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Endothelial dysfunction is not a predictor of outcome in chronic obstructive pulmonary disease

Respiratory Research volume 21, Article number: 90 (2020) Cite this article

Abstract

Background

Local airway inflammation may cause systemic changes which result in endothelial dysfunction. Only a few studies have used reactive hyperemia peripheral arterial tonometry (RH-PAT) in patients with chronic obstructive pulmonary disease (COPD) in order to measure their endothelial dysfunction.

Objective

To determine the efficacy of endothelial dysfunction, measured by RH-PAT, in assessing disease severity and systemic burden in a cohort of COPD patients.

Methods

In this prospective, monocentric study, 157 patients with moderate to very severe COPD (GOLD class II-IV) were examined for endothelial dysfunction using RH-PAT (Itamar medical Ltd., Caesarea, Israel). In a nested-cohort, examination was repeated at exacerbation. The association between reactive hyperemia index (RHI), augmentation index (AI) and disease severity and outcome parameters was analysed.

Results

57% of the COPD patients had a dysfunctional endothelium and the median (IQR) RHI was 1.42 (1.27–1.53). Exacerbation of COPD was not associated with a significant change in RHI (p = 0.625) or ΑΙ (p = 0.530). None of the diagnostic or clinical outcomes of COPD was associated with RHI or arterial stiffness.

Conclusion

Endothelial dysfunction is common in COPD. However, it does not seem to be a predictor neither of disease severity, nor of outcome and does not change during exacerbations of the disease.

Background

Although preventable and treatable, chronic obstructive pulmonary disease (COPD) is one of the leading causes of mortality worldwide [1,2,3]. It is associated with extra-pulmonary comorbid conditions, such as peripheral vascular disease, osteoporosis, skeletal muscle dysfunction, reduced exercise capacity, erectile dysfunction, chronic depression, lung cancer and diabetes [4, 5]. These conditions are responsible for the poor outcome of advanced COPD and may reflect the systemic manifestation of COPD [6]. Cardiovascular comorbidities contribute to the morbidity and mortality of COPD and can be detected independently of traditional risk factors in about one third of COPD patients, accounting for about 50% of deaths [7]. That is because a spill-over of local airway inflammatory mediators into the systemic circulation may result in vascular changes leading to endothelial dysfunction [8]. Endothelial dysfunction may additionally be caused due to a decrease in the availability of nitric oxide (ΝΟ) and due to inflammatory-mediated changes in the structure of the vessel walls, such as the replacement of degraded elastic fibres by collagen, which increases arterial stiffness [8]. Interestingly, endothelial dysfunction is often described as a common feature of COPD and it seems to be positively correlated with the degree of airway obstruction, thus suggesting a mechanistic link between chronic airway obstruction and cardiovascular risk [9,10,11,12].

The main method of determining endothelial dysfunction in patients with COPD is by measuring the flow-mediated dilation (FMD) of the brachial artery. Reactive hyperemia-peripheral arterial tonometry (RH-PAT) is a more recent, noninvasive method to evaluate endothelial dysfunction and its use, easier and less operator-dependent, has been rapidly increasing. RH-PAT measures pulsatile volume changes in response to reactive hyperemia, a transient increase in organ blood flow that is dependent on NO synthesis and occurs after a brief period of ischemia [13,14,15]. RH-PAT assesses endothelial dysfunction in relation to the presence of multiple cardiovascular and metabolic risk factors [16] and can successfully predict cardiovascular events in a population with an intermediate cardiac risk profile [17]. Moreover, abnormal RH-PAT results are correlated with ischemic heart disease diagnosed using an invasive method [18].

Endothelial function assessed by digital RH-PAT is expressed as the reactive hyperemia index (RHI). The RHI describes the ratio of average amplitude during reactive hyperemia compared with the pre-occlusion baseline period [19]. A lower RHI is associated with higher complexity of coronary atherosclerotic plaque, larger systemic atherosclerotic plaque burden and adverse cardiovascular events [20,21,22,23]. Tanaka et al. [24] proposed RHI cutoff values 1.67 and 2.10 (< 1.67 for abnormal and ≥ 1.67 and < 2.10 for borderline, ≥2.10 for normal). On the other hand, the augmentation index (AI) is a measurement of arterial stiffness, which is calculated from a pulse waveform analysis of the peripheral arterial tonometry (PAT) signal at baseline and normalized to a heart rate of 75 bpm [25]. Lower AI values reflect better arterial elasticity [25].

