Abstract
Vulnerability to stress-induced inflammation has been linked to a dysfunctional hypothalamus–pituitary–adrenal (HPA) axis. In the present study, patients with known or suspected coronary artery disease (CAD) were assessed with respect to inflammatory and HPA axis response to acute physical exercise. An exercise stress test was combined with SPECT myocardial perfusion imaging. Plasma and saliva samples were collected before and 30 min after exercise. Interleukin (IL)-6 and adrenocorticotropic hormone (ACTH) were measured in plasma, while cortisol was measured in both plasma and saliva. In total, 124 patients were included of whom 29% had a prior history of CAD and/or a myocardial perfusion deficit. The levels of exercise intensity and duration were comparable in CAD and non-CAD patients. However, in CAD patients, IL-6 increased after exercise (p = 0.019) while no differences were seen in HPA axis variables. Conversely, patients without CAD exhibited increased levels of ACTH (p = 0.003) and cortisol (p = 0.004 in plasma, p = 0.006 in saliva), but no change in IL-6. We conclude that the IL-6 response to acute physical exercise is exaggerated in CAD patients and may be out of balance due to HPA axis hypoactivity. It remains to be further investigated whether this imbalance is a potential diagnostic and therapeutic target in CAD.
Similar content being viewed by others
Introduction
Inflammation is a major component of atherosclerosis assumed to play a role in both pathogenesis and prognosis of cardiovascular disease1. Accumulating evidence indicates that elevations of inflammatory biomarkers predict the risk of developing coronary artery disease (CAD) and myocardial infarction (MI) in healthy individuals2,3. In this regard, interleukin 6 (IL-6) and C-reactive protein (CRP), whose production is stimulated by IL-6, have been among the most commonly assayed markers. Moreover, results from two large genetics consortia have provided evidence that the IL-6 signaling pathway has a causal role in the development of CAD4,5. IL-6 is also an independent predictor of recurrent cardiovascular events in patients with stable CAD6. Importantly, modulation of IL-6 by targeting its upstream mediator IL-1 was recently shown to reduce cardiovascular event rates in CAD patients with previous MI and sustained low-grade inflammation defined as a CRP level of ≥ 2 mg/L7.
The sustained inflammatory state in CAD patients does not have one clear underlying cause. It may reflect an ongoing excessive immune response in the arterial wall but also a systemic proinflammatory milieu created by various risk factors, such as obesity, diabetes, smoking and sedentary life style. Overall, there is emerging evidence for an imbalance between pro- and anti-inflammatory actions and a poor control of the inflammatory reaction in atherosclerosis and CAD1. In the clinical setting, acute stress (mental or physical) can be used as a method to investigate the ability to control inflammation8,9. Interestingly, a few previous studies have shown that patients with CAD display an exaggerated inflammatory response to both mental and physical stress compared with healthy controls, as assessed by CRP or IL-6 elevation in plasma10,11. In general, acute exercise has been found to generate a markedly greater IL-6 response than mental stress10.
One major regulator of stress response and inflammation is the hypothalamic–pituitary–adrenal (HPA) axis. Normally, stress-induced release of cytokines, like IL-6, activates the HPA axis resulting in rapid increases of adrenocorticotropic hormone (ACTH) and cortisol12,13,14. Cortisol will, as a feedback, suppress further release of cytokines. In various animal models, a blunted HPA axis response has been associated with susceptibility to autoimmune and inflammatory disorders15. In human disease, inadequately low cortisol response to stress has been reported in chronic inflammatory processes, such as rheumatoid arthritis, chronic obstructive pulmonary disease and depression16. Furthermore, blunted cortisol response to both mental and physical stress has been shown in patients with CAD compared with healthy controls11,17. Whether blunted HPA axis response, assessed by ACTH and cortisol release, is linked to stress-induced release of IL-6 in CAD patients has not been previously investigated.
In the present study, patients with known or suspected CAD were assessed for their ability to control the inflammatory response to stress with focus on the HPA axis response. The hypothesis of inadequate regulation of IL-6 due to blunted HPA axis response is illustrated in Fig. 1. A short bout of exercise on a bicycle ergometer was used as a method to induce a limited inflammatory response. The exercise stress test was combined with SPECT myocardial perfusion imaging (MPI) for the evaluation of exercise-induced ischemia as a potential confounder. The concentrations of IL-6 and ACTH (in plasma) and cortisol (in plasma and saliva) were measured before and after exercise.
