Obstetrics and Gynaecology - Research Publications

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    A molecular staging model for accurately dating the endometrial biopsy
    Teh, WT ; Chung, J ; Holdsworth-Carson, SJ ; Donoghue, JF ; Healey, M ; Rees, HC ; Bittinger, S ; Obers, V ; Sloggett, C ; Kendarsari, R ; Fung, JN ; Mortlock, S ; Montgomery, GW ; Girling, JE ; Rogers, PAW (NATURE PORTFOLIO, 2023-10-06)
    Natural variability in menstrual cycle length, coupled with rapid changes in endometrial gene expression, makes it difficult to accurately define and compare different stages of the endometrial cycle. Here we develop and validate a method for precisely determining endometrial cycle stage based on global gene expression. Our 'molecular staging model' reveals significant and remarkably synchronised daily changes in expression for over 3400 endometrial genes throughout the cycle, with the most dramatic changes occurring during the secretory phase. Our study significantly extends existing data on the endometrial transcriptome, and for the first time enables identification of differentially expressed endometrial genes with increasing age and different ethnicities. It also allows reinterpretation of all endometrial RNA-seq and array data that has been published to date. Our molecular staging model will significantly advance understanding of endometrial-related disorders that affect nearly all women at some stage of their lives, such as heavy menstrual bleeding, endometriosis, adenomyosis, and recurrent implantation failure.
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    Distribution of smooth muscle actin and collagen in superficial peritoneal endometriotic lesions varies from the surrounding microenvironment
    Colgrave, EM ; Keast, JR ; Nowell, CJ ; Healey, M ; Rogers, PAW ; Holdsworth-Carson, SJ ; Girling, JE (ELSEVIER SCI LTD, 2024-03)
    RESEARCH QUESTION: Do different subtypes of superficial peritoneal endometriotic lesions exist, based on the presence and morphology of smooth muscle, collagen fibres and immune cell populations? DESIGN: A retrospective cohort study of 24 patients, from across the menstrual cycle, with surgically and histologically confirmed endometriosis. Immunofluorescence was used to delineate the CD10 stromal area of lesions (n = 271 lesions from 67 endometriotic biopsies), and then smooth muscle actin (SMA) positive tissue and immune cell populations (CD45+ and CD68+) were quantified within and adjacent to these lesions. Second harmonic generation microscopy was used to evaluate the presence and morphology of type-1 collagen fibres within and surrounding lesions. RESULTS: Overall, immune cell numbers and the area of SMA and collagen within endometriotic lesions tended to be low, but a spectrum of presentations significantly varied, particularly in the adjacent tissue microenvironment, based on lesion locations, the morphology of endometriotic gland profiles, or both. Lesions in which collagen fibres formed well aligned capsules around the CD10+ stromal border were identified compared with lesions in which collagen fibre distribution was random. Considerable inter- and intra-patient variability in the morphology of SMA and collagen was observed within and surrounding lesions. CONCLUSION: These data demonstrate considerable diversity in the presence of immune cells and morphology of SMA and collagen within, but even more so, surrounding endometriotic lesions, even within individual patients. This heterogeneity, especially within individual patients, presents a challenge to incorporating these cell and tissue types into any new endometriosis classification systems or prognostic approaches.
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    Extensive heterogeneity in the expression of steroid receptors in superficial peritoneal endometriotic lesions
    Colgrave, EM ; Keast, JR ; Healey, M ; Rogers, PAW ; Girling, JE ; Holdsworth-Carson, SJ (ELSEVIER SCI LTD, 2024-02)
    RESEARCH QUESTION: Is the expression of steroid hormone receptors (oestrogen receptor-α and progesterone receptor A/B) and proliferative markers (Bcl-2 and Ki67) uniform among superficial peritoneal endometriotic lesions? DESIGN: A retrospective cohort study of 24 patients with surgically and histologically confirmed endometriosis. Immunofluorescence was used to determine the proportion of oestrogen receptor-α (ERα), progesterone receptor A/B, Bcl-2 and Ki67 positive cells in 271 endometriotic lesions (defined as endometriotic gland profile/s within an individual region of CD10 stromal immunostaining from a single biopsy) from 67 endometriotic biopsies from 24 patients. Data were analysed to examine associations related to menstrual cycle stage, lesion location and gland morphology. RESULTS: Oestrogen receptor-α and progesterone receptor A/B expression in superficial peritoneal endometriotic lesions was extremely heterogeneous. Bcl-2 immunostaining in endometriotic lesions was also variable, whereas Ki67 immunostaining was minimal. Menstrual cycle stage associations were limited in steroid hormone receptor and Bcl-2 expression in lesions. Patterns in progesterone receptor A/B and Bcl-2 immunostaining were associated with lesion location. Bcl-2 was differentially expressed, based on lesion gland morphology. CONCLUSIONS: These data demonstrate considerable diversity in the expression of steroid hormone receptors and Bcl-2 between lesions, even within an individual patient.
