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Prediction of pregnancy after frozen‐thawed embryo transfer via in vivo intrauterine oxidation‐reduction potential measurements: a pilot study

PURPOSE: During the implantation period, the uterus goes through many complex, orchestrated changes, including alterations of the glycocalyx that are due to sialylation, sulfation, and fucosylation. A previous mouse study showed that the in vivo intrauterine oxidation‐reduction potential (ORP) aided...

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Autores principales: Nakamura, Hitomi, Hosono, Takayoshi, Taniguchi, Takeshi, Kumasawa, Keiichi, Goa, Satoko, Ono, Masaaki, Kimura, Tadashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6046527/
https://www.ncbi.nlm.nih.gov/pubmed/30013426
http://dx.doi.org/10.1002/rmb2.12098
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author Nakamura, Hitomi
Hosono, Takayoshi
Taniguchi, Takeshi
Kumasawa, Keiichi
Goa, Satoko
Ono, Masaaki
Kimura, Tadashi
author_facet Nakamura, Hitomi
Hosono, Takayoshi
Taniguchi, Takeshi
Kumasawa, Keiichi
Goa, Satoko
Ono, Masaaki
Kimura, Tadashi
author_sort Nakamura, Hitomi
collection PubMed
description PURPOSE: During the implantation period, the uterus goes through many complex, orchestrated changes, including alterations of the glycocalyx that are due to sialylation, sulfation, and fucosylation. A previous mouse study showed that the in vivo intrauterine oxidation‐reduction potential (ORP) aided in determining the alterations in the uterine endometrium that are suitable for implantation and for evaluating prospective uterine receptivity, while the in vivo intrauterine pH did not. It was assessed if the in vivo intrauterine ORP could be a useful parameter to predict pregnancy in women. METHODS: A prospective cohort study was conducted for patients who had received a frozen‐thawed single embryo transfer in a programmed, hormonally controlled cycle. The in vivo intrauterine ORP was measured 3 times during the treatment cycle, at cycle days 9‐10, 1 day before progesterone administration and immediately before the embryo transfer. RESULTS: The amount of in vivo intrauterine ORP at 9‐10 days after the start of menstrual bleeding was significantly lower in the pregnant group than in the non‐pregnant group. A receiver‐operator characteristic curve analysis of the intrauterine ORP as a predictor of non‐conception showed an area under the curve of 0.80. CONCLUSION: The in vivo intrauterine ORP could be a useful parameter to predict pregnancy for the frozen‐thawed embryo transfer treatment cycle.
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spelling pubmed-60465272018-07-16 Prediction of pregnancy after frozen‐thawed embryo transfer via in vivo intrauterine oxidation‐reduction potential measurements: a pilot study Nakamura, Hitomi Hosono, Takayoshi Taniguchi, Takeshi Kumasawa, Keiichi Goa, Satoko Ono, Masaaki Kimura, Tadashi Reprod Med Biol Original Articles PURPOSE: During the implantation period, the uterus goes through many complex, orchestrated changes, including alterations of the glycocalyx that are due to sialylation, sulfation, and fucosylation. A previous mouse study showed that the in vivo intrauterine oxidation‐reduction potential (ORP) aided in determining the alterations in the uterine endometrium that are suitable for implantation and for evaluating prospective uterine receptivity, while the in vivo intrauterine pH did not. It was assessed if the in vivo intrauterine ORP could be a useful parameter to predict pregnancy in women. METHODS: A prospective cohort study was conducted for patients who had received a frozen‐thawed single embryo transfer in a programmed, hormonally controlled cycle. The in vivo intrauterine ORP was measured 3 times during the treatment cycle, at cycle days 9‐10, 1 day before progesterone administration and immediately before the embryo transfer. RESULTS: The amount of in vivo intrauterine ORP at 9‐10 days after the start of menstrual bleeding was significantly lower in the pregnant group than in the non‐pregnant group. A receiver‐operator characteristic curve analysis of the intrauterine ORP as a predictor of non‐conception showed an area under the curve of 0.80. CONCLUSION: The in vivo intrauterine ORP could be a useful parameter to predict pregnancy for the frozen‐thawed embryo transfer treatment cycle. John Wiley and Sons Inc. 2018-03-23 /pmc/articles/PMC6046527/ /pubmed/30013426 http://dx.doi.org/10.1002/rmb2.12098 Text en © 2018 The Authors. Reproductive Medicine and Biology published by John Wiley & Sons Australia, Ltd on behalf of Japan Society for Reproductive Medicine. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Articles
Nakamura, Hitomi
Hosono, Takayoshi
Taniguchi, Takeshi
Kumasawa, Keiichi
Goa, Satoko
Ono, Masaaki
Kimura, Tadashi
Prediction of pregnancy after frozen‐thawed embryo transfer via in vivo intrauterine oxidation‐reduction potential measurements: a pilot study
title Prediction of pregnancy after frozen‐thawed embryo transfer via in vivo intrauterine oxidation‐reduction potential measurements: a pilot study
title_full Prediction of pregnancy after frozen‐thawed embryo transfer via in vivo intrauterine oxidation‐reduction potential measurements: a pilot study
title_fullStr Prediction of pregnancy after frozen‐thawed embryo transfer via in vivo intrauterine oxidation‐reduction potential measurements: a pilot study
title_full_unstemmed Prediction of pregnancy after frozen‐thawed embryo transfer via in vivo intrauterine oxidation‐reduction potential measurements: a pilot study
title_short Prediction of pregnancy after frozen‐thawed embryo transfer via in vivo intrauterine oxidation‐reduction potential measurements: a pilot study
title_sort prediction of pregnancy after frozen‐thawed embryo transfer via in vivo intrauterine oxidation‐reduction potential measurements: a pilot study
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6046527/
https://www.ncbi.nlm.nih.gov/pubmed/30013426
http://dx.doi.org/10.1002/rmb2.12098
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