Journal of Reproductive Medicine Gynaecology & Obstetrics Category: Medical Type: Review Article

Endometriosis - Pathogenesis and Sequelae

Razan Asally1*, Robert Markham2 and Frank Manconi2
1 Discipline Of Obstetrics, Gynaecology And Neonatology, The University Of Sydney, New South Wales, Medical Foundation Building, Australia
2 Discipline Of Obstetrics, Gynaecology And Neonatology, The University Of Sydney, New South Wales, Australia

*Corresponding Author(s):
Razan Asally
Discipline Of Obstetrics, Gynaecology And Neonatology, The University Of Sydney, New South Wales, Medical Foundation Building, Australia
Tel:+61 0290363129,
Fax:+61 0290363188

Received Date: Jul 09, 2018
Accepted Date: Aug 10, 2018
Published Date: Aug 24, 2018


Endometriosis is a gynaecological disorder characterised by the presence of endometrial-like tissue outside the uterus. It affects 10-15% of women during their reproductive age. Endometriosis is a highly variable condition in terms of presenting symptoms, anatomical extent of disease, rate of progression, incidence of infertility, response to treatment and the likelihood of recurrence. The aetiology and the pathogenesis of the disease are poorly understood. Endometriosis has a wide range of symptoms or can be asymptomatic, this makes the diagnosis of the disease difficult. The definitive diagnosis is surgical, usually via laparoscopy with histological confirmation. There is often a long delay in diagnosis, 8-12 years, from the onset of symptoms till a definitive diagnosis is made. Endometriosis is a progressive disease and long delays before effective treatment allows the disease to advance.


Diagnostic; Endometriosis; Neuronal; Nerve fibres; Pain


Endometriosis is an oestrogen-dependent gynaecological disorder that is characterized by the presence of endometrial-like tissue outside the uterus [1]. Endometriosis affects 10-15% of women during their reproductive age, 50 to 60% of women and teenage girls with pelvic pain and up to 50% of women with infertility [2,3].

Endometriosis is considered as a highly variable condition in terms of symptoms, anatomical extent of the disease, rate of progression, incidence of infertility, response to treatment and likelihood of recurrence [3]. Endometriotic lesions can be spread through many areas, and are usually multiple. They are usually found in pelvic peritoneal and visceral surfaces, ovaries and rectovaginal septum [4]. They also can be rarely found in the pancreas, pleura, lung, umbilicus, on sciatic nerve roots, fallopian tubes, thorax and the kidneys, the vertebrae, the extremities or even the brain [5,6].

There are several factors that have been suggested that play a role in the establishment and development of endometriosis. These factors could be related to the genetic profile, inflammation, immune dysfunction, oxidative stress, hormonal activity, menstrual cyclicity, burden and immunological factors [7,8]. There are three symptomatic groups that are usually compared; these are asymptomatic patients, symptomatic (with pain) and infertile patients [9]. As a result the accurate, true prevalence and incidence of endometriosis in the general female population remains unclear, as some women with the disease can be completely asymptomatic, allied with the difficulty of a confirming diagnosis of the disease, which can only be reliably done by laparoscopy together with histological confirmation [3].


The definitive cause and the pathogenesis of endometriosis remains unclear. Many theories have been proposed to explain the development and establishment of endometriosis [8]. Three main theories have been proposed to explain this anomaly and are discussed below.

Retrograde menstruation/implantation theory

This is the oldest theory and the most widely accepted theory and was first hypothesised by Sampson in 1927. He suggested that the origin of endometriosis was from refluxed menstrual tissue and cells which implanted on the surface of the organs in the peritoneal cavity [10]. However, this theory was neglected as retrograde menstruation which occurs in 76-90% of women with fallopian tube disorders and not all of these women have endometriosis [11]. In addition, this theory failed to explain the existence of the disease in early puberty and also rarely in newborns and in women affected by the Mayer-Rokitansky-Küster-Hauser, a syndrome characterized by congenital aplasia of the uterus and the upper part of the vagina and in male endometriosis [12-16].

Coelomic metaplasia theory

This theory proposed that endometriosis initiated from abnormally trans-differentiated mesothelial lining of the visceral and abdominal peritoneum, which transformed into endometrial cells by metaplasia. This could be caused by infectious, hormonal, or other inductive stimuli [17]. The occurrence of endometriosis in prepubertal and adolescent girls, or in women who never menstruated and in unusual sites, including pleural cavity have often been considered as clinical evidence of the metaplasia theory [18-22].

Induction theory

This theory can be considered as an extension of the coelomic metaplasia theory. It was proposed by Levander and Norman. This theory was built on the assumption that several endogenous biochemical or immunological factors could induce the transformation of undifferentiated peritoneal cells to differentiated endometrial tissue [23].


The clinical presentation of endometriosis has been highly variable which has led to a wide spectrum of symptoms. Symptoms that could be influenced by many factors such as age of presentation, anatomical extent of disease, incidence of infertility, response to treatment, likelihood of recurrence, rate of progression and natural long-term history of the condition. Some women will suffer from many symptoms, while others will have minimal symptoms and a small group of women with endometriosis will not present with any symptoms or will not be aware of any substantial symptoms [3]. It is unclear if this great variability in the symptoms presentation has been influenced by the genetic characteristics of the disease or other factors such as lifestyle and environment [24]. Although the symptoms are highly variable, the majority of women with advance endometriosis will suffer from some form of pelvic pain [3].


Pelvic pain is the key symptom in endometriosis; and is the main reason why the patient consults her doctor [25,26]. There are common and classical forms of pelvic pain symptoms that women with endometriosis suffer from, these include: menstrual pain (dysmenorrhoea) which is often characterised as intense, unbearable, miserable, cramping, gnawing, crushing or pressing and pain during intercourse (dyspareunia) [27]. In addition, women with endometriosis may also suffer from pelvic pain with defaecation (dyschezia) and chronic pelvic pain [28].


Endometriosis may cause infertility and up to 50% of women with endometriosis may present with subfertility [29]. Despite a strong association between endometriosis and infertility, a true cause and effect relationship has yet to be established. It seems implausible to many that mild endometriosis could be the sole cause of long-standing infertility [30]. Some of the mechanisms that account for the adverse effects that endometriosis may have on fertility are listed in (Table 1) [31].

Ovarian-Tubal Dysfunction

Anatomical distortion of ovary and tube

               Ovulation failure


               LUF (Luteinized Un-ruptured Follicle)

               Abnormal follicle development

               Reduced follicle development

               Decreased estrogen production

               Increased apoptosis of granulosa cells

Immunological disorder

               Anti-endometrial antibody

Abnormal peritoneal environment

               Increased peritoneal fluids and high concentration of cytokines

                Activated macrophage

Dysregulated endometrial function

Table 1: Pathophysiology of endometriosis associated infertility.


Endometriotic lesions in the pelvic cavity can be classified into three types, these are (a) Peritoneal implants, (b) Deep infiltrating or adenomyomatous disease and (c) Endometriomas, which are chocolate brown like fluid-filled endometriotic cysts generally associated with the ovaries (Figure 1) [1,16].
Figure 1: Peritoneal lesions and an ovarian endometrioma due to endometriosis.

Panel A shows an endometriotic implant (red lesion), adhesions, and hyperemia in the peritoneum. Panel B shows peritoneal implants, including red and blue-black lesions and adhesions. Panel C shows extensive adhesions distorting the normal pelvic anatomy. Panel D shows an endometrioma adherent to the posterior uterus and distending the ovarian capsule.

