4.7 Article

Evidence in Support for the Progressive Nature of Ovarian Endometriomas

期刊

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
卷 105, 期 7, 页码 2189-2202

出版社

ENDOCRINE SOC
DOI: 10.1210/clinem/dgaa189

关键词

adrenergic receptor beta 2; endometriosis; epithelial-mesenchymal transition; fibroblast-to-myofibroblast transdifferentiation; fibrogenesis; progression

资金

  1. National Science Foundation of China [81530040, 81771553, 81671436, 81871144]
  2. Excellence in Centers of Clinical Medicine grant from the Science and Technology Commission of Shanghai Municipality [2017ZZ01016]

向作者/读者索取更多资源

Context: Whether endometriosis is a progressive disease is a highly contentious issue. While progression is reported to be unlikely in asymptomatic deep endometriosis, progression in symptomatic deep endometriosis has recently been reported, especially in menstruating women. However, pathophysiological reasons for these differences are unclear. Objective: This study was designed to investigate whether ovarian endometrioma (OE) is progressive or not. Setting, Design, Patients, Intervention and Main Outcome Measures: Thirty adolescent patients, aged 15 to 19 years, and 32 adult patients, aged 35 to 39 years, all laparoscopically and histologically diagnosed with OE, were recruited into this study after informed consent. Their demographic and clinical information were collected. Their OE tissue samples were collected and subjected to immunohistochemical analysis for E-cadherin, alpha-smooth muscle actin (alpha-SMA), desmin, and adrenergic receptor beta 2 (ADRB2), as well as quantification of lesional fibrosis by Masson trichrome staining. Results: OE lesions from the adolescent and adult patients are markedly different, with the latter exhibiting more extensive and thorough progression and more extensive fibrosis, suggesting that lesions in adults progressed to a more advanced stage. Adult lesions and higher staining level of alpha-SMA and ADRB2 are positively associated with the extent of lesional fibrosis, while the lesion size and the E-cadherin staining are negatively associated. Conclusions: Our data provide a more definitive piece of evidence suggesting that OE is a progressive disease, since the adult lesions have had a longer time to progress. In addition, the pace of progression depends on lesional age as well as the severity of endometriosis-associated dysmenorrhea, if any.

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