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Case Report

Angina Simultaneously Diagnosed with the Recurrence of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome

1
Department of General Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama 700-8558, Japan
2
Center for Graduate Medical Education, Okayama University Hospital, Okayama 700-8558, Japan
*
Author to whom correspondence should be addressed.
Submission received: 10 February 2021 / Revised: 1 March 2021 / Accepted: 4 March 2021 / Published: 6 March 2021
(This article belongs to the Section Pathology and Molecular Diagnostics)

Abstract

:
Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) mainly affects young adults and can have a potential impact on social functioning. As this syndrome is associated with endothelial dysfunction, the heart can be damaged via ischemia due to endothelial damage. This might potentially lead to heart failure, which accounts for approximately 20% of deaths among patients with ME/CFS. While cardiac ischemia is thought be a pathophysiologically important manifestation of this syndrome, this is not yet reported. Herein, we present a case of a young female with newly diagnosed vasospastic or microvascular angina and concurrent exacerbation of ME/CFS severity. Her anginal symptoms, including exertional chest pain and transient chest discomfort, mimicked those of ME/CFS but were relieved after the administration of a calcium channel blocker. We emphasize the possibility of concurrent angina and exacerbation of ME/CFS and the importance of detecting cardiac ischemia to avoid unfavorable outcomes.

1. Introduction

Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is characterized by extreme fatigue that lasts at least 6 months, and post-exertional malaise [1]. There are several diagnostic criteria like the Fukuda Case definition for CFS [1], Canadian Consensus Criteria for ME/CFS [2], and the Institute of Medicine 2015 Diagnostic Criteria [3]. For a diagnosis to be made, some associated symptoms such as autonomic symptoms (e.g., orthostatic hypotension), neurocognitive symptoms (e.g., impaired memory and attention deficit), immune symptoms (e.g., lymphadenopathy, sore throat, and fever), and other symptoms (e.g., sleep disturbance, headache, muscle pain, and multi-joint pain) are often required, along with ruling out the presence of any medical conditions that could explain the presence of fatigue.
In terms of epidemiology, more than 1% of the population might be affected by ME/CFS, which preferentially affects the younger female population. Prior studies conducted in Norway reported two peaks for the age of onset—10–19 and 30–39 years [4,5].
While it is well-established that ME/CFS imposes a profound burden on society, its etiology and pathophysiology are not yet fully understood. Endothelial dysfunction is a pathological manifestation that is associated with this disease, and it plays a major role in the development of angina and other coronary diseases [6]. Previous studies also suggest that ME/CFS is a potential cause of cardiac ischemia [7,8]. Lerner et al. reported repeated negative T-wave changes among patients with ME/CFS [9]. However, to our knowledge, no prior studies reported the new diagnosis of coronary disease in patients with preexisting ME/CFS. Herein, we report a case of ME/CFS in which microvascular angina or vasospastic angina with an electrocardiogram (ECG) change was newly diagnosed in a patient with concurrent exacerbation of ME/CFS. This report highlights the importance of cardiac investigation for obtaining a better insight into this condition and assessing subsequent patient prognosis.