Minet et al. investigated endothelial dysfunction in patients with COPD using RH-PAT, but their cohort consisted of only 44 patients [26]. Our objective was, therefore, to investigate endothelial dysfunction using RH-PAT in a larger and well-characterised cohort of COPD patients, so that we could determine the importance of endothelial dysfunction in assessing disease severity and systemic burden in COPD.

Methods

Τhe PREVENT study [27] is an investigator-initiated and –driven study compiled to the Declaration of Helsinki and Good Clinical Practice Guidelines. The study was approved by the responsible ethics committee (EKNZ 306/10) and was registered at www.controlled-trials.com (identifier ISRCTN 45572998). All patients were recruited from in- and out-patients referred for clinical evaluation and lung function tests to the Clinic of Pneumology, University Hospital of Basel and provided written consent before any study assessments were initiated.

The current study included a nested cohort of the PREVENT study (n = 136) and 21 COPD patients from a cohort of 365 patients that were admitted for a planned pulmonary workup during a period of 4 months (Fig. 1). The inclusion criteria were as follows: age ≥ 40 years; smoking history ≥10 pack-years; moderate to very severe COPD (GOLD class II-IV); clinically relevant disease, as defined by a history of exacerbations in the previous 12 months; stable disease (free of exacerbation) for ≥4 weeks prior to the start of the study. GOLD grades are based on FEV1% predicted: I ≥ 80%; 50% ≤ II < 80%; 30% ≤ III < 50%; and IV < 30%. The exclusion criteria were as follows: pulmonary condition other than COPD; rapid lethal disease; severe immunosuppression including manifested AIDS, organ transplantation or neutropenia (< 500 × 109/L), pregnancy or breastfeeding and known allergy or intolerance to the study medicine. In addition, 14 patients were re-evaluated within 48 h after an acute exacerbation of COPD (AECOPD).

Fig. 1
figure 1

Schematic representation of the study design

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The assessments for each patient included a detailed history, blood sample collection, a physical examination and a measurement of vital signs and lung function. The 6-min walking test (6MWT) [28], the St. George’s respiratory questionnaire (SGRQ), and the COPD assessment test (CAT) were additionally required. Specifically, the 6MWT is a submaximal exercise test that entails measurement of distance walked over a span of 6 min and assesses the performance ability in a variety of cardiopulmonary diseases [29]. The SGRQ measures the impact of COPD on overall health, daily life and perceived well-being [30]. It scores from 0 to 100, with higher scores indicating more limitations [30]. The CAT is a patient-completed questionnaire, assessing the impact of COPD (cough, sputum, dyspnoea, chest tightness) on health status [31]. It scores from 0 to 40 and higher scores denote a more severe impact of COPD on a patient’s life [31].

Information regarding exacerbations were additionally acquired from the patients for the year preceding the baseline measurements and were classified as mild (requiring medical care and increased dose of short-acting β2 agonists), moderate (requiring either antibiotics and/or parenteral corticosteroids) or severe (requiring hospitalization or resulting in death).

Endothelial function was assessed by a trained and certified study nurse at scheduled and unscheduled visits, measuring reactive hyperemia with finger plethysmography, according to the recommendations of the manufacturer (Itamar medical Ltd., Caesarea, Israel) [25]. The device also measured AI.

CT-scans were analysed for emphysema and sub-classified as centrilobular emphysema and paraseptal emphysema.

For our statistical analysis, the SPSS (Statistical Package for Social Sciences) Release 22.0 software package program (SPPS, Inc., Chicago, IL) was utilized. We based our analysis on the data for FMD obtained by Moro et al. [32]. Correlation of RH-PAT values with other measurable disease-relevant parameters was analysed using the Spearman rho coefficient. A comparison of RH-PAT values during stable disease and AECOPD in the same 14 individuals (paired samples) was performed using Mann-Whitney analysis. The predictive value of RH-PAT for adverse outcome events (AECOPD, hospitalisations, cardiovascular events, death) was analysed by uni- and multivariable cox-regression proportional analysis. Adjustment for confounding variables like age, gender and cardiovascular risk factors was pre-defined according to the literature [26]. All tests were two-tailed and the level of statistical significance was set at 0.05. Results were expressed as mean (standard deviation) or median (interquartile range), unless otherwise stated.

