donnell, D. E., Chau, L. K., and Webb, K. A. (1998). Qualitative aspects of exertional dyspnea in patients with interstitial lung disease. J. Appl. Physiol. 84, 2000–2009. doi: 10.1152/jappl.1998.84.6.2000

PubMed Abstract | CrossRef Full Text | Google Scholar

Palange, P., Ward, S. A., Carlsen, K. H., Casaburi, R., Gallagher, C. G., Gosselink, R., et al. (2007). Recommendations on the use of exercise testing in clinical practice. Eur. Respir. J. 29, 185–209. doi: 10.1183/09031936.00046906

PubMed Abstract | CrossRef Full Text | Google Scholar

Panagiotou, M., Church, A. C., Johnson, M. K., and Peacock, A. J. (2017). Pulmonary vascular and cardiac impairment in interstitial lung disease. Eur. Respir. Rev. 26:160053. doi: 10.1183/16000617.0053-2016

PubMed Abstract | CrossRef Full Text | Google Scholar

Panagiotou, M., Polychronopoulos, V., and Strange, C. (2016). Respiratory and lower limb muscle function in interstitial lung disease. Chron. Respir. Dis. 13, 162–172. doi: 10.1177/1479972315626014

PubMed Abstract | CrossRef Full Text | Google Scholar

Parker, C. M., Fitzpatrick, M. F., and O’Donnell, D. E. (2011). “Physiology of interstitial lung disease,” in Interstitial Lung Disease, 5 Edn, eds M. I. Schwarz and T. E. King (Beijing: People’s Medical Publishing House), 61–84.

Google Scholar

Puente-Maestu, L., Palange, P., Casaburi, R., Laveneziana, P., Maltais, F., Neder, J. A., et al. (2016). Use of exercise testing in the evaluation of interventional efficacy: an official ERS statement. Eur. Respir. J. 47, 429–460. doi: 10.1183/13993003.00745-2015

PubMed Abstract | CrossRef Full Text | Google Scholar

Raghu, G., Collard, H. R., Egan, J. J., Martinez, F. J., Behr, J., Brown, K. K., et al. (2011). An official ATS/ERS/JRS/ALAT statement: idiopathic pulmonary fibrosis: evidence-based guidelines for diagnosis and management. Am. J. Respir. Crit. Care Med. 183, 788–824. doi: 10.1164/rccm.2009-040GL

PubMed Abstract | CrossRef Full Text | Google Scholar

Reichenberger, F., Voswinckel, R., Schulz, R., Mensch, O., Ghofrani, H. A., Olschewski, H., et al. (2009). Noninvasive detection of early pulmonary vascular dysfunction in scleroderma. Respir. Med. 103, 1713–1718. doi: 10.1016/j.rmed.2009.05.004

PubMed Abstract | CrossRef Full Text | Google Scholar

Richeldi, L., Launders, N., Martinez, F., Walsh, S. L. F., Myers, J., Wang, B., et al. (2019). The characterisation of interstitial lung disease multidisciplinary team meetings: a global study. ERJ Open Res. 5:00209-2018. doi: 10.1183/23120541.00209-2018

PubMed Abstract | CrossRef Full Text | Google Scholar

Schaeffer, M. R., Molgat-Seon, Y., Ryerson, C. J., and Guenette, J. A. (2017a). Supplemental oxygen and dypsnoea in interstitial lung disease: absence of evidence is not evidence of absence. Eur. Respir. Rev. 26:170072. doi: 10.1183/16000617.0033-2017

PubMed Abstract | CrossRef Full Text | Google Scholar

Schaeffer, M. R., Ryerson, C. J., Ramsook, A. H., Molgat-Seon, Y., Wilkie, S. S., Dhillon, S. S., et al. (2017b). Effects of hyperoxia on dyspnoea and exercise endurance in fibrotic interstitial lung disease. Eur. Respir. J. 49:1602494. doi: 10.1183/13993003.02494-2016