Results
Patient population and results of exercise stress test
In total, 124 patients were included. Their demographic and clinical characteristics, including medication are shown in Table 1. Thirty patients (24%) had documented CAD, defined by coronary angiography as one or more lesions with > 50% diameter stenosis. Among them, 25 had a history of prior myocardial infarction (MI) and 5 had a history of coronary revascularization (percutaneous coronary intervention or coronary by-pass surgery) due to stable or unstable angina. Results of the exercise stress test and SPECT MPI in all patients are shown in Table 2. At maximal exercise, heart rate and systolic blood pressure showed significant increases (both p < 0.001) compared with baseline. Exercise-induced chest pain was reported by 17 patients (14%). A myocardial perfusion deficit was observed in 19 patients (15%) of whom 4 patients had an irreversible perfusion deficit and 15 patients had an ischemic total perfusion deficit (TPD) ≥ 5%. Among those who reported exercise-induced chest pain, only one exhibited ischemic TPD ≥ 5%.
Biochemical measures before and after exercise are presented in Table 3. All patients showed a significant increase in IL-6, ACTH and cortisol after exercise. Also, fatty acid-binding protein 4 (FABP4) levels increased significantly after exercise. FABP4 was used as a potential surrogate marker of exercise-induced activation of the sympathetic nervous system, as described by Iso et al.18.
Patients with or without documented CAD
The patients were divided into two groups: one group with documented CAD and/or the presence of myocardial perfusion deficit (CAD, n = 36) and one group without documented CAD, i.e. no history of prior CAD events and normal SPECT MPI (non-CAD, n = 88). Table 1 shows the descriptive information for CAD and non-CAD patients. There was a dominance of females in the non-CAD group but, otherwise, no differences in variables such as age, BMI, smoking, hypertension, diabetes and plasma levels of creatinine and CRP. Not unexpectedly, the use of cardiovascular medications, including statins, beta-blockers, angiotensin converting enzyme (ACE) inhibitors/angiotensin receptor blockers and low-dose aspirin (75 mg daily) was lower in the non-CAD group, while the use of anti-depressive agents did not differ (CAD 8.3%, non-CAD 11%). Results of the exercise stress tests and SPECT MPI in the CAD and non-CAD groups are also given in Table 2. Heart rate and blood pressure at rest and maximal exercise were similar in the two groups, and so was exertion level, defined by maximal watt load and exercise duration. The prevalence of exercise-induced chest pain was also similar in CAD and non-CAD patients. There was a higher proportion of individuals with reduced left ventricular ejection fraction (< 50%) in the CAD group.
In the non-CAD group, the indications for SPECT MPI were in the majority of cases atypical chest pain or dyspnea and inconclusive results of exercise test. Other indications included pathological electrocardiogram (ECG) findings and family history of premature CAD. Diagnoses obtained after SPECT MPI included palpitations, anxiety, asthma, myalgia and gastroesophageal reflux disease. In 31 cases (34%), no diagnosis was obtained.
As shown in Table 3, the IL-6, ACTH and cortisol response patterns differed between CAD and non-CAD groups. In all CAD patients, IL-6 increased significantly after exercise while no difference was seen in HPA axis variables. If we included only CAD patients with prior MI (n = 25) a similar pattern was seen, i.e. IL-6 increased from 2.9 (2.4–3.9) to 3.2 (2.6–4.2) pg/mL, p = 0.013) while no significant changes occurred in HPA axis variables. In contrast, the non-CAD patients exhibited significant increases in HPA axis variables but no change in IL-6. FABP4 increased in both CAD and non-CAD groups further supporting that adrenergic responses to the exercise test were similar.
In order to evaluate the influence of sex on IL-6, ACTH and cortisol levels, we compared the 45 males and 43 females in the non-CAD group. Females had lower ACTH and salivary cortisol levels at baseline. However, the IL-6, ACTH and cortisol response patterns were similar in males and females (see Table 1, Supplements).