Superficial endometriosis

These occur in the form of peritoneal implants or lesions on the outer surfaces of the ovary. The peritoneal implants can be categorized into intraepithelial and sub-mesothelial lesions consisting of stromal and glandular tissue, which respond to menstrual cycle hormones. Adhesions can sometimes accompany them. Depending on the severity of adhesion formation, the adhesions in the ovary can be sometimes intense and haemorrhagic in nature [1].

Deep infiltrating endometriosis

Also, known as adenomatous endometriosis, this type are mainly comprised of proliferative fibromuscular tissue with sparse glandular and stromal tissue with no surface epithelium. This deep infiltrating type does not obviously respond to menstrual cycle hormones. It is frequently seen in the uterosacral and rectovaginal ligaments [1].

Ovarian endometriomas

An ovarian cyst, when encapsulated by endometriotic tissue, is known as an endometrioma. It is filled with a brown, almost chocolate-coloured fluid, resulting from metabolism of recurrent bleeding from the endometriotic surface implants. With time, this endometriotic tissue slowly gets replaced by fibrotic tissue causing the histological glandular appearance of the endometrioma to wane. The cyst wall is often found to consist of large scarred areas mixed with haemorrhagic, hyper vascularised endometriotic lesions [32].At surgery, it can be difficult to distinguish visually an endometrioma from a cyst of the corpus luteum, a haemorrhagic cyst, or a simple cyst. Although the cyst fluid in endometriomas is thick and dark brown because it contains haemosiderin (hence, the name “chocolate cysts”), this colour is not completely specific to endometriomas. Who acquired the images courtesy of Dr Christopher Herndon, University of California, San Francisco [1].

Diagnosis of endometriosis

There is a lack of simple non-invasive tests for the diagnosis of endometriosis that could be applied in clinical practice. Although clinical history and pelvic examination can increase the possibility of a diagnosis of endometriosis, the usage of traditional clinical parameters to detect women with endometriosis has been limited [33]. The pain originally linked with menstruation causes delay in the time that women approach physicians about their gynaecological concerns [34]. From studying the narrative interviews of women with endometriosis-associated pelvic pain, there was a delay in the diagnosis and course of the treatment as the women believed that their pain was a natural biological side effect of being female [35].


A definitive diagnosis of endometriosis can be accomplished by laparoscopy and histological biopsy, which provides direct visualisation and histological confirmation [36,37]. However, laparoscopy is an invasive intervention and associated with considerable side effects and high costs [34]. Despite the controversy in the literature in regard to the advantage of one surgical modality over another in treating pelvic pathology, there is accumulative evidence suggesting that laparoscopy is the preferred technique to evaluate the pelvis and abdomen and to treat benign conditions such as ovarian endometriomas [33].

Non-Invasive diagnostic imaging

Magnetic Resonance Imaging (MRI) and Ultrasonography (USS) (which includes transabdominal, transvaginal and transrectal approaches) have been used as diagnostic tools to identify endometriosis [34]. However, the primary role of USS in the diagnosis of endometriosis is to customize the management of patients. As the correct recording of endometriotic lesions may notify the surgeon on the presence of lesions that are not readily recognized at laparoscopy. It should be noted that superficial peritoneal endometrioses such as peritoneal bleb and “gunshot” lesions are too small to be detected at ultrasound examination [38]. These two techniques provide good options for the diagnosis of ovarian endometriosis (80-90% sensitivity and 60-98% specificity) however, are limited in detecting lesions outside the peritoneum, adhesions and infiltrations [39]. In addition, Doppler ultrasonography is a tool that may assist in the diagnosis of ovarian endometriosis; the blood flow changes according to the presence or absence of endometriomas [40].

The need for biomarkers for the non-invasive diagnosis of endometriosis

In the last few years, many studies have been conducted or review articles published to discover a biomarker to detect the disease earlier and to avoid the use of laparoscopy [33,41-53]. The search for serum protein markers for endometriosis had commenced over several decades ago [54]. During this period, several proteins had been identified, however, despite extensive research no reliable blood tests currently exist for the diagnosis of endometriosis [55]. Research into urinary biomarkers is an emerging field of research and little is currently known, despite published works [56-59]. A consensus of the World Endometriosis Society has been that the development of a reliable non-invasive diagnostic test is one of the top priories in endometriosis [60]. A reliable biomarker must have high specificity, sensitivity and be inexpensive [34]. To date, there are no molecules that have been proven to be reliable biomarkers to be used in the diagnose of endometriosis [45]. Over the last 25 years, more than 100 possible biomarkers have been investigated for potential diagnostic tests for endometriosis, however, none have proven to be clinically useful [61]. In symptomatic women, the use of CA 125≥30 units/ml is highly specific for diagnosing endometriosis, however, a CA 125 <30 units/ml does not exclude endometriosis and further investigation is required [62].


The approaches to manage endometriosis can be classified into surgical and pharmacological. As the aetiology of the disease is not well understood, to-date there is no prevention or cure for endometriosis. Rather, the aim of the treatment options is mainly to manage the symptoms or to improve fertility rates [63].

Surgical management of endometriosis

The aim of the surgical approach is to address both pain and fertility. Laparoscopy facilitates the removal of endometrial lesions and scar tissue, which may help to reduce pain and improve fertility.
Laparotomy (open surgery) was considered the standard method for surgical therapy of endometriosis prior to the improvements in laparoscopic techniques [30]. In severe endometriosis, it was found that laparotomy and laparoscopy perform equally in treating pain and infertility problems, yet there was a trend towards a higher pregnancy rate and lower dyspareunia recurrence rate after laparotomy compared with laparoscopy in the 1990s [64]. This appeared to have been improved with developments in laparoscopic equipment, techniques and skill.
Laparoscopy is considered as the gold standard for treating mild and moderate stages of endometriosis [65]. Laparoscopy offers several advantages when compared with laparotomy procedures including decreased recovery time and cost [66]. Surgical procedures involve excision, fulguration, or laser ablation of endometriotic implants on the peritoneum, excision, drainage or ablation of endometriomas, resection of rectovaginal nodules, lysis of adhesions and interruption of nerve pathways [1]. Resection is preferred and is usually more effective in healing both pain and infertility. There are risks will all surgery, with laparoscopy, problems are rare, however can be severe.
Radical surgery
Radical surgery involves total abdominal hysterectomy with or without bilateral oophorectomy [67]. This option may suit women with chronic pelvic pain with endometriosis who have completed their families and have undergone other medical and or conservative surgical treatments without complete symptom relief. However, this approach may not always alleviate pain symptoms especially in deep endometriotic disease [67].


Medical therapies are proposed as a temporary relief for pain management [68]. The effect of pharmacological treatment on fertility has been minimal and has been considered as ineffective in some cases such as ovarian endometriomas [69]. Medical treatments for endometriosis include hormonal suppression and analgesic management that are discussed below.

Oral contraceptives

Combined oral contraceptive pills have been used to control endometriosis-related symptoms such as pelvic pain and dysmenorrhea [70]. Whilst the cyclical use of oral contraceptives has been used to manage heavy bleeding associated with endometriosis, the continuous use of oral contraceptives have been more effective in managing pelvic pain [71-73].


Progestogens, which include Medroxyprogesterone Acetate (MPA) and 19-nortestosterone derivatives, help to control the pain associated with endometriosis by two mechanisms. It either stimulates decidualisation and atrophy of endometrial tissue, and inhibits matrix metalloproteinase-enzymes that play a fundamental role in the development and implantation of ectopic endometrium [74,75].

