I had a healthy 8 year old, but then had a miscarriage. I am now 37 and preparing for my first embryo transfer.
Should I screen embryos to have a healthy baby? In which cases can embryo screening be done? (P Huong Linh, Hanoi )
Reply:
Preimplantation genetic testing or Preimplantation Genetic Testing (PGT) is a genetic analysis technique before embryo transfer. Through testing, doctors can help couples choose good genetic quality embryos before the embryo is transferred into the mother's uterus. This test helps avoid the risk of transferring abnormal embryos, improving the chance of having a healthy baby.
In your case, there are a number of factors that may consider preimplantation screening. If embryo screening is needed, couples need to discuss with a specialist for a comprehensive assessment of the indications for the procedure, and full advice on the benefits and risks of this method. It should not be done en masse.
There are three types of preimplantation genetic screening: PGT-M, PGT-SR, and PGT-A.
PGT-M is a diagnostic test for single-gene diseases. The doctor will determine if the embryo has a genetic disease inherited from parents carrying a mutated gene, such as Huntington's disease, cystic fibrosis, thalassemia, Duchenne muscular dystrophy, congenital adrenal hyperplasia, etc.
PGT-SR screening test helps couples have normal pregnancies without abnormalities due to chromosomal structural abnormalities.
PGT-A is a preimplantation genetic test that helps avoid the risk of transferring abnormal embryos with aneuploidy and chromosomal abnormalities, improving the ability to give birth to a healthy baby.
Doctor Le Thuy examines and consults a client. Photo: IVFTA
Preimplantation genetic screening PGT-M or PGT-SR is indicated for couples with genetic abnormalities (carrying disease genes or having structural chromosome abnormalities). PGT-A is often indicated for couples with the mother's age of 35 years or older; a history of multiple miscarriages/stillbirths (especially cases of consecutive miscarriages of 2 or more); a history of multiple implantation failures; severe male infertility; a history of pregnancy or birth defects and wanting to have a healthy next child.
Currently, the new gene sequencing technology NGS has been deployed at Tam Anh General Hospital in Hanoi. This method can detect abnormalities down to the smallest chromosome segment. Accordingly, doctors will select embryos with good genetic quality, increase the live birth rate, reduce the risk of miscarriage, and minimize the rate of children born with genetic defects.
It should be noted that PGT testing can only screen for genetic abnormalities within the specific testing range, but cannot completely rule out genetic abnormalities that may occur in the embryo. Therefore, with IVF pregnancies that have undergone embryo screening, the pregnant woman must still undergo routine prenatal testing.
Doctor Nguyen Le Thuy
Reproductive Support Center, Tam Anh General Hospital Hanoi
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