Abstract

BackgroundPregnant women with a history of acquired thrombotic thrombocytopenic purpura (TTP) are considered at risk for disease recurrence and might be at risk for miscarriage, similar to other autoimmune disorders. However, the exact entity of these risks and their causes are unknown. The aim of this study was to evaluate risk factors associated with adverse pregnancy outcome, in terms of both gravidic TTP and miscarriage, in women affected by previous acquired TTP.MethodsWe conducted a nested case–control study in women with a history of acquired TTP enrolled in the Milan TTP registry from 1994 to October 2012, with strict inclusion criteria to reduce referral and selection bias.ResultsFifteen out of 254 women with acquired TTP were included, namely four cases with gravidic TTP, five with miscarriage, and six controls with uncomplicated pregnancy. In the cases, ADAMTS13 activity levels in the first trimester were moderately-to-severely reduced (median levels <3% in gravidic TTP and median levels 20% [range 14-40%] in the women with miscarriage) and anti-ADAMTS13 antibodies were invariably present, while in the control group ADAMTS13 activity levels were normal (median 90%, range 40-129%), with absence of detectable anti-ADAMTS13 antibodies. Reduced levels of ADAMTS13 activity (<25%) in the first trimester were associated with an over 2.9-fold increased risk for gravidic TTP and with an over 1.2-fold increased risk for miscarriage (lower boundary of the confidence interval of the odds ratio). In addition, the presence of anti-ADAMTS13 antibodies during pregnancy was associated with an over 6.6-fold increased risk for gravidic TTP and with an over 4.1-fold increased risk for miscarriage.ConclusionsADAMTS13 activity evaluation and detection of anti-ADAMTS13 antibody could help to predict the risk of complications in pregnant women with a history of acquired TTP.

Highlights

  • Pregnant women with a history of acquired thrombotic thrombocytopenic purpura (TTP) are considered at risk for disease recurrence and might be at risk for miscarriage, similar to other autoimmune disorders

  • Thrombotic Thrombocytopenic Purpura (TTP) is an acute, life-threatening thrombotic microangiopathy caused by deficient activity of the von Willebrand factor (VWF) cleaving protease ADAMTS13

  • The highest odds ratios were associated with reduced ADAMTS13 activity levels in the first trimester, with lower boundary of the confidence interval of the odds ratio over 2.9 for gravidic TTP (OR ∞, 95% CI 2.9 to ∞) and over 1.2 for miscarriage (OR ∞, 95% CI 1.2 to ∞), and with the presence of anti-ADAMTS13 antibodies during pregnancy, with lower boundary of the confidence interval of the odds ratio over 6.6 for gravidic TTP (OR ∞, 95% CI 6.6 to ∞) and over 4.1 for miscarriage (OR ∞, 95% CI 4.1 to ∞)

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Summary

Introduction

Pregnant women with a history of acquired thrombotic thrombocytopenic purpura (TTP) are considered at risk for disease recurrence and might be at risk for miscarriage, similar to other autoimmune disorders. The aim of this study was to evaluate risk factors associated with adverse pregnancy outcome, in terms of both gravidic TTP and miscarriage, in women affected by previous acquired TTP. Thrombotic Thrombocytopenic Purpura (TTP) is an acute, life-threatening thrombotic microangiopathy caused by deficient activity of the von Willebrand factor (VWF) cleaving protease ADAMTS13 (a disintegrin and metalloprotease with thrombospondin type 1 motif, 13th member). Almost half of TTP cases occur in women in childbearing age and 12-25% of acute episodes are reported in association with pregnancy or puerperium [3,4,5,6,7]. VWF levels increase during the last trimester of normal pregnancy and ADAMTS13 levels progressively reduce, reaching values of as low as 25-30% in some women in the third trimester [8,9,10]

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