2. Case Presentation

A 23-year-old single woman, who was previously healthy and used to play football, was referred and admitted to our department for the investigation of chronic fatigue, which persisted for 9 months. She first started to feel an excessive fatigue even when resting, which often prevented her from stepping out, 9 months earlier. She complained that daily activities such as shopping and housework were enough to deteriorate the fatigue. In addition to fatigue, she had insufficient sleep, mood disturbances, and difficulty in concentrating as neurocognitive symptoms; a slight fever as the only immune symptom; myalgia, multi-joint pain, and headache which does not respond to NSAIDs, dyspnea, and palpitations. There were no signs of sore throat or lymphadenopathy. The results of her ECG, chest X-ray, and blood tests (including liver function test, thyroid function test, and adrenal function test) were all within the normal ranges on admission. There were no signs of infection, organ failure, rheumatologic disease, or malignancy. A diagnosis of depression was ruled out by a psychiatrist. Schizophrenia, manic-depressive illness, substance abuse, eating disorder, and proven organic brain disease were also excluded. The 30-min head-up tilt test indicated that the patient had an orthostatic disorder as an autonomic manifestation. Meeting all of the Fukuda criteria, Canadian Consensus criteria for ME/CFS, and the Institute of Medicine criteria, she was eventually diagnosed with ME/CFS [1,2,3]. Her performance status (PS) (Table 1) was classified as 5, considering that she was not able to work or play football as usual [10]. Kampo medicine was subsequently prescribed, and her condition gradually improved. She recovered 9 months after admission and was able to resume work. She also married about 2 months after resuming work. However, the symptoms recurred 1 year after her initial admission, and her fatigue worsened. She experienced transient chest pain associated with relatively light labor, such as shopping; she did not initially seek treatment, as she thought that these symptoms were due to an exacerbation of ME/CFS.
Her symptoms continued to worsen, and her activities of daily living were significantly impaired; for example, she reported being only able to eat a small portion of her regular meal every day. She was re-admitted to our department for the second time to improve her nutritional status, 18 months after the first admission. The results of her ECG (Figure 1), chest X-ray, and blood tests remained normal on her second admission. Her PS had increased to 8, and ibudilast, vitamin C, and coenzyme Q10 were prescribed. During the second hospitalization, she complained of transient chest discomfort lasting 1 to 2 h, which repeatedly occurred at night or early in the morning; negative ST changes in leads II, III, and aVF were observed on ECG (Figure 2), and the serum troponin was negative. Plasma brain natriuretic peptide level was 4 pg/mL, and echocardiography finding was almost normal. She was then referred to a cardiologist for further investigations. Twenty-four-hour holter monitoring showed ST depression with tachycardia, when the patient felt an exacerbation of fatigue from the baseline (Figure 3). A two-step exercise provoked wide ST depression and negative T waves on ECG (Figure 4). A coronary angiogram was not performed, as it was considered too invasive for an emaciated patient; furthermore, the patient did not consent to this procedure. She was diagnosed with vasospastic or microvascular angina and prescribed a calcium channel blocker, in addition to previous Kampo medicines. Although other ME/CFS symptoms remained, the patient was discharged after approximately 1 month of hospitalization, as she gradually showed slight improvement in food intake, as well as decrease in anginal symptoms.

3. Discussion

In this report, we presented a case of successfully diagnosed angina masked by ME/CFS deterioration. Endothelial dysfunction was previously correlated to ME/CFS and shown to reflect disease severity [11]. While the pathophysiology of ME/CFS is not yet fully elucidated [12,13], autonomic nervous system dysregulation, immunological disturbance, viral infections, and metabolic changes were proposed as underlying mechanisms of this malady [14,15,16,17]. Indeed, previous studies cited all mechanisms as being responsible for endothelial dysfunction [18,19,20,21]. On the other hand, endothelial damage is also correlated with vasospastic or microvascular angina. Endothelial dysfunction might lead to hyperreactivity of vascular smooth muscle cells via downregulation of vasodilators (e.g., nitric monoxide) and upregulation of vasoconstrictors (e.g., endothelin-1), resulting in coronary spasm [18].
Thus, ME/CFS might be associated with an ischemic heart disease, as a malfunctioning endothelium is associated with ME/CFS, and is also closely related to the development of coronary disease [6,7,8]. In fact, a prior study reported that a significantly larger proportion of patients with ME/CFS with angina-like symptoms showed a negative T-wave on 24-h ECG monitoring, compared to patients with the same symptoms but without ME/CFS [9]. Furthermore, any ECG changes are indicative of a higher risk of coronary heart disease and chronic heart failure. Indeed, heart failure accounts for approximately one-fifth of deaths among patients with ME/CFS [7,19].
Notably, in the present case, an ECG change attributed to angina was recorded in concurrence with the recurrence of ME/CFS (which had a 3-year history) and deterioration of PS. Endothelial dysfunction was reported to reduce cerebral blood flow, which is correlated with disease severity [20,21], and results in further fatigue [22]. Therefore, endothelial function might be potentially used to assist the diagnosis of ME/CFS, and serve as an indicator of its severity and the risk of complications [7,11]. The early initiation of treatment is important to improve the prognosis in patients with angina [23].
Additionally, in the present case, exacerbated fatigue was associated with ECG changes, instead of chest discomfort. Although exhaustion is the central symptom of ME/CFS, patients might commonly complain of angina-like symptoms [24]. This suggests that coronary involvement is overlooked in cases of ME/CFS, as the symptoms of ME/CFS might mimic angina, and vice versa. Therefore, physicians should conduct cardiac examinations, including ECG, not only when patients complain of chest pain but also when excessive exhaustion is evident. Such examinations should also be routinely conducted to avoid the potential risk of missing the diagnosis of heart ischemia.
In conclusion, we experienced an interesting case in which vasospastic or microvascular angina was detected along with concurrent exacerbation of ME/CFS severity. This suggested that cardiac manifestations can appear as a result of deterioration. As the symptoms experienced by patients with ME/CFS might mimic those of angina, diagnosis of the latter might be easily missed. Thus, it is pertinent that cardiac examinations be conducted in such patients to rule out the possibility of heart ischemia.

