Preimplantation Genetic Testing at RMSCVA
Patients facing known genetic disease risks for having a healthy baby or patients wanting to screen for common chromosomal abnormalities now have treatment options through in vitro fertilization. Preimplantation genetic testing (PGT) is a laboratory procedure performed at RMSCVA that, when coupled with IVF, can provide information about the genetic health of an embryo prior to placement in the patient’s uterus in an attempt to establish pregnancy.
Preimplantation Genetic Testing for Aneuploidies (PGT-A)
Preimplantation genetic testing for aneuploidies (PGT-A, formerly referred to as preimplantation genetic screening or PGS) is performed to screen for embryonic abnormalities in chromosome number (aneuploidy) or structure (translocation) which commonly lead to implantation failure, pregnancy loss or birth defects. As women age, the incidence of these aneuploidies increases and is a primary reason for age-related decline in fertility. By using PGT-A, couples can identify those embryos with the correct number of chromosomes, greatly increasing their chance of a successful pregnancy.
Preimplantation Genetic Testing for Monogenic Diseases (PGT-M)
Preimplantation genetic testing for monogenic diseases (PGT-M, formerly referred to as preimplantation genetic diagnosis or PGD) is performed to diagnose single-gene (monogenic) defects in embryos from couples known to be carriers of a genetic disease. It can be used to test for autosomal recessive diseases (e.g. cystic fibrosis), autosomal dominant diseases (e.g. Huntington disease), X-linked diseases (e.g. Fragile X syndrome) and others such as Rh factor incompatibility. PGT-M requires the construction of DNA probes or materials specific to the genetic profiles of the parents and possibly grandparents which can take weeks to months prior to commencing treatment. Accordingly, fees for PGT-M are generally higher than for PGT-A. PGT-A is frequently combined with PGT-M to screen for aneuploidies in the same embryo.
Both PGT-A and PGT-M require the biopsy of a small number of cells from each embryo 5 to 6 days after fertilization at the blastocyst stage of development. At this stage cells can be taken from what will become the placenta, avoiding the portion of the embryo that will form the fetus. The cells are sent to a genetic testing lab while the embryo is cryopreserved and remains in storage at the RMSCVA Laboratory. Once the genetic results are obtained, appropriate embryos can be thawed and transferred into the uterus of the patient or a gestational carrier.