Department of Obstetrics and Gynecology, University of British Columbia, Vancouver, V6H 3N1, Canada.
Sex Med Rev. 2023 Sep 27;11(4):323-332. doi: 10.1093/sxmrev/qead033.
Endometriosis is a common cause of deep dyspareunia, while provoked vestibulodynia is a common cause of superficial dyspareunia. The etiology of dyspareunia in both conditions is multifactorial and may include the role of local nerve growth (neurogenesis or neuroproliferation) that sensitizes pelvic structures and leads to pain with contact.
To review the evidence for neuroproliferative dyspareunia in endometriosis and provoked vestibulodynia.
Narrative review.
The pelvic peritoneum and vulvar vestibule receive somatic and autonomic innervation. Various markers have been utilized for nerve subtypes, including pan-neuronal markers and those specific for sensory and autonomic nerve fibers. The nerve growth factor family includes neurotrophic factors, such as nerve growth factor and brain-derived neurotrophic factor, and their receptors. Studies of endometriosis and provoked vestibulodynia have demonstrated the presence of nerve fibers around endometriosis epithelium/stroma in the pelvic peritoneum and within the vulvar vestibule. The number of nerve fibers is higher in these pain conditions as compared with control tissue. Nerve growth factor expression by endometriosis stroma and by immune cells in the vulvar vestibule may be involved in local neuroproliferation. Local inflammation is implicated in this neuroproliferation, with potential roles of interleukin 1β and mast cells in both conditions. Several studies have shown a correlation between nerve fibers around endometriosis and dyspareunia severity, but studies are lacking in provoked vestibulodynia. There are several possible clinical ramifications of neuroproliferative dyspareunia in endometriosis and provoked vestibulodynia, in terms of history, examination, biopsy, and surgical and medical treatment.
A neuroproliferative subtype of dyspareunia may be implicated in endometriosis and provoked vestibulodynia. Additional research is needed to validate this concept and to integrate it into clinical studies. Neuroproliferative pathways could serve as novel therapeutic targets for the treatment of dyspareunia in endometriosis and provoked vestibulodynia.
子宫内膜异位症是深部性交痛的常见原因,而诱发性外阴痛是浅部性交痛的常见原因。这两种情况下性交痛的病因是多因素的,可能包括局部神经生长(神经发生或神经增殖)的作用,这种作用使骨盆结构敏感,并导致接触时疼痛。
综述子宫内膜异位症和诱发性外阴痛中神经增殖性性交痛的证据。
叙述性综述。
盆腔腹膜和外阴前庭接受躯体和自主神经支配。已经利用各种标志物来标记神经亚型,包括神经元标志物和那些专门用于感觉和自主神经纤维的标志物。神经生长因子家族包括神经营养因子,如神经生长因子和脑源性神经营养因子及其受体。子宫内膜异位症和诱发性外阴痛的研究表明,在盆腔腹膜的子宫内膜异位症上皮/基质和外阴前庭内存在神经纤维。与对照组织相比,这些疼痛情况下的神经纤维数量更高。子宫内膜异位症基质和外阴前庭中的免疫细胞表达神经生长因子,可能参与局部神经增殖。局部炎症与这种神经增殖有关,白细胞介素 1β和肥大细胞在这两种情况下都可能发挥作用。几项研究表明,子宫内膜异位症周围的神经纤维与性交痛的严重程度之间存在相关性,但在诱发性外阴痛中缺乏研究。神经增殖性性交痛在子宫内膜异位症和诱发性外阴痛中有几个可能的临床影响,包括病史、检查、活检、手术和药物治疗。
神经增殖性性交痛可能与子宫内膜异位症和诱发性外阴痛有关。需要进一步的研究来验证这一概念,并将其纳入临床研究。神经增殖途径可作为子宫内膜异位症和诱发性外阴痛治疗性交痛的新的治疗靶点。