Author Contributions

K.L. treated the patient and wrote the manuscript. Y.O., Y.N., D.O., K.H., and K.U. also treated the patient and revised the manuscript. M.O., H.K. and F.O. revised the manuscript. All authors have read and agreed to the published version of the manuscript.

Funding

The research received no external funding.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Written informed consent has been obtained from the patient(s) to publish this paper.

Data Availability Statement

The data presented in this study are available on request from the corresponding author.

Acknowledgments

We are grateful to Hirohiko Kuratsune for his clinical advice.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Fukuda, K.; Straus, S.E.; Hickie, I.; Sharpe, M.C.; Dobbins, J.G.; Komaroff, A. The Chronic fatigue syndrome: A comprehensive approach to its definition and study. Interantional Chronic Fatigue Syndrome Study Group. Ann. Intern. Med. 1994, 121, 953–959. [Google Scholar] [CrossRef] [PubMed]
  2. Carruthers, B.M.; Jain, A.K.; De Meirleir, K.L.; Peterson, D.L.; Klimas, N.G.; Lerner, A.M.; Bested, A.C.; Flor-Henry, P.; Joshi, P.; Powles, A.C.P.; et al. Myalgic Encephalomyelitis/Chronic Fatigue Syndrome. J. Chronic Fatigue Syndr. 2003, 11, 7–115. [Google Scholar] [CrossRef]
  3. Clayton, E.W. Beyond Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: An IOM Report on Redefining an Illness. JAMA 2015, 313, 1101–1102. [Google Scholar] [CrossRef]
  4. Kawakami, N.; Iwata, N.; Fujihara, S.; Kitamura, T. Prevalence of chronic fatigue syndrome in a community population in Japan. Tohoku J. Exp. Med. 1998, 186, 33–41. [Google Scholar] [CrossRef] [Green Version]
  5. Bakken, I.J.; Tveito, K.; Gunnes, N.; Ghaderi, S.; Stoltenberg, C.; Trogstad, L.; Håberg, S.E.; Magnus, P. Two age peaks in the incidence of chronic fatigue syndrome/myalgic encephalomyelitis: A population-based registry study from Norway 2008–2012. BMC Med. 2014, 12, 167. [Google Scholar] [CrossRef] [Green Version]
  6. Matsuzawa, Y.; Lerman, A. Endothelial dysfunction and coronary artery disease: Assessment, prognosis, and treatment. Coron. Artery Dis. 2014, 25, 713–724. [Google Scholar] [CrossRef] [Green Version]
  7. Maes, M.; Twisk, F.N.M. Why myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) may kill you: Disorders in the inflammatory and oxidative and nitrosative stress (IO&NS) pathways may explain cardiovascular disorders in ME/CFS. Neuro Endocrinol. Lett. 2009, 51, 677–693. [Google Scholar]
  8. Newton, D.J.; Kennedy, G.; Chan, K.K.F.; Lang, C.C.; Belch, J.J.F.; Khan, F. Large and small artery endothelial dysfunction in chronic fatigue syndrome. Int. J. Cardiol. 2012, 154, 335–336. [Google Scholar] [CrossRef] [PubMed]
  9. Lerner, A.M.; Lawrie, C.; Dworkin, H.S. Repetitively negative changing T waves at 24-h electrocardiographic monitors in patients with the chronic fatigue syndrome. Left ventricular dysfunction in a cohort. Chest 1993, 104, 1417–1421. [Google Scholar] [CrossRef] [Green Version]
  10. Miwa, K. Variability of postural orthostatic tachycardia in patients with myalgic encephalomyelitis and orthostatic intolerance. Heart Vessels 2016, 31, 1522–1528. [Google Scholar] [CrossRef]
  11. Scherbakov, N.; Szklarski, M.; Hartwig, J.; Sotzny, F.; Lorenz, S.; Meyer, A.; Grabowski, P.; Doehner, W.; Scheibenbogen, C. Peripheral endothelial dysfunction in myalgic encephalomyelitis/chronic fatigue syndrome. ESC Heart Fail. 2020, 7, 1064–1071. [Google Scholar] [CrossRef]
