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Plasmatic estradiol concentration in the mid-luteal phase is a good prognostic factor for clinical and ongoing pregnancies, during stimulated cycles of in vitro fertilization

OBJECTIVE: To evaluate the predictive efficiency of serum estradiol (E(2)) concentration in the mid-luteal phase regarding chemical, clinical, and ongoing pregnancies, in patients subjected to IVF/ICSI with fresh embryo transfer. METHODS: One hundred and forty-three patients undergoing IVF/ICSI met...

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Autores principales: Florêncio, Rodopiano S., Meira, Melaynne S. B., da Cunha, Marcos V., Camarço, Mylena N. C. R., Castro, Eduardo C., Finotti, Marta C. C. F., de Oliveira, Vinicius A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Brazilian Society of Assisted Reproduction 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5844653/
https://www.ncbi.nlm.nih.gov/pubmed/29338136
http://dx.doi.org/10.5935/1518-0557.20180005
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author Florêncio, Rodopiano S.
Meira, Melaynne S. B.
da Cunha, Marcos V.
Camarço, Mylena N. C. R.
Castro, Eduardo C.
Finotti, Marta C. C. F.
de Oliveira, Vinicius A.
author_facet Florêncio, Rodopiano S.
Meira, Melaynne S. B.
da Cunha, Marcos V.
Camarço, Mylena N. C. R.
Castro, Eduardo C.
Finotti, Marta C. C. F.
de Oliveira, Vinicius A.
author_sort Florêncio, Rodopiano S.
collection PubMed
description OBJECTIVE: To evaluate the predictive efficiency of serum estradiol (E(2)) concentration in the mid-luteal phase regarding chemical, clinical, and ongoing pregnancies, in patients subjected to IVF/ICSI with fresh embryo transfer. METHODS: One hundred and forty-three patients undergoing IVF/ICSI met all the inclusion criteria for the present study. Most of the patients used antagonists, final maturation was achieved with recombinant chorionic gonadotrophin (HCG), and embryo transfer took place on days 3 to 5, but mostly on day 4. The luteal phase was supplemented with estradiol valerate 6 mg/day and vaginal micronized progesterone 600 mg/day. There was no exclusion of patients in the embryo transfer group due to age or ovarian reserve. All patients with estradiol and chorionic gonadotrophin (βHCG) dosage on the day of transfer, day 7, were included. We assessed the following variables, initially regarding age: number of eggs collected, formed embryos, embryos transferred, day of transfer, transfer type, estradiol and chorionic gonadotropin. Next, we evaluated these elements at three different ranges of estradiol concentrations (<200 pg/ml, 200-500 pg/ml, and >500 pg/ml), comparing these parameters in pregnant (P) and non-pregnant (NP) patients. RESULTS: Data analysis by age group in P and NP patients showed significant differences in the mean values of the variables E(2) and βHCG, TD7. Mean serum estradiol levels in P and NP in the three age groups were: <35years, 835/417 p=0.0006, 35-39 years 833/434 p=0.0118, >39 years, 841/394 p=0.0012. There was also a significant difference in pregnancy rates in the group >500 pg/ml of estradiol concentration (63.4%, p=0.0096). The likelihood of chemical and clinical abortions for the estradiol ranges were: 38.46%, involving the two first ranges versus 15.15% for a concentration >500 pg/ml, p=0.0412 and 5.26% for a concentration >900 pg/ml, p=0.0105. The Pearson correlation coefficient for HCG and estradiol was r = 0.5108. CONCLUSION: This study showed the prognostic value of E(2) in the mid-luteal phase (TD7) for chemical, clinical, and ongoing pregnancies, and its concentration suggested that there is a moderately positive correlation with βHCG levels.
