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Recurrent IVF failure and hereditary thrombophilia
Leila Safdarian1, Zahra Najmi2, Ashraf Aleyasin1
1Department of Infertility, Shariati Hospital, Tehran University of Medical Sciences, Tehran, Iran.
Hereditary thrombophilia is more common in women experiencing recurrent in-vitro fertilization (IVF) failures. Specific thrombophilias, including Factor V Leiden and MTHFR mutations, increase the risk of IVF failure.
Area of Science:
- Reproductive Medicine
- Genetics
- Hematology
Background:
- Recurrent implantation failure is a major cause of in-vitro fertilization (IVF) cycle failure.
- Hereditary thrombophilia is a known risk factor for placental dysfunction and may contribute to recurrent IVF failures.
Purpose of the Study:
- To investigate the prevalence of hereditary thrombophilia in women with recurrent IVF failures.
- To determine if specific inherited thrombophilias are associated with recurrent IVF failure.
Main Methods:
- A case-control study was conducted with 96 women experiencing recurrent IVF failure (cases) and 95 fertile women (controls).
- Participants were tested for inherited thrombophilias: Factor V Leiden, methylenetetrahydrofolate reductase (MTHFR) mutation, prothrombin mutation, homocysteine levels, Protein S and C deficiency, antithrombin III (AT-III) deficiency, and plasminogen activator inhibitor-1 (PAI-1) mutation.
Main Results:
- Women with recurrent IVF failure had a significantly higher prevalence of at least one thrombophilia (OR=3.15, p=0.00).
- Factor V Leiden mutation (OR=3.06, p=0.01) and homozygous MTHFR mutation (OR=12.33, p=0.05) were identified as significant risk factors for recurrent IVF failure.
- No significant differences were found for other tested inherited thrombophilias.
Conclusions:
- Inherited thrombophilia is more prevalent in women with recurrent IVF failure compared to fertile controls.
- The presence of any thrombophilia, Factor V Leiden mutation, and homozygous MTHFR mutation are confirmed risk factors for recurrent IVF failure.
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