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Immune System Sex Differences May Bridge the Gap Between Sex and Gender in Fibromyalgia

Research Output: Contribution to journal Article Peer-review

Open access

Publication metrics

Metrics

SciVal
FWCI
1.24
SciVal
Author count
3
SciVal
Citations
28
SciVal
Paper percentile
78
Scopus
Citations

Abstract

The fibromyalgia syndrome (FMS) is characterized by chronic widespread pain, sleep disturbances, fatigue, and cognitive alterations. A limited efficacy of targeted treatment and a high FMS prevalence (2–5% of the adult population) sums up to high morbidity. Although, altered nociception has been explained with the central sensitization hypothesis, which may occur after neuropathy, its molecular mechanism is not understood. The marked female predominance among FMS patients is often attributed to a psychosocial predisposition of the female gender, but here we will focus on sex differences in neurobiological processes, specifically those of the immune system, as various immunological biomarkers are altered in FMS. The activation of innate immune sensors is compatible with a neuropathy or virus-induced autoimmune diseases. Considering sex differences in the immune system and the clustering of FMS with autoimmune diseases, we hypothesize that the female predominance in FMS is due to a neuropathy-induced autoimmune pathophysiology. We invite the scientific community to verify the autoimmune hypothesis for FMS.

Publication Information

Output type

Research Output: Contribution to journal Article Peer-review

Original language

English

Article number

1414

Pages from-to (Number of pages)

Pages 1414

Journal (Volume, Issue Number)

Frontiers in Neuroscience (Volume 13)

Publication milestones

  • Submitted - 2019
  • Published - 17/01/2020

Publication status

Published - 17/01/2020

ISSN

1662-4548

Publication IDs

  • Scopus: 85078993819
  • Scopus: 85078993819
  • PubMed: 32009888

Funding Details

The authors thank Dr. David Hafner for reviewing the document and the University of Monterrey (UDEM) for grant UIN17536. Funding. This work was supported by the University of Monterrey (UDEM); grant number UIN17536.
FundersFunding numbers
Universidad de Monterrey
-
UDEM
UIN17536