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spelling pubmed-58446532018-03-22 Plasmatic estradiol concentration in the mid-luteal phase is a good prognostic factor for clinical and ongoing pregnancies, during stimulated cycles of in vitro fertilization Florêncio, Rodopiano S. Meira, Melaynne S. B. da Cunha, Marcos V. Camarço, Mylena N. C. R. Castro, Eduardo C. Finotti, Marta C. C. F. de Oliveira, Vinicius A. JBRA Assist Reprod Original Article OBJECTIVE: To evaluate the predictive efficiency of serum estradiol (E(2)) concentration in the mid-luteal phase regarding chemical, clinical, and ongoing pregnancies, in patients subjected to IVF/ICSI with fresh embryo transfer. METHODS: One hundred and forty-three patients undergoing IVF/ICSI met all the inclusion criteria for the present study. Most of the patients used antagonists, final maturation was achieved with recombinant chorionic gonadotrophin (HCG), and embryo transfer took place on days 3 to 5, but mostly on day 4. The luteal phase was supplemented with estradiol valerate 6 mg/day and vaginal micronized progesterone 600 mg/day. There was no exclusion of patients in the embryo transfer group due to age or ovarian reserve. All patients with estradiol and chorionic gonadotrophin (βHCG) dosage on the day of transfer, day 7, were included. We assessed the following variables, initially regarding age: number of eggs collected, formed embryos, embryos transferred, day of transfer, transfer type, estradiol and chorionic gonadotropin. Next, we evaluated these elements at three different ranges of estradiol concentrations (<200 pg/ml, 200-500 pg/ml, and >500 pg/ml), comparing these parameters in pregnant (P) and non-pregnant (NP) patients. RESULTS: Data analysis by age group in P and NP patients showed significant differences in the mean values of the variables E(2) and βHCG, TD7. Mean serum estradiol levels in P and NP in the three age groups were: <35years, 835/417 p=0.0006, 35-39 years 833/434 p=0.0118, >39 years, 841/394 p=0.0012. There was also a significant difference in pregnancy rates in the group >500 pg/ml of estradiol concentration (63.4%, p=0.0096). The likelihood of chemical and clinical abortions for the estradiol ranges were: 38.46%, involving the two first ranges versus 15.15% for a concentration >500 pg/ml, p=0.0412 and 5.26% for a concentration >900 pg/ml, p=0.0105. The Pearson correlation coefficient for HCG and estradiol was r = 0.5108. CONCLUSION: This study showed the prognostic value of E(2) in the mid-luteal phase (TD7) for chemical, clinical, and ongoing pregnancies, and its concentration suggested that there is a moderately positive correlation with βHCG levels. Brazilian Society of Assisted Reproduction 2018 /pmc/articles/PMC5844653/ /pubmed/29338136 http://dx.doi.org/10.5935/1518-0557.20180005 Text en http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Florêncio, Rodopiano S.
Meira, Melaynne S. B.
da Cunha, Marcos V.
Camarço, Mylena N. C. R.
Castro, Eduardo C.
Finotti, Marta C. C. F.
de Oliveira, Vinicius A.
Plasmatic estradiol concentration in the mid-luteal phase is a good prognostic factor for clinical and ongoing pregnancies, during stimulated cycles of in vitro fertilization
title Plasmatic estradiol concentration in the mid-luteal phase is a good prognostic factor for clinical and ongoing pregnancies, during stimulated cycles of in vitro fertilization
title_full Plasmatic estradiol concentration in the mid-luteal phase is a good prognostic factor for clinical and ongoing pregnancies, during stimulated cycles of in vitro fertilization
title_fullStr Plasmatic estradiol concentration in the mid-luteal phase is a good prognostic factor for clinical and ongoing pregnancies, during stimulated cycles of in vitro fertilization
title_full_unstemmed Plasmatic estradiol concentration in the mid-luteal phase is a good prognostic factor for clinical and ongoing pregnancies, during stimulated cycles of in vitro fertilization
title_short Plasmatic estradiol concentration in the mid-luteal phase is a good prognostic factor for clinical and ongoing pregnancies, during stimulated cycles of in vitro fertilization
title_sort plasmatic estradiol concentration in the mid-luteal phase is a good prognostic factor for clinical and ongoing pregnancies, during stimulated cycles of in vitro fertilization
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5844653/
https://www.ncbi.nlm.nih.gov/pubmed/29338136
http://dx.doi.org/10.5935/1518-0557.20180005
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