Abstract

Depression is often associated with local and/or systemic diseases. Chronic inflammation, pain and depression are a clinical triad increasingly recognized as co-morbid. Peripheral and central inflammation can alter neuronal activity, thereby contributing to the psych emotional and somatic symptoms of depression. Preliminary evidence suggests that mast cells direct the immune pathways mediating this triad. Chronic pelvic pain in women could be a paradigm of the triad, and of considerable clinical relevance. Mast cells are immune cells which contribute to and modulate inflammation and immunity. Upon stimulation mast cells release an array of mediators, cytokines, and growth factors to orchestrate an inflammatory response. These mediators can directly initiate tissue responses on resident cells, and may also regulate the activity of other immune cell functions, including central nervous system immune cells like microglia. Mast cell mediators can interact also with neurons, either alone or in concert with other immune cells. New evidence supports the involvement of peripheral and central mast cells in the development of pain processes, in the transition from acute, nociceptive to chronic and neuropathic pain and in the depressive states associated with them. A significant increase of pro-inflammatory cytokines is evident in depression associated with chronic diseases. Marked increases of tissue mast cells and pro-inflammatory cytokines have been documented in disorders associated with chronic pelvic pain presenting as well with significant affective comorbidities (anxiety and depression). Mast cells could be thus considered as a target of therapeutic approaches which aim to reduce inflammation and the chronicization of pain. The present review analyzes current evidence on co-morbidity between depression with peripheral and central inflammation associated with chronic pelvic pain in women. The analysis will briefly focus on key mechanisms of inflammation and role of mast cells as a common denominator of depression and chronic pain. The goal is to offer mental health professionals a biologicallyoriented contribution in the pathophysiologic reading of co-morbidities between depression and chronic pelvic pain in women. Results underline the increasing evidence supporting a role of inflammatory pathways/mechanisms, orchestrated by activated mast cells, as common denominators contributing to co-morbidity between depression and chronic pelvic pain in women.

Highlights

  • Depression, once considered a major psychological disorder is evolving into a more biologically-oriented pathophysiologic description [1,2]

  • Depression was detected in 86% of women with Chronic Pelvic Pain (CPP) associated with symptomatic endometriosis [20], while it was present in a significantly lower percentage (38%) in patients with asymptomatic endometriosis

  • Among diseases with CPP, current irritable bowel syndrome (IBS) in women was consistently associated with anxiety and mood disorders (27.5%) as well as lifetime IBS (50.5%) [27]

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Summary

Introduction

Depression, once considered a major psychological disorder is evolving into a more biologically-oriented pathophysiologic description [1,2]. Chronic pain and underlying inflammation frequently co-occur with mood disorders such as anxiety and depression and show a high prevalence in women affected by pelvic/gynecologic pathologies [6,7,8,9,10]. This is probably due to the greater vulnerability of women to developing depression as compared to men. Alterations in pain perception and tolerance to pain were reported in depressed patients not suffering from chronic pain [12]

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