Results

In this study, we included 157 patients with stable COPD (Fig. 1), 69% of which were male and 42% were smokers (Table 1). The patients were classified as follows: 68% GOLD II, 22% GOLD III, and 10% GOLD IV. The most common cardiovascular comorbidities were arterial hypertension (64%) and coronary artery disease (28%). Accordingly, 42% were on statin medication and 56% were taking aspirin.

Table 1 Baseline characteristics of the patients included in the study
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Additionally, 57% of the COPD patients had a dysfunctional endothelium. The median (IQR) RHI score was 1.42 (1.27–1.53) and none of the diagnostic or clinical outcomes of COPD was associated with the RHI or arterial stiffness (Table 2). The RHI had no significant effect on time to exacerbation up to 3.3 years after inclusion in the study (Hazard Ratio = 1.001, 95% CI 0.436–2.300, p = 0.998).

Table 2 Linear regression looking at the effect of various variables on RHI values
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Significantly, more male than female and more patients with diabetes as a comorbidity had a dysfunctional endothelium (Table 3). The COPD patients with dysfunctional endothelium had significantly higher BMI than those with normal endothelial function. There were no other differences between the two groups of patients and no association with other cardiovascular comorbidities. Moreover, there was no association between RHI and aspirin (Beta = − 0.052, 95% CI -0.271 – 0.140; p = 0.530) nor between endothelial dysfunction and aspirin (OR = 1.342, p = 0.378).

Table 3 COPD patients with dysfunctional endothelium compared to COPD patients with normal endothelial function
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There was no significant difference in RHI between patients with emphysema and those without (median 1.6 vs. 1.6, p = 0.89), with centrilobular emphysema or without (median 1.6 vs. 1.7; p = 0.87) nor with paraseptal emphysema or without (1.6 vs. 1.7; p = 0.89). Linear regression adjusting for confounding factors such as age, BMI, gender, statin use, diabetes, arterial hypertension, FEV1, smoking status, and pack years, showed no association between emphysema, any type of emphysema and RHI (Table 4). A chi-squared test showed no association between emphysema (p = 0.85), centrilobular emphysema (p = 0.94), paraseptal emphysema (p = 0.32) and the absence or presence of endothelial dysfunction.

Table 4 Association of emphysema with reactive hyperemia index and arterial stiffness
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Arterial stiffness, as represented by AI, was 10.50 in COPD patients. The factors associated with arterial stiffness were age (Spearman rho = 0.236; p = 0.001), heart rate (Spearman rho = − 0.406; p < 0.001) and systolic blood pressure (Spearman rho = 0.273; p < 0.001). The predictors for arterial stiffness in patients with COPD were heart rate (Beta = − 0.409, 95% CI -0.862 - -0.408, p < 0.001), systolic blood pressure (Beta = 0.346, 95% CI 0.187–0.506; p < 0.001), BMI (Beta = − 0.175, 95% CI -0.944 - -0.89; p = 0.018) and gender (Beta = 0.264, 95% CI 4.911–16.679; p < 0.001). Arterial stiffness had no effect on time to exacerbation (Hazard ratio = 0.996, 95% CI 0.975–1.017, p = 0.706). Interestingly, there was no significant difference in RHI (p = 0.625, Fig. 2a) and AI (p = 0.530, Fig. 2b) when we compared patients during a stable phase of COPD and the same patients during an acute exacerbation of COPD.

Fig. 2
figure 2

a Reactive hyperemia index (RHI) and (b) arterial stiffness, as measured by the augmentation index (AI) remained unchanged during stable state and exacerbation, as assessed by the paired t-test (p = 0.625 and p = 0.530 accordingly)

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Arterial stiffness did not change significantly between patients with emphysema compared to those without emphysema (median 11 vs. 10: p = 0.46), with centrilobular emphysema and those without (10 vs. 13; p = 0.65) and between those with paraseptal emphysema and those without (9 vs. 11; p = 0.88). A significant association was seen in univariate and multivariate analysis between arterial stiffness and paraseptal emphysema (Table 4).

Discussion

Up-to-date, this is the largest study evaluating endothelial dysfunction in COPD and the first to evaluate potential changes in endothelial dysfunction between stable state and exacerbation of COPD using RH-PAT. We found that 57% of the patients with COPD had endothelial dysfunction. This is comparable to the results of Minet et al. [26], who indicated endothelial dysfunction in 50% of their COPD patients. Malerba et al. [33] reported a higher incidence of endothelial dysfunction (75%) in COPD patients and a lower RHI score (1.31). This might potentially be attributable to the small sample size of their study (n = 16).

