Searchable abstracts of presentations at key conferences in endocrinology

ea0090ep1155 | Late Breaking | ECE2023

Family building after diagnosis of premature ovarian insufficiency - a cross-sectional survey in 324 women

Cambray Solange , Dubreuil Sophie , Tejedor Isabelle , Dulon Jerome , Touraine Philippe

Objective: The diagnosis of premature ovarian insufficiency (POI) is a traumatic event for many patients that involves poor fertility prognosis. After such diagnosis spontaneous pregnancies are rare. The alternatives for building a family are oocyte donation, embryo donation and adoption. However, we have few information on how many women with POI finally built a family after the diagnosis and which alternative they chose.Design: We performed a cross-sec...

ea0022oc5.5 | Reproduction & Thyroid | ECE2010

Predictive factors of intermittent ovarian function in patients with premature ovarian failure

Bidet Maud , Bissauge Estelle , Dulon Jerome , Bachelot Anne , Touraine Philippe

Objective: Premature ovarian failure (POF) is not an early menopause and intermittent ovarian function can be spontaneously observed in POF patients. We sought to characterize these patients and determine which factors were predictors of intermittent ovarian function.Patients and methods: Among 391 patients with idiopathic POF followed from 1997 in our department, 67 (17.1%) patients (Group 1) had POF fluctuating criteria: FSH <15 IU/l, resumed spont...

ea0020p645 | Reproduction | ECE2009

A monocentric study of 360 consecutive patients presenting with premature ovarian failure

Bachelot Anne , Rouxel Agnes , Massin Nathalie , Dulon Jerome , Courtillot Carine , Kuttenn Frederique , Touraine Philippe

Premature ovarian failure (POF) encompasses a heterogeneous spectrum of conditions, with phenotypic variability among patients. The etiology of POF remains unknown in most cases. This led us to set up a French network on POF for the purpose of better characterizing POF patients and understanding the mechanisms involved in this pathology. Over the last 10 years, we have evaluated 360 women who were referred to our center with a diagnosis of POF, and performed a study of clinica...

ea0022oc4.5 | Adrenals | ECE2010

Effects of mitotane on testicular adrenal rest tumors size, sperm count and adrenal steroidogenesis in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Bachelot Anne , Salenave Sylvie , Renard Raphaelle , Rocher Laurence , Dulon Jerome , Coussieu Christiane , Brailly-Tabard Sylvie , Morel Yves , Touraine Philippe , Young Jacques

Testicular adrenal rest tumors (TART), described in patients with classic congenital adrenal hyperplasia (CAH) secondary to 21-hydroxylase deficiency, are responsible for Leydig cell failure and impaired spermatogenesis. These tumors, often unresponsive to intensified glucocorticoid therapy and surgical resection, may lead to infertility or even sterility. Here, we studied the effects of long term treatment with mitotane (Lysodren), a specific adrenolytic agent, on TART in 4 C...

ea0016p18 | Adrenal | ECE2008

Impact of total cumulative glucocorticoid dose on bone mineral density in patients with 21-hydroxylase deficiency

Zeina Chakhtoura , Anne Bachelot , Dinane Samara-Boustani , Jean-Charles Ruiz , Bruno Donadille , Jerome Dulon , Sophie Christin-Maitre , Claire Bouvattier , Marie-Charles Raux-Demay , Philippe Bouchard , Jean-Claude Carel , Juliane Leger , Frederique Kuttenn , Michel Polak , Philippe Touraine

Introduction: There are contradictory results concerning bone mineral density status in adult patients with congenital adrenal hyperplasia. To resolve this issue, we hypothesized that there could be a correlation between BMD and a total cumulative glucocorticoid dose from the diagnosis in early infancy to adulthood. We then conducted a retrospective in a referral centers for CAH. Thirty-eight adult patients (28 women, 10 men, aged 16–39 years) suffering from CAH and treat...