Reduced heart rate variability predicts fatigue severity in individuals with chronic fatigue syndrome/myalgic encephalomyelitis.

Rosa María Escorihuela, Lluís Capdevila, Juan Ramos Castro, María Cleofé Zaragozà, Sara Maurel, José Alegre, Jesús Castro-Marrero
Author Information
  1. Rosa María Escorihuela: Departament de Psiquiatria i Medicina Legal, Institut de Neurosciències, Universitat Autònoma de Barcelona, Facultat de Medicina, Avinguda Can Domènech, s/n, 08193, Bellaterra, Barcelona, Spain. rosamaria.escorihuela@uab.cat.
  2. Lluís Capdevila: Laboratory of Sport Psychology, Department of Basic Psychology, Universitat Autònoma de Barcelona, Barcelona, Spain.
  3. Juan Ramos Castro: Department of Electronic Engineering, Biomedical and Electronic Instrumentation Group, Universitat Politécnica de Catalunya, Barcelona, Spain.
  4. María Cleofé Zaragozà: Clinical Research Department, Laboratorios Viñas, Barcelona, Spain.
  5. Sara Maurel: Department of Medicine, Universitat Autònoma de Barcelona, Barcelona, Spain.
  6. José Alegre: CFS/ME Unit, Vall d'Hebron University Hospital Research Institute, Universitat Autònoma de Barcelona, Passeig de Vall d'Hebron 119-129, 08035, Barcelona, Spain.
  7. Jesús Castro-Marrero: CFS/ME Unit, Vall d'Hebron University Hospital Research Institute, Universitat Autònoma de Barcelona, Passeig de Vall d'Hebron 119-129, 08035, Barcelona, Spain. jesus.castro@vhir.org. ORCID

Abstract

BACKGROUND: Heart rate variability (HRV) is an objective, non-invasive tool to assessing autonomic dysfunction in chronic fatigue syndrome/myalgic encephalomyelitis (CFS/ME). People with CFS/ME tend to have lower HRV; however, in the literature there are only a few previous studies (most of them inconclusive) on their association with illness-related complaints. To address this issue, we assessed the value of different diurnal HRV parameters as potential biomarker in CFS/ME and also investigated the relationship between these HRV indices and self-reported symptoms in individuals with CFS/ME.
METHODS: In this case-control study, 45 female patients who met the 1994 CDC/Fukuda definition for CFS/ME and 25 age- and gender-matched healthy controls underwent HRV recording-resting state tests. The intervals between consecutive heartbeats (RR) were continuously recorded over three 5-min periods. Time- and frequency-domain analyses were applied to estimate HRV variables. Demographic and clinical features, and self-reported symptom measures were also recorded.
RESULTS: CFS/ME patients showed significantly higher scores in all symptom questionnaires (p < 0.001), decreased RR intervals (p < 0.01), and decreased HRV time- and frequency-domain parameters (p < 0.005), except for the LF/HF ratio than in the healthy controls. Overall, the correlation analysis reached significant associations between the questionnaires scores and HRV time- and frequency-domain measurements (p < 0.05). Furthermore, separate linear regression analyses showed significant relationships between self-reported fatigue symptoms and mean RR (p = 0.005), RMSSD (p = 0.0268) and HFnu indices (p = 0.0067) in CFS/ME patients, but not in healthy controls.
CONCLUSIONS: Our findings suggest that ANS dysfunction presenting as increased sympathetic hyperactivity may contribute to fatigue severity in individuals with ME/CFS. Further studies comparing short- and long-term HRV recording and self-reported outcome measures with previous studies in larger CFS/ME cohorts are urgently warranted.

Keywords

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MeSH Term

Case-Control Studies
Fatigue Syndrome, Chronic
Female
Heart Rate
Humans
Self Report
Surveys and Questionnaires

Word Cloud

Created with Highcharts 10.0.0HRVCFS/MEfatigueself-reportedp < 0ratevariabilitydysfunctionencephalomyelitisstudiesindividualspatientshealthycontrolsRRfrequency-domainp = 0Heartchronicsyndrome/myalgicpreviousparametersalsoindicessymptomsintervalsrecordedanalysessymptommeasuresshowedscoresquestionnairesdecreasedtime-005significantseverityBACKGROUND:objectivenon-invasivetoolassessingautonomicPeopletendlowerhoweverliteratureinconclusiveassociationillness-relatedcomplaintsaddressissueassessedvaluedifferentdiurnalpotentialbiomarkerinvestigatedrelationshipMETHODS:case-controlstudy45femalemet1994CDC/Fukudadefinition25age-gender-matchedunderwentrecording-restingstatetestsconsecutiveheartbeatscontinuouslythree5-minperiodsTime-appliedestimatevariablesDemographicclinicalfeaturesRESULTS:significantlyhigher00101exceptLF/HFratioOverallcorrelationanalysisreachedassociationsmeasurements05FurthermoreseparatelinearregressionrelationshipsmeanRMSSD0268HFnu0067CONCLUSIONS:findingssuggestANSpresentingincreasedsympathetichyperactivitymaycontributeME/CFScomparingshort-long-termrecordingoutcomelargercohortsurgentlywarrantedReducedheartpredictsAutonomicChronicsyndromeFatigueMyalgic

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