Preimplantation genetic testing (PGT) involves screening cells from embryos for genetic diseases and chromosomal disorders. This testing is performed with in-vitro fertilization (IVF) and occurs prior to embryo transfer, before a pregnancy is established. PGT-A for aneuploidy offers at-risk couples the opportunity to select embryos for transfer with a normal number of chromosomes. The goal of PGT-A is to identify chromosomal abnormal embryos so they will not be transferred, leaving unaffected embryos with a normal number of chromosomes to be selected for transfer that are more likely to make healthy babies.

PGT-SR refers to preimplantation genetic testing for chromosomal structural rearrangements such as chromosomal translocations (rearrangements of parts of chromosomes) and PGT-M refers to preimplantation genetic testing for monongenic/single-gene disorders (genetic diseases that are the result of a single mutated gene). There are over 4,000 single-gene disorders. The most common diseases tested for are Cystic Fibrosis, Spinal Muscular Atrophy, Tay Sachs, Fragile X, Myotonic Dystrophy and Thalassemia.

PGT-A technology can also be used to determine the sex of the embryo prior to the transfer into the uterus. Sex selection is offered to couples interested in family balancing who already have at least one child.

For those people with recurrent pregnancy loss or those interested in defining chromosomal normalcy prior to implantation, PGT-A applies the technology from PGT to improve their chances for a successful pregnancy. Embryos are screened for aneuploidy (missing or additional numbers of chromosomes), which is a leading cause of miscarriage and implantation failure (failure of the embryo to implant into the uterus). The goal of PGT is to identify chromosomally normal embryos, so they can be transferred increasing the chance of pregnancy significantly.

Who should have PGT?

PGT is an extremely useful tool for couples in which one or both of the partners are carriers of an inherited genetic disorder. Depending on the inheritance pattern of the disease, the risk of creating an affected child can be as high as 50%. PGT-M significantly reduces this risk.

PGT-A can be applied to any blastocyst embryo produced during an IVF cycle. We anticipate 30% chance of all embryos in women less than 35 years will be chromosomally abnormal. PGT-A can define embryos with a normal number of chromosomes, and thus, the patient does not need to undergo multiple embryo transfer cycles.

The accuracy, sensitivity and specificity for these techniques are nearly 98%. Currently, because there exists the possibility of error, PGT is not considered a replacement for prenatal testing.

What are the risks of PGT?

The largest risk of PGT is not having embryos available for transfer and/or a negative pregnancy test. The results of the PGT procedure may show that all of the embryos are abnormal. In these circumstances, no embryos are transferred and the cycle is cancelled.

There is a small (0.1%) risk that the embryo may be damaged during the biopsy procedure. The risk of not obtaining a diagnosis on a biopsy also exists, although, at the Fertility Centers of New England this risk is less than 1%. Misdiagnosis is also a possible risk of PGT. It is possible when performing PGT-A that one cell in the embryo may have different chromosome numbers than the other cells in the biopsy. This is referred to as mosaicism and will result in a misdiagnosis due to the fact that the information from the biopsied cell is not reflective of the entire embryo. Because PGT is the diagnosis or screening of an embryo based on the results from a single cell, there are limitations involved in using this technology, and PGT is not considered a replacement for prenatal testing.

The PGT Process

Initial Evaluationexpand

If PGT-M or PGT-SR is recommended and you decide to proceed with PGT, you will work closely with our Fertility Centers of New England PGT coordinator. You will need to have the same lab work and tests performed as required for an IVF cycle. You and your partner may also need to have your blood drawn in order to make DNA probes from which to test the cells. A genetic counselor from one of our referring centers will meet with you to answer all your questions and discuss your specific case, the PGT procedure, and your options. A representative from our insurance department will also work with you in order to determine if PGT is a covered benefit under your insurance policy.

IVFexpand

PGT is performed in conjunction with IVF. Patients will undergo ovarian hyperstimulation, oocyte retrieval and IVF in order to produce the maximum number of embryos that can be evaluated. Intra-cytoplasmic sperm injection (ICSI) is required.

Embryo biopsy and cell preparationexpand

Representative cells removed from embryos at the blastocyst stage of development on day 5 (or day 6) of culture. Embryos that have not developed to the blastocyst stage of development can not be used for PGT. The biopsied cells are then transferred to a small tube for PGT analysis. Once the biopsy is performed, the embryos are vitrified (frozen) and stored in our facility for later transfer once the results of the biopsy are known.

PGT analysisexpand

The biopsied cells are sent to one of our referring cytogenetic laboratories to be analyzed. Polymerase Chain Reaction (PCR) is used to identify single gene disorders. PCR is used to amplify the DNA from the single biopsied cell to identify the mutant gene sequence. PGT-A will be performed for some patients using new emerging techniques such as CGH and next generation sequencing to screen for all 22 pairs and the sex chromosomes. The results are reported back to us within a few days.

Embryo transferexpand

The physician and the embryologist review the PGT results with the patient. As these embryos are blastocysts (day 5 embryos), they will be transferred during a frozen embryo transfer cycle in a simulated cycle. The endometrium is prepared and monitored and most often progesterone is administered for final preparation for implantation. The selected, cryopreserved embryo is thawed and assisted hatching is performed. Assisted hatching allows the embryo to free itself from the protective zona shell, which is necessary for implantation. The embryo is then guided into the uterine cavity via ultrasound to maximize implantation efficacy.

What are the chances of a successful pregnancy following PGT?expand

Many factors go into making a successful pregnancy. Your chance of a successful pregnancy will depend upon your age, the number and quality of your embryos, the results of the biopsies, and other fertility-related factors based on your individual situation. While pregnancy success cannot be guaranteed, in general, a 60% to 70% success rate may be expected (depending on your individual circumstances) related to having PGT.