GnRH agonists

GnRH agonists bind to pituitary receptors and have a longer half-life than native GnRH [76]. It stimulates the down-regulation of the pituitary-ovarian axis causing hypoestrogenism, which stimulates amenorrhea and endometrial atrophy [75]. In addition, the uses of GnRH analogue treatments have helped to reduce bleeding more than the IUD-administered progestin treatment [76]. Side effects of GnRH agonists, such as vasomotor symptoms and accelerated bone loss, limit treatment duration to six months. However, treatment can be extended beyond six months if add-back therapy is combined with the GnRH agonist [77].


Danazol is an androgen that is derived from 17α-ethinyl testosterone and can be used as a treatment to manage the pain associated with endometriosis. It inhibits steroidogenesis and the LH surge leading to an increase in the level free testosterone. Danazol has androgenic side effects such as weight gain, acne and edema [78].

Aromatase inhibitors

Aromatase is an enzyme, which converts steroidal precursors into estrogens. The estrogens trigger the growth of ectopic tissue, which leads to the onset of pelvic pain [79]. The inhibition of aromatase decreases the estrogen production [80]. The reduction of estrogen level in premenopausal women leads to an increase in FSH levels, which may cause ovarian follicular cysts [81]. Consequently, an “add-back therapy” and oral contraceptives are recommended to be used with aromatase inhibitors [81]. This combination therapy notably reduces abdominal and pelvic pain and shrinks endometriotic lesions at second-look surgery [81,82].


Nonsteroidal Anti-Inflammatory Drugs (NSAIDs) have been indicated to be a reliable option for treating primary dysmenorrhea and they have an anti-inflammatory effect in endometriosis [83-85]. Although NSAIDs have been the most frequently used medications for pelvic pain, their efficacy in treating pain associated with endometriosis to date is not definite [86].


Recent evidence suggest that antioxidant supplements may reduce pelvic pain in patients with endometriosis [87,88].


The existence of close and complex a relationship between chronic pelvic pain and endometriosis has been widely recognised by gynaecologists. It is one of the consequences of the disease that most women with endometriosis complain about [26]. It affects the quality of life of women and has a negative impact on their ability to work, self-esteem and their personal relationships. The International Association for the Study of Pain has defined pain as “unpleasant sensory and emotional experience associated with actual or potential tissue damage, or described in terms of such damage” [89]. Different types of pain are associated with endometriosis, which include dysmenorrhoea, dyspareunia and inter-menstrual pain, often over long periods and often considered as Chronic Pelvic Pain (CPP) [90]. Although there has been much research into the pain mechanisms of endometriosis, the associations between the severity of pain, extent of the disease and site of the lesions are still unclear and the mechanisms are still poorly understood [24,91].

Prostaglandins (PGs) have an important role in the pathogenesis of the symptom of pain in endometriosis due to an excess in the amount of PGs secreted from the endometrium during menstruation. Among PGs, PGFα is considered the most potent causal factor of pain [92]. Chronically elevated catecholamine levels are associated with pain and inflammatory disease, both often are associated with endometriosis [93-96]. Medina and Lebovic reported that Substance P (SP) and Calcitonin Gene-Related Peptide (CGRP) were both involved in the inflammatory and pain responses and both were present in the myometrial layer, this was reported as being indicative of the occurrence of sensory C and Aδ fibres [97]. Bulletti observed a greater contractility at the time of menstruation in endometriosis subjects in comparison with control subjects, this was postulated as the possible roles of SP and CGRP nerve fibres in relation to the generation of pain in endometriosis and dysmenorrhea [98].


Sensory nerves are afferent nerves carrying nerve impulses from peripheral receptors to the Central Nervous System (CNS) [99]. Peripheral nerve fibers are also classified into three types according to their sizes (Table 2), which includes chemo-, mechano-, photo- and thermo-receptors, as well as nociceptors [100]. The perception of pain occurs as a result of crosstalk between the CNS and the Peripheral Nervous System (PNS) which is exerted by afferent and efferent nerves.

Type of Fibers



Axonal Diameter (μm)

Conduction Velocity (m/s)

Direction of Conduction

A (Myelinated)


Proprioception, muscle contraction



Afferent and efferent


Touch-Pressure, vibration



Afferent and efferent


Intrafusal fibers contraction





Pain (acute, shallow), temperature
(cold receptors), touch-pressure




B (Myelinated)


Preganglionic fibers of ANS





Fibers of dorsal roots

Pain (chronic, deep), temperature (warmth receptors), touch-pressure (tactile or mechanoreceptors)





Postganglionic fibers  of sympathetic nerves




Table 2: Different types of peripheral nerve fibers. Source: Yan et al., [99]; Compiled from: Laverdet et al., [100] and Purves, 2012 [101].

Neurotrophins and their receptors role in neurogenesis and pain

Neurotrophins are a family of structurally and functionally related proteins that play a role in regulating the growth, maintenance and apoptosis of neurons in the developing nervous system as well as injured neurons [102-104]. Neurotrophins consist of four members including Nerve Growth Factor (NGF), Brain-Derived Neurotrophic Factor (BDNF), Neurotrophin 3 (NT-3) and Neurotrophin 4 with the latter also known as Neurotrophin-5 (NT-4 or NT4/5) [102,103].

The biological effects of neurotrophins are facilitated through two major receptors including neurotrophic tyrosine kinase (Trks) receptors and the pan neurotrophin receptor at 75 kDa (p75NTR) [105]. Each neurotrophins binds with a specific Trk receptor in particular, NGF binds with TrkA, BDNF and NT-4 bind with TrkB, and NT-3 to TrkC [105]. NT-3 also binds with TrkA and TrkB however, with lower affinities and all four mature NTs bind with similar affinity to the p75NTR [106,107] (Figure 2).
Figure 2: Neurotrophins and their receptors. Each neurotrophin binds with a specific Trk receptor. NGF binds with TrkA, BDNF and NT-4 bind with TrkB, and NT-3 to TrkC. Trk: Tropomyosin Related Kinase; NGF: Neuronal Growth Factor; BDNF: Brain-Derived Neurotrophic Factor; NT: Neurotrophin. Source: Arevalo et al., [107] and Sanchez-Sanchez et al., [108].

In addition, Glial cell line-Derived Neurotrophic Factor (GDNF) family, which includes GDNF, Neurturin, Artemin and Persephin and other neurotrophic factors that are crucial for the development, survival of the nervous system [109,110]. The activation of all GDNF family members are facilitated by binding with multicomponent GDNF Family ligand Receptor (GFR) α [110]. GDNF binds to GFRα1 and also interacts with GFRα2 and GFRα3 at lower affinities, Neurturin to GFRα2, Artemin to GFRα3 and Persephin to GFRα4 [110].

There is strong evidence that neurotrophins, specially NGF and BDNF, act as mediators and modulators of pain in different conditions [111]. Nociceptors express NGF receptors activating NGF that leads to the sensitisation of these nociceptors. In addition, BDNF is released from the spinal terminals of activated nociceptors. BDNF modulate and alter the effectiveness of the central nociceptive signals. NT3 and NT-4/5 has been shown to play reasonably modest roles in pain processing in most conditions [111]. Moreover, almost one-half of the nociceptor population has receptor components for GDNF, suggesting an important role for GDNF in the activation and maintenance of nociceptors [112,113].

Neuronal guidance molecules and their receptors role in neurogenesis and pain

In the last two decades, work has led to the discovery of proteins that help to facilitate neuronal circuits through the guiding of neuronal axons to their specific targets during their development [114]. Neuronal guidance molecules can act as attractants or repellents. They can either guide axons towards a specific target or divert them away from a specific area. In addition, these molecules can be membrane-associated molecules and act with a limited effect or as secreted molecules with a wider range of effects [114]. Neuronal guidance molecules are divided into five families of canonical guidance proteins including Semaphorins, Netrins, Slits, Repulsive Guidance Molecules (RGMs) and Ephrins [115,116].

