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Five mutations to watch for: VTE risk and thrombogenic mutations in pregnancy.(Obstetrics)

OB GYN News

| September 01, 2004 | Brunk, Doug | COPYRIGHT 2004 International Medical News Group. This material is published under license from the publisher through the Gale Group, Farmington Hills, Michigan.  All inquiries regarding rights should be directed to the Gale Group. (Hide copyright information)Copyright

LAS VEGAS -- There are six key thrombogenic mutations to be concerned about in pregnant patients, Dr. Charles Lock-wood said at the Fifth World Congress on Controversies in Obstetrics, Gynecology, and Infertility.

These include:

* Factor V Leiden mutation. About 80% of women with activated C-reactive protein resistance have this mutation. Both men and women with factor V Leiden mutation face a 30% lifetime risk of venous thromboembolism (VTE), and the prevalence in Europeans ranges from 5% to 15%. The prevalence of the mutation in the United States is about 5%, said Dr. Lockwood, who chairs the department of obstetrics, gynecology, and reproductive sciences at Yale University, New Haven.

About 40% of VTE events in pregnancy are caused by factor V Leiden mutation. Women with the mutation face a 10-fold increased risk of VTE during pregnancy.

However, this risk remains low in asymptomatic heterozygotes, at 0.2%, whereas the risk is far higher in homozygotes, at 16%-17%.

* Prothrombin gene mutation. Patients with this mutation also face a 30% lifetime risk of VTE; the prevalence is 2%-3%.

About 17% of VTE events in pregnancy are caused by the prothrombin gene mutation, and those who have it face a 15-fold increased risk of VTE during pregnancy. The risk of VTE in heterozygotes is just 0.5%, but the risk in homozygotes is 15%.

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