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    The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions
    Rahmioglu, N ; Mortlock, S ; Ghiasi, M ; Moller, PL ; Stefansdottir, L ; Galarneau, G ; Turman, C ; Danning, R ; Law, MH ; Sapkota, Y ; Christofidou, P ; Skarp, S ; Giri, A ; Banasik, K ; Krassowski, M ; Lepamets, M ; Marciniak, B ; Noukas, M ; Perro, D ; Sliz, E ; Sobalska-Kwapis, M ; Thorleifsson, G ; Topbas-Selcuki, NF ; Vitonis, A ; Westergaard, D ; Arnadottir, R ; Burgdorf, KS ; Campbell, A ; Cheuk, CSK ; Clementi, C ; Cook, J ; De Vivo, I ; DiVasta, A ; Dorien, O ; Donoghue, JF ; Edwards, T ; Fontanillas, P ; Fung, JN ; Geirsson, RT ; Girling, JE ; Harkki, P ; Harris, HR ; Healey, M ; Heikinheimo, O ; Holdsworth-Carson, S ; Hostettler, IC ; Houlden, H ; Houshdaran, S ; Irwin, JC ; Jarvelin, M-R ; Kamatani, Y ; Kennedy, SH ; Kepka, E ; Kettunen, J ; Kubo, M ; Kulig, B ; Kurra, V ; Laivuori, H ; Laufer, MR ; Lindgren, CM ; MacGregor, S ; Mangino, M ; Martin, NG ; Matalliotaki, C ; Matalliotakis, M ; Murray, AD ; Ndungu, A ; Nezhat, C ; Olsen, CM ; Opoku-Anane, J ; Padmanabhan, S ; Paranjpe, M ; Peters, M ; Polak, G ; Porteous, DJ ; Rabban, J ; Rexrode, KM ; Romanowicz, H ; Saare, M ; Saavalainen, L ; Schork, AJ ; Sen, S ; Shafrir, AL ; Siewierska-Gorska, A ; Slomka, M ; Smith, BH ; Smolarz, B ; Szaflik, T ; Szyllo, K ; Takahashi, A ; Terry, KL ; Tomassetti, C ; Treloar, SA ; Vanhie, A ; Vincent, K ; Vo, KC ; Werring, DJ ; Zeggini, E ; Zervou, M ; Stefansson, K ; Nyegaard, M ; Uimari, O ; Yurttas-Beim, P ; Tung, JY ; Adachi, S ; Buring, JE ; Ridker, PM ; D'Hooghe, T ; Goulielmos, GN ; Hapangama, DK ; Hayward, C ; Horne, AW ; Low, S-K ; Martikainen, H ; Chasman, D ; Rogers, PAW ; Saunders, PT ; Sirota, M ; Spector, T ; Strapagiel, D ; Whiteman, DC ; Giudice, LC ; Velez-Edwards, DR ; Kraft, P ; Salumets, A ; Nyholt, DR ; Magi, R ; Becker, CM ; Steinthorsdottir, V ; Missmer, SA ; Montgomery, GW ; Morris, AP ; Zondervan, KT (NATURE PORTFOLIO, 2023-03)
    Endometriosis is a common condition associated with debilitating pelvic pain and infertility. A genome-wide association study meta-analysis, including 60,674 cases and 701,926 controls of European and East Asian descent, identified 42 genome-wide significant loci comprising 49 distinct association signals. Effect sizes were largest for stage 3/4 disease, driven by ovarian endometriosis. Identified signals explained up to 5.01% of disease variance and regulated expression or methylation of genes in endometrium and blood, many of which were associated with pain perception/maintenance (SRP14/BMF, GDAP1, MLLT10, BSN and NGF). We observed significant genetic correlations between endometriosis and 11 pain conditions, including migraine, back and multisite chronic pain (MCP), as well as inflammatory conditions, including asthma and osteoarthritis. Multitrait genetic analyses identified substantial sharing of variants associated with endometriosis and MCP/migraine. Targeted investigations of genetically regulated mechanisms shared between endometriosis and other pain conditions are needed to aid the development of new treatments and facilitate early symptomatic intervention.
