Your new experience awaits. Try the new design now and help us make it even better

REVIEW article

Front. Neurol.

Sec. Headache and Neurogenic Pain

This article is part of the Research TopicExploring gender-related phenotypic differences in neuropathic and nociplastic painView all 3 articles

Disentangling Sex-Specific Mechanisms in Neuropathic and Nociplastic Chronic Pain. A review

Provisionally accepted
  • 1School of Psychology, Trinity College Dublin, Dublin, Ireland
  • 2University of Otago, Dunedin, New Zealand

The final, formatted version of the article will be published soon.

Chronic pain is a multidimensional condition shaped by sex-specific biological and sociocultural factors, leading to distinct vulnerabilities, mechanisms, and treatment experiences in men and women. While women consistently exhibit lower pain thresholds, more unpleasantness, and higher prevalence of chronic pain syndromes, these differences extend beyond sensory experience and reflect qualitative divergences in immune signalling, hormonal modulation, brain network engagement, and psychosocial processing. Emerging preclinical and clinical evidence demonstrates that neuropathic pain in males is predominantly driven by microglia-dependent neuroinflammation, whereas in females it is sustained by adaptive immune mechanisms involving T-cell signalling. In nociplastic pain syndromes—such as fibromyalgia—women-biased hormonal fluctuations, limbic hyperconnectivity, and stress–immune interactions amplify central sensitization and affective suffering. Genetic studies further reveal largely non-overlapping sex-specific risk loci and gene expression patterns in pain-related tissues, supporting divergent molecular trajectories toward chronic pain. Despite these mechanistic differences, current treatments largely target sex-indifferent nociceptive circuits, resulting in comparable analgesic outcomes but sex-specific side-effect profiles and device tolerability. This review synthesizes converging evidence across genetic, neural, immune, hormonal, psychosocial, and clinical domains to propose a dual-framework model: chronic pain emerges from shared core pathways but is differentially modulated by sex-specific upstream mechanisms. Recognizing these distinctions opens a path toward hybrid treatment strategies that combine universal interventions with sex-tailored adjuncts, offering a foundation for precision pain therapeutics.

Keywords: Chronic Pain, neuropathic pain, Nociplastic pain, precision pain therapeutics, sex differences

Received: 22 Oct 2025; Accepted: 08 Dec 2025.

Copyright: © 2025 Vanneste, Castejon, Arulchelvan and De Ridder. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence: Sven Vanneste

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.