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1.
Turk J Obstet Gynecol ; 13(2): 95-98, 2016 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-28913100

RESUMO

Although around 1-4% of human zygotes have been found to be tripronuclear, there is little information about the subsequent development and chromosomal composition of embryos that derive from these zygotes. Herein, we report a pregnancy and subsequent delivery of a healthy newborn after the transfer of a blastocyst that developed from a tripronuclear zygote that had a euploid microarray result.

2.
Arch Gynecol Obstet ; 291(1): 185-91, 2015 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-25078054

RESUMO

PURPOSE: The aim of this study was to compare the incidence of ectopic pregnancy in GnRH agonist triggered IVF cycles with intensive luteal support versus hCG triggered IVF cycles. METHODS: This study was conducted as a retrospective cohort analysis of women who underwent IVF treatment employing GnRH agonist or recombinant hCG (rhCG) triggers during 2-year period. The medical charts of women who achieved pregnancies were reviewed and their demographic characteristics, infertility reasons and IVF data were recorded. A multiple logistic regression analysis was performed to estimate the association between the triggering medication used to stimulate final oocyte maturation (GnRHa or rhCG) and EP, with adjustment for important confounders: the day of embryo transfer (ETD), the etiology of infertility and estrogen level at the time of triggering. RESULTS: The number of metaphase II oocytes, fertilized oocytes and good quality embryos were significantly higher in the GnRH agonist triggered group compared with the hCG triggered group (p < 0.001 for all). The clinical pregnancy and implantation rates in the hCG triggered cycles were 38.6 and 31.1 %, respectively and 24.7 and 22 %, respectively in the triptorelin triggered cycles. The ectopic pregnancy rates were 5.3 % in the triptorelin triggered group and 1.4 % in the hCG triggered group. The trigger medication and the day of embryo transfer were found to have a significant effect on the probability of developing ectopic pregnancy (p = 0.028, p = 0.046 respectively). However, the estrogen level was not found to have a significant effect on the probability of developing ectopic pregnancy (p = 0.447). CONCLUSIONS: The reasons for higher ectopic pregnancy rates in GnRH agonist triggered cycles relative to hCG triggered cycles may be the decreased receptivity of the endometrium due to insufficient luteal support and higher implantation potential of embryos in correlation with a higher number of good quality embryos obtained in these cycles.


Assuntos
Gonadotropina Coriônica/uso terapêutico , Fertilização in vitro/métodos , Hormônio Liberador de Gonadotropina/agonistas , Gravidez Ectópica/epidemiologia , Adulto , Estudos de Coortes , Implantação do Embrião , Transferência Embrionária/métodos , Endométrio/metabolismo , Feminino , Hormônio Liberador de Gonadotropina/antagonistas & inibidores , Gonadotropinas/uso terapêutico , Antagonistas de Hormônios/uso terapêutico , Humanos , Oócitos/metabolismo , Oogênese , Gravidez , Taxa de Gravidez , Estudos Retrospectivos , Pamoato de Triptorrelina/uso terapêutico
3.
J Turk Ger Gynecol Assoc ; 15(3): 156-60, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-25317043

RESUMO

OBJECTIVE: To compare the outcomes of embryos that were given a dynamic score based on a preconstructed embryo scoring model and to analyze whether this model complies with our data. MATERIAL AND METHODS: A total of 910 transferred embryos with known implantation data were retrospectively analyzed in this study. All of the embryos were given a dynamic score based on the preconstructed hierarchical embryo scoring model. RESULTS: The highest pregnancy rate was seen in groups C+ and A- (48.2% for each), and the lowest was observed in Group E (19.7%). When implantation and clinical pregnancy rates were compared between groups, it was found that the highest and statistically significant implantation and clinical pregnancy rates were seen in group C+ (32.7% for each, p=0.000). They were dropped down to 29.4% in Group A-. CONCLUSION: The outcomes of the embryos based on the dynamic score do not comply with the results of the preconstructed model. Each IVF laboratory is unique based on its practice. Therefore, we suggest that each IVF laboratory should determine its own embryo selection criteria based on its own data instead of using a preconstructed model.

