Preimplantation Genetic Diagnosis (PGD)
Preimplantation Genetic Diagnosis (PGD)
Also known as Preimplantation Genetic Screening, the purpose of this process is to evaluate the chromosomal makeup of an egg/embryo. Because the majority of miscarriages are due to chromosomal abnormalities, many couples undergo Preimplantation Genetic Diagnosis in order to select embryos that are chromosomally “normal” and increase their chances of IVF success. An egg/embryo with too many or too few chromosomes will either 1) fail to implant in the uterus, 2) lead to a miscarriage, or 3) result in a chromosomal birth defect such as Down Syndrome or Turner Syndrome.
Another reason for performing PGD is for family balancing through gender selection. Because the gender chromosomes are identified during PGD, it is possible to select a “male” or “female” embryo for transfer to the uterus.
There are several methods of PGD, the most common of which is known as Fluorescence In Situ Hybridization (FISH). This method screens 8-12 pairs of chromosomes. After the egg is fertilized and progresses to the embryo stage, one or more cells are removed from each embryo to be tested. The cells are then analyzed via the FISH process and any extra or missing chromosomes are revealed (an extra or missing chromosome is referred to as Aneuploidy).
The shortcoming of FISH as a method of PGD is in the fact that it only screens 8-12 pairs of an embryo’s 23 pairs of chromosomes, so it is far from 100% accurate. Until recently, FISH was virtually the only way to screen embryos for Aneuploidy prior to IVF embryo transfer. A new method refined by Sher Institutes known as Comparative Genomic Hybridization (CGH) evaluates all 23 pairs of chromosomes for a far more comprehensive analysis. CGH is available at only a handful of clinics throughout the country, primarily SIRM offices. Extensive information on this remarkable breakthrough is available by clicking here.
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