Preimplantation genetic diagnosis after 20 years

被引:34
作者
Handyside, Alan H. [1 ,2 ]
机构
[1] Gynaecol & Genet Ctr, London, England
[2] Univ Leeds, Fac Biol Sci, Inst Integrat & Comparat Biol, Leeds, W Yorkshire, England
关键词
aneuploidy; cost-benefit analysis; preimplantation genetic diagnosis; single gene defect; CYSTIC-FIBROSIS; AMPLIFICATION; CYCLES; SINGLE; PGD;
D O I
10.1016/j.rbmo.2010.07.007
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Preimplantation genetic diagnosis (PGD) should not be an option only for the few couples at risk of serious genetic conditions who can afford it. We appear to have lost sight of the original driving force behind the development of PGD, which is that most couples who carry a serious genetic disorder find it more acceptable to choose to conceive with healthy embryos tested in-vitro at preimplantation stages of development within the first week following fertilization, even if that means discarding those diagnosed as affected. It has been shown using cystic fibrosis as an example, that the cost savings to the US healthcare system of providing free IVF-PGD to all carrier couples compared to the lifetime costs of medical treatment for patients affected by this disease, run to dozens of billions of dollars. With the increasing emphasis in medicine on early diagnosis and prevention of disease together with the availability of new molecular genetic diagnostic tools, a national IVF-PGD programme seems to be the next step in modern health care. (C) 2010, Reproductive Healthcare Ltd. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:280 / 282
页数:3
相关论文
共 12 条
[1]   Multiple micromanipulations for preimplantation genetic diagnosis do not affect embryo development to the blastocyst stage [J].
Cieslak-Janzen, Jeanine ;
Tur-Kaspa, Ilan ;
Ilkevitch, Yuri ;
Bernal, Alejandra ;
Morris, Randy ;
Verlinsky, Yury .
FERTILITY AND STERILITY, 2006, 85 (06) :1826-1829
[2]   Strategies and clinical outcome of 250 cycles of Preimplantation Genetic Diagnosis for single gene disorders [J].
Fiorentino, F ;
Biricik, A ;
Nuccitelli, A ;
De Palma, R ;
Kahraman, S ;
Iacobelli, M ;
Trengia, V ;
Caserta, D ;
Bonu, MA ;
Borini, A ;
Baldi, M .
HUMAN REPRODUCTION, 2006, 21 (03) :670-684
[3]   ESHRE PGD Consortium data collection IX: cycles from January to December 2006 with pregnancy follow-up to October 2007 [J].
Goossens, V. ;
Harton, G. ;
Moutou, C. ;
Traeger-Synodinos, J. ;
Van Rij, M. ;
Harper, J. C. .
HUMAN REPRODUCTION, 2009, 24 (08) :1786-1810
[4]   PREGNANCIES FROM BIOPSIED HUMAN PREIMPLANTATION EMBRYOS SEXED BY Y-SPECIFIC DNA AMPLIFICATION [J].
HANDYSIDE, AH ;
KONTOGIANNI, EH ;
HARDY, K ;
WINSTON, RML .
NATURE, 1990, 344 (6268) :768-770
[5]   Isothermal whole genome amplification from single and small numbers of cells: a new era for preimplantation genetic diagnosis of inherited disease [J].
Handyside, AH ;
Robinson, MD ;
Simpson, RJ ;
Omar, MB ;
Shaw, MA ;
Grudzinskas, JG ;
Rutherford, A .
MOLECULAR HUMAN REPRODUCTION, 2004, 10 (10) :767-772
[6]   BIRTH OF A NORMAL GIRL AFTER INVITRO FERTILIZATION AND PREIMPLANTATION DIAGNOSTIC TESTING FOR CYSTIC-FIBROSIS [J].
HANDYSIDE, AH ;
LESKO, JG ;
TARIN, JJ ;
WINSTON, RML ;
HUGHES, MR .
NEW ENGLAND JOURNAL OF MEDICINE, 1992, 327 (13) :905-909
[7]  
HANDYSIDE AH, J MED GENET IN PRESS
[8]   Let parents decide [J].
Handyside, Alan .
NATURE, 2010, 464 (7291) :978-979
[9]   Preclinical validation of a microarray method for full molecular karyotyping of blastomeres in a 24-h protocol [J].
Johnson, D. S. ;
Gemelos, G. ;
Baner, J. ;
Ryan, A. ;
Cinnioglu, C. ;
Banjevic, M. ;
Ross, R. ;
Alper, M. ;
Barrett, B. ;
Frederick, J. ;
Potter, D. ;
Behr, B. ;
Rabinowitz, M. .
HUMAN REPRODUCTION, 2010, 25 (04) :1066-1075
[10]   Report on a consecutive series of 581 children born after blastomere biopsy for preimplantation genetic diagnosis [J].
Liebaers, I. ;
Desmyttere, S. ;
Verpoest, W. ;
De Rycke, M. ;
Staessen, C. ;
Sermon, K. ;
Devroey, P. ;
Haentjens, P. ;
Bonduelle, M. .
HUMAN REPRODUCTION, 2010, 25 (01) :275-282