Cardiovascular characteristics of chronic fatigue syndrome

  • Authors:
    • Sara Bozzini
    • Andrea Albergati
    • Enrica Capelli
    • Lorenzo Lorusso
    • Carmine Gazzaruso
    • Gabriele Pelissero
    • Colomba Falcone
  • View Affiliations

  • Published online on: November 28, 2017     https://doi.org/10.3892/br.2017.1024
  • Pages: 26-30
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Abstract

Patients with chronic fatigue syndrome (CFS) commonly exhibit orthostatic intolerance. Abnormal sympathetic predominance in the autonomic cardiovascular response to gravitational stimuli was previously described in numerous studies. The aim of the current study was to describe cardiological and clinical characteristics of Italian patients with CFS. All of the patients were of Caucasian ethnicity and had been referred to our center, the Cardiology Department of the University Hospital of Pavia (Pavia, Italy) with suspected CFS. A total of 44 patients with suspected CFS were included in the present study and the diagnosis was confirmed in 19 patients according to recent clinical guidelines. The characteristics at baseline of the population confirm findings from various previous reports regarding the prevalence in females with a female to male ratio of 4:1, the age of onset of the pathology and the presence of previous infection by the Epstein-Barr virus, cytomegalovirus and other human herpesviruses. Despite the current data indicating that the majority of the cardiological parameters investigated are not significantly different in patients with and without CFS, a significant association between the disease and low levels of blood pressure was identified. Other pilot studies revealed a higher prevalence of hypotension and orthostatic intolerance in patients with CFS. Furthermore, many of the CFS symptoms, including fatigue, vertigo, decreased concentration, tremors and nausea, may be explained by hypotension.

Introduction

Chronic fatigue syndrome (CFS) is characterized by a strong and permanent fatigue of unknown cause, which limits functional capacity and produces varying degrees of disability (1). CFS is associated, in addition to fatigue, to a wide spectrum of symptoms, including joint and muscle pain, headaches, anxiety, depressive symptoms, cognitive and sleep disorders and intolerance to physical exertion. Establishing a diagnosis has long been inhibited due to the lack of knowledge regarding the etiopathogenesis of CFS, and the difficulty in obtaining an objective and quantitative assessment of the symptoms. In recent years, due to the variety of established criteria, it has been possible to more accurately delineate CFS, which has contributed to an improved understanding of its clinical picture, and the development of potential novel therapeutic interventions (2,3).

Specific investigations are required for the cardiovascular and respiratory systems. Patients with CFS commonly exhibit orthostatic intolerance, and abnormal sympathetic predominance in the autonomic cardiovascular response to gravitational stimuli was previously described (4). In addition, certain studies investigate the role of sympathetic activity in CFS patients via the analysis of heart rate variability; however, the results are inconclusive (5). Furthermore, a small left ventricular size with a low cardiac output was observed in patients with CFS, in whom orthostatic intolerance appears to be extremely common (6). In addition, in adolescents, CFS was characterized by reduced systolic blood pressure variability and sympathetic predominance of baroreflex heart rate control during orthostatic stress (7).

Thus, the aim of the present study was to evaluate the cardiological characteristics of Italian patients with suspected CFS to identify potential diagnostic parameters. An improved understanding of these characteristics is important for detecting potential risk factors and predictors associated with CFS, and to improve health care prevision.

Materials and methods

Patients

The patients recruited for the present study were all of Caucasian ethnicity, and were referred from March 2011 to December 2014 to the Cardiology Department of the University Hospital of Pavia (Italy) with suspected CFS. For inclusion in the current study, fatigue must have been present for at least 6 months. Any accompanying symptoms should not have preceded the onset of fatigue and be persistent or recurring for at least 6 months. The current study was in accordance with the guidelines of the Helsinki Declaration for Human Research, and was approved by the ethics committee of the University of Pavia. Subjects exhibiting a chronic disease (such as an allergy, skin disease, vascular disease or diabetes), diagnosis of fibromyalgia, irritable bowel syndrome or using drugs on a regular basis were excluded. Written informed consent was obtained from all the participants.

