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The Infertility Center of St. Louis

Pre-Implantation Genetic Diagnosis General Information on PGD

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If you have any questions, you may call us at  (314) 576-1400.

Pre-implantation genetic diagnosis discussed on St. Louis network television. December, 2002

Pre-implantation genetic diagnosis discussed on St. Louis network television. December, 2002.

  PGD1

Pre-implantation genetic diagnosis discussed on St. Louis network television. July, 2002.

 
Embryo biopsy for genetic diagnosis. [technical video]

Embryo biopsy for genetic diagnosis. [technical video]

  Marfan’s Syndrome Report on St. Louis network Television. March 23, 2003

Marfan's Syndrome Report on St. Louis network Television. March 23, 2003.

WHAT IS PRE-IMPLANTATION GENETIC DIAGNOSIS (PGD)?

Most of the twenty-five thousand or so genes in the human genome have now been identified and their DNA sequenced. Molecular analysis of genes is becoming simpler and more efficient. As a consequence, PGD with IVF, can now prevent couples from having to face the difficulty of giving birth to children with almost any of the genetic defects such as Down syndrome, cystic fibrosis, muscular dystrophy, sickle cell anemia, Tay-Sachs, Gaucher’s disease, mental retardation, etc., that are a concern to every woman who ever gets pregnant. With PGD, we can also better understand the problem of recurrent, early miscarriage and the genetic errors that arise in pregnancies of older mothers.

PGD should not be construed as creating “designer babies,” an incorrect term used only by the press and not by physicians. We could not manipulate (even if we wanted to) the features or characteristics of an offspring. That is just pure fiction. All we can do is eliminate heartbreaking and devastating genetic disease.

Figure 1: 8 Cell Embryo Ready for Biopsy (i.e. Remove One Cell)
Figure 1: 8 Cell Embryo Ready for Biopsy (i.e. Remove One Cell)

WHAT IS EMBRYO BIOPSY?

When an embryo reaches the third day of development, it normally has eight cells. One or two of these cells, called “blastomeres,” can be removed from the embryo with micromanipulation technique. The embryo is usually unharmed, and can go on to develop just as though this one cell were never removed. You can then subject those one or two cells to genetic analysis, and know the chromosomal composition of the embryos, and if they carry a specific disease-producing mutation.

Figure 2: Removing One Cell for DNA Analysis
Figure 2: Removing One Cell for DNA Analysis

BASIC GENETIC LESSONS

DNA Testing and Single Gene Disease

Everything we are physically is determined by approximately 25,000 genes located in our DNA. Your entire body is made up of many thousands of different proteins whose structure and orientation determine the incredible machinery of your body and brain. However, these many thousands of different proteins are in turn composed of just twenty amino acids. The variety of amino acids that theoretically could be expected to exist is unlimited. Chemists can synthesize many thousands of them. However, living nature is composed of only twenty specific amino acids, which are absolutely the same for all living things on earth. The differences between living creatures lie in the differences in the sequences of these twenty amino acids, which make up all the different proteins of which they are composed. In turn, this sequence of amino acids has been determined by the sequence of the 4 basic letters that comprise our DNA. The entire human genome represents 3 billion base pairs, or letters, of DNA. A specific set of combinations of three DNA letters are codes for each one of the twenty amino acids. Therefore, the order in which the DNA letters occurs on the chromosome determines the sequence of amino acids, and this, in turn, determines the proteins, which determine everything in our body. A single error in an amino acid sequence in any protein can cause a dramatic change in its structure, and a severe genetic disease like cystic fibrosis or Tay Sachs. These errors in DNA sequence can be diagnosed by a process (carried out in a test tube) called PCR, and that is the basis of PGD for single gene genetic disease.

Chromosome Testing and Aneuploidy Screening

All of our 6 billion DNA “letters” are located on forty-six chromosomes, which are coiled up inside the nucleus of every single cell in your body and are divided into twenty-three pairs, twenty-two “autosomal” pairs and one “sex” chromosome pair, the “X” and the “Y”. The child who has two X chromosomes will be a girl, and one with one Y chromosome and one X chromosome will be a boy.