Similar to the vast majority of COPD patients, our patients had several cardiovascular comorbidities. Indeed, we found an association between endothelial dysfunction and diabetes mellitus. However, we found no association between dysfunctional endothelium and other cardiovascular comorbidities or aspirin, a medication considered to influence endothelial function [34]. This is surprising and could point to a technical fault, yet, the RHI measured for patients with arterial hypertension (RHI = 1.8 ± 0.7) was similar to that reported by Weisrock et al. (RHI = 1.7 ± 0.4 to 1.8 ± 0.4) [35]. Additionally, we confirmed the finding of van der Heijden et al. [36] that BMI is associated with endothelial dysfunction. On the other hand, more than half of the patients assessed in our study had arterial hypertension. Weisrock et al. [35] indicated that PAT is not a reliable method for measuring endothelial dysfunction in patients with arterial hypertension. This could, therefore, explain why we found no association between RHI and most cardiovascular comorbidities or aspirin in our study.

Unlike Marchetti et al. [37], Ozben et al. [38] and Urban et al. [39], in our study endothelial dysfunction was similar at stable state and exacerbation of COPD. This finding is rather intriguing, as exacerbations of COPD are linked to bacterial and viral infections, increase in local and systemic inflammation, hypoxia, pulmonary arterial hypertension and congestive heart failure; all these conditions are independently related to endothelial dysfunction [40,41,42]. Furthermore, there is a well-known increase in cardiovascular risk associated with exacerbation of COPD [43, 44]. On the other hand, although Marchetti et al. [37] and Ozben et al. [38] found lower FMD during exacerbation compared to the recovery period, they found no difference between patients with COPD in recovery and controls. They also found no difference in brachial artery diameter during exacerbation and recovery and no association between FMD and lung function [10, 37, 38]. That said, considering the small sample size used for the exacerbation analysis, it would be prudent to look at endothelial dysfunction before and after exacerbation in a larger cohort.

In two previous studies, Minet et al. [26] and Malerba et al. [33] found an association between RHI and FEV1. However, the current results suggest no association between RHI and any COPD parameter i.e. airflow limitation, exercise capacity, BODE index, GOLD status or modified Medical Research Council (mMRC) dyspnoea scale. These differences could lie in the fact that both previous studies had relatively small populations (n = 44 and n = 16, respectively). In addition, the discrepancies in the findings may be attributed to the fact that: 1) our study only excluded COPD patients with other pulmonary conditions, rapid lethal disease and severe immunosuppression and therefore affords a more reasonable representation of the general COPD population, while, on the other hand, Malerba et al. [33] excluded patients with a history of any cardiovascular disease except arterial hypertension, diabetes mellitus and if the patient had an exacerbation in the previous 6months; and 2) in the study of Malerba et al. [33], patients had less severe COPD than the patients in our study. In a number of studies, both FMD and RHI are lower in COPD patients than in controls, but the association with COPD parameters is tenuous [45, 46]. Eickhoff et al. [10] found an association between FMD and FEV1% predicted in a univariate analysis, but no significant association between FMD and GOLD status. Moro et al. [32] found an association between FMD and airflow limitation (FEV1/VC), however, they did not measure or adjust for brachial artery diameter. Barr et al [47] found an association between FMD and FEV1, but this association was present both in COPD and non-COPD patients. Clarenbach et al. [48] demonstrated that a change in FMD was associated with a change in FEV1 in COPD patients after lung volume reduction surgery. However, they did not look at the relationship between FMD and FEV1 at baseline, nor did they take COPD medication into account. Importantly, Barr et al. [47] found that COPD medication is associated with large differences in FMD.

Unlike Bhatt et al. [49], we found no association between RHI or AI and centrilobular emphysema. This could be because coronary calcification, which was used in the analysis by Bhatt et al. [49], is an independent process with different pathways compared to endothelial dysfunction [50]. There was, however, an association between paraseptal emphysema and arterial stiffness. Patients with paraseptal emphysema are at higher risk of developing lung cancer [51]. Arterial stiffness is associated with haematological malignancies [52], but its role in lung cancer is unknown.

Our study has several limitations. It was a monocentric study including patients with COPD receiving extensive treatment for their disease. In addition, we did not exclude patients with cardiovascular comorbidities. Strengths included the full characterisation of the study population, the multivariable adjustment for several confounding factors and the inclusion of a large COPD population with commonly encountered comorbidities, which assures the generalizability of our results.

