You may have heard about genetic testing of embryos but don’t really understand who needs it, why people would opt for it, or what is involved? Here’s your questions answered.
By Dr Stephen Lane, Specialist, City Fertility Centre Adelaide
Genetic screening can be beneficial for a range of people including those suffering recurrent miscarriage, of advanced maternal age, with a family history of chromosomal disorders, or have experienced previous unsuccessful IVF cycles.
What is genetic screening of embryos?
Genetic screening of embryos in IVF is known as pre-implantation diagnosis or PGD for short. It involves genetically testing the embryo prior to it being implanted.
Put simply, genetic screening is used to detect anomalies in the number or structure of chromosomes in embryos. In some instances just the eggs can be genetically tested before fertilisation occurs.
Normal human cells (embryonic cells) contain 46 chromosomes in 23 pairs. We receive 23 chromosomes from each parent. If an error occurs, and the egg or sperm has an extra or missing chromosome, the embryo created will also have an extra or missing chromosome resulting in what is scientifically called aneuploidy. The most common aneuploidy is Down Syndrome however there are many others.
Why is it useful to carry out genetic testing?
When embryos have abnormal chromosomes it may prevent implantation to the uterine lining, lead to pregnancy loss, or result in the birth of a child with disabilities.
The potential benefits of advanced embryo selection and choosing only chromosomally normal embryos include reducing the risk of a child with a chromosomal abnormality, reducing the incidence of miscarriage, increasing chances of IVF success, reducing the number of IVF cycles required to achieve a successful outcome.
How is it done?
The most common embryo testing method is Embryo or Blastomere Biopsy, whereby some blastomeres or embryonic cells are carefully removed on the fifth day of embryo development and tested.
A second test is available. A Polar Body Biopsy is where the maturing egg produces two small cells known as polar bodies, which degenerate after fertilisation. The polar bodies are carefully removed and the chromosomal content tested. This is rarely performed and is used to check egg quality.
How are the cells analysed?
The biopsied cells are then analysed via an Advanced Embryo Selection (AES) technique called Comparative Genomic Hybridisation (CGH) or Fluorescence In Situ Hybridisation (FISH).
The CGH testing method looks at all chromosomes including the X and Y and compares them with a sample of “normal” DNA. A computerised scanner interprets the results of the slide, which are then verified by a scientist. CGH can test all 23 pairs of chromosomes.
The FISH method uses probes labelled with different fluorescent dyes. The number of chromosomes are counted and the geneticist can distinguish the normal cells and those with aneuploidy (an extra or missing chromosome). FISH is only able to test a limited number of chromosomes.
What happens next?
While the PGD testing of the cells is taking place the embryos are kept in a culture in an incubator and are then frozen and kept in storage.
If the testing reveals normal embryos then the best quality embryo is chosen to be transferred. The remaining viable embryos will be frozen for future use if required.
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This article is reproduced with permission from City Fertility.