Performance and Diagnostic Value of Genome-Wide Noninvasive Prenatal Testing in Multiple Gestations

OBJECTIVE: To evaluate the accuracy and diagnostic value of genome-wide noninvasive prenatal testing (NIPT) for the detection of fetal aneuploidies in multiple gestations, with a focus on dichorionic-diamniotic twin pregnancies. METHODS: We performed a retrospective cohort study including data from...

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Veröffentlicht in:OBSTETRICS AND GYNECOLOGY 2021-06, Vol.137 (6), p.1102-1108
Hauptverfasser: van Riel, Margot, Brison, Nathalie, Baetens, Machteld, Blaumeiser, Bettina, Boemer, Francois, Bourlard, Laura, Bulk, Saskia, De Leener, Anne, Desir, Julie, Devriendt, Koenraad, Dheedene, Annelies, Duquenne, Armelle, Fieremans, Nathalie, Fieuw, Annelies, Gatot, Jean-Stephane, Grisart, Bernard, Janssens, Sandra, Khudashvili, Nairi, Lannoo, Lore, Marichal, Axel, Meunier, Colombine, Palmeira, Leonor, Parijs, Ilse, Pichon, Bruno, Roets, Ellen, Sammels, Eva, Smits, Guillaume, Suenaert, Marion, Sznajer, Yves, Van den Bogaert, Kris, Vancoillie, Leen, Vandeputte, Lotte, Vantroys, Elise, Vermeesch, Joris Robert, Janssens, Katrien
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container_title OBSTETRICS AND GYNECOLOGY
container_volume 137
creator van Riel, Margot
Brison, Nathalie
Baetens, Machteld
Blaumeiser, Bettina
Boemer, Francois
Bourlard, Laura
Bulk, Saskia
De Leener, Anne
Desir, Julie
Devriendt, Koenraad
Dheedene, Annelies
Duquenne, Armelle
Fieremans, Nathalie
Fieuw, Annelies
Gatot, Jean-Stephane
Grisart, Bernard
Janssens, Sandra
Khudashvili, Nairi
Lannoo, Lore
Marichal, Axel
Meunier, Colombine
Palmeira, Leonor
Parijs, Ilse
Pichon, Bruno
Roets, Ellen
Sammels, Eva
Smits, Guillaume
Suenaert, Marion
Sznajer, Yves
Van den Bogaert, Kris
Vancoillie, Leen
Vandeputte, Lotte
Vantroys, Elise
Vermeesch, Joris Robert
Janssens, Katrien
description OBJECTIVE: To evaluate the accuracy and diagnostic value of genome-wide noninvasive prenatal testing (NIPT) for the detection of fetal aneuploidies in multiple gestations, with a focus on dichorionic-diamniotic twin pregnancies. METHODS: We performed a retrospective cohort study including data from pregnant women with a twin or higher-order gestation who underwent genome-wide NIPT at one of the eight Belgian genetic centers between November 1, 2013, and March 1, 2020. Chorionicity and amnionicity were determined by ultrasonography. Follow-up invasive testing was carried out in the event of positive NIPT results. Sensitivity and specificity were calculated for the detection of trisomy 21, 18, and 13 in the dichorionic-diamniotic twin cohort. RESULTS: Unique NIPT analyses were performed for 4,150 pregnant women with a multiple gestation and an additional 767 with vanishing gestations. The failure rate in multiple gestations excluding vanishing gestations ranged from 0% to 11.7% among the different genetic centers. Overall, the failure rate was 4.8%, which could be reduced to 1.2% after single resampling. There were no common fetal trisomies detected among the 86 monochorionic-monoamniotic and 25 triplet cases. Two monochorionic-diamniotic twins had an NIPT result indicative of a trisomy 21, which was confirmed in both fetuses. Among 2,716 dichorionic-diamniotic twin gestations, a sensitivity of 100% (95% CI 74.12-100%) and a specificity of 100% (95% CI 99.86-100%) was reached for trisomy 21 (n=12). For trisomy 18 (n=3), the respective values were 75% (95% CI 30.06-95.44%) sensitivity and 100% (95% CI 99.86-100%) specificity, and for trisomy 13 (n=2), 100% (95% CI 20.65-100%) sensitivity and 99.96% (95% CI 99.79-99.99%) specificity. In the vanishing gestation group, 28 NIPT results were positive for trisomy 21, 18, or 13, with only five confirmed trisomies. CONCLUSION: Genome-wide NIPT performed accurately for detection of aneuploidy in dichorionic-diamniotic twin gestations.