Conclusions

In conclusion, we found that 57% of patients with COPD had an incidence of endothelial dysfunction with a median (IQR) RHI of 1.42 (1.27–1.53). However, RHI was not associated to any COPD-related outcome and endothelial dysfunction was similar at stable state and at exacerbation of COPD. In addition, endothelial dysfunction, as measured using RH-PAT, is neither a predictor of disease severity nor outcome in COPD.

Availability of data and materials

The datasets used and analysed during the current study are available from the corresponding author on reasonable request.

Abbreviations

6MWT:

6-min walking test

6MWD:

6-min walking distance

AI:

Augmentation index

BMI:

Body mass index

COPD:

Chronic obstructive pulmonary disease

FEV1 :

Forced expiratory volume in 1 s

FMD:

Flow-mediated dilation

RHI:

Reactive hyperemia index

RH-PAT:

Reactive hyperemia peripheral arterial tonometry

References

  1. World Health Organisation. The top 10 causes of death; 2014. www.who.int/mediacentre/factsheets/fs310/en/.

    Google Scholar 

  2. Organisation WH. Chronic obstructive pulmonary disease; 2016. www.who.int/mediacentre/factsheets/fs315/en:.

    Google Scholar 

  3. Mathers CD, Loncar D. Projections of global mortality and burden of disease from 2002 to 2030. PLoS Med. 2006;3:11.

    Article  Google Scholar 

  4. Sin DD, Man SF. Why are patients with chronic obstructive pulmonary disease at increased risk of cardiovascular diseases? The potential role of systemic inflammation in chronic obstructive pulmonary disease. Circulation. 2003;107(11):1514–9.

    Article  PubMed  Google Scholar 

  5. Celli BR, MacNee W. ATS/ERS task force. Standards for the diagnosis and treatment of patients with COPD: a summary of the ATS/ERS position paper. Eur Respir J. 2004;23(6):932–46.

    Article  CAS  PubMed  Google Scholar 

  6. Boschetto P, Beghe B, Fabbri LM, Ceconi C. Link between chronic obstructive pulmonary disease and coronary artery disease: implication for clinical practice. Respirology. 2012;17:422–31.

    Article  PubMed  Google Scholar 

  7. Nussbaumer-Ochsner Y, Rabe KF. Systemic manifestations of COPD. Chest. 2011;139(1):165–73.

    Article  PubMed  Google Scholar 

  8. Seals DR, Tanaka H, Clevenger CM, Monahan KD, Reiling MJ, Hiatt WR, et al. Blood pressure reductions with exercise and sodium restriction in postmenopausal women with elevated systolic pressure: role of arterial stiffness. J Am Coll Cardiol. 2001;38:506–13.

    Article  CAS  PubMed  Google Scholar 

  9. Clarenbach CF, Senn O, Sievi NA, Camen G, van Gestel AJ, Rossi VA, et al. Determinants of endothelial function in patients with COPD. Eur Respir J. 2013;42:1194–204.

    Article  CAS  PubMed  Google Scholar 

  10. Eickhoff P, Valipour A, Kiss D, Schreder M, Cekici L, Geyer K, et al. Determinants of systemic vascular function in patients with stable chronic obstructive pulmonary disease. Am J Respir Crit Care Med. 2008;178:1211–8.

    Article  CAS  PubMed  Google Scholar 

  11. Maclay JD, McAllister DA, Mills NL, Paterson FP, Ludlam CA, Drost EM, et al. Vascular dysfunction in chronic obstructive pulmonary disease. Am J Respir Crit Care Med. 2009;180:513–20.

    Article  PubMed  Google Scholar 

  12. Mills NL, Miller JJ, Anand A, Robinson SD, Frazer GA, Anderson D, et al. Increased arterial stiffness in patients with chronic obstructive pulmonary disease: a mechanism for increased cardiovascular risk. Thorax. 2008;63:306–11.

    Article  CAS  PubMed  Google Scholar 

  13. Bonetti PO, Pumper GM, Higano ST, Holmes DR Jr, Kuvin JT, Lerman A. Noninvasive identification of patients with early coronary atherosclerosis by assessment of digital reactive hyperemia. J Am Coll Cardiol. 2004;44(11):2137–41.

    Article  PubMed  Google Scholar 

  14. Kuvin JT, Patel AR, Sliney KA, Pandian NG, Sheffy J, Schnall RP, et al. Assessment of peripheral vascular endothelial function with finger arterial pulse wave amplitude. Am Heart J. 2003;146(1):168–74.

