ABSTRACT
Thrombophilia by definition represents acquired and/or genetic conditions that predispose
patients to both venous and arterial thromboembolic events. Thrombosis is the most
common cause of death worldwide. On the arterial side, myocardial infarction and stroke
result in significant morbidity and mortality. Venous thromboembolic events most commonly
involve the deep veins of the lower extremity with potential complications of pulmonary
emboli. Pregnancy is a hypercoagulable state, and thromboembolism is the leading cause
of antepartum and postpartum maternal mortality. With the description by Dahlback
in 1993 of a condition initially labeled activated protein C resistance, significant
advances have rapidly followed. Activated protein C resistance was linked to an underlying
point mutation resulting in coagulation factor V (factor V Leiden). Recent attention
has focused on certain inherited thrombophilic factors that may predispose to arterial
and/or venous thromboses and their possible association with pregnancy complications,
including early pregnancy loss. These include a group of mostly autosomal dominant,
inherited gene mutations leading to a hypercoagulable state, such as factor V Leiden
G1691A, factor II or prothrombin G20210A, and hyperhomocysteinemia associated with
methylenetetrahydrofolate reductase C677T mutation. In addition, deficiencies in protein
S, protein C, and antithrombin can lead to a hypercoagulable state. Although some
studies of recurrent pregnancy loss patients with a positive test for an inherited
thrombophilia are conflicting, a case-control study of untreated recurrent miscarriage
patients who were heterozygous for the factor V Leiden mutation revealed a lower success
rate than the controls who had a history of idiopathic recurrent miscarriage. With
the identification of genetic risk factors, there has been synergistic amplification
of thrombotic risk when one has an abnormal gene (e.g., factor V Leiden) plus environmental
issues (e.g., pregnancy). Current understanding indicates that a combination of risk
factors, including multiple inherited thrombophilic defects associated with secondary
hypercoagulable states, have a particularly strong association with adverse pregnancy
outcome.
KEYWORDS
Recurrent pregnancy loss - thrombophilias - coagulation abnormalities - miscarriage
- antiphospholipid antibodies
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William H KuttehM.D. Ph.D. H.C.L.D.
Professor of Obstetrics and Gynecology, Director of Reproductive Endocrinology and
Infertility, Director of Reproductive Immunology, University of Tennessee, Memphis
80 Humphreys Center, Suite 307, Memphis, TN 38120-2363
eMail: wkutteh@utmem.edu