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Association between serum estradiol level on the human chorionic gonadotrophin administration day and clinical outcome
BACKGROUND: Estradiol, as an important hormone in follicular development and endometrial receptivity, is closely related to clinical outcomes of fresh in vitro fertilization embryo transfer (IVF-ET) cycles. The aim of this retrospective study was to evaluate the association between elevated serum es...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Wolters Kluwer Health
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6511421/ https://www.ncbi.nlm.nih.gov/pubmed/30973445 http://dx.doi.org/10.1097/CM9.0000000000000251 |
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author | Li, Xin Zeng, Cheng Shang, Jing Wang, Sheng Gao, Xue-Lian Xue, Qing |
author_facet | Li, Xin Zeng, Cheng Shang, Jing Wang, Sheng Gao, Xue-Lian Xue, Qing |
author_sort | Li, Xin |
collection | PubMed |
description | BACKGROUND: Estradiol, as an important hormone in follicular development and endometrial receptivity, is closely related to clinical outcomes of fresh in vitro fertilization embryo transfer (IVF-ET) cycles. The aim of this retrospective study was to evaluate the association between elevated serum estradiol (E(2)) levels on the day of human chorionic gonadotrophin (hCG) administration and IVF-ET pregnancy and birth outcomes. METHODS: A total of 1771 infertile patients with their first fresh IVF-ET cycles were analyzed retrospectively between January 2011 and January 2016 in Peking University First Hospital. Patients were categorized by serum E(2) levels on the day of hCG administration into six groups: group 1 (serum E(2) levels ≤ 1000 pg/mL, n = 205), group 2 (serum E(2) levels 1001–2000 pg/mL, n = 457), group 3 (serum E(2) levels 2001–3000 pg/mL, n = 425), group 4 (serum E(2) levels 3001–4000 pg/mL, n = 310), group 5 (serum E(2) levels 4001–5000 pg/mL, n = 237), and group 6 (serum E(2) levels > 5000 pg/mL, n = 137). The retrieved oocyte and MII oocyte numbers and implantation and clinical pregnancy rates of the groups were compared as the first objective of the study. For the 360 women with singleton births among all patients, the area under the corresponding receiver operating characteristic curve (ROC curve) was calculated to assess the predictive value of the E(2) change for the probability of low birth weight (LBW) infants as the second objective. RESULTS: The retrieved oocyte and MII oocyte numbers and implantation and clinical pregnancy rates gradually increased from groups 1 to 5 but decreased in group 6. The parameters of group 1 were statistically worse than those of the other groups, from group 2 to group 6 (the number of retrieved oocytes, t = 13.096, t = 23.307, t = 23.086, t = 26.376, t = 19.636, P < 0.003; the number of retrieved MII oocytes, t = 10.856, t = 20.868, t = 21.874, t = 23.374, t = 19.092, P < 0.003; the implantation rate, χ(2) = 12.179, χ(2) = 22.239, χ(2) = 23.993, χ(2) = 23.344, χ(2) = 16.758, P < 0.003; the clinical pregnancy rate, χ(2) = 16.415, χ(2) = 28.074, χ(2) = 35.387, χ(2) = 37.025, χ(2) = 24.590, P < 0.003). ROC analysis revealed that when a serum peak E(2) of 3148 pg/mL was used to predict LBW. CONCLUSIONS: The results indicate that serum E(2) levels have a concentration-dependent effect on clinical outcomes. The optimal range of the E(2) level during a fresh IVF-ET cycle is 1000 to 3148 pg/mL. |
format | Online Article Text |