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    Gene expression of the endocannabinoid system in endometrium through menstrual cycle
    Tanaka, K ; Amoako, AA ; Mortlock, S ; Rogers, PAW ; Holdsworth-Carson, SJ ; Donoghue, JF ; Teh, WT ; Montgomery, GW ; McKinnon, B (NATURE PORTFOLIO, 2022-06-07)
    Endocannabinoids mediate cellular functions and their activity is controlled by a complex system of enzymes, membrane receptors and transport molecules. Endocannabinoids are present in endometrium, a cyclical regenerative tissue requiring tightly regulated cellular mechanisms for maturation. The objective of this study was to investigate the gene expression of key elements involved in the endocannabinoid system across the menstrual cycle. RNA was isolated from endometrial tissue and genome-wide gene expression datasets were generated using RNA-sequencing. An a priori set of 70 genes associated with endocannabinoid system were selected from published literature. Gene expression across the menstrual cycle was analyzed using a moderated t test, corrected for multiple testing with Bonferroni's method. A total of 40 of the 70 genes were present in > 90% of the samples, and significant differential gene expression identified for 29 genes. We identified 4 distinct regulation patterns for synthesizing enzymes, as well as a distinct regulation pattern for degradations and transporting enzymes. This study charts the expression of endometrial endocannabinoid system genes across the menstrual cycle. Altered expression of genes that control endocannabinoid may allow fine control over endocannabinoid concentrations and their influence on cellular function, maturation and differentiation as the endometrium matures through the menstrual cycle.
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    Obstetric Outcome After Surgical Treatment of Endometriosis: A Review of the Literature
    Mooney, SSS ; Ross, V ; Stern, C ; Rogers, PAW ; Healey, M (FRONTIERS MEDIA SA, 2021-12-24)
    A diagnosis of endometriosis is associated with increased risks of adverse pregnancy outcomes including placenta praevia and preterm birth. Some studies have also suggested associations with gestational hypertension, foetal growth restriction, gestational diabetes, perinatal death, and obstetric haemorrhage. This review aims to assess the impact of pre-pregnancy surgical treatment of endometriosis on future obstetric outcomes. A search of the Medline, Embase and PubMed electronic databases was performed to identify studies reporting pre-pregnancy surgery for endometriosis and subsequent pregnancy outcome compared to controls with unresected endometriosis. Three studies met the inclusion criteria. The studies were heterogenous in design, definition of study groups and outcome measures. All three studies were judged at critical risk of bias. Pre-pregnancy excision of endometriosis was associated with an increased risk of caesarean section in one of two studies, OR 1.72 (95% CI 1.59-1.86) and OR 1.79 (95% CI 0.69-4.64). Placenta praevia rates were also increased in one of two studies OR 2.83 (95% CI 0.56-12.31) and OR 2.04 (95% CI 1.66-2.52). One study found increased risks of preterm birth, small for gestational age, gestational hypertension, and antepartum and postpartum haemorrhage (all p < 0.05) with pre-pregnancy excision of endometriosis. There is insufficient evidence examining the role of pre-pregnancy endometriosis surgery in ameliorating adverse pregnancy outcomes, and thus reliable conclusions cannot be drawn. Prospectively designed studies are needed to assess the relationship between surgical treatments for endometriosis and obstetric outcome and examine potential confounders such as comorbid adenomyosis and infertility.
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    A multi-level investigation of the genetic relationship between endometriosis and ovarian cancer histotypes
    Mortlock, S ; Corona, R ; Kho, PF ; Pharoah, P ; Seo, J-H ; Freedman, ML ; Gayther, SA ; Siedhoff, MT ; Rogers, PAW ; Leuchter, R ; Walsh, CS ; Cass, I ; Karlan, BY ; Rimel, BJ ; Montgomery, GW ; Lawrenson, K ; Kar, SP (CELL PRESS, 2022-03-15)
    Endometriosis is associated with increased risk of epithelial ovarian cancers (EOCs). Using data from large endometriosis and EOC genome-wide association meta-analyses, we estimate the genetic correlation and evaluate the causal relationship between genetic liability to endometriosis and EOC histotypes, and identify shared susceptibility loci. We estimate a significant genetic correlation (rg) between endometriosis and clear cell (rg = 0.71), endometrioid (rg = 0.48), and high-grade serous (rg = 0.19) ovarian cancer, associations supported by Mendelian randomization analyses. Bivariate meta-analysis identified 28 loci associated with both endometriosis and EOC, including 19 with evidence for a shared underlying association signal. Differences in the shared risk suggest different underlying pathways may contribute to the relationship between endometriosis and the different histotypes. Functional annotation using transcriptomic and epigenomic profiles of relevant tissues/cells highlights several target genes. This comprehensive analysis reveals profound genetic overlap between endometriosis and EOC histotypes with valuable genomic targets for understanding the biological mechanisms linking the diseases.