These neuronal guidance molecules are activated through binding to their specific receptors to trigger the intracellular signalling cascades, which cause axon routing through stimulation of changes in the growth-cone cytoskeleton [114,115]. Semaphorin family, which have attractant and repellent effects, bind to receptors from the plexin and neuropilin protein families [117]. Netrin molecules are activated through binding to DCC receptors and UNC-5 receptors to produce attractive and repulsive effects respectively [118]. Slit molecules have repellent effects which prevent axons re-crossing and through binding to the roundabout (Robo) family receptors [119]. RGMs have also repellent affects that signal through binding to Neogenin receptor [120]. While tethered to the membrane Ephrin A molecules interact with class A Eph receptors, the transmembrane Ephrin B interact with class B Eph receptors and both play a well-known role in organising axon connections between the eye and the brain [121] (Figure 3).
Figure 3: Five families of identified neuronal guidance molecules (top) and their binding receptors (bottom). Semaphorins binds to receptors from the Plexin and neuropilin protein families; Netrin molecules binds to DCC receptors and UNC-5 receptors; Slit molecules binds to the roundabout (Robo) family receptors, Repulsive Guidance Molecules (RGMs) binds to their receptors Neogenin; Ephrin A molecules interact with class A Eph receptors and Ephrin B interacts with class B Eph receptors. Source: Van Battum et al., [114].


Pain associated with endometriosis is as complex as the disease itself. As endometriosis is identified by the presence of lesions outside uterus, this suggests that the sensation of pain associated with endometriosis starts with sensory nerves that transduce noxious mediators, which are produced by lesions and other cells in their microenvironment, to CNS which is perceived as pain [1,99]. Interestingly, there is increasing evidence suggesting that the presence of nerve fibres in ectopic and eutopic endometrium play a possible role in the pain associated with endometriosis [122-124]. In addition, the relationship between endometriotic lesions and nerve fibers is bidirectional, as endometriotic lesions and nerve fibers are engaged in active cross-talks, which lead to the development of endometriosis and pain [99]. Numerous studies on pain associated with endometriosis have focused on the identification of nerve fibers and other factors that play a role in the development and maintenance of nerve fibres, to explain their possible role in pain triggering. Brief basic facts on nerve fibers and the possible role of nerve fibres in pain associated with endometriosis are discussed below.
Nerve fibres in peritoneal endometriosis
Tulandi was the first study that investigated the presence of the nerve fibres in peritoneal endometriotic lesions compared to normal peritoneum in women with endometriosis using an antibody against Neurofilament (NF) protein [125]. However, no differences in the density of nerve fibres in peritoneal endometriotic lesions compared to normal peritoneum were detected. On the other hand, Tokushige demonstrated a higher density of small unmyelinated nerve fibres stained with protein gene product 9.5 (PGP 9.5) in peritoneal endometriotic lesions of women with endometriosis compared with normal peritoneum in women without endometriosis [122]. In addition, the density of nerve fibres was higher near endometriotic glands and blood vessels compared to the stroma [122]. Another study confirmed these results by finding nerve fibres stained with NF and Substance P (SP) in direct contact with endometriotic lesions in 74.5% (79/106) of the samples [123]. However, there were no significant differences in the total mean nerve scores in the peritoneum tissue from women with and without the disease. In another study by the same group demonstrated that the density of nerve fibres stained with NF and PGP 9.5 was significantly higher in the peritoneum of women with higher pain scores for dysmenorrhoea and pelvic pain in comparison with the peritoneum from women with a lower pain score. However, there was no correlation between the nerve fibre density and dyspareunia, dyschezia or dysuria [124].

In addition, some studies have also investigated the effect of hormonal treatment on nerve fibre density. Tokushige reported a decrease in the density of nerve fibres stained with PGP 9.5 in peritoneal endometriotic lesions of hormone-treated women in comparison to endometriotic lesion of untreated women [126]. However, Wang et al., showed no differences in the density of nerve fibres stained with NF or PGP 9.5 through different stages of the menstrual cycle [127].
Nerves fibers in endometrium and myometrium
It has been suggested that endometrial biopsies could be used as a potential biomarker assay, due to the accessibility of it through a semi-invasive procedure [61,128]. A preliminary study on samples from the lower one half of the uterus collected after hysterectomy, reported an increase of nerve fibres stained with anti-S100 in the myometrium of patients with endometriosis or chronic pelvic pain, however, without endometriosis in comparison with controls [129]. In another study Tokushige demonstrated the presence of nerve fibres in the basal and functional layer of the endometrium in all patients of endometriosis [130]. In addition, no nerve fibres were found in the functional layer of the endometrium of women without endometriosis [130]. These results were confirmed by a subsequent study showing the presence of nerve fibres in the functional endometrial layer stained with Vasoactive Intestinal Peptide (VIP), Neuropeptide Y (NPY), SP and Calcitonin Gene-Related Peptide (CGRP), which suggest the presence of a mixture of sensory, adrenergic and cholinergic fibres [131]. Nerve fibres were also found in the myometrium of women with and without endometriosis. The density of endometrial nerve fibres has been suggested to be hormone dependent [132]. There was a decrease in density of the nerve fibres in the functional and basal endometrial layers of women using hormonal treatment in comparison to untreated women with endometriosis [132].

The results of previous studies have supported using endometrial nerve fibres as potential biomarkers for endometriosis [61]. Al-Jefout et al., was the first study to investigate this hypothesis. In this study nerve fibers were stained with PGP 9.5 and were reportedly detected with a specificity and sensitivity of 100% in the endometrial biopsies [128]. A further double-blinded study assessed efficacy of the detection of nerve fibres stained with PGP 9.5 in endometrial biopsies compared to laparoscopically verified endometriosis. This result demonstrated a specificity and sensitivity of 83% and 98%, respectively, with a positive predictive value of 91% and negative predictive value of 96% [133]. In addition, women with endometriosis and pain symptoms showed a significantly higher nerve fibre density compared to women with endometriosis and without [133]. However, the following studies have contradicted these encouraging results and it remains unclear why recent studies have disproved previous studies. Possible explanations could be the heterogeneity of the endometriosis, variability in tissue collection and processing protocols [134-138]. To find definite answers to the usefulness of the presence of nerve fibres in eutopic endometrium as a biomarker for endometriosis, the standardisation of these variable factors in large Randomized Controlled Trials (RCTs) with specific emphasis on minimal and mild endometriosis is needed [43,139].


There is evidence that neurotrophins and their receptors are involved in nerve fibre growth and are expressed in endometrial tissue and Peritoneal Fluid (PF) of women with endometriosis. Previous studies have shown that NT-3, NGF and their receptors: p75 and TrkA (respectively), are expressed in endometrial glands and stroma of peritoneal lesions, ovarian and Deep Infiltrating Endometrial (DIE) lesions [122,140,141]. In addition, Barcena de Arellano investigated the possible role of neurotrophins in eutopic endometrium and demonstrated that NGF, BDNF and NT-3 are expressed in the endometrium of women with and without endometriosis and there were no differences detected [142]. However, another study showed that the levels of NT-4/5 and BDNF were higher in the endometrium of women with endometriosis compared with controls, and there were no differences in the NGF level observed between the two study groups [143]. 

