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Wednesday, 4 June 2014

Designer babies #Pint2014 Review by Debbie

My Dear Sexy Readers,

I'm sure you are all sexilly aware by now of Pint Of Science festival that happened this year all over the world between the 19th and 21st of May (my review on the liver talk, my review on the probiotics talk). You can also look up #pint2014 on here or on your favourite platform.

Because so many talks were happening at the same type all across my city - London - it was impossible to be everywhere, so I asked a few friends to report to me on what they learnt down their local pub ;)

May I introduce to you Sexy Debbie who went to the Imperial College Union Bar to a talk entitled 'Creating Life: Test Tubes and Ethics'. Here is her review, and don't forget to leave your thoughts in the comments box:

"When does life begin? Who has the right to decide on the fate of an embryo? Is genetic enhancement necessarily a bad thing? These are hotly debated issues surrounded by controversies and impassioned views. They are not easy questions and they have no easy answers, yet they are just some of the many contentious issues faced by the field of medical ethics and reproductive science.

At a sold-out Pint of Science event I was lucky enough to be in the audience for Mr Stuart Lavery and Professor Raanan Gillon’s talks on ‘Creating life: test tubes and ethics’, in the unlikely surroundings of the pub. Mr Stuart Lavery is the director of IVF Hammersmith, one of the world’s largest IVF units, and Professor Raanan Gillon is Emeritus Professor in Medical Ethics at Imperial College London. Together they are two of the world’s foremost professors in the field of medical ethics and reproductive science.

IVF Hammersmith has pioneered the reproductive technology of preimplantation genetic diagnosis, whereby couples undergoing IVF can have their embryos screened for genetic diseases so that only embryos free from the genetic mutations will be implanted. On a scientific level, the procedure is ground-breaking. By removing just one cell from an 8-cell stage embryo, enough DNA can be extracted for genetic screening and the embryo will continue to develop unharmed. At IVF Hammersmith, every member of lab staff has been genetically screened so that if any of their cells accidentally fall into the vials they are working with their DNA will be detected and not confused with that of the embryo.

Baby Designer Healthy Happy Mother SSS
'All parents hope for a healthy baby'


All parents hope for a healthy baby and will do what they can to help minimise any risks, giving up smoking, alcohol and caffeine for example. Selecting an embryo that is not predisposed to a genetic disease is another means of increasing the chance of having a healthy baby. The concerns and objections tend to arise based on the fate of the embryos that do have genetic mutations and when the possibilities of what the technology is capable of are considered.





Preimplantation genetic diagnosis currently screens for specific serious genetic diseases. This isn’t because that is all that the science is capable of, this is because that is all that is legal in the UK. It is possible to screen embryos for risk factors for particular diseases, such as the risk gene for breast cancer. Would it be right to select against embryos that may get a disease when they equally may not get it? Likewise, it is possible to select for a female or male embryo, to screen for eye colour or hair colour, and even to genetically modify the DNA of the embryo and develop so-called designer babies. As more genes are identified, personality traits could also be screened for. What is the line? Who should decide where to draw it? Should legislation be the same across different countries? Should legislation be in place at all, should public committees be used to make ethical decisions or should parents have the right to decide?

As much as the right of the parents is respected, this was over-ridden in the case of a deaf couple who requested for their IVF embryos to be screened for the deaf gene. They felt they could raise a deaf child better than a hearing child, but it was decided that this did not value the welfare of the child and so the request was rejected. The process of reaching ethical verdicts such as this was explained by Professor Raanan Gillon, who described four principles that provide a moral framework within which to make ethical decisions.

This was a fascinating evening full of discussion and debate. I came away with many more questions than I started with. Clearly the development of reproductive technologies has increased the options for couples at risk of having a child with a serious genetic disorder. However, the use of techniques such as preimplantation genetic diagnosis is expanding, creating new ethical and legal dilemmas in need of regulation and legal frameworks.

How often do you get to discuss such hot topics in the pub with two world experts?! Thanks Pint of Science, I will definitely be back again next year!"

Useful links/further reading 
Preimplantation genetic diagnosis
A guide to preimplantation genetic diagnosis
IVF Hammersmith
Pint of Science
Professor Raanan Gillon Imperial College profile

I hope you all Sexy Readers enjoyed Debbie's review on this super hot topic and let me know what you think in the comments :)

Stay tuned for Sexy Phil and his review on the Big Bang Theory talk by none other than Prof John Ellis, one of the most famous theoretical physicist of our time (a real - slightly older - Sheldon if you like ;))!

See you Soon for more Sexy Science,


12 comments:

  1. Wow, I think you hurt my brain! lol! Bit heavy for a sunday morning, hehe!

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  2. Oh noooo ;) Thanks for dropping by and taking the time to comment!

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  3. The Pint of Science sounds like the place to be if you want to learn something new.
    Love the idea of it.
    Maybe see you there next year

    Pint of Science
    Pint of Science

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  4. The Pint of Science sounds like the place to be if you want to learn something new.
    Love the idea of it.
    Maybe see you there next year

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  5. Preimplantation genetic diagnosis is just the natural progression of research into devastating diseases. I think PGD is no different in combating a disease than a child undergoing a stem-cell transplant once they are born with said disorder - expect there will be zero suffering with PGD for the child and family. It's a no-brainer.

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  6. Those are some weighty things to discuss. I'm afraid I always end up on the fence with a lot of things as I can see so many ifs and buts I go around in circles.

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  7. Hi Agata, I will definitely be there next year. My friends are organizing it so I'm kept in the loop of what's happening! I can't wait to see how many more new countries and cities they will reach next year!!!!!

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  8. Thank you Jessica for your comment. Indeed as long as there are some rules over what can be done, we can safely say it's a no brainer! You might be interested in reading a previous article of mine on Banking your baby's umbilical cord blood and tissue for those all important and precious stem cells. I hope to see you soon

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  9. After studying psychology as my degree I found the whole correlation/causation thing to be infuriating - so many overlaps and confusion with people assuming a correlated relationship is also a cause.

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  10. After I read your post I had a look at the web and I was shocked to discover how many countries took part in it this year.
    I would love to join in next year round.
    I bookmarked the page and put myself a reminder for next April :-)

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  11. Indeed, it's difficult to stay calm in those circumstances. At the moment I'm struggling with Anti-vaxxers (parents who refuse to vaccinate their children)!!!

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  12. Oh well my friends will be happy to hear this, thank you for them. If you are based in London, I also know of a similar science cafe that runs once a month, in case you are thirsty for some science and can't wait a whole year ;)

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