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METHODS: We performed a retrospective cohort study including data from pregnant women with a twin or higher-order gestation who underwent genome-wide NIPT at one of the eight Belgian genetic centers between November 1, 2013, and March 1, 2020. Chorionicity and amnionicity were determined by ultrasonography. Follow-up invasive testing was carried out in the event of positive NIPT results. Sensitivity and specificity were calculated for the detection of trisomy 21, 18, and 13 in the dichorionic-diamniotic twin cohort. RESULTS: Unique NIPT analyses were performed for 4,150 pregnant women with a multiple gestation and an additional 767 with vanishing gestations. The failure rate in multiple gestations excluding vanishing gestations ranged from 0% to 11.7% among the different genetic centers. Overall, the failure rate was 4.8%, which could be reduced to 1.2% after single resampling. There were no common fetal trisomies detected among the 86 monochorionic-monoamniotic and 25 triplet cases. Two monochorionic-diamniotic twins had an NIPT result indicative of a trisomy 21, which was confirmed in both fetuses. Among 2,716 dichorionic-diamniotic twin gestations, a sensitivity of 100% (95% CI 74.12-100%) and a specificity of 100% (95% CI 99.86-100%) was reached for trisomy 21 (n=12). For trisomy 18 (n=3), the respective values were 75% (95% CI 30.06-95.44%) sensitivity and 100% (95% CI 99.86-100%) specificity, and for trisomy 13 (n=2), 100% (95% CI 20.65-100%) sensitivity and 99.96% (95% CI 99.79-99.99%) specificity. In the vanishing gestation group, 28 NIPT results were positive for trisomy 21, 18, or 13, with only five confirmed trisomies. 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METHODS: We performed a retrospective cohort study including data from pregnant women with a twin or higher-order gestation who underwent genome-wide NIPT at one of the eight Belgian genetic centers between November 1, 2013, and March 1, 2020. Chorionicity and amnionicity were determined by ultrasonography. Follow-up invasive testing was carried out in the event of positive NIPT results. Sensitivity and specificity were calculated for the detection of trisomy 21, 18, and 13 in the dichorionic-diamniotic twin cohort. RESULTS: Unique NIPT analyses were performed for 4,150 pregnant women with a multiple gestation and an additional 767 with vanishing gestations. The failure rate in multiple gestations excluding vanishing gestations ranged from 0% to 11.7% among the different genetic centers. Overall, the failure rate was 4.8%, which could be reduced to 1.2% after single resampling. There were no common fetal trisomies detected among the 86 monochorionic-monoamniotic and 25 triplet cases. Two monochorionic-diamniotic twins had an NIPT result indicative of a trisomy 21, which was confirmed in both fetuses. Among 2,716 dichorionic-diamniotic twin gestations, a sensitivity of 100% (95% CI 74.12-100%) and a specificity of 100% (95% CI 99.86-100%) was reached for trisomy 21 (n=12). For trisomy 18 (n=3), the respective values were 75% (95% CI 30.06-95.44%) sensitivity and 100% (95% CI 99.86-100%) specificity, and for trisomy 13 (n=2), 100% (95% CI 20.65-100%) sensitivity and 99.96% (95% CI 99.79-99.99%) specificity. In the vanishing gestation group, 28 NIPT results were positive for trisomy 21, 18, or 13, with only five confirmed trisomies. CONCLUSION: Genome-wide NIPT performed accurately for detection of aneuploidy in dichorionic-diamniotic twin gestations.