Chronic fatigue syndrome in childhood
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Published on: July 3, 2026
1Department of Child Development, Kumamoto University School of Medicine, Japan. tomo@kaiju.medic.kumamoto-u.ac.jp
Insights
Pediatric chronic fatigue syndrome (CFS) involves abnormal brain function, indicated by altered cerebral blood flow and elevated choline/creatine ratios. These findings suggest a neurological basis for CFS symptoms in children and adolescents.
Area of Science:
- Pediatric Neurology
- Neuroimaging
- Metabolic Psychiatry
Background:
- Chronic fatigue syndrome (CFS) presents a diagnostic challenge in pediatric practice.
- Understanding the underlying pathophysiology of pediatric CFS is crucial for effective treatment.
Observation:
- Three pediatric cases of CFS (ages 11-13) presented with fatigue, fever, sleep disturbance, and functional decline.
- Neuroimaging techniques, including SPECT and Xe-CT, assessed regional cerebral blood flow (rCBF).
- MR spectroscopy (MRS) evaluated brain metabolic profiles.
Findings:
- Reduced rCBF in the left temporal and occipital lobes was observed in two cases (using corticocerebellar ratio).
- Elevated rCBF in the left basal ganglia and thalamus was noted in one case.
- Significantly increased choline/creatine ratios were detected via MRS in CFS patients, indicating altered brain metabolism. No structural abnormalities were found on MRI.
Implications:
- Abnormal brain function, including altered perfusion and metabolism, is implicated in pediatric CFS.
- These neurobiological findings may explain the diverse clinical manifestations of CFS in young individuals.
- Further research into brain function abnormalities could lead to targeted therapeutic strategies for pediatric CFS.
Abstract:
Chronic fatigue occurring in previously healthy children and adolescents is one of the most vexing problems encountered by pediatric practitioners. We report three cases, 11, 12 and 13-year-old children, with chronic fatigue syndrome (CFS). They initially developed a low grade fever and generalized fatigue, followed by sleep disturbance and psychosomatic symptoms, and their performance ability deteriorated. They were diagnosed as having CFS on the basis of criteria. To investigate the brain function in CFS patients, we examined the regional cerebral blood flow by single-photon emission-computed tomography (SPECT) with 111 MBq [123I]-iodoamphetamine (123I-IMP) or xenon-computed tomography (Xe-CT), and brain metabolic levels by MR spectroscopy (MRS). Blood flow, expressed as the corticocerebellar ratio (CCR), in the left temporal and occipital lobes was markedly lower in cases 2 and 3 than that in healthy subjects reported by another investigator. In case 1, however, blood flow in the left basal ganglia and thalamus was markedly higher than in healthy subjects. The MR spectroscopy (MRS) study revealed remarkable elevation of the choline/creatine ratio in the patients with CFS. None of our patients exhibited evidence of focal structural abnormalities on MRI. These findings suggest that the various clinical symptoms in CFS patients may be closely related to an abnormal brain function.
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