69 research outputs found

    A picture of medically assisted reproduction activities during the COVID-19 pandemic in Europe

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    STUDY QUESTION: How did coronavirus disease 2019 (COVID-19) impact on medically assisted reproduction (MAR) services in Europe during the COVID-19 pandemic (March to May 2020)? SUMMARY ANSWER: MAR services, and hence treatments for infertile couples, were stopped in most European countries for a mean of 7 weeks. WHAT IS KNOWN ALREADY: With the outbreak of COVID-19 in Europe, non-urgent medical care was reduced by local authorities to preserve health resources and maintain social distancing. Furthermore, ESHRE and other societies recommended to postpone ART pregnancies as of 14 March 2020. STUDY DESIGN, SIZE, DURATION: A structured questionnaire was distributed in April among the ESHRE Committee of National Representatives, followed by further information collection through email. PARTICIPANTS/MATERIALS, SETTING, METHODS: The information was collected through the questionnaire and afterwards summarised and aligned with data from the European Centre for Disease Control on the number of COVID-19 cases per country. MAIN RESULTS AND THE ROLE OF CHANCE: By aligning the data for each country with respective epidemiological data, we show a large variation in the time and the phase in the epidemic in the curve when MAR/ART treatments were suspended and restarted. Similarly, the duration of interruption varied. Fertility preservation treatments and patient supportive care for patients remained available during the pandemic. LARGE SCALE DATA: N/A. LIMITATIONS, REASONS FOR CAUTION: Data collection was prone to misinterpretation of the questions and replies, and required further follow-up to check the accuracy. Some representatives reported that they, themselves, were not always aware of the situation throughout the country or reported difficulties with providing single generalised replies, for instance when there were regional differences within their country. WIDER IMPLICATIONS OF THE FINDINGS: The current article provides a basis for further research of the different strategies developed in response to the COVID-19 crisis. Such conclusions will be invaluable for health authorities and healthcare professionals with respect to future similar situations.peer-reviewe

