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      Antiphospholipid Antibodies in Stillbirth

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          Abstract

          Objective

          To compare antiphospholipid antibodies in deliveries with and without stillbirth using a multicenter, population-based case-control study of stillbirths and live births.

          Methods

          Maternal sera were assayed for IgG and IgM anticardiolipin and anti-β 2-glycoprotein-I antibodies. Assays were performed in 582 stillbirth deliveries and 1,547 live birth deliveries.

          Results

          Elevated levels of IgG anticardiolipin and IgG anti-β 2-glycoprotein-I antibodies were associated with an approximate threefold increased odds of stillbirth; crude odds ratio (OR) 3.43 (95% confidence interval [CI] 1.79, 6.60) (3.8% versus 1.1%) and OR 3.17 (95% CI 1.30, 7.72) (1.9% versus 0.6%), respectively when all deliveries with stillbirth were compared with all deliveries with live birth. When the subset of stillbirths not associated with fetal anomalies or obstetric complications were compared with term live births, elevated IgG anticardiolipin antibodies were associated with stillbirth (5.0% versus 1.0%) (OR 5.30, 95% CI 2.39–11.76); IgG anti-β 2-glycoprotein-I antibodies (1.9% versus 0.6%) had an OR of 3.00 (95% CI 1.01–8.90) and IgM anticardiolipin antibodies (6.0% versus 3.0%) had an OR of 2.03 (95% CI 1.09–3.76). Elevated levels of anticardiolipin and anti-β 2-glycoprotein-I antibodies were associated with a threefold to fivefold increased odds of stillbirth.

          Conclusions

          Our data support consideration of testing for antiphospholipid antibodies in cases of otherwise unexplained stillbirth.

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          Author and article information

          Journal
          0401101
          6204
          Obstet Gynecol
          Obstet Gynecol
          Obstetrics and gynecology
          0029-7844
          1873-233X
          1 November 2017
          September 2013
          14 November 2017
          : 122
          : 3
          : 641-657
          Affiliations
          [1 ]University of Utah School of Medicine, Salt Lake City, Utah
          [2 ]RTI International, Research Triangle Park, North Carolina
          [3 ]Pregnancy and Perinatology Branch, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland
          [4 ]Columbia University, New York, New York
          [5 ]Brown University School of Medicine, Providence, Rhode Island
          [6 ]University of Texas Health Science Center at San Antonio
          [7 ]University of Texas Medical Branch at Galveston
          [8 ]Emory University School of Medicine, Atlanta, Georgia
          [9 ]Rollins School of Public Health, Emory University, Atlanta, Georgia
          Author notes
          Correspondence: Robert M. Silver, MD, Department of Obstetrics and Gynecology, University of Utah School of Medicine, 30 North 1900 East, Room 2B308, Salt Lake City, Utah 84132; bsilver@ 123456hsc.utah.edu ; phone: (801) 585-3857, fax: (801) 585-2594
          Article
          PMC5684877 PMC5684877 5684877 nihpa508217
          10.1097/AOG.0b013e3182a1060e
          5684877
          23921873
          4c3cb220-4141-400c-b77b-999f83a17b5b
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