Barcena de Arellano also showed elevated levels of NGF, NT-3, but none in BDNF in the PF of women with peritoneal endometriosis compared with adenomyosis, adhesions or asymptomatic controls [144]. However, the concentrations of these neurotrophins did not show a correlation with the pain symptoms in any of the groups. Kajitani et al., demonstrated contrasting results, with a significant correlation between high NGF levels and the severity of dysmenorrhoea and moderate or severe dyspareunia in women with peritoneal or ovarian endometriosis [145]. Moreover, women with endometriosis showed elevated BDNF in their plasma [146]. These results are suggestive that neurotrophins may stimulate a differential nerve fibre growth pattern in women with endometriosis and potentially contributing to pain mechanisms associated with endometriosis.


Elevated neuronal guidance molecules activities were observed in women with endometriosis. Women with endometriosis showed a significantly higher Semaphorin 3A in endometrium, Semaphorin 3C in the endometrium and peritoneal endometriotic lesions and Semaphorin 3F in peritoneal endometriotic lesions [147-149]. Shen et al., reported a higher expression of Slit and Robo1 proteins, as well as an increased microvascular density, in cases of endometrioma recurrence [150]. The results of these studies suggested the possible role of neuronal guidance molecules in nerve fibres growth in women with endometriosis and potentially contributing to pain mechanisms associated with endometriosis.


To-date the aetiology and the pathogenesis of the disease are still poorly understood. As discussed endometriosis has a wide range of symptoms or can be asymptomatic, this makes the diagnosis of the disease difficult. The definitive diagnosis is surgical, usually via laparoscopy with histological confirmation. There is often a long delay in diagnosis, 8-12 years, from the onset of symptoms till a definitive diagnosis is made. Endometriosis is a progressive disease and the long delays before effective treatment allows the disease to advance. Ideally there is a need for the discovery of a biomarker to detect the disease earlier and to avoid the use of laparoscopy.


The authors declare that there is no conflict of interest.