Data collection

The entire population underwent the following examinations: Medical history and family anamnesis, blood test, physical examination, blood pressure measurement, echocardiographic examination, basal 12-lead electrocardiogram and continuous electrocardiographic monitoring for 24 h, stress testing cycle ergometer and blood pressure monitoring 24 h. All patients then underwent neurological examination, which established the diagnosis of CFS.

Sociodemographic data included patient age, sex, body mass index and ethnicity. Outcomes of interest regarding onset of the illness included age of onset (age at which the patient first experienced symptoms) and the duration of illness (time in years elapsed since the onset of illness). In addition, the current study accounted for the events and exposure to infectious agents that the participants were subjected to prior to illness.

Ergometric stress test

Exercise stress testing was performed as previously described (8). Briefly, a multistage-bicycle-ergometer exercise stress test was performed with the patients in the supine position with an initial workload of 25 W and successive increments of 25 W every 3 min at a pedalling frequency of 60 rpm. A standard 12-lead electrocardiography was taken before and at the end of each stage, and at the end of the exercise. Leads V4, V5, V6 were monitored during exercise. The systolic and diastolic blood pressures were measured using a sphygmomanometer at basal conditions, at the end of each interval, at the maximum quantity of work and every 3 min in the recovery phase. During the test, the patients were interrogated continuously regarding their symptoms in terms of pain, dyspnea, vertigo and tachycardia, as well as other symptoms. The test was interrupted if one of these conditions manifested: Appearance of chest pain and/or dyspnea, exhaustion, ST segment elevation ≥1 mm without diagnostic Q waves, ST-segment depression ≥2 mm, repetitive arrhythmias or a drop in systolic blood pressure >10 mmHg. The test was considered positive in the presence of down sloping ST-segment depression ≥1 mV below the baseline, at least 0.06–0.08 sec after the QRS complex J point in multiple leads or ST-segment elevation.

Prior to the exercise test, a pharmacological washout was performed. Calcium-channel antagonists and nitrates were halted 48 h before the test. β-Blockers were gradually reduced and subsequently stopped 1 week before the examination. Patients who were taking Digitalis were not included in the current study.

Heart rate variability (HRV) parameters

Twenty-four-hour Holter electrocardiogram (ECG) monitoring was performed in all patients enrolled in the study, using a three-channel tape recorder (Cardioline Click Holter Recorder; Cardioline SpA, Trento, Italy). Each tape was manually corrected for noise and ectopic beats. Mean RR intervals and the following HRV parameters were calculated as 24-h values: Standard deviation of all NN interval, square root of the mean of the sum of the square of the differences between adjacent NN intervals and number of adjacent NN intervals differing by >50 msec divided by the total number of all NN intervals (pNN50).

Echocardiography

Conventional echocardiography and tissue EcocolorDoppler imaging were performed. M-mode, two-dimensional and Doppler echocardiographic examinations were performed using an ultrasonographic system (MyLab™30Gold Cardiovascular; Esaote SpA, Genoa, Italy) equipped with a multi-frequency transduction. The left ventricle (LV) ejection fraction was calculated from apical two- and four-chamber views using LV volumes according to the modified biplane Simpson's rule. LV end-diastolic volume and LV end-systolic volume were indexed to body surface area. Peak early (E) and late (A) filling velocities, the E:A ratio, and E velocity deceleration time were measured from the LV-inflow pattern at the tips of the mitral valve at the end of expiration. Measurement of systolic pulmonary artery pressure was performed using the maximal regurgitant velocity at the tricuspid valve via continuous wave Doppler.

Statistical analysis

Continuous variables were expressed as means ± standard deviation for normally distributed data and they were expressed as medians ± standard deviation otherwise. Discrete data were instead analyzed using the χ2 test. P<0.05 was considered to indicate a statistically significant difference.

