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Current status of preimplantation genetic diagnosis in Japan

This is a retrospective study aimingto clarify the current status of preimplantation genetic diagnosis (PGD) in Japan. Our data were collected from 12 facilities between September 2004 and September 2012, and entered into a database. A majority of PGD in Japan was performed for balanced structural c...

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Autores principales: Sato, Kenji, Sueoka, Kou, Iino, Kotaro, Senba, Hiroshi, Suzuki, Mariko, Mizuguchi, Yuki, Izumi, Yoko, Sato, Suguru, Nakabayashi, Akira, Tanaka, Mamoru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Biomedical Informatics 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4464542/
https://www.ncbi.nlm.nih.gov/pubmed/26124570
http://dx.doi.org/10.6026/97320630011254
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author Sato, Kenji
Sueoka, Kou
Iino, Kotaro
Senba, Hiroshi
Suzuki, Mariko
Mizuguchi, Yuki
Izumi, Yoko
Sato, Suguru
Nakabayashi, Akira
Tanaka, Mamoru
author_facet Sato, Kenji
Sueoka, Kou
Iino, Kotaro
Senba, Hiroshi
Suzuki, Mariko
Mizuguchi, Yuki
Izumi, Yoko
Sato, Suguru
Nakabayashi, Akira
Tanaka, Mamoru
author_sort Sato, Kenji
collection PubMed
description This is a retrospective study aimingto clarify the current status of preimplantation genetic diagnosis (PGD) in Japan. Our data were collected from 12 facilities between September 2004 and September 2012, and entered into a database. A majority of PGD in Japan was performed for balanced structural chromosomal abnormalities in couples with recurrent miscarriage. PGD for monogenic diseases was performed only in two facilities. The average maternal age was 38 years for monogenic diseases and 40 years for chromosomal abnormalities. Overall there have been671 cycles to oocyte retrieval reported. Of these cycles, 85% (572 cycles)were for chromosomal abnormalities, and 15% (99 cycles) for monogenic diseases. Diagnosis rates in the current study were 70.8% for monogenic diseases and 94.0% for chromosomal abnormalities. Rates of embryo transfer of PGD were 62.7% for monogenic diseases and 25.5% for chromosomal abnormalities. Clinical pregnancy rates per embryo transfer were 12.0% for monogenic diseases and 35.6% for chromosomal abnormalities. Our study is the first PGD report from all facilities which had the approval of the ethics committee of the Japanese Society of Obstetrics and Gynecology. We have built a basis for gathering continuous PGD data in Japan.
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spelling pubmed-44645422015-06-29 Current status of preimplantation genetic diagnosis in Japan Sato, Kenji Sueoka, Kou Iino, Kotaro Senba, Hiroshi Suzuki, Mariko Mizuguchi, Yuki Izumi, Yoko Sato, Suguru Nakabayashi, Akira Tanaka, Mamoru Bioinformation Hypothesis This is a retrospective study aimingto clarify the current status of preimplantation genetic diagnosis (PGD) in Japan. Our data were collected from 12 facilities between September 2004 and September 2012, and entered into a database. A majority of PGD in Japan was performed for balanced structural chromosomal abnormalities in couples with recurrent miscarriage. PGD for monogenic diseases was performed only in two facilities. The average maternal age was 38 years for monogenic diseases and 40 years for chromosomal abnormalities. Overall there have been671 cycles to oocyte retrieval reported. Of these cycles, 85% (572 cycles)were for chromosomal abnormalities, and 15% (99 cycles) for monogenic diseases. Diagnosis rates in the current study were 70.8% for monogenic diseases and 94.0% for chromosomal abnormalities. Rates of embryo transfer of PGD were 62.7% for monogenic diseases and 25.5% for chromosomal abnormalities. Clinical pregnancy rates per embryo transfer were 12.0% for monogenic diseases and 35.6% for chromosomal abnormalities. Our study is the first PGD report from all facilities which had the approval of the ethics committee of the Japanese Society of Obstetrics and Gynecology. We have built a basis for gathering continuous PGD data in Japan. Biomedical Informatics 2015-05-28 /pmc/articles/PMC4464542/ /pubmed/26124570 http://dx.doi.org/10.6026/97320630011254 Text en © 2015 Biomedical Informatics This is an open-access article, which permits unrestricted use, distribution, and reproduction in any medium, for non-commercial purposes, provided the original author and source are credited.
spellingShingle Hypothesis
Sato, Kenji
Sueoka, Kou
Iino, Kotaro
Senba, Hiroshi
Suzuki, Mariko
Mizuguchi, Yuki
Izumi, Yoko
Sato, Suguru
Nakabayashi, Akira
Tanaka, Mamoru
Current status of preimplantation genetic diagnosis in Japan
title Current status of preimplantation genetic diagnosis in Japan
title_full Current status of preimplantation genetic diagnosis in Japan
title_fullStr Current status of preimplantation genetic diagnosis in Japan
title_full_unstemmed Current status of preimplantation genetic diagnosis in Japan
title_short Current status of preimplantation genetic diagnosis in Japan
title_sort current status of preimplantation genetic diagnosis in japan
topic Hypothesis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4464542/
https://www.ncbi.nlm.nih.gov/pubmed/26124570
http://dx.doi.org/10.6026/97320630011254
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