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WOMAM® MTR is a genetic test specifically designed to assess the risk of thrombophilia and reproductive complications in women with gestational desire in both, natural and assisted reproduction processes. In the DNA extracted from a woman´s blood sample, 9 polymorphic variants of 7 genes are evaluated. These variants are a risk factor for thrombophilia and have also been associated with pregnancy complications such as miscarriage, recurrent fetal loss, preeclamsia, intrauterine growth restriction or placental failure.

METHODOLOGY

WOMAM®MTR (MISCARRIAGE & THROMBOSIS RISK)

Blood simple extraction (4ml)

WOMAM®MTR (MISCARRIAGE & THROMBOSIS RISK)

Mantainance of blood samples at 4°C until shipping

WOMAM®MTR (MISCARRIAGE & THROMBOSIS RISK)

Shipping at room temperature

WOMAM®MTR (MISCARRIAGE & THROMBOSIS RISK)

WOMAM® MTR genotyping

WOMAM®MTR (MISCARRIAGE & THROMBOSIS RISK)

Results in 20 working days

WHAT IS THROMBOPHILIA?

Thrombophilia is a disease caused by the alteration of blood clotting mechanisms, which predisposes to developing thrombotic phenomena, such as the formation of clots that can obstruct the blood vessels. In many cases, women are unaware that they have thrombophilia until it manifests a related symptom, such as repeated miscarriages. Thrombophilia is one of the main causes of repeated pregnancy loss. 

In pregnancy, the risk of thrombosis increases due to natural physiological phenomena. However, pregnant women suffering from thrombophilia have an increased risk. These women are more likely to develop clots that obstruct blood vessels and make it difficult for oxygen and nutrients to reach the fetus, risking the continuation of the pregnancy.

WHAT IS HEREDITARY OR GENETIC THROMBOPHILIA?

Hereditary or genetic thrombophilia is a genetic predisposition to abnormal blood clotting. It is a type of thrombophilia whose cause lies in the presence of genetic variants in the genes of the clotting proteins that alter their function, increasing the risk of developing clots.

This type of thrombophilia has a prevalence of up to 10% of the population depending on the affected gene. This disease can be studied through the genetic analysis of the clotting factors that can be altered.

Thrombosis is a complex disease and, as such, it is the result of the interaction between environmental factors, genetic predisposition and risk factors of the patient. However, genetics contributes in approximately 60% to the development of thromboembolic events. Therefore, the genetic study is key for the diagnosis of thrombophilia.

WHAT IS WOMAM® MTR?

WOMAM®MTR is a genetic study that includes the analysis of 9 polymorphic variants of 7 genes (F2, F5, F12, F13A1, FGB, MTHFR, SERPINE1) that constitute a risk factor for thrombophilia and have been associated with pregnancy complications such as spontaneous abortion, recurrent fetal loss, preeclampsia, intrauterine growth restriction and/or placental insufficiency. 

In this test, the polymorphisms and genes of interest are genotyped through an analysis of SNPs by quantitative PCR. It is therefore possible to determine the presence of risk allelic variants for a particular patient and, consequently, to establish the risks of thrombophilia and associated pregnancy complications. 

HOW IS WOMAM® MTR PERFORMED?

A blood sample from the patient is required to perform the test. This sample is sent to our laboratory at room temperature where we will extract the DNA from the sample and analyse the genetic variants selected in the panel.

WHO CAN BENEFIT FROM WOMAM® MTR TESTING?

Most women are unaware that they suffer from thrombophilia. This test is indicated for: 

  • Women who have experienced pregnancy loss, fetal growth retardation or intrauterine fetal death.
  • Women who have experienced placental abruption, preeclampsia or implantation failure.
  • Women exposed to risk factors such as muscle and blood vessel injuries, obesity, tobacco use, chronic diseases or major surgeries.
  • Women who are experiencing difficulties to conceive. 

WHAT ARE THE ADVANTAGES OF WOMAM® MTR PANEL?

WOMAM®MTR is the first genetic panel for thrombophilia specifically designed for the analysis of the most informative gene variants responsible for hereditary thrombophilia and reproductive risk. Genetic variants classified as pathological and influencing human reproduction have been carefully selected, including variants associated with recurrent miscarriage preeclampsia, intrauterine fetal growth retardation, placental abruption, or intrauterine fetal death. The WOMAM®MTR panel can help in the diagnosis and orientation of the most indicated treatment in women who are experiencing difficulties in conceiving and want to avoid pregnancy risks and complications.

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