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    Dilated Thin-Walled Blood and Lymphatic Vessels in Human Endometrium: A Potential Role for VEGF-D in Progestin-Induced Break-Through Bleeding (vol 7, e30916, 2012)
    Donoghue, JF ; McGavigan, CJ ; Lederman, FL ; Cann, LM ; Fu, L ; Dimitriadis, E ; Girling, JE ; Rogers, PAW (PUBLIC LIBRARY SCIENCE, 2021-10-26)
    [This corrects the article DOI: 10.1371/journal.pone.0030916.].
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    Peripheral, Central, and Cross Sensitization in Endometriosis-Associated Pain and Comorbid Pain Syndromes.
    McNamara, HC ; Frawley, HC ; Donoghue, JF ; Readman, E ; Healey, M ; Ellett, L ; Reddington, C ; Hicks, LJ ; Harlow, K ; Rogers, PAW ; Cheng, C (Frontiers Media S.A., 2021)
    Endometriosis-associated pain and the mechanisms responsible for its initiation and persistence are complex and difficult to treat. Endometriosis-associated pain is experienced as dysmenorrhea, cyclical pain related to organ function including dysuria, dyschezia and dyspareunia, and persistent pelvic pain. Pain symptomatology correlates poorly with the extent of macroscopic disease. In addition to the local effects of disease, endometriosis-associated pain develops as a product of peripheral sensitization, central sensitization and cross sensitization. Endometriosis-associated pain is further contributed to by comorbid pain conditions, such as bladder pain syndrome, irritable bowel syndrome, abdomino-pelvic myalgia and vulvodynia. This article will review endometriosis-associated pain, its mechanisms, and its comorbid pain syndromes with a view to aiding the clinician in navigating the literature and terminology of pain and pain syndromes. Limitations of our current understanding of endometriosis-associated pain will be acknowledged. Where possible, commonalities in pain mechanisms between endometriosis-associated pain and comorbid pain syndromes will be highlighted.
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    Prevalence and incidence of endometriosis in Australian women: a data linkage cohort study
    Rowlands, IJ ; Abbott, JA ; Montgomery, GW ; Hockey, R ; Rogers, P ; Mishra, GD (WILEY, 2021-03)
    OBJECTIVE: To estimate the prevalence and incidence of endometriosis among Australian women. DESIGN: Population-based cohort study linked to administrative health records. SETTING: Secondary analysis of seven surveys collected between 2000 and 2018 from a population-based cohort study. POPULATION: A total of 13 508 Australian women, born 1973-78, from a prospective cohort study of 14 247 women conducted between 1996 and 2018. METHODS: During 2000 and 2018, self-reported longitudinal survey data were linked to three administrative health databases to separately identify women with clinically confirmed or suspected endometriosis across the multiple data sources. MAIN OUTCOME MEASURES: Prevalence and incidence of clinically confirmed endometriosis in the cohort were first estimated using national hospital data. Data were then combined with other administrative health databases and the survey data to capture all clinically confirmed and suspected diagnoses of endometriosis. RESULTS: The cumulative prevalence of clinically confirmed endometriosis was 6.0% (95% CI 5.8-6.2%) by age 40-44 years. The cumulative prevalence increased to 11.4% (95% CI 11.1-11.7%) when adding diagnoses of clinically suspected endometriosis. Age-specific incidence estimates peaked to 6 per 1000 person-years at age 30-34 years. CONCLUSIONS: Among 13 508 Australian women followed for 20 years, one in nine women had clinically confirmed or suspected endometriosis by the age of 44, with most diagnosed during their early thirties. Endometriosis is a significant public health issue requiring increased surveillance, clinical awareness and management. Efforts to expand knowledge on the aetiology of the disease and optimal methods for disease management are crucial to women's health. TWEETABLE ABSTRACT: In a national study of 13 508 Australian women, one in nine women were diagnosed with endometriosis by age 44.