  1. Giudice LC (2010) Endometriosis. N Engl J Med 362: 2389-2398.
  2. Eskenazi B, Warner ML (1997) Epidemiology of endometriosis. Obstet and Gynecol Clin North Am 24: 235-258.
  3. Fraser IS (2008) Recognising, understanding and managing endometriosis. J Hum Reprod Sci 1: 56-64.
  4. Olive DL, Pritts EA (2001) Drug therapy: Treatment of endometriosis. New England Journal of Medicine 345: 266-275.
  5. Jubanyik KJ, Comite F (1997) Extrapelvic endometriosis. Obstet Gynecol Clin North Am 24: 411-440.
  6. Saad A (2008) Endometriosis. Obstet Gynaecol amp; Reprod Med 18: 126-133.
  7. Mu F, Rich-Edwards J, Rimm EB, Spiegelman D, Missmer SA (2016) Endometriosis and risk of coronary heart disease. Circ Cardiovasc Qual Outcomes 9: 257-264.
  8. Sourial S, Tempest N, Hapangama DK (2014) Theories on the pathogenesis of endometriosis. International Journal of Reproductive Medicine 179515.
  9. McLeod BS, Retzloff MG (2010) Epidemiology of endometriosis: An assessment of risk factors. Clin Obstet Gynecol 53: 389-396.
  10. Sampson JA (1927) Peritoneal endometriosis due to the menstrual dissemination of endometrial tissue into the peritoneal cavity. Am J Obstet Gynecol 14: 422-469.
  11. Sasson IE, Taylor HS (2008) Stem Cells and the Pathogenesis of Endometriosis. Ann N Y Acad Sci 1127: 106-115.
  12. Ebert AD, Fuhr N, David M, Schneppel L, Papadopoulos T (2009) Histological con?rmation of endometriosis in a 9-year-old girl suffering from unexplained cyclic pelvic pain since her eighth year of life. Gynecol Obstet Invest 67: 158-161.
  13. Marsh EE, Laufer MR (2005) Endometriosis in premenarcheal girls who do not have an associated obstructive anomaly. Fertil Steril 83: 758-760.
  14. Díez García R, Prieto Díez M, Aguilar Tremoya F (1996) Neonatal ovarian endometriosis. Its conservative treatment. An Esp Pediatr 44: 397-398.
  15. Balci O, Karatayli R, Capar M (2008) An incidental coexistence of Mayer-Rokitansky-Kuster-Hauser syndrome with pelvic ectopic kidney and perirenal endometrioma. Saudi Med J 29: 1340-1341.
  16. Bulun SE (2009) Endometriosis. N Engl J Med 360: 268-279.
  17. Metzger DA, Haney AF (1989) Etiology of endometriosis. Obstet Gynecol Clin North Am 16: 1-14.
  18. Clark AH (1948) Endometriosis in a young girl. J Am Med Assoc 136: 690.
  19. Schifrin BS, Erez S, Moore JG (1973) Teen-age endometriosis. Am J Obstet Gynecol 116: 973-980.
  20. EL-Mahgoub S, Yaseen S (1980) A positive proof for the theory of coelomic metaplasia. Am J Obstet Gynecol 137: 137-140.
  21. Hobbs JE, Bortnick AR (1940) Endometriosis of the lungs: An experimental and clinical study. Am J Obstet Gynecol 40: 832-843.
  22. Cassina PC, Hauser M, Kacl G, Imthurn B, Schröder S, et al. (1997) Catamenial hemoptysis - Diagnosis with MRI. Chest 111: 1447-1450.
  23. Seli E, Berkkanoglu M, Arici A (2003) Pathogenesis of endometriosis. Obstet Gynecol Clin North Am 30: 41-61.
  24. Vercellini P, Fedele L, Aimi G, Pietropaolo G, Consonni D, et al. (2007) Association between endometriosis stage, lesion type, patient characteristics and severity of pelvic pain symptoms: a multivariate analysis of over 1000 patients. Hum Reprod 22: 266-271.
  25. Fraser IS (2010) Mysteries of endometriosis pain: Chien-Tien Hsu Memorial Lecture 2009. J Obstet Gynaecol Res 36: 1-10.
  26. Sinaii N, Plumb K, Cotton L, Lambert A, Kennedy S, et al. (2008) Differences in characteristics among 1,000 women with endometriosis based on extent of disease. Fertil Steril 89: 538-545.
  27. Markham R (2002) Endometriosis symptoms in australian women (phd thesis). The university of Sydney, Austraila.
  28. Evans S, Moalem-Taylor G, Tracey DJ (2007) Pain and endometriosis. Pain 132: 22-25.
  29. D'Hooghe TM, Debrock S, Hill JA, Meuleman C (2003) Endometriosis and subfertility: is the relationship resolved? Semin Reprod Med 21: 243-254.
  30. Candiani GB, Fedele L, Vercellini P (1989) Laparotomy versus laparoscopy in the surgical treatment of endometriosis: the end of an era? Acta Eur Fertil 20: 163-166.
  31. Khine YM, Taniguchi F, Harada T (2016) Clinical management of endometriosis-associated infertility. Reprod Med Biol 15: 217-225.
  32. Amer S (2008) Endometriosis. Obstet Gynecol Reprod Med 18: 126-133.
  33. Nisenblat V, Farquhar C, Akoum A, Fraser I, Bossuyt PMM (2012) Non?invasive tests for the diagnosis of endometriosis. Cochrane Database of Systematic Reviews, John Wiley & Sons, New Jersey, United States.
  34. Gupta S, Harlev A, Agarwal A, Ellis-Kahana J, Cirenza C (2015) Diagnosis of endometriosis. Endometriosis: A Comprehensive update. Cham: Springer International Publishing, Switzerland.
  35. Manderson L, Warren N, Markovic M (2008) Circuit breaking: pathways of treatment seeking for women with endometriosis in australia. Qual Health Res18: 522-534.
  36. Somigliana E, Vercellini P, Vigano' P, Benaglia L, Crosignani PG, et al. (2010) Non-invasive diagnosis of endometriosis: the goal or own goal? Hum Reprod 25: 1863-1868.
  37. Mehedintu C, Plotogea M N, Ionescu S, Antonovici M (2014) Endometriosis still a challenge. J Med Life 7: 349-357.
  38. Van den Bosch T, Van Schoubroeck D (2018) Ultrasound diagnosis of endometriosis and adenomyosis: State of the art. Best Pract Res Clin Obstet Gynaecol 1521.
  39. Brosens I, Puttemans P, Campo R, Gordts S, Kinkel K (2004) Diagnosis of endometriosis: pelvic endoscopy and imaging techniques. Best Pract Res Clin Obstet Gynaecol 18: 285-303.
  40. Seckin B, Oruc AS, Turkcapar F, Ugur M (2013) The relation of pelvic pain and dense adhesions to Doppler ultrasound findings in patients with ovarian endometriomas. Arch Gynecol Obstet 287: 723-728.
  41. Ahn SH, Singh V, Tayade C (2017) Biomarkers in endometriosis: challenges and opportunities. Fertil Steril 107: 523-532.
  42. Fassbender A, Burney RO, O DF, D'Hooghe T, Giudice L (2015) Update on Biomarkers for the Detection of Endometriosis. Biomed Res Int 2015: 130854.
  43. Fassbender A, Vodolazkaia A, Saunders P, Lebovic D, Waelkens E, et al. (2013b) Biomarkers of endometriosis. Fertil Steril 100: 20-20.
  44. Fassbender A, Vodolazkaia A, Saunders P, Lebovic D, Waelkens E, et al. (2013a) Biomarkers of endometriosis. Fertil Steril 99: 1135-1145.
  45. Gupta D, Hull ML, Fraser I, Miller L, Bossuyt PM, et al. (2016) Endometrial biomarkers for the non-invasive diagnosis of endometriosis. Cochrane Database Syst Rev 4: 012165.
  46. Nisenblat V, Bossuyt PM, Shaikh R, Farquhar C, Jordan V, et al. (2016) Blood biomarkers for the non-invasive diagnosis of endometriosis. Cochrane Database Syst Rev 1: 012179.
  47. Nisenblat V, Prentice L, Bossuyt PM, Farquhar C, Hull ML, et al. (2016) Combination of the non-invasive tests for the diagnosis of endometriosis. Cochrane Database Syst Rev 7: 012281.
  48. Reis FMD, Monteiro CDS, Carneiro MM (2017) Biomarkers of Pelvic Endometriosis. Rev Bras Ginecol Obstet 39: 091-093.
  49. Worku DA (2017) The Role of Biomarkers in the Early Diagnosis of Endometriosis. Invest Gynecol Res Women’s Health 1: 1-4.
  50. Johnson NP, Hummelshoj L (2013) Consensus on current management of endometriosis. Hum Reprod 28: 3163-3164.
  51. Johnson NP, Hummelshoj L; World Endometriosis Society Montpellier Consortium (2013) Consensus on current management of endometriosis. Hum Reprod 28: 1552-1568.
  52. Nisenblat V, Bossuyt PM, Farquhar C, Johnson N, Hull ML (2016) Imaging modalities for the non-invasive diagnosis of endometriosis. Cochrane Database Syst Rev 2: 009591.
  53. Johnson NP, Hummelshoj L, Nisenblat V, Bush D, Kiesel L, et al. (2014) 12th world congress on endometriosis. World endometriosis society, Sao paulo, Brazil.
  54. Joshi SG, Zamah NM, Raikar RS, Buttram VC Jr, Henriques ES, et al.(1986) Serum and peritoneal fluid proteins in women with and without endometriosis. Fertil Steril 46: 1077-1082.
  55. Kingsmore SF (2006) Multiplexed protein measurement: technologies and applications of protein and antibody arrays. Nat Rev Drug Discov 5: 310-320.