PubMed Abstract | CrossRef Full Text | Google Scholar

Schaeffer, M. R., Ryerson, C. J., Ramsook, A. H., Molgat-Seon, Y., Wilkie, S. S., Dhillon, S. S., et al. (2018). Neurophysiological mechanisms of exertional dyspnoea in fibrotic interstitial lung disease. Eur. Respir. J. 51, 1701726. doi: 10.1183/13993003.01726-2017

PubMed Abstract | CrossRef Full Text | Google Scholar

Schwaiblmair, M., Behr, J., and Fruhmann, G. (1996). Cardiorespiratory responses to incremental exercise in patients with systemic sclerosis. Chest 110, 1520–1525. doi: 10.1378/chest.110.6.1520

PubMed Abstract | CrossRef Full Text | Google Scholar

Seeger, W., Adir, Y., Barbera, J. A., Champion, H., Coghlan, J. G., Cottin, V., et al. (2013). Pulmonary hypertension in chronic lung diseases. J. Am. Coll. Cardiol. 62, D109–D116. doi: 10.1016/j.jacc.2013.10.036

PubMed Abstract | CrossRef Full Text | Google Scholar

Tonelli, R., Cocconcelli, E., Lanini, B., Romagnoli, I., Florini, F., Castaniere, I., et al. (2017). Effectiveness of pulmonary rehabilitation in patients with interstitial lung disease of different etiology: a multicenter prospective study. BMC Pulm. Med. 17:130. doi: 10.1186/s12890-017-0476-5

PubMed Abstract | CrossRef Full Text | Google Scholar

Vainshelboim, B., Kramer, M. R., Izhakian, S., Lima, R. M., and Oliveira, J. (2016). Physical activity and exertional desaturation are associated with mortality in idiopathic pulmonary fibrosis. J. Clin. Med. 5:73. doi: 10.3390/jcm5080073

PubMed Abstract | CrossRef Full Text | Google Scholar

Van Meerhaeghe, A., Scano, G., Sergysels, R., Bran, M., and De Coster, A. (1981). Respiratory drive and ventilatory pattern during exercise in interstitial lung disease. Bull. Eur. Physiopathol. Respir. 17, 15–26.

Google Scholar

Watanabe, F., Taniguchi, H., Sakamoto, K., Kondoh, Y., Kimura, T., Kataoka, K., et al. (2013). Quadriceps weakness contributes to exercise capacity in nonspecific interstitial pneumonia. Respir. Med. 107, 622–628. doi: 10.1016/j.rmed.2012.12.013

PubMed Abstract | CrossRef Full Text | Google Scholar

Wehr, K. L., and Johnson, R. L. (1976). Maximal oxygen consumption in patients with lung disease. J. Clin. Invest. 58, 880–890. doi: 10.1172/JCI108541

PubMed Abstract | CrossRef Full Text | Google Scholar

Younes, M. (1984). Interpretation of clinical exercise testing in respiratory disease. Clin. Chest Med. 5, 189–206.

Google Scholar

Young, I. H., and Bye, P. T. (2011). Gas exchange in disease: asthma, chronic obstructive pulmonary disease, cystic fibrosis, and interstitial lung disease. Compr. Physiol. 1, 663–697. doi: 10.1002/cphy.c090012

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: dyspnea, exercise capacity, hypoxemia, idiopathic pulmonary fibrosis, ventilatory limitation

Citation: Molgat-Seon Y, Schaeffer MR, Ryerson CJ and Guenette JA (2020) Cardiopulmonary Exercise Testing in Patients With Interstitial Lung Disease. Front. Physiol. 11:832. doi: 10.3389/fphys.2020.00832

Received: 15 April 2020; Accepted: 22 June 2020;
Published: 10 July 2020.

Edited by:

Denis Eunan O’Donnell, Queen’s University, Canada

Reviewed by:

Nicolle Jasmin Domnik, Queen’s University, Canada
Gabriele Valli, Azienda Ospedaliera San Giovanni Addolorata, Italy

Copyright © 2020 Molgat-Seon, Schaeffer, Ryerson and Guenette. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Yannick Molgat-Seon, y.molgat-seon@uwinnipeg.ca

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.