As an alternative approach, we divided the patients into IL-6 high responders and IL-6 low responders defined as above or below the median value of IL-6 (0.19 pg/mL), see Table 2, Supplements. The proportions of females were similar, 39% and 40%, respectively. As shown in Fig. 2, being a high IL-6 responder was significantly more common among CAD patients, defined as a history of prior MI and/or coronary revascularization and/or a myocardial perfusion deficit, compared with non-CAD patients. The similar result was obtained if only patients with prior MI (n = 25) were included in the analysis. After adjusting for sex, the odds ratio (OR) for documented CAD was 2.03 (p = 0.045) in IL-6 high responders compared with IL-6 low responders. Similarly, using history of prior MI as dependent variable, the OR was 2.70 (p = 0.045) after sex adjustment. If myocardial perfusion deficit was used as dependent variable, the OR for ischemic myocardial perfusion deficit was 1.23 (p = 0.220) in IL-6 high responders compared with IL-6 low responders.
As expected, cortisol levels in plasma and saliva were strongly correlated, p < 0.001, as were ACTH and cortisol in plasma, p < 0.001, whereas IL-6 or CRP levels did not correlate with either ACTH or cortisol levels in the whole study population. However, in the non-CAD group, ACTH and IL-6 levels showed weak but significant inverse correlations at baseline, r = -0.211, p = 0.046, and after exercise, r = -0.246, p = 0.021. Also, ACTH after exercise correlated inversely with CRP, r = -0.267, p = 0.012, in the non-CAD group. There were no correlations between inflammatory markers, ACTH or cortisol in the CAD group. The IL-6, ACTH or cortisol responses did not show any significant correlations with exertion level, left ventricular ejection fraction or degree of myocardial perfusion deficit (data not shown).
We also divided the whole study cohort into subgroups based on medication; statins, beta-blockers, low-dose aspirin or ACE inhibitors/angiotensin receptor blockers, but found no significant differences in IL-6, ACTH and cortisol levels, neither before or after stress (data not shown).
Discussion
The main findings of the present study indicate an unbalanced relationship between IL-6 and HPA axis variables in patients with documented CAD. A single bout of maximal exercise caused a significant rise in IL-6 but no increase in ACTH and cortisol whereas the opposite pattern was seen in patients without any signs of CAD.
In the whole study cohort, IL-6, ACTH and cortisol increased significantly after exercise. This is in line with previous studies showing that acute exercise is a useful method to investigate stress-induced inflammation. An increase in IL-6 has been reported to be the earliest and most prominent of the cytokine responses to exercise, though strongly related to intensity and duration of the exercise19,20. It is also well known that transient elevations in IL-6 induce increased levels of ACTH and cortisol in humans, as part of a normal stress response12,13,14. Thus, for most people, the inflammatory response to acute exercise should be blunted almost immediately by anti-inflammatory mediators stimulated simultaneously by the bout of physical exercise.
However, the IL-6 response to a single bout of maximal exercise varied substantially among study participants, being larger in those with CAD compared to non-CAD despite comparable levels of exercise intensity and duration. The findings agree with previous work reporting that inflammatory response to acute physical exercise, assessed by IL-6 or CRP, is exaggerated in CAD patients compared with healthy controls10,11. One plausible explanation of stress-induced inflammatory response in CAD patients could be myocardial ischemia. Two previous studies have examined the inflammatory response to mental stress in relation to inducible myocardial ischemia in CAD patients but found no relationship21,22. Neither did we find any evidence that exercise-induced ischemia per se was linked to an exaggerated IL-6 response.
Another striking difference between CAD and non-CAD patients was the lack of increase in ACTH and cortisol in CAD patients after exercise. In line with this finding, a few previous studies have reported that the cortisol response to acute physical or mental stress is blunted in CAD patients compared with healthy subjects11,23. Furthermore, there is evidence of other manifestations of HPA axis dysfunctions in patients with CAD, characterized by elevated evening levels and flattening of the diurnal cortisol slope11,24. A flattened diurnal cortisol slope before coronary artery bypass graft surgery has been shown to identify those who are at risk of adverse cardiac events and death after surgery25. Also, population-based studies have demonstrated that a flattened diurnal cortisol slope is associated with both coronary calcification and increased risk of cardiovascular disease mortality26,27.
One intriguing question is whether the lack of ACTH and cortisol response in the CAD group represents a hypoactive HPA axis and thereby a disrupted homeostasis. Several experimental studies have demonstrated an association between abnormally low glucocorticoid response to stress and susceptibility to inflammation15. Impaired cortisol response to acute physical exercise has also been described in human chronic inflammatory disorders, such as rheumatoid arthritis and chronic obstructive pulmonary disease16. The lack of ACTH response in CAD patients along with the lost association between ACTH and IL-6 levels further highlight the possibility of imbalance between cytokine and cortisol response to stress. Interestingly, Silverman et al.28 investigated the role of ACTH in adrenal glucocorticoid response to infection in a mouse model and found that IL-6 failed to elicit glucocorticoid response in the absence of ACTH.