    Article  PubMed  Google Scholar 

  15. Nohria A, Gerhard-Herman M, Creager MA, Hurley S, Mitra D, Ganz P. Role of nitric oxide in the regulation of digital pulse volume amplitude in humans. J Appl Physiol. 2006;101(2):545–8.

    Article  CAS  PubMed  Google Scholar 

  16. Hamburg NM, Keyes MJ, Larson MG, Vasan RS, Schnabel R, Pryde MM, et al. Cross-sectional relations of digital vascular function to cardiovascular risk factors in the Framingham heart study. Circulation. 2008;117:2467–74.

    Article  PubMed  PubMed Central  Google Scholar 

  17. Korkmaz H, Akbulut M, Ozbay Y, Koc M. A new noninvasive method of evaluating the endothelial function: the measurement of the resistive index after reactive hyperemia of the brachial artery. Echocardiography. 2010;27:873–7.

    Article  PubMed  Google Scholar 

  18. Targonski PV, Bonetti PO, Pumper GM, Higano ST, Holmes DR, Lerman A. Coronary endothelial dysfunction is associated with an increased risk of cerebrovascular events. Circulation. 2003;107:2805–9.

    Article  PubMed  Google Scholar 

  19. Bruyndonckx L, Radtke T, Eser P, Vrints CJ, Ramet J, Wilhelm M, et al. Methodological considerations and practical recommendations for the application of peripheral arterial tonometry in children and adolescents. Int J Cardiol. 2013;168(4):3183–90.

    Article  PubMed  Google Scholar 

  20. Maeda H, Sugiyama S, Jinnouchi H, Matsuzawa Y, Fujisue K, Hirata Y, et al. Advanced peripheral microvascular endothelial dysfunction and polyvascular disease in patients with high cardiovascular risk. J Cardiol. 2016;67(5):455–62.

    Article  PubMed  Google Scholar 

  21. Matsuzawa Y, Li J, Aoki T, Guddeti RR, Kwon TG, Cilluffo R, et al. Predictive value of endothelial function by noninvasive peripheral arterial tonometry for coronary artery disease. Coron Artery Dis. 2015;26(3):231–8.

    Article  PubMed  PubMed Central  Google Scholar 

  22. Matsuzawa Y, Sugiyama S, Sumida H, Sugamura K, Nozaki T, Ohba K, et al. Peripheral endothelial function and cardiovascular events in high-risk patients. J Am Heart Assoc. 2013;2(6):e000426.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  23. Rubinshtein R, Kuvin JT, Soffler M, Lennon RJ, Lavi S, Nelson RE, et al. Assessment of endothelial function by non-invasive peripheral arterial tonometry predicts late cardiovascular adverse events. Eur Heart J. 2010;31(9):1142–8.

    Article  PubMed  Google Scholar 

  24. Tanaka A, Tomiyama H, Maruhashi T, Matsuzawa Y, Miyoshi T, Kabutoya T, et al. Physiological diagnostic criteria for vascular failure. Hypertension. 2018;72(5):1060–71.

    Article  CAS  PubMed  Google Scholar 

  25. Brant LCC, Barreto SM, Passos VMA, Ribeiro ALP. Reproducibility of peripheral arterial tonometry for the assessment of endothelial function in adults. J Hypertens. 2013;31:1984–90.

    Article  CAS  PubMed  Google Scholar 

  26. Minet C, Vivodtzev I, Tamisier R, Arbib F, Wuyam B, Timsit J-F, et al. Reduced six-minute walking distance, high fat-free-mass index and hypercapnia are associated with endothelial dysfunction in COPD. Respir Physiol Neurobiol. 2012;183:128–34.

    Article  PubMed  Google Scholar 

  27. Stolz D, Hirsch HH, Schilter D, Louis R, Rakic J, Boeck L, et al. Intensified therapy with inhaled corticosteroids and long-acting beta2-agonists at the onset of upper respiratory tract infection to prevent chronic obstructive pulmonary disease exacerbations. A multicenter, randomized, double-blind, placebo-controlled trial. Am J Respir Crit Care Med. 2018;197(9):1136–46.

    Article  CAS  PubMed  Google Scholar 

  28. Enright PL, Sherrill DL. Reference equations for the six-minute walk in healthy adults. Am J Respir Crit Care Med. 1998;158:1384–7.