id | pubmed-6511421 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-65114212019-07-30 Association between serum estradiol level on the human chorionic gonadotrophin administration day and clinical outcome Li, Xin Zeng, Cheng Shang, Jing Wang, Sheng Gao, Xue-Lian Xue, Qing Chin Med J (Engl) Original Articles BACKGROUND: Estradiol, as an important hormone in follicular development and endometrial receptivity, is closely related to clinical outcomes of fresh in vitro fertilization embryo transfer (IVF-ET) cycles. The aim of this retrospective study was to evaluate the association between elevated serum estradiol (E(2)) levels on the day of human chorionic gonadotrophin (hCG) administration and IVF-ET pregnancy and birth outcomes. METHODS: A total of 1771 infertile patients with their first fresh IVF-ET cycles were analyzed retrospectively between January 2011 and January 2016 in Peking University First Hospital. Patients were categorized by serum E(2) levels on the day of hCG administration into six groups: group 1 (serum E(2) levels ≤ 1000 pg/mL, n = 205), group 2 (serum E(2) levels 1001–2000 pg/mL, n = 457), group 3 (serum E(2) levels 2001–3000 pg/mL, n = 425), group 4 (serum E(2) levels 3001–4000 pg/mL, n = 310), group 5 (serum E(2) levels 4001–5000 pg/mL, n = 237), and group 6 (serum E(2) levels > 5000 pg/mL, n = 137). The retrieved oocyte and MII oocyte numbers and implantation and clinical pregnancy rates of the groups were compared as the first objective of the study. For the 360 women with singleton births among all patients, the area under the corresponding receiver operating characteristic curve (ROC curve) was calculated to assess the predictive value of the E(2) change for the probability of low birth weight (LBW) infants as the second objective. RESULTS: The retrieved oocyte and MII oocyte numbers and implantation and clinical pregnancy rates gradually increased from groups 1 to 5 but decreased in group 6. The parameters of group 1 were statistically worse than those of the other groups, from group 2 to group 6 (the number of retrieved oocytes, t = 13.096, t = 23.307, t = 23.086, t = 26.376, t = 19.636, P < 0.003; the number of retrieved MII oocytes, t = 10.856, t = 20.868, t = 21.874, t = 23.374, t = 19.092, P < 0.003; the implantation rate, χ(2) = 12.179, χ(2) = 22.239, χ(2) = 23.993, χ(2) = 23.344, χ(2) = 16.758, P < 0.003; the clinical pregnancy rate, χ(2) = 16.415, χ(2) = 28.074, χ(2) = 35.387, χ(2) = 37.025, χ(2) = 24.590, P < 0.003). ROC analysis revealed that when a serum peak E(2) of 3148 pg/mL was used to predict LBW. CONCLUSIONS: The results indicate that serum E(2) levels have a concentration-dependent effect on clinical outcomes. The optimal range of the E(2) level during a fresh IVF-ET cycle is 1000 to 3148 pg/mL. Wolters Kluwer Health 2019-05-20 2019-05-20 /pmc/articles/PMC6511421/ /pubmed/30973445 http://dx.doi.org/10.1097/CM9.0000000000000251 Text en Copyright © 2019 The Chinese Medical Association, produced by Wolters Kluwer, Inc. under the CC-BY-NC-ND license. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0 |
spellingShingle | Original Articles Li, Xin Zeng, Cheng Shang, Jing Wang, Sheng Gao, Xue-Lian Xue, Qing Association between serum estradiol level on the human chorionic gonadotrophin administration day and clinical outcome |
title | Association between serum estradiol level on the human chorionic gonadotrophin administration day and clinical outcome |
title_full | Association between serum estradiol level on the human chorionic gonadotrophin administration day and clinical outcome |
title_fullStr | Association between serum estradiol level on the human chorionic gonadotrophin administration day and clinical outcome |
title_full_unstemmed | Association between serum estradiol level on the human chorionic gonadotrophin administration day and clinical outcome |
title_short | Association between serum estradiol level on the human chorionic gonadotrophin administration day and clinical outcome |
title_sort | association between serum estradiol level on the human chorionic gonadotrophin administration day and clinical outcome |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6511421/ https://www.ncbi.nlm.nih.gov/pubmed/30973445 http://dx.doi.org/10.1097/CM9.0000000000000251 |
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