Fibromyalgia (FM) is a very common but mysterious pain disorder characterized by chronic widespread muscular pain. Fatigue, anxiety and depression are common comorbidities. The syndrome is commonly associated with several symptoms, including fatigue, sleeping disturbance, cognitive impairment, and comorbid pain syndrome, especially irritable bowel symptoms and temporomandibular disease. Anxiety and depression are common psychiatric co-morbidies. Daily stress is believed to trigger or aggravate pain conditions. These symptoms can markedly affect patients' quality of life, and even lead to disability. So far, the etiology and pathogenesis are largely unknown, and diagnostic biomarkers and curative treatment remain to be developed. Recent technological advances enable scientists to explore mechanisms by genetic, transcriptomic, proteomic, and metabolomic researches. However, no definitive result has been concluded for clinical practice so far. In this study, the investigators use tailored questionnaires to evaluate fibromyalgia and associated symptoms, including numeric rating scale for soreness, widespread soreness index, Fibromyalgia impact questionnaire, Hospital Anxiety and Depression Scale, and perceived stress scale. The investigators also use metabolomics and lipidomic approach to probe the potential pathophysiology of fibromyalgia. In our prior translation research (PMID: 32907805), the investigators found that excessive LPC16:0 resulting from lipid oxidization inflicts psychological stress-induced chronic non-inflammatory pain via activating ASIC3. In this content, our prior translational research identified a potential nociceptive ligand that causes fibromyalgia symptoms, which is likely to function as biomarkers for diagnosis or disease monitor. In the current clinical investigation, the investigators aim to reversely translate the novel findings in animal studies and validate the bio-significance of LPC16:0 for fibromyalgia with clinical approaches.
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Questionnaire: Numeric rating scale (NRS) for pain and soreness
Timeframe: Changes from baseline NRS at 2 weeks are assessed
Questionnaire: Numeric rating scale (NRS) for pain and soreness
Timeframe: Changes from baseline NRS at 4 weeks are assessed
Questionnaire: widespread pain index and widespread soreness index
Timeframe: Change from baseline widespread index at 2 weeks are assessed
Questionnaire: widespread pain index and widespread soreness index
Timeframe: Change from baseline widespread index at 4 weeks are assessed
Questionnaire: Fibromyalgia impact questionnaire (FIQR)
Timeframe: Change from baseline FIQR at 2 weeks are assessed
Questionnaire: Fibromyalgia impact questionnaire (FIQR)
Timeframe: Change from baseline FIQR at 4 weeks are assessed
Questionnaire: Hospital Anxiety and Depression Scale (HADS)
Timeframe: Change from baseline HADS at 2 weeks are assessed
Questionnaire: Hospital Anxiety and Depression Scale (HADS)
Timeframe: Change from baseline HADS at 4 weeks are assessed
Questionnaire: The Pittsburgh Sleep Quality Index (PSQI)
Timeframe: Change from baseline PSQI at 2 weeks are assessed
Questionnaire: The Pittsburgh Sleep Quality Index (PSQI)
Timeframe: Change from baseline PSQI at 4 weeks are assessed
Questionnaire: Perceived stress scale (PSS)
Timeframe: Change from baseline PSS at 2 weeks are assessed
Questionnaire: Perceived stress scale (PSS)
Timeframe: Change from baseline PSS at 4 weeks are assessed
Metabolomics investigation
Timeframe: Change from baseline metabolomics at 3 months are assessed
Lipidomics investigation
Timeframe: Change from baseline metabolomics at 3 months are assessed
Metabolomics investigation
Timeframe: Change from baseline metabolomics at 6 months are assessed
Lipidomics investigation
Timeframe: Change from baseline metabolomics at 6 months are assessed
Metabolomics investigation
Timeframe: Change from baseline metabolomics at 9 months are assessed
Lipidomics investigation
Timeframe: Change from baseline metabolomics at 9 months are assessed
Metabolomics investigation
Timeframe: Change from baseline metabolomics at 12 months are assessed
Lipidomics investigation
Timeframe: Change from baseline metabolomics at 12 months are assessed