Previous research has described the development of HPA axis hyporeactivity in individuals exposed to chronic stress or suffering from stress-related bodily disorders29,30. There is emerging evidence that psychological factors may play a role in the development of HPA axis hypoactivity in CAD. According to Nikkheslat et al.17, depressed CAD patients had higher levels of IL-6 gene expression in blood mononuclear cells and lower plasma and saliva cortisol levels compared with non-depressed CAD patients under resting conditions, suggesting that the inflammatory state in depressed CAD patients might be inadequately restrained by endogenous glucocorticoids. In line with this, Waller et al.23 reported that depressed CAD patients had a more blunted cortisol response to mental stress than non-depressed CAD patients. In the present study, data on psychosocial stress variables, such as depression, were not available. Only, it was noted that the use of anti-depressive agents was equally low in CAD and non-CAD patients as well as in IL-6 high and low responders.
Another relevant question is whether the increased use of drugs, such as statins or beta blockers, in CAD patients had any suppressive effect on the HPA axis response. As inhibitor of steroid biosynthesis, statins can thereotically influence steroid hormone production. However, levels or rhythms of ACTH and cortisol seem to be unaffected by statin treatment, as recently stated in a Scientific Statement from American Heart Association31. Also, the effect of beta blockers on cortisol response to stress has been investigated previously. Compared with placebo, beta blockade resulted in higher cortisol levels after mental stress as well as after short-term maximal dynamic exercise32,33. In the present study, neither the use of statins, nor beta blockers seemed to influence the HPA axis response.
Finally, some major limitations of our study should be addressed. Firstly, samples were collected at one single time point 30 min after exercise. This time point was chosen based on data from previous studies using acute bicycle exercise11,34 but still, it leaves us unaware of very early transient changes as well as delayed responses. Secondly, the exercise tests took place in the morning between 08 am and 12 noon, raising the possibility that basal cortisol circadian rhythm might influence the cortisol stress response. However, as shown previously35,36, there is no evidence of association between cortisol diurnal decline and the magnitude of cortisol stress response. Furthermore, a reanalysis of five independent studies led to the conclusion that the HPA axis response to psychosocial stress was similar in the morning and afternoon37. Thirdly, we did not include healthy asymptomatic sex- and age-matched controls. Even if we were able to define non-CAD patients as individuals without a documented history of CAD and a normal SPECT MPI, they were still patients with different types of chest discomfort. The higher proportion of women in the non-CAD group was not an unexpected finding since symptoms of atypical chest pain as well as inconclusive exercise stress tests are known to be more common in women than men38. Yet, we found no evidence that the IL-6 or HPA axis stress response differed between men and women,
Conclusion
By using an exercise test combined with SPECT MPI as a model for stress-induced inflammation, we show that an exaggerated IL-6 response occurred more frequently in patients with documented CAD. The IL-6 response was not related to either exercise intensity and duration or myocardial ischemia. Instead, the findings indicate that the IL-6 response in CAD patients could be out of balance due to HPA axis hypoactivity. Further work needs to be done to establish whether this imbalance is a marker of vulnerability and a potential diagnostic and therapeutic target in CAD.
Methods
Patient population
Patients referred for a bicycle ergometry exercise test combined with SPECT MPI were consecutively recruited at the Department of Clinical Physiology, Linköping University Hospital from September 2018 to April 2019. The referral for stress testing was at the clinical discretion of a cardiologist. Subjects were excluded only if they were using oral or parenteral treatment with nonsteroidal anti-inflammatory drugs or any other immunosuppressive agent, such as glucocorticoids or cytostatic agents. Baseline demographic data and medical history were collected retrospectively from medical records, whereas test results were recorded prospectively. The research protocol was approved by the Regional Ethical Review Board in Linköping, Sweden, and informed consent was obtained from all participants. All procedures performed in the study were carried out in accordance with relevant guidelines and regulations that comply with institutional, national, or international gudielines.