  12. Cortes Rivera, M.; Mastronardi, C.; Silva-Aldana, C.T.; Arcos-Burgos, M.; Lidbury, B.A. Myalgic encephalomyelitis/chronic fatigue syndrome: A comprehensive review. Diagnostics 2019, 9, 91. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  13. Komaroff, A.L. Advances in understanding the pathophysiology of chronic fatigue syndrome. JAMA 2019, 322, 499–500. [Google Scholar] [CrossRef] [PubMed]
  14. Komaroff, A.L.; Cho, T.A. Role of infection and neurologic dysfunction in chronic fatigue syndrome. Semin. Neurol. 2011, 31, 325–337. [Google Scholar] [CrossRef] [Green Version]
  15. Naviaux, R.K.; Naviaux, J.C.; Li, K.; Bright, A.T.; Alaynick, W.A.; Wang, L.; Baxter, A.; Nathan, N.; Anderson, W.; Gordon, E. Metabolic features of chronic fatigue syndrome. Proc. Natl. Acad. Sci. USA 2016, 113, E5472–E5480. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  16. Amiya, E.; Watanabe, M.; Komuro, I. The relationship between vascular function and the autonomic nervous system. Ann. Vasc. Dis. 2014, 7, 109–119. [Google Scholar] [CrossRef] [Green Version]
  17. Jernigan, P.L.; Makley, A.T.; Hoehn, R.S.; Edwards, M.J.; Pritts, T.A. The role of sphingolipids in endothelial barrier function. Biol. Chem. 2015, 396, 681–691. [Google Scholar] [CrossRef] [PubMed]
  18. Hubert, A.; Seitz, A.; Pereyra, V.M.; Bekeredjian, R.; Sechtem, U.; Ong, P. Coronary artery spasm: The interplay between endothelial dysfunction and vascular smooth muscle cell hyperreactivity. Eur. Cardiol. 2020, 15, e12. [Google Scholar] [CrossRef]
  19. De Bacquer, D.; De Backer, G.; Kornitzer, M.; Blackburn, H. Prognostic value of ECG findings for total, cardiovascular disease, and coronary heart disease death in men and women. Heart 1998, 80, 570–577. [Google Scholar] [CrossRef] [Green Version]
  20. Sabayan, B.; Westendorp, R.G.; van der Grond, J.; Stott, D.J.; Sattar, N.; van Osch, M.J.P.; van Buchem, M.A.; de Craen, A.J.M. Markers of endothelial dysfunction and cerebral blood flow in older adults. Neurobiol. Aging 2014, 35, 373–377. [Google Scholar] [CrossRef] [PubMed]
  21. Van Campen, C.L.M.C.; Rowe, P.C.; Visser, F.C. Cerebral blood flow is reduced in severe myalgic encephalomyelitis/chronic fatigue syndrome patients during mild orthostatic stress testing: An exploratory study at 20 degrees of head-up tilt testing. Healthcare 2020, 8, 169. [Google Scholar] [CrossRef] [PubMed]
  22. Fan, J.L.; Kayser, B. Fatigue and exhaustion in hypoxia: The role of cerebral oxygenation. High Alt. Med. Biol. 2016, 17, 72–84. [Google Scholar] [CrossRef] [PubMed]
  23. Yasue, H.; Takizawa, A.; Nagao, M.; Nishida, S.; Horie, M.; Kubota, J.; Omote, S.; Takaoka, K.; Okumura, K. Long-term prognosis for patients with variant angina and influential factors. Circulation 1988, 78, 1–9. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  24. Jason, L.A.; Torres-Harding, S.R.; Carrico, A.W.; Taylor, R.R. Symptom occurrence in persons with chronic fatigue syndrome. Biol. Psychol. 2002, 59, 15–27. [Google Scholar] [CrossRef]
Figure 1. Resting electrocardiogram on second admission. No abnormal electrocardiogram changes were detected on admission.
Figure 1. Resting electrocardiogram on second admission. No abnormal electrocardiogram changes were detected on admission.
Diagnostics 11 00460 g001
