Infertility and Inherited Thrombophilia
نویسندگان
چکیده
Infertility is a condition that affects between one-fifth and one-sixth of couples of reproductive age. It is defined as a reduction in or a lack of ability to reproduce and its cause may lie either in the male or female partner (Stedman, 2006). According to the American Society for Reproductive Medicine, infertility should be considered when pregnancy fails to occur after one year of regular sexual activity without the use of any contraceptive method. In view of its high incidence, infertility currently constitutes a significant health issue. The social structure prevalent today in which women are conditioned to consider motherhood at a later age results in an increase in the number of couples seeking medical assistance to fulfill their dream of having children (Neuspiller, 2003). Nevertheless, the forms of treatment available today within the realm of assisted reproduction result in a pregnancy rate of approximately 40%, an unsatisfactory percentage, since it means that the majority of couples are still denied the opportunity to conceive (Qublan, 2006; Vaquero et al., 2006). In 30% of the couples currently undergoing treatment for infertility, the factors preventing them from becoming pregnant have yet to be identified (Grandone, 2005). The majority of the studies conducted to evaluate failure to conceive in assisted reproduction have focused on the problems that occur following laboratory fertilization, i.e. implantation of the embryo in the woman’s uterus (Vaquero et al., 2006). Various studies have concentrated on improving factors associated with the embryo, such as the quality and quantity of embryos, and on female factors. Some that need to be taken into consideration include improving endometrial receptivity and identifying intervening factors associated with immunological response and the genetic characteristics of the woman, including her potential for coagulation during pregnancy and implantation of the embryo (Glueck, 2000). Because of the success rate of 34%, the assisted reproduction clinics try to improve the pregnancy rate by transferring more than one embryo. This procedure has as a consequence, another problem of great significance and social impact, which is the multiple pregnancy (Haggarty, 2006). Recently, a hypothesis has been raised that the same factors associated with the occurrence of recurrent pregnancy loss may also affect the early phase of the embryo implantation process (Vaquero et al., 2006). The possible causes for a failure in embryo implantation have been widely investigated; however, there is no consensus in the literature on this subject.
منابع مشابه
Inherited Genetic Markers for Thrombophilia in Northeastern Iran (a Clinical-Based Report)
Background: Thrombophilia is a main predisposition to thrombosis due to a procoagulant state. Several point mutations play key roles in blood-clotting disorders, which are grouped under the term thrombophilia. These thrombophilic mutations are methylenetetrahydrofolate reductase (MTHFR, C677T, and A1298C), factor V Leiden (G1691A), prothrombin gene mutation (factor II, G20210A), and plasminogen...
متن کاملP-102: Recurrent In Vitro Fertilization Failure and Hereditary Thrombophilia
a:4:{s:10:"Background";s:363:"The largest percentage of failed in vitro fertilization (IVF) cycles are due to lack of implantation. As hereditary thrombophilia can cause in placentation failure, it may have a role in recurrent IVF failure. The aim of this case-control study was to determine whether or not hereditary thrombophilia is more prevalent in women with recurrent IVF failures.";s:19:"Ma...
متن کاملIncreased rates of thrombophilia in women with repeated IVF failures.
BACKGROUND We investigated whether hereditary thrombophilia is more prevalent in women with recurrent IVF-embryo transfer failures. METHODS This case-control study was conducted in an academic tertiary care hospital and compared 45 women with a history of four or more failed IVF cycles (group A) with 44 apparently healthy women matched for age and ethnic origin (group B). All participants wer...
متن کاملInherited genetic markers for thrombophilia in northeastern Iran (a clinical-based report).
BACKGROUND Thrombophilia is a main predisposition to thrombosis due to a procoagulant state. Several point mutations play key roles in blood-clotting disorders, which are grouped under the term thrombophilia. These thrombophilic mutations are methylenetetrahydrofolate reductase (MTHFR, C677T, and A1298C), factor V Leiden (G1691A), prothrombin gene mutation (factor II, G20210A), and plasminogen ...
متن کاملThe effect of trombophilia on pregnancy outcome and IVF success.
Thrombophilia is a group of inherited and acquired coagulation disorders often associated with an increased risk of thrombosis. Over the last decade, inherited thrombophilia is often referred as a possible cause of recurrent miscarriages and in vitro fertilisation (IVF) failure. However, many studies in this area still give conflicting results, so the goal of our study was to determine the effe...
متن کاملPrevalence of inherited thrombophilia in patients with severe ovarian hyperstimulation syndrome.
BACKGROUND AND OBJECTIVE To determine the prevalence of markers of inherited thrombophilia in patients with severe form of ovarian hyperstimulation syndrome (OHSS) DESIGN AND METHODS: Blood samples were analysed for markers of thrombophilia (mutation of factor V - Leiden, mutation of methylentetrahydrofolat reductase (MTHFR) C677T and mutation of prothrombin G20210A). The study group consisted ...
متن کامل