  56. El-Kasti MM, Wright C, Fye HK, Roseman F, Kessler BM, et al. (2011) Urinary peptide profiling identifies a panel of putative biomarkers for diagnosing and staging endometriosis. Fertility and sterility 95: 1-6.
  57. Tokushige N, Markham R, Crossett B, Ahn SB, Nelaturi VL, et al (2011) Discovery of a novel biomarker in the urine in women with endometriosis. Fertil Steril 95: 46-49.
  58. Cho S, Choi YS, Yim SY, Yang HI, Jeon YE, et al. (2012) Urinary vitamin D-binding protein is elevated in patients with endometriosis. Hum Reprod 27: 515-22.
  59. Yun BH, Lee YS, Chon SJ, Jung YS, Yim SY, et al. (2014) Evaluation of elevated urinary enolase I levels in patients with endometriosis. Biomarkers 19: 16-21.
  60. Rogers PA, D'Hooghe TM, Fazleabas A, Giudice LC, Montgomery GW (2013) Defining future directions for endometriosis research: workshop report from the 2011 World Congress of Endometriosis In Montpellier, France. Reprod Sci 20: 483-499.
  61. May KE, Conduit-Hulbert SA, Villar J, Kirtley S, Kennedy SH, et al. (2010) Peripheral biomarkers of endometriosis: A systematic review. Hum Reprod Update 16: 651-674.
  62. Hirsch M, Duffy JMN, Davis CJ, Plana MN, Khan KS, et al. (2016) Diagnostic accuracy of cancer antigen 125 for endometriosis: A systematic review and meta-analysis. BJOG 123: 1761-1768.
  63. Platteeuw L1 D'Hooghe T (2014) Novel agents for the medical treatment of endometriosis. Curr Opin Obstet Gynecol 26: 243-252.
  64. Crosignani PG, Vercellini P, Biffignandi F, Costantini W, Cortesi I , et al. (1996) Laparoscopy versus laparotomy in conservative surgical treatment for severe endometriosis. Fertil Steril 66: 706-711.
  65. Afors K, Murtada R, Centini G, Fernandes R, Meza C, et al. (2014) Employing laparoscopic surgery for endometriosis. Women's Health 10: 431-443.
  66. Duffy JM, Arambage K, Correa FJ, Olive D, Farquhar C, et al. (2014) Laparoscopic surgery for endometriosis. Cochrane Database of Syst Rev 011031.
  67. Al-Jefout M (2011) Brief update on endometriosis treatment. Middle East Fertility Society Journal 16: 167-174.
  68. Dunselman GA, Vermeulen N, Becker C, Calhaz-Jorge C, D'Hooghe T, et al. (2014) ESHRE guideline: management of women with endometriosis. Hum Reprod 29: 400-412.
  69. Muzii L, Panici PB (2010) Combined technique of excision and ablation for the surgical treatment of ovarian endometriomas: the way forward? Reprod Biomed Online 20: 300-302.
  70. Somigliana E , Vigano P , Barbara G , Vercellini P (2009) Treatment of endometriosis-related pain: options and outcomes. Frontiers in Bioscience (Elite Edition) 1: 455-465.
  71. Vercellini P, Somigliana E, Viganò P, Abbiati A, Daguati R, et al. (2008) Endometriosis: current and future medical therapies. Best Pract Res Clin Obstet Gynaecol 22: 275-306.
  72. Sulak PJ, Cressman BE, Waldrop E, Holleman S, Kuehl TJ (1997) Extending the duration of active oral contraceptive pills to manage hormone withdrawal symptoms. Obstet Gynecol 89: 179-183.
  73. Coffee AL, Sulak PJ, Kuehl TJ (2007) Long-term assessment of symptomatology and satisfaction of an extended oral contraceptive regimen. Contraception 75: 444-449.
  74. Practice Committee of The American Society for Reproductive (2006) Treatment of pelvic pain associated with endometriosis. Fertil Steril 86: 18-27.
  75. Olive DL (2003) Medical therapy of endometriosis. Semin Reprod Med 21: 209-222.
  76. Gupta S, Harlev A, Agarwal A, Rakhit M, Ellis-Kahana, et al. (2015b) Management of endometriosis. Endometriosis: A comprehensive update. Cham: Springer International Publishing, Switzerland.
  77. Hornstein MD, Gibbons WE (2018) Endometriosis: Long-term treatment with gonadotropin-releasing hormone agonists. Wolters Kluwer, Alphen aan den Rijn, The Netherlands.
  78. Selak V, Farquhar C, Prentice A, Singla A (2007) Danazol for pelvic pain associated with endometriosis. Cochrane Database Syst Rev 17: 000068.
  79. Velasco I, Rueda J, Acien P (2006) Aromatase expression in endometriotic tissues and cell cultures of patients with endometriosis. MHR: Basic science of reproductive medicine 12: 377-381.
  80. Pavone ME, Bulun SE(2012) Aromatase Inhibitors For The Treatment Of Endometriosis: A Review. Fertil Steril 98: 1370-1379.
  81. Ailawadi RK, Jobanputra S, Kataria M, Gurates B, Bulun SE (2004) Treatment of endometriosis and chronic pelvic pain with letrozole and norethindrone acetate: a pilot study. Fertil Steril 81: 290-296.
  82. Remorgida V, Abbamonte HL, Ragni N, Fulcheri E, Ferrero S (2007 Letrozole and norethisterone acetate in rectovaginal endometriosis. Fertil Steril 88: 724-726.
  83. Hamann GO (1980) Severe, primary dysmenorrhea treated with naproxen. A prospective, double-blind, crossover investigation. Prostaglandins 19: 651-657.
  84. Hanson FW, Izu A, Henzl MR (1978) Naproxen sodium in dysmenorrhea. Its influence in allowing continuation of work/school activities. Obstet Gynecol 52: 583-587.
  85. Zito G, Luppi S, Giolo E, Martinelli M, Venturin, et al. (2014) Medical treatments for endometriosis-associated pelvic pain. Biomed Res Int 2014: 191967.
  86. Brown J, Crawford TJ, Allen C, Hopewell S, Prentice A (2009) Nonsteroidal anti-inflammatory drugs for pain in women with endometriosis. Cochrane Database Syst Rev 1: 00487.
  87. Sinha A, Gupta S (2017) The Role of Antioxidant Supplementation in Endometriosis Therapy. J Gynecol Women’s Health 3: 1-3.
  88. Santanam N, Kavtaradze N, Murphy A, Dominguez C, Parthasarathy S (2013) Antioxidant supplementation reduces endometriosis-related pelvic pain in humans. Transl Res 161: 189 - 195.
  89. Howard FM (2009) Endometriosis and mechanisms of pelvic pain. J Minim Invasive Gynecol 16: 540-550.
  90. Vercellini P, Fedele L, Molteni P, Arcaini L, Bianchi S, et al. (1990) Laparoscopy in the diagnosis of gynecologic chronic pelvic pain. Int J Gynaecol Obstet 32: 261-265.
  91. Whiteside JL, Falcone T (2003) Endometriosis-related pelvic pain: what is the evidence? Clin Obstet Gynecol 46: 824-830.
  92. Harada T (2013) Dysmenorrhea and endometriosis in young women. Yonago Acta Med 56: 81-84.
  93. Chrousos GP (2009) Stress and disorders of the stress system. Nat Rev Endocrinol 5: 374-381.
  94. Huether G, Doering S, Rüger U, Rüther E, Schüssler G (1996) [Psychological stress and neuronal plasticity. An expanded model of the stress reaction process as the basis for understand central nervous system adaptation processes]. Z Psychosom Med Psychoanal 42: 107-127.
  95. Lundberg U (2002) Psychophysiology of work: stress, gender, endocrine response, and work-related upper extremity disorders. Am J Ind Med 41: 383-392.
  96. Paiva S1, Carneiro MM (2013) Complementary and Alternative Medicine in the Treatment of Chronic Pelvic Pain in Women: What Is the Evidence?. ISRN Pain 2013: 469575.
  97. Medina MG, Lebovic DI (2009) Endometriosis-associated nerve fibers and pain. Acta Obstet Gynecol Scand 88: 968-975.
  98. Bulletti C, De Ziegler D, Polli V, Del Ferro E, Palini S, et al. (2002) Characteristics of uterine contractility during menses in women with mild to moderate endometriosis. Fertil Steril 77: 1156-1161.
  99. Yan D, Liu X, Guo SW (2017) Nerve fibers and endometriotic lesions: partners in crime in inflicting pains in women with endometriosis. Eur J Obstet Gynecol Reprod Biol 209: 14-24.
  100. Laverdet B, Danigo A, Girard D, Magy L, Demiot C, et al. (2015) Skin innervation: important roles during normal and pathological cutaneous repair. Histol Histopathol 30: 875-892.
  101. Purves D (2012) Neuroscience, Sunderland (Massachusetts), Sinauer Associates.
  102. Ceni C, Unsain N, Zeinieh MP, Barker PA (2014) Neurotrophins in the regulation of cellular survival and death. Handb Exp Pharmacol 220: 193-221.
  103. Skaper SD (2012) The neurotrophin family of neurotrophic factors: an overview. Methods Mol Biol 846: 1-12.
  104. Davies AM (2008) Neurotrophins giveth and they taketh away. Nature Neuroscience 11: 627-628.
  105. Patapoutian A, Reichardt LF (2001) Trk receptors: mediators of neurotrophin action. Curr Opin Neurobiol 11: 272-280.