Exercise stress test and sampling procedure
The MPI SPECT tests took place between 08 am and 12 noon. Patients were continued on their daily medication regimen, including anti-ischemic drugs, but were instructed to avoid tooth brushing, smoking, eating and drinking for at least 2 h before the test. The exercise stress test was performed on the electronically braked bicycle Ergometer Ebike Basic Comfort (GE Healthcare, Freiburg, Germany) until exhaustion. The exercise protocol was determined based on estimation of the individual´s capacity, starting at 30–50 W and continuously increased by 10–20 W/min. Heart rate and blood pressure were monitored and recorded before and during each stage of exercise. General exhaustion, anginal chest pain and dyspnea were recorded every minute according to the 20 (general exhaustion and leg fatigue) or 10 (anginal chest pain and dyspnea) graded Borg scale. Continuous 12-lead electrocardiogram (ECG) monitoring was performed before, during and 3–5 min after exercise.
Baseline saliva and blood samples were collected prior to the exercise test (after at least 20 min of rest) and post-exercise saliva and blood samples were collected 30 min after the completion of exercise test. First, saliva was collected with Salimetrics Oral Swabs (Salimetrics via Electrabox, Stockholm, Sweden) placed under the tongue for 2 min. The saliva samples were then immediately placed on ice. Thereafter, whole blood was collected in 9 mL EDTA tubes (BD Biosciences) and plasma was obtained after centrifugation for 10 min at 1500 × g. Centrifugation had to be started within 30 min after blood collection. Saliva and plasma samples were frozen at -70 °C until analysis.
Myocardial perfusion imaging
MPI was performed according to the European Association of Nuclear Medicine guidelines39. At the highest work load and exercise level, technetium-99 m (99mTc) tetrofosmin was injected whereon the patient continued to cycle for 1–2 min. Imaging was performed in upright and supine position with at least 1 million myocardial counts for each imaging session using a semiconductor cadmium-zinc-telluride (CZT) SPECT camera (Spectrum Dynamics, Israel). If the stress imaging studies showed normal perfusion, no additional resting imaging studies were required. In the remaining cases, the patients were asked to return for a resting image two days later. 99mTc tetrofosmin was then administered during rest, followed by SPECT image acquisition after approximately 1 h. Visual analysis was performed by three different nuclear medicine consultants (each with at least 10 years experience in MPI) to assess left ventricular myocardial perfusion during stress and rest and the degree to which the deficit was reversible, according to current guidelines40. Ischemic TPD was calculated from the difference between the stress and rest TPD scores using quantitative perfusion software (QPS, version 2012, Cedars-Sinai Medical Center) and the normal databases supplied by the vendour (Spectrum Diagnostic). An abnormal criterion for ischemic TPD was defined as 5% or more41. Results close to 5% as well as ambiguous results were assessed and classified by a second nuclear medicine consultant.
Left ventricular ejection fraction was measured by using ECG-gated imaging with 8 frames per cardiac cycle (Quantitative Gated SPECT (QGS) software version 2012, Cedars-Sinai Medical Center). Stress images were used in the analyses.
Plasma measurements
IL-6 in plasma was analyzed with Luminex Performance Human High Sensitivity Cytokine Panel (Biotechne, Abingdon, UK). FABP4 in plasma was analyzed with Human Premixed Multi-Analyte Kit (Biotechne). The analyses were performed according to the manufacturer’s instructions. The inter-assay coefficients of variation (CV) were 6.4 and 1.0% for IL-6 and FABP4, respectively and the ranges of the standard curves were 0,83 – 3400 pg/mL and 0,61 – 148 ng/mL, respectively. CRP was measured at the Department of Clinical Chemistry at the Linköping University hospital using an immunoturbidimetric assay with a Roche Cobas C502 analyzer (Roche Diagnostics, Scandinavia AB), with a CV of 2.2%.
ACTH and cortisol in plasma were analyzed at the Department of Clinical Chemistry at the Linköping University hospital using an electrochemiluminescence immunoassay with a Roche Cobas e602 (Roche diagnostics) with CV of 1.1 and 3.4%, respectively.
Free cortisol was measured in saliva. After thawing, the samples were centrifuged at 2000 × g for 10 min at 4 °C before 300 µl was mixed with deuterated internal standard D4-cortisol. After extraction with ethyl acetate the organic phase was collected and evaporated under nitrogen. Samples were finally diluted in 10% methanol and then analyzed with liquid chromatography-mass spectrometry (LC–MS/MS)42. Four standards with concentrations between 0.625 – 40 nmol/L were used. The intra-assay precision was 6.6% (CV).
