Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: A Neurological Entity?

• Published in: Medicina (Kaunas, Lithuania) Lithuania), 2021-09, Vol.57 (10), p.1030
• Main Authors: Murga Gandasegui, Iñigo, Aranburu Laka, Larraitz, Gargiulo, Pascual-Ángel, Gómez-Esteban, Juan-Carlos, Lafuente Sánchez, José-Vicente
• Format: Article
• Language: English
• Subjects: Autonomic Nervous System; Biomarkers; Chronic fatigue syndrome; Chronic Fatigue Syndrome (CFS); Disease; dysautonomia; Encephalomyelitis; Fatigue Syndrome, Chronic - diagnosis; Fibromyalgia; Heart Rate; Humans; Hypothalamus; International Classification of Diseases; Magnetic resonance imaging; Medical imaging; Metabolism; Metabolites; Myalgic Encephalomyelitis (ME); neuroimaging; Pain; Pathology; Psychosis; Review; Sleep; Spectrum analysis
• ISSN: 1648-9144; 1010-660X; 1648-9144
• DOI: 10.3390/medicina57101030

Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) is a disorder of unknown physiopathology with multisystemic repercussions, framed in ICD-11 under the heading of neurology (8E49). There is no specific test to support its clinical diagnosis. Our objective is to review the evidence in neuroimaging and dysautonomia evaluation in order to support the neurological involvement and to find biomarkers serving to identify and/or monitor the pathology. The symptoms typically appear acutely, although they can develop progressively over years; an essential trait for diagnosis is "central" fatigue together with physical and/or mental exhaustion after a small effort. Neuroimaging reveals various morphological, connectivity, metabolic, and functional alterations of low specificity, which can serve to complement the neurological study of the patient. The COMPASS-31 questionnaire is a useful tool to triage patients under suspect of dysautonomia, at which point they may be redirected for deeper evaluation. Recently, alterations in heart rate variability, the Valsalva maneuver, and the tilt table test, together with the presence of serum autoantibodies against adrenergic, cholinergic, and serotonin receptors were shown in a subgroup of patients. This approach provides a way to identify patient phenotypes. Broader studies are needed to establish the level of sensitivity and specificity necessary for their validation. Neuroimaging contributes scarcely to the diagnosis, and this depends on the identification of specific changes. On the other hand, dysautonomia studies, carried out in specialized units, are highly promising in order to support the diagnosis and to identify potential biomarkers. ME/CFS orients towards a functional pathology that mainly involves the autonomic nervous system, although not exclusively.