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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Biomedical Informatics
2015
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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. |
format | Online Article Text |
id | pubmed-4464542 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Biomedical Informatics |
record_format | MEDLINE/PubMed |
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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