Statistics
IBM SPSS Statistics 25 was used for statistical analyses. Paired sample t-test (for normally distributed data) or Wilcoxon Signed rank test (for non-normally distributed data) were used to compare paired samples. Student´s t-test or Mann–Whitney U test were used for comparisons between groups, and Chi square for comparison of categorical data. Correlation analyses were performed by using Spearman ́s rank correlation or logistic regression analysis. Two-tailed p values < 0.05 were considered significant. Numerical data are consistently presented as median (inter-quartile range).
Data availability
The datasets used and analysed during the current study are available from the corresponding author on reasonable request.
References
Hansson, G. K., Libby, P. & Tabas, I. Inflammation and plaque vulnerability. J. Intern. Med. 278, 483–493. https://doi.org/10.1111/joim.12406 (2015).
Danesh, J. et al. C-reactive protein and other circulating markers of inflammation in the prediction of coronary heart disease. N. Engl. J. Med. 350, 1387–1397. https://doi.org/10.1056/NEJMoa032804 (2004).
Pai, J. K. et al. Inflammatory markers and the risk of coronary heart disease in men and women. N. Engl. J. Med. 351, 2599–2610. https://doi.org/10.1056/NEJMoa040967 (2004).
Sarwar, N. et al. Interleukin-6 receptor pathways in coronary heart disease: a collaborative meta-analysis of 82 studies. Lancet 379, 1205–1213. https://doi.org/10.1016/s0140-6736(11)61931-4 (2012).
Swerdlow, D. I. et al. The interleukin-6 receptor as a target for prevention of coronary heart disease: a mendelian randomisation analysis. Lancet 379, 1214–1224. https://doi.org/10.1016/s0140-6736(12)60110-x (2012).
Held, C. et al. Inflammatory biomarkers interleukin-6 and C-reactive protein and outcomes in stable coronary heart disease: experiences from the stability (stabilization of atherosclerotic plaque by initiation of darapladib therapy) trial. J. Am. Heart Assoc. https://doi.org/10.1161/jaha.116.005077 (2017).
Ridker, P. M. et al. Antiinflammatory therapy with canakinumab for atherosclerotic disease. N. Engl. J. Med. 377, 1119–1131. https://doi.org/10.1056/NEJMoa1707914 (2017).
Shephard, R. J. & Shek, P. N. Cold exposure and immune function. Can. J. Physiol. Pharmacol. 76, 828–836. https://doi.org/10.1139/cjpp-76-9-828 (1998).
Steptoe, A., Hamer, M. & Chida, Y. The effects of acute psychological stress on circulating inflammatory factors in humans: a review and meta-analysis. Brain Behav. Immun. 21, 901–912. https://doi.org/10.1016/j.bbi.2007.03.011 (2007).
Kop, W. J. et al. Effects of acute mental stress and exercise on inflammatory markers in patients with coronary artery disease and healthy controls. Am. J. Cardiol. 101, 767–773. https://doi.org/10.1016/j.amjcard.2007.11.006 (2008).
Nijm, J., Kristenson, M., Olsson, A. G. & Jonasson, L. Impaired cortisol response to acute stressors in patients with coronary disease. Implications for inflammatory activity. J. Intern. Med. 262, 375–384. https://doi.org/10.1111/j.1365-2796.2007.01817.x (2007).
Bethin, K. E., Vogt, S. K. & Muglia, L. J. Interleukin-6 is an essential, corticotropin-releasing hormone-independent stimulator of the adrenal axis during immune system activation. Proc. Natl. Acad. Sci. USA 97, 9317–9322. https://doi.org/10.1073/pnas.97.16.9317 (2000).
Steensberg, A., Fischer, C. P., Keller, C., Moller, K. & Pedersen, B. K. IL-6 enhances plasma IL-1ra, IL-10, and cortisol in humans. Am. J. Physiol. Endocrinol. Metab. 285, E433–E437. https://doi.org/10.1152/ajpendo.00074.2003 (2003).
Stouthard, J. M. et al. Endocrinologic and metabolic effects of interleukin-6 in humans. Am. J. Physiol. 268, E813–E819. https://doi.org/10.1152/ajpendo.1995.268.5.E813 (1995).
