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Neuroinflammation in fibromyalgia and CRPS is multifactorial


In his Review article (Neurogenic neuroinflammation in fibromyalgia and complex regional pain syndrome. Nat. Rev. Rheumatol. 11, 639–648; 2015)1, Geoffrey Littlejohn ascribes neuroinflammation to a “neurogenic” origin, presumably triggered by pain and stress. However, attribution of neuroinflammation and central sensitization to a primary neurogenic origin is premature without integrating the well-documented coexistence of small intestine bacterial overgrowth (SIBO, one type of gastrointestinal dysbiosis), vitamin D deficiency, and mitochondrial dysfunction.

Littlejohn1 notes that chronic pain has been associated with lipopolysaccharide (LPS)–stimulated proinflammatory cytokines (particularly IFN-γ and TNF); however, he does not pursue this line of thought to connect it to relevant literature showing clear evidence of gastrointestinal dysbiosis and increased intestinal permeability in patients with fibromyalgia and complex regional pain syndrome (CRPS). The gastrointestinal tract is the most abundant source of LPS, systemic absorption of which is increased by SIBO and increased intestinal permeability. In 1999, Pimentel et al.2 showed that oral administration of antibiotics led to alleviation of pain and other clinical measures of fibromyalgia. In 2004, Pimentel et al.3 showed that among 42 fibromyalgia patients, all (100%) showed laboratory evidence of SIBO, severity of which correlated positively with severity of fibromyalgia. In that same year, Wallace and Hallegua4 showed that eradication of SIBO with antimicrobial therapy led to clinical improvements in fibromyalgia patients in direct proportion to antimicrobial efficacy. In 2008, Goebel et al.5 documented that patients with fibromyalgia and CRPS have intestinal hyperpermeability; mucosal “leakiness” was highest in patients with CRPS, indicating a strong gastrointestinal component to the illness. In 2013, Reichenberger et al.6 showed that CRPS patients have a distinct alteration in their gastrointestinal microbiome characterized by reduced diversity and significantly increased levels of Proteobacteria. LPS from Gram-negative bacteria is powerfully proinflammatory and is known to trigger microglial activation via Toll-like receptor 4; experimental studies have shown that LPS promotes muscle mitochondrial impairment, peripheral hyperalgesia, and central sensitization7.

Vitamin D deficiency is prevalent in chronic pain and fibromyalgia patients and promotes pain sensitization, myalgia and bone pain (osteomalacia)8. Human clinical trials have shown that vitamin D supplementation can alleviate inflammation9, intestinal hyperpermeability10, fibromyalgia pain11 and other neuromusculoskeletal pain. Vitamin D reduces experimental microglial activation12, a component of neuroinflammation and central sensitization.

Mitochondrial dysfunction, noted in fibromyalgia13 and CRPS14, may be triggered by gastrointestinal dysbiosis via LPS, D-lactate, hydrogen sulfide, and inflammation; mitochondrial dysfunction exacerbates and perpetuates microglial activation and glutaminergic neurotransmission15, thereby promoting pain sensitization centrally while also contributing to muscle pain peripherally7. Treatment of mitochondrial dysfunction with ubiquinone alleviates many biochemical and clinical manifestations of fibromyalgia13.

Thus, neuroinflammation in fibromyalgia and CRPS has biological contributions including gastrointestinal dysbiosis, vitamin D deficiency, and mitochondrial dysfunction. These independent contributions commonly co-exist, and each of these is additive/synergistic with the others in the promotion of peripheral and central hyperalgesia. The consistent pain-alleviating benefits of treatments for intestinal dysbiosis (antibiotics), vitamin D deficiency (supplementation) and mitochondrial dysfunction (ubiquinone) establish that these painful conditions are multifactorial and maintained by ongoing physiologic insults, each of which is treatable.


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Correspondence to Alex Vasquez.

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The author declares that he has worked as a consultant for Biotics Research Corporation (a nutraceutical company based in the USA), and that he has lectured and written for this company on various topics, including fibromyalgia.

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Vasquez, A. Neuroinflammation in fibromyalgia and CRPS is multifactorial. Nat Rev Rheumatol 12, 242 (2016).

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