    Cell signalling and serum marker of cell proliferation in adenomyosis

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    L’adĂ©nomyose est une pathologie chronique bĂ©nigne de l’utĂ©rus caractĂ©risĂ©e par une infiltration du myomĂštre par du tissu endomĂ©trial composĂ© de glandes et de stroma avec une hypertrophie et une hyperplasie des cellules musculaires lisses adjacentes. Cette maladie frĂ©quente de la femme en Ăąge de procrĂ©er cause des symptĂŽmes invalidants comme des dysmĂ©norrhĂ©es, des saignements utĂ©rins anormaux et une infertilitĂ©. L’adĂ©nomyose utĂ©rine est souvent associĂ©e Ă  d’autres pathologies gynĂ©cologiques bĂ©nignes ƓstrogĂ©no-dĂ©pendantes comme les lĂ©iomyomes utĂ©rins et l’endomĂ©triose. Les options thĂ©rapeutiques mĂ©dicamenteuses sont purement symptomatiques et non-curatives et l’adĂ©nomyose reste une cause majeure d’hystĂ©rectomie. Les mĂ©canismes physiopathologiques qui aboutissent au dĂ©veloppement de l’adĂ©nomyose sont probablement multifactoriels et ne sont que partiellement compris actuellement. Selon la thĂ©orie la plus communĂ©ment admise, l’adĂ©nomyose trouve son origine dans la couche basale de l’endomĂštre avec une invagination de cellules entre les faisceaux musculaires et/ou le long de vaisseaux lymphatiques. De multiples facteurs pourraient ĂȘtre impliquĂ©s dans l’initiation de cette invasion, notamment une rĂ©sistance Ă  l’action de la progestĂ©rone, une production intra-lĂ©sionnelle d’ƓstrogĂšnes par activation de l’aromatase, des anomalies myomĂ©triales prĂ©disposant Ă  l’invasion, des lĂ©sions tissulaires induites par la grossesse, l’accouchement, le dyspĂ©ristaltisme utĂ©rin ou iatrogĂšnes et des anomalies de l’endomĂštre le prĂ©disposant Ă  l’invasion. Dans un premier temps nous dĂ©taillons, dans un article de revue, les traitements mĂ©dicamenteux actuellement utilisĂ©s pour traiter les symptĂŽmes causĂ©s par l’adĂ©nomyose et discutons les mĂ©canismes physiopathologiques qui pourraient ĂȘtre la cible de nouveaux traitements mĂ©dicamenteux. Ensuite, nous exposons les rĂ©sultats de l’étude in vitro des voies de signalisation cellulaires des mitogen-activated protein kinases (MAPKs) et phosphatidylinositol 3 kinase/Akt/mammalian target of rapamycin (PI3K/mTOR/Akt) dans les cellules musculaires lisses utĂ©rines issues de femmes avec de l’adĂ©nomyose et de tĂ©moins sans adĂ©nomyose. Nous montrons une augmentation de la prolifĂ©ration des cellules myomĂ©triales avec une activation in vitro de la voie MAPK/ERK chez les femmes avec de l’adĂ©nomyose en comparaison avec les tĂ©moins. L’activation de la voie PI3K/mTOR/Akt n’est pas significativement diffĂ©rente. La production de dĂ©rivĂ©s rĂ©actifs de l’oxygĂšne et leurs voies de dĂ©toxification ne sont pas diffĂ©rentes dans les cellules myomĂ©triales de femmes avec de l’adĂ©nomyose et celles de tĂ©moins, ce qui suggĂšre une activation de la voie des MAPK/ERK indĂ©pendante des dĂ©rivĂ©s rĂ©actifs de l’oxygĂšne. Nos rĂ©sultats montrent que des inhibiteurs des protĂ©ines kinases et le rapanalogue temsirolimus contrĂŽlent la prolifĂ©ration des cellules myomĂ©triales in vitro, ce qui suggĂšre une implication des voies de signalisation MAPK/ERK et PI3K/mTOR/Akt dans la prolifĂ©ration des cellules musculaires lisses dans l’adĂ©nomyose et les lĂ©iomyomes. Finalement, nous avons Ă©tudiĂ© l’ostĂ©opontine comme biomarqueur sĂ©rique dans une cohorte de femmes en Ăąge de procrĂ©er opĂ©rĂ©es pour des pathologies gynĂ©cologiques bĂ©nignes. La prĂ©sence d’endomĂ©triose a Ă©tĂ© dĂ©terminĂ©e chirurgicalement et les lĂ©sions endomĂ©triosiques ont Ă©tĂ© confirmĂ©es histologiquement et classĂ©es en lĂ©sions superficielles, endomĂ©triomes ou lĂ©sions invasives profondes. La prĂ©sence d’adĂ©nomyose a Ă©tĂ© dĂ©terminĂ©e par imagerie par rĂ©sonance magnĂ©tique prĂ©opĂ©ratoire et deux types d’adĂ©nomyose ont Ă©tĂ© caractĂ©risĂ©s : l’adĂ©nomyose diffuse, l’adĂ©nomyose focale avec ou sans lĂ©sions diffuses associĂ©es. L’ostĂ©opontine sĂ©rique est diminuĂ©e en cas d’adĂ©nomyose focale et de lĂ©sions d’endomĂ©triose profonde en comparaison avec des tĂ©moins sains et augmentĂ©e dans l’endomĂ©triose superficielle en comparaison avec l’endomĂ©triose profonde. (...)Adenomyosis is chronic benign uterine disease characterized by myometrial infiltration by endometrial tissue – both glands and stroma – with hypertrophy and hyperplasia of surrounding smooth muscle cells. This frequent disease occurring in reproductive age women causes invalidating symptoms such as dysmenorrhoea, abnormal uterine bleeding and infertility. Adenomyosis is frequently associated with other estrogen-dependant gynaecologic diseases such as uterine leiomyomas and endometriosis. Medical treatments are non-curative and act purely by alleviating symptoms and adenomyosis remains a major cause of hysterectomy. Physiopathological mechanisms underlying the disease are probably multifactorial and currently not fully elucidated. According to the most widely accepted theory adenomyosis originates from the basal layer of the endometrium which invaginates between smooth muscle cell bundles and/or along lymphatic vessels. Multiple factors could be implicated in triggering this invasion, amongst others resistance to progesterone, intra-lesional production of estrogens through aromatase activation, myometrial anomalies predisposing to invasion, tissue lesions induced by pregnancy, labour, uterine dysperistaltism or iatrogenic and endometrial anomalies predisposing to invasion. First, in a clinical review article, we detail current medical therapies used to alleviate adenomyosis-associated symptoms and discuss physiopathological mechanisms that could be targets for novel medical treatments. We then describe an in vitro study on the activation of the mitogen-activated protein kinases (MAPKs) and phosphatidylinositol three kinase/mammalian target of rapamycin/Akt (PI3K/mTOR/Akt) signalling pathways in uterine smooth muscle cells derived from women with adenomyosis and from adenomyosis-free controls. We show an increased proliferation of uterine smooth muscle cells related to the in vitro activation of the MAPK/ERK pathway in women with adenomyosis compared to controls. The activation of PI3K/mTOR/Akt was not significantly different. The production of reactive oxygen species and their detoxification enzymes were not different in uterine smooth muscle cells of women with adenomyosis compared to controls suggesting a reactive oxygen species independent activation of the MAPK/ERK pathway. Our results also show that inhibitors of protein kinases and the rapanalogue temsirolimus control the in vitro proliferation of uterine smooth muscle cells suggesting an implication of both MAPK/ERK and PI3K/mTOR/Akt in the proliferation of uterine smooth muscle cells in adenomyosis and leiomyomas. Finally, we studied osteopontin as a serum biomarker in a cohort of reproductive-age women undergoing surgery for benign gynaecological conditions. The presence of endometriosis was determined surgically and endometriosis lesions were confirmed histologically and classified into superficial lesions, endometriomas and deep infiltrating lesions. The presence of adenomyosis was determined by magnetic resonance imaging before surgery and women were classified according to two types of adenomyosis: diffuse adenomyosis, focal adenomyosis with or without associated diffuse lesions. Osteopontin levels were decreased in case of focal adenomyosis and deep infiltrating endometriosis compared to disease-free women and increased in superficial endometriosis compared to deep infiltrating endometriosis. Osteopontin, a secreted glycoprotein implicated in inflammation and in tumor-metastasis, is not a biomarker of disease severity in endometriosis and adenomyosis but could reflect events implicated in peritoneal dissemination of endometriosis lesions

