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1.
JBRA Assist Reprod ; 22(2): 148-156, 2018 Jun 01.
Article de Anglais | MEDLINE | ID: mdl-29488367

RÉSUMÉ

OBJECTIVE: To identify, appraise, and summarize the evidence from randomized controlled trials (RCTs) comparing oral dydrogesterone to vaginal progesterone capsules for luteal-phase support (LPS) in women offered fresh or frozen embryo transfers following in vitro fertilization. METHODS: Two independent authors screened the literature for papers based on titles and abstracts, then selected the studies, extracted data, and assessed the risk of bias. Dydrogesterone and progesterone were compared based on risk ratios (RR) and the precision of the estimates was assessed through the 95% confidence interval (CI). RESULTS: An electronic search performed on June 7, 2017 retrieved 376 records, nine of which were papers deemed eligible and included in this systematic review and quantitative analysis. Good quality evidence indicates that oral dydrogesterone provided at least similar results than vaginal progesterone capsules on live birth/ongoing pregnancy (RR=1.08, 95%CI=0.92-1.26, I2=29%, 8 RCTs, 3,386 women) and clinical pregnancy rates (RR 1.10, 95% CI 0.95 to 1.27; I2=43%; 9 RCTs; 4,061 women). Additionally, moderate quality evidence suggests there is no relevant difference on miscarriage rates (RR=0.92, 95%CI=0.68-1.26, I2=6%, 8 RCTs, 988 clinical pregnancies; the quality of the evidence was downgraded because of imprecision). CONCLUSIONS: Good quality evidence from RCTs suggest that oral dydrogesterone provides at least similar reproductive outcomes than vaginal progesterone capsules when used for LPS in women undergoing embryo transfers. Dydrogesterone is a reasonable option and the choice of either of the medications should be based on cost and side effects.


Sujet(s)
Dydrogestérone/usage thérapeutique , Transfert d'embryon , Progestérone/usage thérapeutique , Progestines/usage thérapeutique , Administration par voie vaginale , Administration par voie orale , Adulte , Maintien du corps jaune/effets des médicaments et des substances chimiques , Dydrogestérone/administration et posologie , Dydrogestérone/effets indésirables , Femelle , Humains , Grossesse , Progestérone/administration et posologie , Progestérone/effets indésirables , Progestines/administration et posologie , Progestines/effets indésirables , Essais contrôlés randomisés comme sujet
2.
J Interferon Cytokine Res ; 20(8): 677-83, 2000 Aug.
Article de Anglais | MEDLINE | ID: mdl-10954910

RÉSUMÉ

The gene coding for bovine interferon-omega1 (BoIFN-omega1) was recently cloned and expressed at high levels in the yeast Pichia pastoris. The recombinant BoIFN-omega1 protein shows antiviral activity in different cell lines and has an antiluteolytic effect in cyclic ewes. In this article, we describe a method for purification of BoIFN-omega1 expressed in the methylotrophic yeast P. pastoris and characterization of its activity in vivo. The recombinant protein secreted to the culture medium had low activity because of self-aggregation. BoIFN-omega1 was solubilized using urea and desalting and finally purified by ion exchange chromatography on Q-Sepharose Fast Flow. The yield of purified product was approximately 300 mg/L of fermentation culture, with a specific antiviral activity of 10(8) IU/mg. Its purity was at least 80%. The biologic characterization of purified BoIFN-omega1 was determined by induction of an antiviral state on ewes challenged with 100 lethal doses (LD) of Aujeszky virus and by the extension of the corpus luteum life span and interestrous interval in cyclic cows. Ewes treated with 2 x 106 IU/kg BoIFN-omega1 were protected from Aujeszky virus infection. In cows receiving an intrauterine infusion of 1 mg BoIFN-omega1, equally distributed between the two uterine horns, twice daily from day 14 to day 22 of the experimental estrous cycle, the lifespan of the corpus luteum (25 vs. 19 days) and the interestrous intervals (26 vs. 21 days) were extended when compared with a control group (p < 0.05). We show that recombinant BoIFN-omega1 purified from P. pastoris has high antiviral activity and is an effective antiluteolytic agent in cattle.


Sujet(s)
Interféron de type I/pharmacologie , Animaux , Antiviraux/pharmacologie , Bovins , Lignée cellulaire , Maintien du corps jaune/effets des médicaments et des substances chimiques , Oestrus/effets des médicaments et des substances chimiques , Femelle , Techniques in vitro , Interféron de type I/génétique , Interféron de type I/isolement et purification , Mâle , Pichia/génétique , Grossesse , Maladie d'Aujeszky/prévention et contrôle , Protéines recombinantes , Ovis
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