</description><issn>0029-7844</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>FZOIL</sourceid><recordid>eNqNjLsOgkAQAK_QRHz8w3YWhuQQBK_22WgojJZkAws5PfcMdxA_Xws_wGqamRmIQMqlCrN1kozE2Lm7lDJKVRyIMqe2tu0TuSRArmCrsWHrvC7hiqYjsDUciO2TwpuuCM6WNffodE-Qt8To0cCFvgE3oBlOnfH6ZegbOY9eW3ZTMazROJr9OBHz_e6yOYaPzlDXExeVe2FJRbSMk1WarVWRZomKVDwRi__Mwr99_P_3A0ymVCs</recordid><startdate>202106</startdate><enddate>202106</enddate><creator>van Riel, Margot</creator><creator>Brison, Nathalie</creator><creator>Baetens, Machteld</creator><creator>Blaumeiser, Bettina</creator><creator>Boemer, Francois</creator><creator>Bourlard, Laura</creator><creator>Bulk, Saskia</creator><creator>De Leener, Anne</creator><creator>Desir, Julie</creator><creator>Devriendt, Koenraad</creator><creator>Dheedene, Annelies</creator><creator>Duquenne, Armelle</creator><creator>Fieremans, Nathalie</creator><creator>Fieuw, Annelies</creator><creator>Gatot, Jean-Stephane</creator><creator>Grisart, Bernard</creator><creator>Janssens, Sandra</creator><creator>Khudashvili, Nairi</creator><creator>Lannoo, Lore</creator><creator>Marichal, Axel</creator><creator>Meunier, Colombine</creator><creator>Palmeira, Leonor</creator><creator>Parijs, Ilse</creator><creator>Pichon, Bruno</creator><creator>Roets, Ellen</creator><creator>Sammels, Eva</creator><creator>Smits, Guillaume</creator><creator>Suenaert, Marion</creator><creator>Sznajer, Yves</creator><creator>Van den Bogaert, Kris</creator><creator>Vancoillie, Leen</creator><creator>Vandeputte, Lotte</creator><creator>Vantroys, Elise</creator><creator>Vermeesch, Joris Robert</creator><creator>Janssens, Katrien</creator><general>LIPPINCOTT WILLIAMS &amp; 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METHODS: We performed a retrospective cohort study including data from pregnant women with a twin or higher-order gestation who underwent genome-wide NIPT at one of the eight Belgian genetic centers between November 1, 2013, and March 1, 2020. Chorionicity and amnionicity were determined by ultrasonography. Follow-up invasive testing was carried out in the event of positive NIPT results. Sensitivity and specificity were calculated for the detection of trisomy 21, 18, and 13 in the dichorionic-diamniotic twin cohort. RESULTS: Unique NIPT analyses were performed for 4,150 pregnant women with a multiple gestation and an additional 767 with vanishing gestations. The failure rate in multiple gestations excluding vanishing gestations ranged from 0% to 11.7% among the different genetic centers. Overall, the failure rate was 4.8%, which could be reduced to 1.2% after single resampling. There were no common fetal trisomies detected among the 86 monochorionic-monoamniotic and 25 triplet cases. Two monochorionic-diamniotic twins had an NIPT result indicative of a trisomy 21, which was confirmed in both fetuses. Among 2,716 dichorionic-diamniotic twin gestations, a sensitivity of 100% (95% CI 74.12-100%) and a specificity of 100% (95% CI 99.86-100%) was reached for trisomy 21 (n=12). For trisomy 18 (n=3), the respective values were 75% (95% CI 30.06-95.44%) sensitivity and 100% (95% CI 99.86-100%) specificity, and for trisomy 13 (n=2), 100% (95% CI 20.65-100%) sensitivity and 99.96% (95% CI 99.79-99.99%) specificity. In the vanishing gestation group, 28 NIPT results were positive for trisomy 21, 18, or 13, with only five confirmed trisomies. CONCLUSION: Genome-wide NIPT performed accurately for detection of aneuploidy in dichorionic-diamniotic twin gestations.</abstract><pub>LIPPINCOTT WILLIAMS &amp; WILKINS</pub></addata></record>
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title Performance and Diagnostic Value of Genome-Wide Noninvasive Prenatal Testing in Multiple Gestations
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