For conception to occur, twenty-three chromosomes from the husband’s set of forty-six, and twenty-three chromosomes from the wife’s set of forty-six, must meet at the moment of fertilization and become an embryo with a new normal set of forty-six chromosomes. The process whereby primitive sperm cells and primitive eggs lose half of their chromosome number as they become sperm and mature eggs ready for fertilization is called “meiosis.” The aging process of eggs makes it harder for them to undergo the meiosis process than sperm. That is why the eggs from older women are less likely to result in a viable embryo, and that is also why older women are more infertile than younger women, and why older women have higher rates of miscarriage and of babies with abnormalities such as Down’s syndrome.

If there is an error in division of the egg’s chromosomes and one of the pairs of chromosomes fails to separate, then the egg will have twenty-four chromosomes instead of twenty-three. In Down’s syndrome, for example, the embryo has a total of forty-seven chromosomes instead of forty-six because it has three sets of chromosome 21 instead of the normal two sets. This kind of a chromosome error, in which one of the chromosomes has three copies instead of the proper two copies, is called “trisomy.” All of these chromosomal errors, including trisomies, monosomies, and various combinations can occur in virtually any of the chromosomes, and these errors, as a group, are called “aneuploidy.” These numerical chromosomal erros in a cell can be diagnosed by counting color signals on a slide by a process called FISH.

Most of these chromosomal defects that occur in human embryos are lethal and result in either failure of the embryo to implant, or result in a miscarriage. Only occasional chromosomal defects such as trisomy 21, or Down syndrome result in the actual birth of an abnormal baby, and even in that event (trisomy 21), only 20% of the time. Nothing about in vitro fertilization (IVF) or ICSI, increases the risk of these chromosomal abnormalities.

Criticisms and Limitations of PGD

Single gene defects are the rare genetic diseases like cystic fibrosis or Tay Sachs (there are thousands of them), which occur in the offspring of otherwise fertile couples who are carriers, and which are diagnosed by PCR. PGD for such couples is extremely accurate today because for verification, multiple DNA sequences near the defective gene (linked markers) can be tested for, as well as the mutation itself. PGD is also very accurate for recurrent miscarriage caused by chromosomal translocations for which about 1.5% of infertile couples are carriers.

However, PGD (referred to as PGS in Europe) for routine aneuploidy screening during IVF for infertile couples has recently come under severe criticism in Europe owing to several prospective, randomized control studies in Holland and Belgium. PGS has failed to show any improvement in IVF clinical outcome per initiated cycle for advanced maternal age, nor for recurrent implantation failure.

In European studies of even younger, infertile couples, only 36% of embryos subject to PGD were found to be chromosomally normal (where two embryos are removed and tested rather than one). When embryos diagnosed as chromosomally abnormal on Day 3 (and, therefore, not transferred to the patient) were re-examined on Day 5, only 54% turned out to have that abnormality. The error rate for the FISH technique has been clearly shown to be as low as 5%. Therefore, this 50% discordance appears to be mostly due to the wide prevalence of embryo mosaicism. This means that some of the cells in many embryos are normal and some are abnormal. About 50% of embryos in the European studies have thus been found to be mosaic. Therefore, the use of PGS may result in good embryos being discarded (diagnosed as abnormal) and abnormal embryos (diagnosed as normal) being transferred.

However, there is still some benefit to PGS in certain cases. Firstly, if two cells are tested instead of one, and both reveal chromosomal errors, the diagnosis of abnormal embryo is very likely to be correct. Likewise, the diagnosis of normal embryo using two cells also is likely to be correct. (However, the problem is that removing two cells is more likely to hurt the embryo than removing one cell.)

Secondly, for recurrent miscarriage in younger women, even with removing and testing only one cell, PGS is likely to reduce the miscarriage rate. (However, unfortunately, with PGS there are certain to be some normal embryos that are discarded as abnormal.) PGS can also vastly reduce the risk of a Downs Syndrome conception.

Thirdly, it may be useful in counseling for cases who consistently produce all chromosomally abnormal embryos in order to understand their problem better.

Our experience with PGS and PGD is extensive, and we can counsel you on whether it is a good idea or not for your particular IVF cycle. In general it is best reserved for carriers of single gene disease who do not want an offspring to have such disease, and for recurrent miscarriage.

Related Information:

"Genetic screening for disorder offers hope: Woman with Marfan’s didn’t want to pass it on"

Possibility of selectively transferring embryos, by preimplantation genetic diagnosis (PGD/PGS) determined to be chromosomally abnormal

If you have any questions, you may call us at  (314) 576-1400.