Results

Clinical and demographic aspects of the study population

A total of 44 patients with suspected CFS were included in the current study (9 males and 35 females; mean age, 40±13 years) as presented in Table I.

Table I.

Clinical characteristics of the included population.

Table I.

Clinical characteristics of the included population.

VariableTotal population (n=44)Patients with confirmed diagnosis of CFS (n=19)Patients without CFS (n=25)
Males, n (%)9 (20%)3 (16%)6 (24%)
Age, years40±1340±1441±12
Body mass index23.7±6.223.6±5.723.8±6.9
Age of onset31±1328±1334±12
Viral infection, n (%)18 (41%)6 (32 %)12 (48 %)

[i] CFS, chronic fatigue syndrome.

The mean age of onset of symptoms was 31±13 years. In the current population, the onset of symptoms was fatigue/weakness in nine patients (20%), fever in five patients (11%), flu-like syndrome in two patients (5%), arthromyalgia in one patient (2%), neurological problems in 30 patients (68%), dyspnea in three patients (7%) and viral infectious episodes in seven patients (16%). In addition, one patient developed symptoms following an intestinal infectious episode and one patient developed symptoms following a surgical intervention. The following were considered as neurological problems: Amnesias, cognitive impairment, difficulty concentrating, confusion, headaches and vertigo.

Persistent symptoms included fatigue in 26 patients (59%); unrefreshing sleep in 10 patients (23%); pain (such as headaches) in eight patients (18%); arthromyalgia/myalgia in 14 patients (32%); fever in nine patients (20%), major depression in 11 patients (25%), and mood disorders and anxiety in 12 patients (27%). Two patients (4%) presented with a sore throat and five patients (11%) exhibited lymphadenopathy. The accompanying symptoms observed in these patients underline the heterogeneity of CFS.

Viral serology testing was performed on 3-ml blood samples of all the patients at the time of recruitment and provided evidence of exposure to the Epstein-Barr virus (EBV), cytomegalovirus (CMV) and other human herpesviridae (HHV). In the present study, the presence of past exposure to EBV was observed in 10 patients, seven patients exhibited previous CMV infection, and five patients exhibited antibodies for EBV and CMV, indicative of previous infection with both.

Table II presents the biochemical parameters that were evaluated in the current study. No differences in the concentration of hemoglobin and hematocrit were observed. Furthermore, thyroid function appears to be similar in the two populations, as were the lipid, glucose and creatinine levels. Certain differences were observed in the muscle profiles, but the differences were not statistically significant.

Table II.

Biochemical characteristics of the study population.

Table II.

Biochemical characteristics of the study population.

VariableTotal population (n=44)Patients with confirmed diagnosis of CFS (n=19)Patients without CFS (n=25)P-value
Hemoglobin (g/dl)13.1±1.612.9±1.212.6 ±1.9Ns
Hematocrit (%)40±3.8%39.7±2.7%40.4±4.6Ns
Free T3 (pg/ml)3.6±0.63.22±0.73.58±0.4Ns
Free T4 (ng/dl)2.7±3.52.4±1.92.9±4.4Ns
Thyroid-stimulating hormone (microUI/ml)2±1.11.96±0.91.96±1.4Ns
Potassium (mEq/l)4.3±0.44.4±0.44.2±0.4Ns
Creatine kinase Mb (U/l)11.5±6.815.5±3.57.5±3.8Ns
Creatine kinase (U/l)66.3±32.861.6±16.272.5±33.1Ns
Lactate dehydrogenase (U/l)283.1±90.6291.3±75.8273.2±114.6Ns
Total cholesterol (mg/dl)193.9±40.7181.6 ±24.9205.16±49.5Ns
High-density lipoprotein cholesterol (mg/dl)62.3±12.657.3±13.765.5±11.3Ns
Triglycerides (mg/dl)77.7±24.879.3±24.276.1±26.6Ns
Glycaemia (mg/dl)89±11.489.4±10.688.6±12.4Ns
Creatinine (mg/dl)0.8±0.20.8±0.20.7±0.1Ns

[i] CFS, chronic fatigue syndrome; Ns, not significant.