    Anti-MĂŒllerian hormone level measurement in gynaecology: Myths and clinical utility

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    Anti-MĂŒllerian hormone (AMH) is a glycoprotein implicated in the regulation of the pace of ovarian follicular recruitment and loss and follicle selection in adult females. AMH predicts the magnitude of the response to controlled ovarian stimulation for assisted reproductive techniques and is used to individualize treatments and avoid ovarian hyperstimulation syndrome. In contrast, AMH levels do not seem to be related to fecundability or time to pregnancy and do not predict the results intrauterine inseminations or natural cycle in vitro fertilisation. AMH fluctuates only in a minor way during the menstrual cycle allowing its measure without regard to the menstrual cycle phase. The impact of hormonal treatments such as the oral contraceptive pill is still debated. AMH levels can also be used to study the impact of medical treatments, surgical procedure or environmental factors on ovarian reserve

    Transcripts for the ENDOFERT STUDY - qualitative part

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    Objective. The aim of the present study is to conduct a qualitative investigation to provide a deeper understanding of women’s views about endometriosis, fertility and their perception of reproductive options.Methods. Semi-structured interviews were conducted by two female psychiatrists, specialized in gynecology and obstetrical consultation-liaison psychiatry, trained in qualitative procedures, with experience in qualitative studies and in psychological support of women attending infertility consultations. No prior relationship with respondents was established before data collection. Interviews were tape-recorded and transcribed. Interviews lasted 45–75 minutes. The transcripts were then analysed using thematic content analysis.</p

    The role of preventive uterine artery occlusion during laparoscopic myomectomy: a review of the literature

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    Surgical myomectomy is currently regarded as the standard conservative treatment for patients who wish to preserve their fertility. However, it presents two main problems: the intra- and postoperative risk of bleeding and the risk of recurrence of leiomyomas. Preventive occlusion of uterine arteries was described during laparoscopic myomectomy as one of the procedures addressing these issues

    Women's lived experience of endometriosis-related fertility issues.

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    ObjectiveThe aim of the present study is to conduct a qualitative investigation to provide a deeper understanding of women's views about endometriosis, fertility and their perception of reproductive options.MethodsSemi-structured interviews were conducted by two female psychiatrists, specialized in gynecology and obstetrical consultation-liaison psychiatry, trained in qualitative procedures, with experience in qualitative studies and in psychological support of women attending infertility consultations. No prior relationship with respondents was established before data collection. Interviews were tape-recorded and transcribed. Interviews lasted 45-75 minutes. The transcripts were then analysed using thematic content analysis.ResultsTwenty-nine women were contacted. Twelve agreed to an interview at the hospital's infertility clinic. Eleven women with diverse sociodemographic characteristics were included. The key findings of thematic content analysis can be grouped into four topics: (1) Diagnostic announcement and initial delay; (2) Negative perceptions of initial care: pre-diagnosis phase; (3) Struggle with endometriosis and its treatment; (4) Issues related to health problems, fertility and reproductive options.ConclusionOur analysis of the interviews corroborates the distressing impact of the trivialization of pain and the uncertainty of or the long quest for diagnosis. The findings also stress various associated issues, from the diagnostic delay to the low success rates of fertility treatments. This qualitative analysis contributes to better understand the accumulation of negative emotions within the illness trajectory and the poor dyadic adjustment within the couple

    Innovations in classical hormonal targets for endometriosis

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    Endometriosis is a chronic disease of unknown etiology that affects approximately 10% of women in reproductive age. Several evidences show that endometriosis lesions are associated to hormonal imbalance, including estrogen synthesis, metabolism and responsiveness and progesterone resistance. These hormonal alterations influence the ability of endometrial cells to proliferate, migrate and to infiltrate the mesothelium, causing inflammation, pain and infertility. Hormonal imbalance in endometriosis represents also a target for treatment. We provide an overview on therapeutic strategies based on innovations of classical hormonal mechanisms involved in the development of endometriosis lesions. The development phase of new molecules targeting these pathways is also discussed. Endometriosis is a chronic disease involving young women and additional biological targets of estrogen and progesterone pharmacological manipulation (brain, bone and cardiovascular tissue) need to be carefully considered in order to improve and overcome current limits of long-term medical management of endometriosis
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