Editer l'article Suivre ce blog Administration + Créer mon blog
3 mai 2012 4 03 /05 /mai /2012 18:40

Paru hier dans la revue scientifique Molecular Genetics, une étude qui montre un taux de succès significativement plus élevé (69.1%) en FIV après sélection des embryons (stade blastocyte) par un test génétique sur les 24 chromosomes.

C'est l'entreprise britannique BlueGnome qui a mis au point cette méthodologie de screening, qui semble beaucoup plus efficace que les tests morphologiques selon lesquels sont habituellement évalués les embryons

On notera, parmi les utilisateurs de ce test, des centres américains, australiens, italiens et britanniques. Et si on déménageait ? Alors Cambridge, Rome ou Melbourne ??! Il paraît que c'est d'autant plus adapté pour les cas d'infertilité complexe et les couples "âgés"...

Ci dessous le communiqué de presse de l'entreprise et pour les plus scientifiques, le lien vers la publication scientifique.


Press release

3rd May 2012, For immediate release


Selecting IVF embryos for normal numbers of chromosomes can significantly increase pregnancy rates - first randomised prospective study shows ongoing pregnancy rate after 20 weeks per cycle started of 69.1% in the 24sure treatment group vs 41.7% in the control group. 


BlueGnome Ltd (Cambridge, UK) is pleased to announce the results of the first randomised prospective IVF study of pre-implantation chromosome analysis using their 24sure array platform. The study, published in The Journal of Molecular Cytogenetics by Yang et al (Pacific Reproductive Center,Torrance, USA) has demonstrated that selectively implanting euploid embryos, with a normal number of chromosomes, significantly increases pregnancy rates.

The study blindly randomised 103 IVF cycles. In the treatment group of 55 cycles, 24sure analysis of day 5 biopsies was used to selectively implant a single euploid embryo (as recommended by IVF regulatory bodies such as the HEFA), while in the control group of 48 cycles single embryos were selected using existing morphological scorecard approaches. The ongoing pregnancy rate, after 20 weeks, per cycle started was 69.1% in the 24sure treatment group vs 41.7% in the control group. This extremely promising result provides direct evidence that 24sure analysis can deliver a 65% increase in pregnancy rates, even in younger patients with more favourable IVF outcomes. Further randomised studies are needed and are underway.

“This study provides crucial evidence that 24 chromosome aneuploidy screening, using 24sure, can offer a dramatic benefit to IVF success rates. While further studies are still needed, this result is incredibly exciting because it indicates for the first time that 24 chromosome screening and single embryo transfer has the potential to become the default standard of care for all IVF cycles worldwide.” Nick Haan, CEO, BlueGnome Ltd, Cambridge, UK


Link to scientific paper


Video of 24sure



Quotes from Key Opinion Leaders


24sure comprehensive chromosomal screening has been clinically proven to be the effective means to select the chromosomally normal embryo(s) for transfer to ensure a healthy pregnancy for infertile patients. As a clinical scientist, I am happy to be a part of the new technology. Dr Zhihong Yang, Executive Director, ART and PGD Laboratories, Pacific Reproductive Center Torrance, CA, USA.

This is a breakthrough clinical study, showing for the first time how this technology, which CARE helped pioneer, can greatly improve IVF success rates for younger patients. Here at Care Fertility we have already shown that pre-implantation genetic screening has benefits for older patients, and those with complex histories, so it is great to see the scope of this technology could benefit many more patients. Prof. Simon Fishel, Managing Director, CARE Fertility Group, UK.

I’m not at all surprised by these fantastic results from the Californian group. They mirror our success at Melbourne IVF using BlueGnome’s 24sure technology. We’ve provided this service to our patients for just over a year and already about 20 babies have been born and another 50 are on the way. It’s a significant breakthrough for patients who are struggling to become pregnant. Dr. Leeanda Wilton, Scientific Director, Preimplantation Genetics, Melbourne IVF, Australia.