4.
Fertil Steril ; 102(4): 1029-1033.e1, 2014 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-25086787

RESUMO

OBJECTIVE: To compare the detection rate of multinucleation with the time-lapse system and conventional control timing proposed by European Society of Human Reproduction and Embryology (ESHRE) consensus and evaluate its impact on pregnancy rates. DESIGN: Retrospective study. SETTING: A private IVF center. PATIENT(S): A total of 686 embryos from 511 intracytoplasmic sperm injection (ICSI) cycles. INTERVENTION(S): None. MAIN OUTCOME MEASURE(S): A time-lapse system was used to acquire embryo images until ET; the stored data were reviewed for the presence and persistence of multinucleation. The detection rate of multinucleation was compared with ESHRE/ALPHA consensus-proposed embryo evaluating times (23 ± 1, 26 ± 1, 44 ± 1 hours). Morphokinetic characteristics of multinucleated embryos and the effect of multinucleation on pregnancy rate were researched. RESULT(S): Multinucleation was detected in 159 embryos of 145 ICSI cycles. Using ESHRE/ALPHA consensus embryo evaluating times, only 44 (27.6%) out of 159 multinucleated embryos could be identified. In cycles with multinucleated ETs compared with cycles with no multinucleated embryos, clinical pregnancy rates (respectively, 23.4 vs. 44) and implantation rates (respectively, 23.3 vs. 43.6) were significantly lower. Time to 2-cell, 4-cell, and 6-cell stage was significantly longer in multinucleated embryos. Patient age (odds ratio [OR], 0.95; confidence interval [CI], 0.92-0.98) and presence of multinucleation (OR, 0.37; CI, 0.24-0.56) were the only significant predictors of clinical pregnancy rate. CONCLUSION(S): The time-lapse monitoring system seems to be a valuable tool to identify all cases with multinucleation. We conclude that the detection of multinucleation by time-lapse monitoring is associated with lower implantation and clinical pregnancy rates.


Assuntos
Núcleo Celular/patologia , Embrião de Mamíferos/patologia , Resultado da Gravidez , Técnicas de Reprodução Assistida , Imagem com Lapso de Tempo , Adulto , Distribuição de Qui-Quadrado , Técnicas de Cultura Embrionária , Implantação do Embrião , Transferência Embrionária , Feminino , Humanos , Modelos Logísticos , Idade Materna , Razão de Chances , Valor Preditivo dos Testes , Gravidez , Técnicas de Reprodução Assistida/efeitos adversos , Estudos Retrospectivos , Fatores de Risco , Injeções de Esperma Intracitoplásmicas , Fatores de Tempo , Resultado do Tratamento
5.
Am J Reprod Immunol ; 64(2): 87-92, 2010 Aug 01.
Artigo em Inglês | MEDLINE | ID: mdl-20175773

RESUMO

PROBLEM: To compare the prevalence of 112T>C point mutations among women experiencing RPL with fertile control women. METHOD OF STUDY: Buccal swabs were obtained from 232 individuals: 136 with a history of >or=2 abortions, 37 with at least 2 live births and 59 with a history of deep vein thrombosis (DVT). DNA was extracted and PCR amplification of Apo E codons was performed. RESULTS: The allelic frequency of a cytosine at position 112 was 11.4% (31/272) among patients experiencing RPL, compared with a frequency of 5.4% (4/74) among the fertile controls (P = 0.19) and 19.5% (23/118) among individuals with a history of DVT. However, significantly more E3/E4 and E4/E4 genotypes were seen among individuals experiencing RPL and DVT than fertile controls (P < 0.05). CONCLUSION: Apo E4 codon 112C point mutation is, by itself, not associated with an elevated risk of recurrent pregnancy loss, but rather codon 112C in association with codon 158C is a risk factor for RPL.


Assuntos
Aborto Habitual/genética , Apolipoproteínas E/genética , Polimorfismo de Nucleotídeo Único , Aborto Habitual/epidemiologia , Adulto , Apolipoproteína E4/genética , Códon , Feminino , Frequência do Gene , Estudos de Associação Genética , Genótipo , Humanos , Mutação Puntual , Reação em Cadeia da Polimerase , Isoformas de Proteínas/genética , Trombose Venosa/complicações , Trombose Venosa/genética
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