    Article  CAS  PubMed  Google Scholar 

  29. Brown AW, Nathan SD. The value and application of the 6-minute-walk test in idiopathic pulmonary fibrosis. Ann Am Thorac Soc. 2018;15(1):3–10.

    Article  PubMed  Google Scholar 

  30. Jones PW, Quirk FH, Baveystock CM, Littlejohns P. A self-complete measure of health status for chronic airflow limitation. The St. George’s respiratory questionnaire. Am Rev Respir Dis. 1992;145(6):1321–7.

    Article  CAS  PubMed  Google Scholar 

  31. Jones PW, Harding G, Berry P, Wiklund I, Chen WH, Kline LN. Development and first validation of the COPD assessment test. Eur Respir J. 2009;34(3):648–54.

    Article  CAS  PubMed  Google Scholar 

  32. Moro L, Pedone C, Scarlata S, Malafarina V, Fimognari F, Antonelli-Incalzi R. Endothelial dysfunction in chronic obstructive pulmonary disease. Angiology. 2008;59(3):357–64.

    Article  CAS  PubMed  Google Scholar 

  33. Malerba M, Radaeli A, Nardin M, Clini E, Carpagnano GE, Sciatti E, et al. Endothelial dysfunction assessment by noninvasive peripheral arterial tonometry in patients with chronic obstructive pulmonary disease compared with healthy subjects. Clin Respir J. 2017;12:1–7.

    Google Scholar 

  34. Dzeshka MS, Shantsila A, Lip GYH. Effects of aspirin on endothelial function and hypertension. Curr Hypertens Rep. 2016;18:83.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  35. Weisrock F, Fritschka M, Beckmann S, Litmeier S, Wagner J, Tahirovic E, et al. Reliability of peripheral arterial tonometry in patients with heart failure, diabetic nephropathy and arterial hypertension. Vasc Med. 2017;22(4):292–300.

    Article  PubMed  Google Scholar 

  36. van der Heijden DJ, van Leeuwen MAH, Janssens GN, Lenzen MJ, van de Ven PM, Eringa EC, et al. Body mass index is associated with microvascular endothelial dysfunction in patients with treated metabolic risk factors and suspected coronary artery disease. J Am Heart Assoc. 2017;6:9.

    Google Scholar 

  37. Marchetti N, Ciccolella DE, Jacobs MR, Crookshank A, Gaughan JP, Kashem MA, et al. Hospitalized acute exacerbation of COPD impairs flow and nitroglycerin-mediated peripheral vascular dilation. J Chron Obstruct Pulmon Dis. 2011;8(2):60–5.

    Article  Google Scholar 

  38. Oezben B, Eryüksel E, Tanrikulu AM, Papila-Topal N, Celikel T, Basaran Y. Acute exacerbation impairs endothelial function in patients with chronic obstructive pulmonary disease. Arch Turk Soc Cardiol. 2010;38(1):1–7.

    Google Scholar 

  39. Urban MH, Valipour A, Kiss D, Eickhoff P, Funk G-C, Burghuber OC. Soluble receptor of advanced glycation end-products and endothelial dysfunction in COPD. Respir Med. 2014;108:891–7.

    Article  PubMed  Google Scholar 

  40. Wedzicha JA, Singh R, Mackay AJ. Acute COPD exacerbations. Clin Chest Med. 2014;35(1):157–63.

    Article  PubMed  Google Scholar 

  41. Rohde G, Wiethege A, Borg I, Kauth M, Bauer TT, Gillissen A, et al. Respiratory viruses in exacerbations of chronic obstructive pulmonary disease requiring hospitalisation: a case-control study. Thorax. 2003;58(1):37–42.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  42. de Miguel DJ, Chancafe MJ, Jimenez GR. The association between COPD and heart failure risk: a review. Int J Chron Obstruct Pulmon Dis. 2013;8:305–12.

    Google Scholar 

  43. Kunisaki KM, Dransfield MT, Anderson JA, Brook RD, Calverley PMA, Celli BR, et al. Exacerbations of chronic obstructive pulmonary disease and cardiac events: a cohort analysis. Am J Respir Crit Care Med. 2018;198(1):51 epub ahead of print.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  44. Smith MC, Wrobel JP. Epidemiology and clinical impact of major comorbidities in patients with COPD. Int J Chron Obstruct Pulmon Dis. 2014;27(9):871–88.

