L. Helmgaard
Ferring Pharmaceuticals
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Publication
Featured researches published by L. Helmgaard.
British Journal of Obstetrics and Gynaecology | 2006
Adam Balen; Peter Platteau; Andersen An; Paul Devroey; Per Sørensen; L. Helmgaard; J.-C. Arce
Objective To assess the influence of body weight on the outcome of ovulation induction in women with World Health Organization (WHO) group II anovulatory infertility.
Reproductive Biomedicine Online | 2013
Etienne Van den Abbeel; Basak Balaban; Søren Ziebe; Kersti Lundin; Maria José Gómez Cuesta; Bjarke Mirner Klein; L. Helmgaard; Joan-Carles Arce
The aim of this study was to assess the ability of three individual blastocyst morphology parameters - expansion and hatching (EH) stage, inner cell mass (ICM) grade and trophectoderm grade - to predict outcome of a cycle with single-blastocyst transfer. The study was a secondary analysis of data prospectively collected in a large multicentre trial. A total of 618 intracytoplasmic sperm injection patients undergoing ovarian stimulation in a gonadotrophin-releasing hormone antagonist cycle with compulsory single-blastocyst transfer on day 5 were included. In the simple logistic regression analysis, all three blastocyst morphology parameters were statistically significantly (P<0.005 for each) associated with positive human chorionic gonadotrophin, clinical and ongoing pregnancy rates and live birth rates, while only the ICM grade was significantly (P=0.033) associated with early pregnancy loss rate. Blastocyst EH stage was the only significant predictor of live birth (P=0.002) in the multiple logistic regression. In conclusion, although all three blastocyst morphology parameters were related to treatment outcome of fresh single-blastocyst cycles, selection of high-quality blastocysts for transfer should consider first the EH stage. Transfer of a blastocyst with ICM grade A may reduce the risk of early pregnancy loss. Choosing the embryo(s) with the best implantation potential is essential for securing each couple the highest chance of achieving pregnancy after assisted reproduction. The selection of embryo(s) for transfer at the blastocyst stage is based on morphology parameters of expansion and hatching stage, inner cell mass grade and trophectoderm grade. The aim of this study was to assess the relative impact of each parameter in predicting the probability of a successful outcome. The study was a secondary analysis of data prospectively collected in a large multicentre trial. A total of 618 patients who underwent single-blastocyst transfer on day 5 were included. Statistical analysis showed that all three blastocyst morphology parameters were significantly associated with positive human chorionic gonadotrophin (βHCG), clinical and ongoing pregnancy rates and live birth rates. Only the inner cell mass grade was significantly associated with early pregnancy loss between the positive βHCG test and confirmation of ongoing pregnancy 10-11weeks after transfer. The expansion and hatching stage was the only significant predictor of live birth in the multiple logistic regression analysis. In conclusion, although all three blastocyst morphology parameters were related to treatment outcome of fresh single-blastocyst cycles, selection of high-quality blastocysts for transfer should consider first the expansion and hatching stage. Transfer of a blastocyst with inner cell mass grade A may reduce the risk of early pregnancy loss.
Human Reproduction | 2008
Anders Nyboe Andersen; Adam Balen; Peter Platteau; Paul Devroey; L. Helmgaard; Joan-Carles Arce
BACKGROUND The objective of this investigation was to establish independent predictors of follicle-stimulating hormone (FSH) threshold dose in anovulatory women undergoing ovulation induction with FSH preparations. METHODS One hundred and fifty-one patients with WHO Group II anovulatory infertility failing to ovulate or conceive on clomiphene citrate underwent ovarian stimulation with FSH-only preparations following a low-dose step-up protocol. The individual FSH threshold dose was defined as the FSH dose when meeting the human chorionic gonadotrophin criteria (one follicle ≥17 mm, or 2–3 follicles ≥15 mm). The influence of demographics, physical characteristics, obstetric and infertility and menstrual cycle history, ovarian ultrasonography, endocrine parameters and type of gonadotrophin preparation on the FSH threshold dose was assessed through multiple regression analysis. RESULTS In the univariate analysis, age, body mass index (BMI), failure to ovulate with clomiphene citrate, menstrual cycle history (amenorrhea, oligomenorrhea or anovulatory cycles of 21–35 days), mean ovarian volume, LH/FSH ratio, testosterone and free androgen index were significant (P < 0.05) predictors of FSH threshold dose. In the multivariate analysis, menstrual cycle history, mean ovarian volume and BMI remained significant (P < 0.001). CONCLUSIONS The individual FSH threshold dose for ovulation induction in anovulatory women can be predicted based on three variables easily determined in clinical practice: menstrual cycle history, mean ovarian volume and BMI. A FSH dosage nomogram was constructed based on these parameters.