The preliminary results of this paper highlight the importance of offering PGS also to good prognosis IVF patients. For years the PGD community has focused only on couples with a specific indication for testing (e.g. advanced maternal age), not considering that aneuploidies may arise in every IVF patient. This is clearly demonstrated from the 45% aneuploidy rate detected also in embryos from young patients, and may explain why many young women fail to achieve a pregnancy even after transfer of good quality embryos. Embryo assessment by PGS has become a crucial component to the clinical success of IVF techniques. The new array-CGH-based comprehensive chromosome screening technology holds great promise for improving IVF clinical outcomes for every infertile patient, by selecting the most competent embryo(s) for transfer. Dr Francesco Fiorentino, Director, Genoma, Rome, Italy.

This well designed study supports what many of us have expected for a long time; aneuploidy is responsible for most IVF failure. Assessment of an embryo’s ability to create a pregnancy is best done not by morphologic examination, rather it is best done by assessing all 24 chromosomes. This approach will result in better patient outcomes. Choosing a single high potential embryo will result in fewer multiple pregnancies, fewer miscarriages and will also help us define the population of patients who make few or no euploid embryos. Jamie A Grifo MD PhD, Program Director NYU Fertility Center, USA.

Many fertilized eggs are genetically affected, even in young infertile couples. This study shows conclusively that those embryos cannot be recognized from microscopic assessment alone. This multi-center study performed in two different countries underscores the importance of removing seriously abnormal embryos before transfer into the uterus using so-called comprehensive screening; a contemporary form of preimplantation genetic screening or PGS. Although the study was relatively modest in size, the results were blinded to observers and embryos were randomized to avoid bias. It opens up the exciting possibility to perform PGS not just in complicated patients such as those with poor ovarian reserve, but also egg donors and young women as abnormal embryos are common at any age. Jacques Cohen, PhD. Director, Tyho-Galileo Research Laboratories, Livingston, NJ, USA.

The work of Dr. Yang is remarkable. We know that chromosome abnormality rates in embryos of young patients are as high as 40%, and increase up to 70% in blastocyst of women >40. Their study means that if young women benefit from blastocyst biopsy, aCGH and day 6 transfer, women of advanced maternal age who have a bigger problem conceiving, would too, provided they produce enough embryos or do banking of embryos. Indeed work by Gary Harton while at Reprogenetics showed that if euploid blastocysts are available for transfer, they implant at the same rate regardless of maternal age. The approach used, day 5 biopsy and day 6 transfer is also more acceptable for patients, since they are less costly than vitrification and patients do not have to wait another cycle for replacement. Santiago Munne, PhD, Director, Reprogenetics, Livingston, NJ, USA.

While this is a small pilot study, it underscores clearly that even younger infertile couples undergoing IVF will benefit significantly by this powerful technology advance. Since nearly half of a patient’s embryos are chromosomally abnormal, the ability to reliably detect the normal ones for uterine transfer will impressively improve the chances that these rather desperate couples can finally have a healthy family – and one baby at a time, which is the ultimate goal for all involved. Professor Mark Hughes, Genesis Genetics Institute, Detroit, MI, USA.

This well done study adds to the growing evidence that 24 chromosome testing by array CGH will allow PGD to finally reach its potential to identify the best embryos with highest implantation and lowest loss rates. The study by Yang et al. confirms that chromosome analysis by array CGH is the best approach to identify developmentally competent embryos for eSET. Harvey J. Stern MD, PhD. Director, Reproductive Genetics, Genetics & IVF Institute, USA.