Sternberg, E. M. Neuroendocrine regulation of autoimmune/inflammatory disease. J. Endocrinol. 169, 429–435. https://doi.org/10.1677/joe.0.1690429 (2001).
Silverman, M. N. & Sternberg, E. M. Glucocorticoid regulation of inflammation and its functional correlates: from HPA axis to glucocorticoid receptor dysfunction. Ann. N. Y. Acad. Sci. 1261, 55–63. https://doi.org/10.1111/j.1749-6632.2012.06633.x (2012).
Nikkheslat, N. et al. Insufficient glucocorticoid signaling and elevated inflammation in coronary heart disease patients with comorbid depression. Brain Behav. Immun. 48, 8–18. https://doi.org/10.1016/j.bbi.2015.02.002 (2015).
Iso, T. et al. Serum levels of fatty acid binding protein 4 and fat metabolic markers in relation to catecholamines following exercise. Clin. Biochem. 50, 896–902. https://doi.org/10.1016/j.clinbiochem.2017.05.021 (2017).
Fischer, C. P. Interleukin-6 in acute exercise and training: what is the biological relevance?. Exerc. Immunol. Rev. 12, 6–33 (2006).
Kasapis, C. & Thompson, P. D. The effects of physical activity on serum C-reactive protein and inflammatory markers: a systematic review. J. Am. Coll. Cardiol. 45, 1563–1569. https://doi.org/10.1016/j.jacc.2004.12.077 (2005).
Hammadah, M. et al. Inflammatory response to mental stress and mental stress induced myocardial ischemia. Brain Behav. Immun. 68, 90–97. https://doi.org/10.1016/j.bbi.2017.10.004 (2018).
Rooks, C. R. et al. Young women post-MI have higher plasma concentrations of interleukin-6 before and after stress testing. Brain Behav. Immun. 51, 92–98. https://doi.org/10.1016/j.bbi.2015.08.008 (2016).
Waller, C. et al. Blunted cortisol stress response and depression-induced hypocortisolism is related to inflammation in patients with CAD. J. Am. Coll. Cardiol. 67, 1124–1126. https://doi.org/10.1016/j.jacc.2015.12.031 (2016).
Tang, A. R. et al. Prolonged hypothalamic-pituitary-adrenal axis activation after acute coronary syndrome in the GENESIS-PRAXY cohort. Eur. J. Prev. Cardiol. 25, 65–72. https://doi.org/10.1177/2047487317734323 (2018).
Ronaldson, A. et al. Diurnal cortisol rhythm is associated with adverse cardiac events and mortality in coronary artery bypass patients. J. Clin. Endocrinol. Metab. 100, 3676–3682. https://doi.org/10.1210/jc.2015-2617 (2015).
Kumari, M., Shipley, M., Stafford, M. & Kivimaki, M. Association of diurnal patterns in salivary cortisol with all-cause and cardiovascular mortality: findings from the Whitehall II study. J. Clin. Endocrinol. Metab. 96, 1478–1485. https://doi.org/10.1210/jc.2010-2137 (2011).
Matthews, K., Schwartz, J., Cohen, S. & Seeman, T. Diurnal cortisol decline is related to coronary calcification: CARDIA study. Psychosom. Med. 68, 657–661. https://doi.org/10.1097/01.psy.0000244071.42939.0e (2006).
Silverman, M. N., Miller, A. H., Biron, C. A. & Pearce, B. D. Characterization of an interleukin-6- and adrenocorticotropin-dependent, immune-to-adrenal pathway during viral infection. Endocrinology 145, 3580–3589. https://doi.org/10.1210/en.2003-1421 (2004).
Carpenter, L. L. et al. Decreased adrenocorticotropic hormone and cortisol responses to stress in healthy adults reporting significant childhood maltreatment. Biol. Psychiatry 62, 1080–1087. https://doi.org/10.1016/j.biopsych.2007.05.002 (2007).
Heim, C., Ehlert, U. & Hellhammer, D. H. The potential role of hypocortisolism in the pathophysiology of stress-related bodily disorders. Psychoneuroendocrinology 25, 1–35. https://doi.org/10.1016/s0306-4530(99)00035-9 (2000).
Newman, C. B. et al. Statin safety and associated adverse events: a scientific statement from the American Heart Association. Arterioscler. Thromb. Vasc. Biol. 39, e38–e81. https://doi.org/10.1161/atv.0000000000000073 (2019).