Figure 2. Electrocardiogram obtained when the patient complained of transient chest discomfort. ST depression and negative T waves were recorded in leads II, III, and aVF.
Figure 2. Electrocardiogram obtained when the patient complained of transient chest discomfort. ST depression and negative T waves were recorded in leads II, III, and aVF.
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Figure 3. 24-h holter monitoring. ST depression and negative T waves with tachycardia were recorded via 24-h holter monitoring; this was concurrent with the patient’s report of exacerbated fatigue.
Figure 3. 24-h holter monitoring. ST depression and negative T waves with tachycardia were recorded via 24-h holter monitoring; this was concurrent with the patient’s report of exacerbated fatigue.
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Figure 4. Two-step exercise electrocardiogram. Two-step exercise provoked wide ST depression and negative T waves on the electrocardiogram. I, II, III, aVL, aVR and aVF are each corresponding to six limb leads, and V1, V2, V3, V4, V5 and V6 are each corresponding to six precordial leads.
Figure 4. Two-step exercise electrocardiogram. Two-step exercise provoked wide ST depression and negative T waves on the electrocardiogram. I, II, III, aVL, aVR and aVF are each corresponding to six limb leads, and V1, V2, V3, V4, V5 and V6 are each corresponding to six precordial leads.
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Table 1. Performance status scoring criteria.
Table 1. Performance status scoring criteria.
PS 0The patient can perform the usual activities of daily living and social activities without malaise.
PS 1The patient often feels fatigue.
PS 2The patient often needs to rest because of general malaise or fatigue.
PS 3The patient cannot work or perform usual activities for a few days in a month.
PS 4The patient cannot work or perform usual activities for a few days in a week.
PS 5The patient cannot work or perform usual activities but can perform light work.
PS 6The patient needs daily rest but can perform light work on a “good day”.
PS 7The patient can take care of himself/herself but cannot perform usual duties.
PS 8The patient needs help to take care of himself/herself.
PS 9The patient needs to rest the whole day and cannot take care of himself/herself without help.
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MDPI and ACS Style

Li, K.; Otsuka, Y.; Nakano, Y.; Omura, D.; Hasegawa, K.; Obika, M.; Ueda, K.; Kataoka, H.; Otsuka, F. Angina Simultaneously Diagnosed with the Recurrence of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome. Diagnostics 2021, 11, 460. https://0-doi-org.brum.beds.ac.uk/10.3390/diagnostics11030460

AMA Style

Li K, Otsuka Y, Nakano Y, Omura D, Hasegawa K, Obika M, Ueda K, Kataoka H, Otsuka F. Angina Simultaneously Diagnosed with the Recurrence of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome. Diagnostics. 2021; 11(3):460. https://0-doi-org.brum.beds.ac.uk/10.3390/diagnostics11030460

Chicago/Turabian Style

Li, Koki, Yuki Otsuka, Yasuhiro Nakano, Daisuke Omura, Kou Hasegawa, Mikako Obika, Keigo Ueda, Hitomi Kataoka, and Fumio Otsuka. 2021. "Angina Simultaneously Diagnosed with the Recurrence of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome" Diagnostics 11, no. 3: 460. https://0-doi-org.brum.beds.ac.uk/10.3390/diagnostics11030460

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