In 19 of the 44 patients with suspected CFS the diagnosis was confirmed according to recent clinical guidelines (9). Of these, three were male and 16 were female (mean age, 40±14 years). The mean age of onset of symptoms was 28±13 years and the cause of this occurrence was viral infection (n=6) and a flu-like episode (n=5). The two groups were comparable regarding sex and gender.

Cardiological characteristics

The mean heart rate at baseline in the patients was 79±13 bpm (82±10 bpm in patients with CFS and 77±15 bpm in patients without CFS).

The Holter ECG over 24 h identified the presence of rare/sporadic ventricular or supraventricular arrhythmias in 14 patients. The HRV in patients with and without confirmed diagnosis of CFS were evaluated using ECG monitoring over 24 h. No significant differences were observed for the HRV parameters between the two subpopulations (Table III).

Table III.

Cardiovascular characteristics of patients grouped according to confirmed diagnosis of CFS.

Table III.

Cardiovascular characteristics of patients grouped according to confirmed diagnosis of CFS.

CharacteristicPatients with confirmed diagnosis of CFS (n=19)Patients without CFS (n=25)P-value
Heart rate at baseline (bpm)82±1077±15Ns
Ejection fraction (%)59±457±16Ns
Low value of BP at 24-h monitoring (n)9 (47%)4 (16%)0.02
Diurnal systolic BP at 24-h monitoring (mmHg)109±5120±110.03
Diurnal diastolic BP at 24-h monitoring (mmHg)69±474±7Ns
Nocturnal systolic BP at 24-h monitoring (mmHg)102±7109±11Ns
Nocturnal diastolic BP at 24-h monitoring (mmHg)62±566±9Ns
Standard deviation of all NN intervals127.8±43.1130.6±47.4Ns
RMSSD45.3±37.639.1±30.4Ns
pNN5016.3±12.718.2±13.8Ns

[i] CFS, chronic fatigue syndrome; BP, blood pressure; RMSSD, square root of the mean of the sum of the square of the differences between adjacent NN intervals; pNN50, number of adjacent NN intervals differing by >50 msec divided by the total number of all NN intervals; Ns, not significant.

EcocolorDoppler in the study population excluded alteration in left ventricular segmental kinetics, four patients exhibited mitral valve prolapse and the mean ejection fraction was 58±12%. With regard to the patients with confirmed diagnosis of CFS, the mean ejection fraction was 59±4%; in three of these patients with confirmed diagnosis, mitral valve prolapse was observed.

The 24-h blood pressure monitoring demonstrated that nine out of 19 patients with CFS had blood pressure at the lower of the normal limits, and only one with high blood pressure. No symptomatic hypotensive episodes were recorded during the 24-h monitoring period and the nocturnal blood pressure was similar in the two subgroups.

Discussion

The profiles of the patients in the current study confirm findings from various previous reports on prevalence in Caucasian females with a female to male ratio of 4:1 (10), the age of onset of the pathology (10) and the presence of previous infection (by EBV, Candida albicans, Borrelia burgdorferi, enterovirus, CMV, other HHV, retrovirus, bornavirus, coxsackievirus B, and the hepatitis C virus) (11,12).

A higher ratio of females is commonly reported within CFS (1315). The prevalence in female patients is found in numerous autoimmune diseases and indicates a different regulation of gene expression between the sexes due to the action of the hormone system. However, although different studies have investigated genetic profiles associated with CFS, data thus far are scarce and different.

As previously described, CFS predominantly affects young adults aged 20–40 years, although the symptoms also exist in childhood, adolescence and in the elderly (16). In the present study, the mean age of onset for patients with confirmed diagnosis of CFS was 28±13 years.

