AI Article Synopsis

  • - Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is a complex illness linked to postviral fatigue, making diagnosis difficult due to vague symptoms and no specific tests available.
  • - The study uses microarray technology to analyze viral RNA levels in immune cells, revealing elevated Torque Teno Mini Virus 9 (TTMV9) in a specific group of ME/CFS patients that differs from other conditions and healthy individuals.
  • - Findings indicate that TTMV9 could serve as a potential biomarker for identifying certain ME/CFS patients, suggesting a need for further research to understand its role in the disease.

Article Abstract

Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is a chronic disorder classified by the WHO as postviral fatigue syndrome (ICD-11 8E49 code). Diagnosing ME/CFS, often overlapping with fibromyalgia (FM), is challenging due to nonspecific symptoms and lack of biomarkers. The etiology of ME/CFS and FM is poorly understood, but evidence suggests viral infections play a critical role. This study employs microarray technology to quantitate viral RNA levels in immune cells from ME/CFS, FM, or co-diagnosed cases, and healthy controls. The results show significant overexpression of the Torque Teno Mini Virus 9 (TTMV9) in a subgroup of ME/CFS patients which correlate with abnormal HERV and immunological profiles. Increased levels of TTMV9 transcripts accurately discriminate this subgroup of ME/CFS patients from the other study groups, showcasing its potential as biomarker for patient stratification and the need for further research into its role in the disease. Validation of the findings seems granted in extended cohorts by continuation studies.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11435283PMC
http://dx.doi.org/10.3390/pathogens13090751DOI Listing

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