Literature DB >> 29259423

Preimplantation genetic diagnosis: an update on current technologies and ethical considerations.

Kou Sueoka1.   

Abstract

The aim of reproductive medicine is to support the birth of healthy children. Advances in assisted reproductive technologies and genetic analysis have led to the introduction of preimplantation genetic diagnosis (PGD) for embryos. Indications for PGD have been a major topic in the fields of ethics and law. Concerns vary by nation, religion, population, and segment, and the continued rapid development of new technologies. In contrast to the ethical augment, technology has been developing at an excessively rapid speed. The most significant recent technological development provides the ability to perform whole genome amplification and sequencing of single embryonic cells by microarray or next-generation sequencing methods. As new affordable technologies are introduced, patients are presented with a growing variety of PGD options. Simultaneously, the ethical guidelines for the indications for testing and handling of genetic information must also rapidly correspond to the changes.

Entities:  

Keywords:  Microarray; Polymerase chain reaction (PCR); Preimplantation genetic diagnosis (PGD); Preimplantation genetic screening (PGS); Whole genome amplification

Year:  2015        PMID: 29259423      PMCID: PMC5715849          DOI: 10.1007/s12522-015-0224-6

Source DB:  PubMed          Journal:  Reprod Med Biol        ISSN: 1445-5781


  55 in total

1.  Detailed investigation of factors influencing amplification efficiency and allele drop-out in single cell PCR: implications for preimplantation genetic diagnosis.

Authors:  Wirawit Piyamongkol; Mercedes G Bermúdez; Joyce C Harper; Dagan Wells
Journal:  Mol Hum Reprod       Date:  2003-07       Impact factor: 4.025

2.  Degenerate oligonucleotide-primed PCR: general amplification of target DNA by a single degenerate primer.

Authors:  H Telenius; N P Carter; C E Bebb; M Nordenskjöld; B A Ponder; A Tunnacliffe
Journal:  Genomics       Date:  1992-07       Impact factor: 5.736

3.  Preimplantation genetic screening to improve in vitro fertilization pregnancy rates: a prospective randomized controlled trial.

Authors:  Jennifer E Mersereau; Eugene Pergament; Xingqi Zhang; Magdy P Milad
Journal:  Fertil Steril       Date:  2007-12-03       Impact factor: 7.329

4.  Preimplantation genetic diagnosis for retinoblastoma predisposition.

Authors:  Seema Dhanjal; Georgia Kakourou; Thalia Mamas; Natasha Saleh; Alpesh Doshi; Sarah Gotts; Sarah Nuttall; Karen Fordham; Paul Serhal; Joy Delhanty; Joyce Harper; Sioban Sengupta
Journal:  Br J Ophthalmol       Date:  2007-08       Impact factor: 4.638

5.  ESHRE PGD Consortium data collection XII: cycles from January to December 2009 with pregnancy follow-up to October 2010.

Authors:  C Moutou; V Goossens; E Coonen; M De Rycke; G Kokkali; P Renwick; S B SenGupta; K Vesela; J Traeger-Synodinos
Journal:  Hum Reprod       Date:  2014-03-11       Impact factor: 6.918

Review 6.  The use of whole genome amplification in the study of human disease.

Authors:  Simon Hughes; Nona Arneson; Susan Done; Jeremy Squire
Journal:  Prog Biophys Mol Biol       Date:  2005-05       Impact factor: 3.667

7.  Two different microarray technologies for preimplantation genetic diagnosis and screening, due to reciprocal translocation imbalances, demonstrate equivalent euploidy and clinical pregnancy rates.

Authors:  Kyle J Tobler; Paul R Brezina; Andrew T Benner; Luke Du; Xin Xu; William G Kearns
Journal:  J Assist Reprod Genet       Date:  2014-04-26       Impact factor: 3.412

8.  Evaluation of targeted next-generation sequencing-based preimplantation genetic diagnosis of monogenic disease.

Authors:  Nathan R Treff; Anastasia Fedick; Xin Tao; Batsal Devkota; Deanne Taylor; Richard T Scott
Journal:  Fertil Steril       Date:  2013-01-09       Impact factor: 7.329

9.  Assessment of numeric abnormalities of X, Y, 18, and 16 chromosomes in preimplantation human embryos before transfer.

Authors:  S Munné; K M Sultan; H U Weier; J A Grifo; J Cohen; Z Rosenwaks
Journal:  Am J Obstet Gynecol       Date:  1995-04       Impact factor: 8.661

10.  High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays.

Authors:  D Pinkel; R Segraves; D Sudar; S Clark; I Poole; D Kowbel; C Collins; W L Kuo; C Chen; Y Zhai; S H Dairkee; B M Ljung; J W Gray; D G Albertson
Journal:  Nat Genet       Date:  1998-10       Impact factor: 38.330

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  3 in total

1.  Preimplantation genetic testing for a family with usher syndrome through targeted sequencing and haplotype analysis.

Authors:  Haining Luo; Chao Chen; Yun Yang; Yinfeng Zhang; Yuan Yuan; Wanyang Wang; Renhua Wu; Zhiyu Peng; Ying Han; Lu Jiang; Ruqiang Yao; Xiaoying An; Weiwei Zhang; Yanqun Le; Jiale Xiang; Na Yi; Hui Huang; Wei Li; Yunshan Zhang; Jun Sun
Journal:  BMC Med Genomics       Date:  2019-11-07       Impact factor: 3.063

Review 2.  Genetic counseling prior to assisted reproductive technology.

Authors:  Yukiko Katagiri; Yuko Tamaki
Journal:  Reprod Med Biol       Date:  2020-12-31

3.  Successful preimplantation genetic diagnosis by targeted next-generation sequencing on an ion torrent personal genome machine platform.

Authors:  Yan Hao; Dawei Chen; Zhiguo Zhang; Ping Zhou; Yunxia Cao; Zhaolian Wei; Xiaofeng Xu; Beili Chen; Weiwei Zou; Mingrong Lv; Dongmei Ji; Xiaojin He
Journal:  Oncol Lett       Date:  2018-01-26       Impact factor: 2.967

  3 in total

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