ADAMTS13, Thrombotic Thrombocytopenic Purpura and Pregnancy

Thrombotic thrombocytopenic purpura (TTP) is a thrombotic microangiopathy (TMA) which pathophysiology mainly relies on a severe deficiency (either acquired or inherited) of ADAMTS13, the specific von Willebrand factor (VWF) protease. TTP is characterized by a feminine predominance and pregnancy is a precipitating factor for TTP boots. Obstetrical TTP represents at least 20% of all TTP occurring in child-bearing age women. In this review, an analyze of the English-language literature from 1955 to 2011 found about 350 cases of obstetrical TTP including about 40 case-reports/-series with well documented ADAMTS13 investigation (32 inherited and 17 acquired TTP with severe ADAMTS13 deficiency). In the 32 patients with inherited TTP, the first pregnancy was systematically associated with a TTP boot, mostly occurring during the third trimester; curative plasma therapy (PT) allowed a good maternal outcome although the fetal outcome was almost systematically bad. In the 17 patients with acquired TTP, TTP also occurred mostly de novo during the first pregnancy and after 20 weeks gestation; curative PT usually allowed a good maternal outcome and the birth of an alive baby in about 2 cases/3. The diagnosis of obstetrical TTP is challenging because it mostly occurs in women with no antecedent of TTP and it has no specific clinical/biological symptoms except a severely deficient ADAMTS13. However, because of the severity of the prognosis in the absence of urgent treatment, any thrombocytopenia +/hemolytic anemia in a pregnant woman with no alternative diagnosis to TMA should be considered as TTP. The management of an obstetrical TTP boot consists in a blood collection for ADAMTS13 investigation followed by an emergency first-line treatment with PT yielding a maternal response rate of about 80% although the global stillbirth rate is likely to be close to 50%. The follow-up of women who recovered from an obstetrical TTP boot should include a complete ADAMTS13 investigation to distinguish between the inherited and the acquired form of TTP, in order to both estimate the risk for relapse and optimize prophylaxis indication during subsequent pregnancies. The relapse rate appears to be 100% in inherited TTP and about 20% in acquired TTP. Early prophylactic PT is thus indicated systematically in inherited TTP as it is clearly beneficial for both the mother and the fetus outcomes. In contrast, the optimal management is still debated in subsequent pregnancies of women with acquired TTP whose clinical and biological monitoring should be very careful. TTP is a very rare complication of pregnancy (about 1/100,000 pregnancies) but it is a life-threatening disease for both the mother and the fetus. Many advances have been performed in the last 10 years in terms of diagnosis and treatment. However, clear guidelines are still needed to optimize the management of subsequent pregnancies, which may be significantly different as a function of the pathophysiology for ADAMTS13 deficiency. *Corresponding author: Pr Agnès Veyradier, MD, PhD, Service d’Hématologie biologique Hôpital Antoine Béclère, 157 rue de la Porte-de-Trivaux, 92140 Clamart France, Tel : +33 1 45 37 43 05 ; Fax : +33 1 45 37 40 95; E-mail : [email protected] Received December 23, 2011; Accepted February 14, 2012; Published February 19, 2012 Citation: Veyradier A, Stepanian A, Coppo P (2012) ADAMTS13, Thrombotic Thrombocytopenic Purpura and Pregnancy. Hereditary Genetics S1:002. doi:10.4172/2161-1041.S1-002 Copyright: © 2012 Veyradier A, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Introduction Thrombotic Thrombocytopenic purpura (TTP) is a thrombotic microangiopathy (TMA) defined by a microangiopathic hemolytic anemia and thrombocytopenia without an alternative cause [1,2]. Clinical manifestations of multivisceral ischemia (neurologic symptoms, renal and cardiac involvement...) are later events. In about half cases, TTP occurs in patients with previously or concomitantly diagnosed other clinical conditions (pregnancy, infections, autoimmune diseases, drugs, hematopoietic stem cell transplantation, cancer, malignant hypertension...) although in the other half of cases, TTP is apparently idiopathic [1,2]. TTP, especially idiopathic forms, is strongly associated with a severe functional deficiency (activity <10%) of ADAMTS13 (A Disintegrin And Metalloprotease with ThromboSpondin type 1 repeats, member 13), the specific metalloprotease that cleaves ultralarge (UL) multimers of von Willebrand factor (VWF), the most hemostatically active species of VWF [3]. Thus, the pathophysiology for about 75% of TTP is explained by the accumulation of platelet-hyperadhesive ULVWF multimers leading to the spontaneous formation of microthrombi within the microcirculation [4,5]. ADAMTS13 severe deficiency may be due either to auto-antibodies to ADAMTS13 (acquired autoimmune TTP) or to recessively inherited bi-allelic mutations of ADAMTS13 gene (hereditary TTP also named Upshaw-Schulman syndrome (USS) [6]. TTP is a rare disease as its prevalence is 4-10 cases/million people/year. In a large majority of cases, TTP is an adult-onset disease characterized by both a feminine predominance (2-3F/1M), a peak between 30 and Citation: Veyradier A, Stepanian A, Coppo P (2012) ADAMTS13, Thrombotic Thrombocytopenic Purpura and Pregnancy. Hereditary Genetics S1:002. doi:10.4172/2161-1041.S1-002