  106. Davies AM, Minichiello L, Klein R (1995) Developmental changes in NT3 signalling via TrkA and TrkB in embryonic neurons. EMBO J 14: 4482-4489.
  107. Arévalo JC, Wu SH (2006) Neurotrophin signaling: many exciting surprises! Cell Mol Life Sci 63: 1523-1537.
  108. Sánchez-Sánchez J, Arévalo JC (2017) A Review on Ubiquitination of Neurotrophin Receptors: Facts and Perspectives. Int J Mol Sci 18: 630.
  109. Saarma M, Sariola H (1999) Other neurotrophic factors: glial cell line-derived neurotrophic factor (GDNF). Microsc Res Tech 45: 292-302.
  110. Airaksinen MS, Saarma M (2002) The GDNF family: Signalling, biological functions and therapeutic value. Nat Rev Neurosci 3: 383-394.
  111. Pezet S, McMahon SB (2006) Neurotrophins: mediators and modulators of pain. Annu Rev Neurosci 29: 507-538.
  112. Snider W D, Mcmahon S B (1998) Tackling pain at the source: new ideas about nociceptors. Neuron 20: 629-632.
  113. Salio C, Ferrini F (2016) BDNF and GDNF expression in discrete populations of nociceptors. Ann Anat 207: 55-61.
  114. Van Battum EY, Brignani S, Pasterkamp RJ (2015) Axon guidance proteins in neurological disorders. Lancet Neurol 14: 532-546.
  115. Kolodkin AL, Tessier-Lavigne M (2011) Mechanisms and molecules of neuronal wiring: a primer. Cold Spring Harb Perspect Biol 3: 001727.
  116. Pasterkamp RJ, Kolodkin AL (2013) SnapShot: Axon Guidance. Cell 153: 494e1-2.
  117. Pasterkamp RJ (2012) Getting neural circuits into shape with semaphorins. Nat Rev Neurosci 13: 605-618.
  118. Lai Wing Sun K, Correia JP, Kennedy TE (2011) Netrins: versatile extracellular cues with diverse functions. Development 138: 2153-2169.
  119. Ypsilanti AR, Zagar Y, Chédotal A (2010) Moving away from the midline: new developments for Slit and Robo. Development 137: 1939-1952.
  120. Severyn CJ, Shinde U, Rotwein P (2009) Molecular biology, genetics and biochemistry of the repulsive guidance molecule family. Biochem J 422: 393-403.
  121. Klein R (2012) Eph/ephrin signalling during development. Development 139: 4105-4109.
  122. Tokushige N, Markham R, Russell P, Fraser IS (2006) Nerve fibres in peritoneal endometriosis. Hum Reprod 21: 3001-3007.
  123. Mechsner S, Schwarz J, Thode J, Loddenkemper C, Salomon DS, et al. (2007) Growth-associated protein 43-positive sensory nerve fibers accompanied by immature vessels are located in or near peritoneal endometriotic lesions. Fertil steril, 88: 581-7.
  124. Mechsner S, Kaiser A, Kopf A, Gericke C, Ebert A, et al. (2009) A pilot study to evaluate the clinical relevance of endometriosis-associated nerve fibers in peritoneal endometriotic lesions. Fertil Steril, 92: 1856-1861.
  125. Tulandi T, Felemban A, Chen MF (2001) Nerve fibers and histopathology of endometriosis-harboring peritoneum. J Am Assoc Gynecol Laparosc 8: 95-98.
  126. Tokushige N, Markham R, Russell P, Fraser IS (2009). Effect of progestogens and combined oral contraceptives on nerve fibers in peritoneal endometriosis. Fertil Steril 92: 1234-1239.
  127. Wang G, Tokushige N, Fraser IS (2011) Nerve fibers and menstrual cycle in peritoneal endometriosis. Fertil Steril 95: 2772-2774.
  128. Al-Jefout M, Andreadis N, Tokushige N, Markham R, Fraser I (2007) A pilot study to evaluate the relative efficacy of endometrial biopsy and full curettage in making a diagnosis of endometriosis by the detection of endometrial nerve fibers. Am J Obstet Gynecol 197: 1-4.
  129. Atwal G, du Plessis D, Armstrong G, Slade R, Quinn M (2005) Uterine innervation after hysterectomy for chronic pelvic pain with, and without, endometriosis. Am J Obstet Gynecol 193: 1650-1655.
  130. Tokushige N, Markham R, Russell P, Fraser IS (2006) High density of small nerve fibres in the functional layer of the endometrium in women with endometriosis. Hum Reprod 21: 782-787.
  131. Tokushige N, Markham R, Russell P, Fraser IS (2007) Different types of small nerve fibers in eutopic endometrium and myometrium in women with endometriosis. Fertil Steril 88: 795-803.
  132. Tokushige N, Markham R, Russell P, Fraser IS (2008) Effects of hormonal treatment on nerve fibers in endometrium and myometrium in women with endometriosis. Fertil Steril 90: 1589-1598.
  133. Al-Jefout M, Dezarnaulds G, Cooper M, Tokushige N, Luscombe GM, et al. (2009) Diagnosis of endometriosis by detection of nerve fibres in an endometrial biopsy: a double blind study. Hum Reprod 24: 3019-3024.
  134. Zhang X, Lu B, Huang X, Xu H, Zhou C, et al. (2009) Endometrial nerve fibers in women with endometriosis, adenomyosis, and uterine fibroids. Fertil Steril 92: 1799-1801.
  135. Zhang X, Yao H, Huang X, Lu B, Xu H, et al. (2010) Nerve fibres in ovarian endometriotic lesions in women with ovarian endometriosis. Hum Reprod 25: 392-397.
  136. Leslie C, Ma T, McElhinney B, Leake R, Stewart CJ (2013) Is the detection of endometrial nerve fibers useful in the diagnosis of endometriosis? Int J Gynecol Pathol 32: 149-55.
  137. Newman TA, Bailey JL, Stocker LJ, Woo YL, Macklon NS, et al. (2013) Expression of neuronal markers in the endometrium of women with and those without endometriosis. Hum Reprod 28: 2502-2510.
  138. Morotti M, Vincent K, Brawn J, Zondervan KT, Becker CM (2014) Peripheral changes in endometriosis-associated pain. Hum Reprod Update 20: 717-736.
  139. D'Hooghe TM, Mihalyi AM, Simsa P, Kyama CK, Peeraer K, et al. (2006) Why we need a noninvasive diagnostic test for minimal to mild endometriosis with a high sensitivity. Gynecol Obstet Invest 62: 136-138.
  140. Anaf V, Simon P, El Nakadi I, Fayt I, Simonart T, et al. (2002) Hyperalgesia, nerve infiltration and nerve growth factor expression in deep adenomyotic nodules, peritoneal and ovarian endometriosis. Hum Reprod 17: 1895-1900.
  141. Tokushige N, Russell P, Black K, Barrera H, Dubinovsky S, et al. (2010) Nerve fibers in ovarian endometriomas. Fertil Steril 94: 1944-1947.
  142. Barcena de Arellano ML, Arnold J, Sacher F, Blöchle M, Staube M, et al. (2012) Eutopic endometrium from women with endometriosis does not exhibit neurotrophic properties. J Neuroimmunol 249: 49-55.
  143. Browne AS, Yu J, Huang RP, Francisco AM, Sidell N, et al. (2012) Proteomic identification of neurotrophins in the eutopic endometrium of women with endometriosis. Fertil Steril 98: 713-719.
  144. Barcena de Arellano ML, Arnold J, Lang H, Vercellino GF, Chiantera V, et al. (2013) Evidence of neurotrophic events due to peritoneal endometriotic lesions. Cytokine 62: 253-261.
  145. Kajitani T, Maruyama T, Asada H, Uchida H, Oda H, et al. (2013) Possible involvement of nerve growth factor in dysmenorrhea and dyspareunia associated with endometriosis. Endocr J 60: 1155-64.
  146. Wessels JM, Kay VR, Leyland NA, Agarwal SK, Foster WG (2016) Assessing brain-derived neurotrophic factor as a novel clinical marker of endometriosis. Fertil Steril 105: 119-128.
  147. Kao LC, Germeyer A, Tulac S, Lobo S, Yang JP, et al. (2003) Expression profiling of endometrium from women with endometriosis reveals candidate genes for disease-based implantation failure and infertility. Endocrinology 144: 2870-2881.
  148. Liang Y, Wang W, Huang J, Tan H, Liu T, et al. (2015) Potential role of semaphorin 3a and its receptors in regulating aberrant sympathetic innervation in peritoneal and deep infiltrating endometriosis. Plos one 10: 0146027.
  149. Scheerer C, Frangini S, Chiantera V, Mechsner S (2017) Reduced Sympathetic Innervation in Endometriosis is Associated to Semaphorin 3C and 3F Expression. Mol Neurobiol 54: 5131-5141.
  150. Shen F, Liu X, Geng JG, Guo SW (2009) Increased immunoreactivity to SLIT/ROBO1 in ovarian endometriomas: a likely constituent biomarker for recurrence. Am J Pathol 175: 479-488.

Citation: Asally R, Markham R, Manconi F (2018) Endometriosis - Pathogenesis and Sequelae. J Reprod Med Gynecol Obstet 3: 010.

Copyright: © 2018  Razan Asally, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

© 2022, Copyrights Herald Scholarly Open Access. All Rights Reserved!