The largest proportion of patients (32%) identified infectious events prior to the onset of their fatigue, such as fever, flu-like syndrome and viral infectious episodes. With regard to noninfectious events prior to illness, neurological problems (amnesias, cognitive impairment, difficulty concentrating, confusion, headaches and vertigo) or undue stress were identified to be the most common. This reflects the pathophysiology proposal for CFS; that it is a multisystem disease, which involves the interaction between the immune and central nervous system, and in which stress potentially reactivates or replicates latent viruses, such as EBV, causing the symptoms of CFS (1721).

As a cross-sectional study, it is not possible to determine whether the weight and obesity were significant predictors for CFS or otherwise. However, only three of the CFS patients were considered overweight or obese. This is considerably less than previously reported (22) and this could be associated with debilitating and chronic nature of the disease, which leads patients to have a more sedentary lifestyle, thus significantly reducing mobility (23).

The majority of studies agree that there is an increase in heart rate in patients with CFS, at rest and under stress. In the present study, mean heart rate at baseline is not significantly different among patients with and without CFS and, during ergometric tests, no abnormalities of ventricular repolarization were observed in all of the patients. Hypothesizing a role of sympathetic/vagal disturbance during stress, the rapidity of vagal withdrawal at onset of exercise was examined in the present study, but no differences were identified in patients with and without CFS. In addition, the Holter ECG monitoring, which enabled analysis of HRV in the two subpopulations of patients, did not indicate any significant difference.

Despite the current data demonstrating that the majority of the cardiological parameters investigated are not significantly different in patients with and without CFS, a significant association between the disease and low blood pressure was found. Other pilot studies have identified a higher prevalence of hypotension and orthostatic intolerance in patients with CFS. Many of the CFS symptoms, including fatigue, vertigo, decreased concentration, tremors and nausea, may be explained by an autonomic dysfunction.

Previous studies have documented an alteration in autonomic cardiovascular control; this appears to be of central origin and may be a fundamental aspect of the underlying pathophysiology of CFS (24). Patients with CFS appear to have, as well as lower systolic blood pressure, exaggerated diurnal variation. The latter, in particular, appears to be inversely correlated with increasing fatigue (25).

Our study reaffirms a previous study that highlights the potential value of non-invasive autonomic parameters, such as an alteration in blood pressure, as clinical diagnostic biomarkers in this disease (26).

The current findings reveal a novel field of research for CFS, which involves the cardiovascular system, in particular blood pressure, which may trigger the symptoms of the disease itself. The hyperactivity of the immune system in response to stress that was observed in patients with this disease, together with the presence of low pressure values, may demonstrate interactions between different pathophysiological environments.

In conclusion, although the present results require confirmation in a larger population, it is apparent that CFS patients have low blood pressure. In these patients, appropriate physiotherapeutic activity ensures that constant physical activity is performed, from which the patients will also benefit from a psychological point of view.

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Bozzini S, Albergati A, Capelli E, Lorusso L, Gazzaruso C, Pelissero G and Falcone C: Cardiovascular characteristics of chronic fatigue syndrome. Biomed Rep 8: 26-30, 2018
APA
Bozzini, S., Albergati, A., Capelli, E., Lorusso, L., Gazzaruso, C., Pelissero, G., & Falcone, C. (2018). Cardiovascular characteristics of chronic fatigue syndrome. Biomedical Reports, 8, 26-30. https://doi.org/10.3892/br.2017.1024
MLA
Bozzini, S., Albergati, A., Capelli, E., Lorusso, L., Gazzaruso, C., Pelissero, G., Falcone, C."Cardiovascular characteristics of chronic fatigue syndrome". Biomedical Reports 8.1 (2018): 26-30.
Chicago
Bozzini, S., Albergati, A., Capelli, E., Lorusso, L., Gazzaruso, C., Pelissero, G., Falcone, C."Cardiovascular characteristics of chronic fatigue syndrome". Biomedical Reports 8, no. 1 (2018): 26-30. https://doi.org/10.3892/br.2017.1024