Andrews, J. & Pruessner, J. C. The combined propranolol/TSST paradigm–a new method for psychoneuroendocrinology. PLoS ONE 8, e57567. https://doi.org/10.1371/journal.pone.0057567 (2013).
Gullestad, L., Dolva, L. O., Kjeldsen, S. E., Eide, I. & Kjekshus, J. Effect of beta-adrenergic blockade on hormonal responses during continuous and intermittent exercise. Cardiovasc. Drugs Ther. 3, 63–71. https://doi.org/10.1007/bf01881530 (1989).
van der Pompe, G., Bernards, N., Meijman, T. F. & Heijnen, C. J. The effect of depressive symptomatology on plasma cortisol responses to acute bicycle exercise among post-menopausal women. Psychiatry Res. 85, 113–117. https://doi.org/10.1016/s0165-1781(98)00132-2 (1999).
Kidd, T., Carvalho, L. A. & Steptoe, A. The relationship between cortisol responses to laboratory stress and cortisol profiles in daily life. Biol. Psychol. 99, 34–40. https://doi.org/10.1016/j.biopsycho.2014.02.010 (2014).
van Eck, M. M., Nicolson, N. A., Berkhof, H. & Sulon, J. Individual differences in cortisol responses to a laboratory speech task and their relationship to responses to stressful daily events. Biol. Psychol. 43, 69–84. https://doi.org/10.1016/0301-0511(95)05159-7 (1996).
Kudielka, B. M., Schommer, N. C., Hellhammer, D. H. & Kirschbaum, C. Acute HPA axis responses, heart rate, and mood changes to psychosocial stress (TSST) in humans at different times of day. Psychoneuroendocrinology 29, 983–992. https://doi.org/10.1016/j.psyneuen.2003.08.009 (2004).
Nguyen, P. K., Nag, D. & Wu, J. C. Sex differences in the diagnostic evaluation of coronary artery disease. J. Nucl. Cardiol. 18, 144–152. https://doi.org/10.1007/s12350-010-9315-2 (2011).
Hyafil, F. et al. EANM procedural guidelines for myocardial perfusion scintigraphy using cardiac-centered gamma cameras. Eur. J. Hybrid Imag. 3, 11. https://doi.org/10.1186/s41824-019-0058-2 (2019).
Slomka, P. J. et al. Automated quantification of myocardial perfusion SPECT using simplified normal limits. J. Nucl. Cardiol. 12, 66–77. https://doi.org/10.1016/j.nuclcard.2004.10.006 (2005).
Nakazato, R. et al. Quantitative upright-supine high-speed SPECT myocardial perfusion imaging for detection of coronary artery disease: correlation with invasive coronary angiography. J. Nucl. Med. 51, 1724–1731. https://doi.org/10.2967/jnumed.110.078782 (2010).
Jensen, M. A., Hansen, A. M., Abrahamsson, P. & Norgaard, A. W. Development and evaluation of a liquid chromatography tandem mass spectrometry method for simultaneous determination of salivary melatonin, cortisol and testosterone. J. Chromatogr. B Analyt. Technol. Biomed. Life Sci. 879, 2527–2532. https://doi.org/10.1016/j.jchromb.2011.07.005 (2011).
Acknowledgements
This study has been financially supported by Heart-Lung Foundation, Sweden (20180436), Swedish Research Council (2018-03232), and Swedish Grandlodge of Freemasonry (20191209-141318). The authors also wish to express their deep gratitude to all the patients who participated in this study.
Funding
Open Access funding provided by Linköping University Library.
Author information
Authors and Affiliations
Contributions
All authors contributed to study design. Z.M., A.D., and A.K.L. collected the data. Z.M., A.D., E.O., P.L., A.K.L. and L.J. analyzed and interpreted the data. Z.M. and L.J. wrote the manuscript. All authors reviewed the manuscript.
Corresponding author
Ethics declarations
Competing interests
The authors declare no competing interests.
Additional information
Publisher's note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary information
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
Mahmood, Z., Davidsson, A., Olsson, E. et al. The effect of acute exercise on interleukin-6 and hypothalamic–pituitary–adrenal axis responses in patients with coronary artery disease. Sci Rep 10, 21390 (2020). https://doi.org/10.1038/s41598-020-78286-2
Received:
Accepted:
Published:
DOI: https://doi.org/10.1038/s41598-020-78286-2
- Springer Nature Limited