Reproductive Biomedicine Online | 2018
Jesper Petersen; Anders Nyboe Andersen; Bjarke Mirner Klein; L. Helmgaard; Joan-Carles Arce
Research has focused on optimizing luteal phase support and endometrial receptivity in ovarian stimulation cycles. In this study, serial endocrine measurements were taken in 600 patients after a gonadotrophin-releasing hormone antagonist stimulation protocol. On the day of blastocyst transfer, serum progesterone and oestradiol were similar irrespective of a subsequent positive or negative pregnancy test (median 99 ng/ml versus 103 ng/ml for progesterone, respectively) or a subsequent live birth or pregnancy loss. Serum progesterone was significantly correlated to each ovarian response parameter (total number of follicles, number of oocytes retrieved and oestradiol concentration; r = 0.45, 0.57 and 0.54 respectively, all P < 0.0001). These correlations were consistent irrespective of clinical outcome. On the day of the pregnancy test, these correlations had vanished except in the live birth subgroup showing a weaker correlation (r = 0.22, 0.27 and 0.32 respectively, all P < 0.005). The lowest HCG and progesterone levels associated with live birth were 59.3 IU/l and 12.3 ng/ml, respectively. Fourteen out of 92 patients (15.2%) with pregnancy loss had normal HCG but low progesterone levels (above and below their respective 5th percentile), and miscarried before the end of the 7th week, when the luteal-placental shift occurs.
Human Reproduction | 2007
Søren Ziebe; Kersti Lundin; Ronny Janssens; L. Helmgaard; Joan-Carles Arce
Human Reproduction | 2006
Peter Platteau; Anders Nyboe Andersen; Adam Balen; Paul Devroey; Per Sørensen; L. Helmgaard; Joan-Carles Arce
Human Reproduction | 2006
Joan-Carles Arce; Søren Ziebe; Kersti Lundin; Ronny Janssens; L. Helmgaard; Per Sørensen
Fertility and Sterility | 2017
Anders Nyboe Andersen; Scott M. Nelson; Bart C.J.M. Fauser; Juan A. Garcia-Velasco; Bjarke Mirner Klein; Joan-Carles Arce; Herman Tournaye; Petra De Sutter; Wim Decleer; Alvaro Petracco; Edson Borges; Caio Parente Barbosa; Jon Havelock; Paul Claman; A. Albert Yuzpe; H. Visnova; Pavel Ventruba; Petr Uher; Milan Mrazek; Ulla Breth Knudsen; Anne Guivarc'h Leveque; Antonio La Marca; Enrico Papaleo; Kuczyński W; Katarzyna Kozioł; Margarita Anshina; Irina Zazerskaya; Alexander Gzgzyan; Elena Bulychova; Victoria Verdú
Human Reproduction | 2007
Adam Balen; Peter Platteau; Anders Nyboe Andersen; Paul Devroey; L. Helmgaard; Joan-Carles Arce
Human Reproduction | 2012
S. Davies; D. Christopikou; E. Tsorva; A. Karagianni; A.H. Handyside; M. Mastrominas; Samer Alfarawati; M. Poli; Dagan Wells; Elpida Fragouli; M. Konstantinidis; S. Jaroudi; E. Van den Abbeel; Basak Balaban; Søren Ziebe; K. Lundin; Bjarke Mirner Klein; L. Helmgaard; Joan-Carles Arce; Y. Yokota; M. Yokota; H. Yokota; S. Sato; M. Nakagawa; M. Sato; I. Anazawa; Y. Araki; N. Lédée; Virginie Gridelet; Stéphanie Ravet