About BlueGnome

BlueGnome is a leading provider of genetic solutions for the screening of chromosomal abnormalities in cytogenetics and IVF

Partager cet article


on est pris en charge à Madrid, où on a de la famille, ça limitera les frais d'hébergement, c'est toujours àa de gagné :)
<br /> <br /> Tiens moi au courant, sur comment cela se passe là bas, si les conditions (techniques, humaines...) sont effectivement ce qu'on en dit et gages de réussite... Vous commencez quand le premier<br /> essai là bas ? Bonne chance dans tous les cas. Apo<br /> <br /> <br /> <br />
merci pour cet article.<br /> Comme quoi, de belles avancées se font ... ailleurs!<br /> tout comme le fameux incubateur à embryons utilisé en espagne depuis 10 ans et qui va enfin être utilisé en france.<br /> mouais ... va falloir rattraper notre retard dans notre bonne vieille france.
<br /> Bonjour Fabienne. Bienvenue au club des vieilles en pma... Je lis ton blog de temps en temps et espère que tes prochains rdv seront concluants. Les larmes à n'en plus finir, l'impression de toucher<br /> le fond, on connaît aussi et je ne me remets pas de l'échec de fiv-icsi 2... Quant au don, à notre grande surprise, le ponte du centre Pma, misogyne et pédant, nous a répondu "don de quoi" sous<br /> entendu direct double don, ie ailleurs quen france... Séjours à Barcelone en vue? La france est lamentablement en retard, ce test ne serait ainsi pas a priori légal hors couple ayant une maladie<br /> génétique avérée. Ceux qui ont pondu ces lois n'ont jamais du faire de pma... Bon courage à nous tous!<br /> <br /> <br />
Bon, l'anglais et moi on est fâchés, mais ceci nous donne grandement espoir pour notre nouveau parcours en fiv dpi ! En cas d'échec espagnol, ça ouvre de nouvelles perspectives... Et l'Australie,<br /> on en rêve un peu déjà.... Faudrait juste que j'apprivoise mon english :)
<br /> Je viens de découvrir ton blog que j'irais donc lire désormais ! Vous Partez donc en Espagne? Barcelone? Tiens moi au courant! Bises. Apo<br /> <br /> <br />
Ca améliore clairement la sélection de l'embryon (et c'est top!) mais il reste la question cruciale de l'implantation et la nidation. Et là, je pense qu'il y a encore des recherches à faire. La<br /> Nature reste très mystérieuse.<br /> Ceci dit, ça donne beaucoup d'espoir des études comme celles-ci pour les futurs couples infertiles. Je doute que nous puissions en bénéficier en revanche...
<br /> Cette impression d'arriver trop tard (par rapport à l'âge) et trop tôt par rapport à la technique et à la législation... Nous reste t il que les yeux pour pleurer comme on dit? apo<br /> <br /> <br />
Toutes ces études et ces progrès me font penser que, dans quelques années, la FIV sera "facile" Je n'arrive pas à trouver de mot plus édéquat... Enfin je veux dire que les résultats positifs seront<br /> plus rapides ... Tu me comprends ??<br /> Bisous
Là, j'avoue, je passe mon tour sur la partie en, anglais!!!<br /> Belle journée à toi
<br /> <br /> C'est pour cela que j'ai fait un petit résumé en français, en gros cette technique de tri (encore faut il en avoir plusieurs...) d'embryons augmente significativement les taux de succes par<br /> rapport au tri morphologique actuellement effectué... C'est encore au stade de la recherche mais laisse des espoirs, malheureusement pas pour nous à moins de partir dans un des centres impliqués<br /> dans le protocole de recherche :((<br /> <br /> <br /> <br />

Un Blog De Fiv...

  • : 6cellules
  • : Un blog de FIV, entre difficultés, doutes et espoirs. Et avec des infos scientifiques sur l'AMP
  • Contact

A Propos De Nous

  • 6cellules
  • A &amp; A, 40 ans et des poussières, trouver, un peu tard, l'amour de sa vie et avoir envie d'un enfant. Mais un cancer il y a 10 ans et distilbène in utero... Se battre contre l'adversité, s'essouffler, s'aimer en espérant le meilleur...