    Article  Google Scholar 

  45. Vaes AW, Spruit MA, Theunis J, Goswami N, Vanfleteren LE, Franssen FME, et al. Endothelial function in patients with chronic obstructive pulmonary disease: a systematic review of studies using flow mediated dilatation. Expert Rev Respir Med. 2017;11(12):1021–31.

    CAS  PubMed  Google Scholar 

  46. Ambrosino P, Lupoli R, Iervolino S, De Felice A, Pappone N, Storino A, et al. Clinical assessment of endothelial function in patients with chronic obstructive pulmonary disease: a systematic review with meta-analysis. Intern Emerg Med. 2017;12:877–85.

    Article  PubMed  Google Scholar 

  47. Barr RG, Mesia-Vela S, Austin JHM, Basner RC, Keller BM, Reeves AP, et al. Impaired flow-mediated dilation is associated with low pulmonary function and emphysema in ex-smokers. Am J Respir Crit Care Med. 2007;176:1200–7.

    Article  PubMed  PubMed Central  Google Scholar 

  48. Clarenbach CF, Sievi NA, Brock M, Schneiter D, Weder W, Kohler M. Lung volume reduction surgery and improvement of endothelial function and blood pressure in patients with chronic obstructive pulmonary disease - a randomized controlled trial. Am J Respir Crit Care Med. 2015;192(3):307–14.

    Article  PubMed  Google Scholar 

  49. Bhatt SP, Nath HP, Kim Y-I, Ramachandran R, Watts JR, Terry NLJ, et al. Centrilobular emphysema and coronary artery calcification: mediation analysis in the SPIROMICS cohort. Respir Res. 2018;19:257.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  50. Han SH, Gerber TC, Suwaidi JA, Eeckhout E, Lennon R, Rubinshtein R, et al. Relationship between coronary endothelial function and coronary calcification in early atherosclerosis. Atherosclerosis. 2010;209(1):197–200.

    Article  CAS  PubMed  Google Scholar 

  51. Mouronte-Roibas C, Fernandez-Villar A, Ruano-Ravina A, Ramos-Hernandez C, Tilve-Gomez A, Rodriguez-Fernandez P, et al. Influence of the type of emphysema in the relationship between COPD and lung cancer. Int J Chron Obstruct Pulmon Dis. 2018;13:3563–70.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  52. Mozos I, Borzak G, Caraba A, Mihaescu R. Arterial stiffness in hematologic malignancies. Onco Targets Ther. 2017;10:1381–8.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

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Acknowledgments

Not applicable.

Funding

This study forms a nested cohort of the PREVENT study, which was primarily funded by a Swiss National Foundation grant to Prof. D. Stolz (PP00-P3_128412/1) and by the Clinic of Pneumology of the University Hospital Basel.

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Author notes

  1. Andreas Scherr and Desiree M. Schumann contributed equally to this work.

Authors and Affiliations

  1. Clinic of Respiratory Medicine and Pulmonary Cell Research, University Hospital of Basel and University of Basel, Petersgraben 4, 4031, Basel, Switzerland

    Andreas Scherr, Desiree M. Schumann, Meropi Karakioulaki, Léo Franchetti, Werner Strobel, Michael Tamm & Daiana Stolz

  2. Clinic of Cardiology, University Hospital Basel, Petersgraben 4, 4031, Basel, Switzerland

    Michael Zellweger

Authors
  1. Andreas Scherr
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  2. Desiree M. Schumann
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  4. Léo Franchetti
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  5. Werner Strobel
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  8. Daiana Stolz
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Contributions

Data collection, accuracy of data, statistical analysis, writing of the manuscript, contribution to the discussion of results, finalization of the manuscript and approval of the submitted article: AS, DMS, ΜΚ, WS, MZ, MT and DS; conception of the research project, contribution in clinical work, integrity and accuracy of data, preparation and approval of the submitted article: DS.

Corresponding author

Correspondence to Daiana Stolz.

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Ethics approval and consent to participate

All patients consent to participate in the study. The study was approved by the ethics committee of the Northwestern and Central Switzerland.

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All patients signed informed consents for publication of their data in the study.

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The authors declare that they have no competing interests.

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Scherr, A., Schumann, D.M., Karakioulaki, M. et al. Endothelial dysfunction is not a predictor of outcome in chronic obstructive pulmonary disease. Respir Res 21, 90 (2020). https://doi.org/10.1186/s12931-020-01345-9

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Keywords

Respiratory Research

ISSN: 1465-993X

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