‘Dual Positivity’ for Neural Tube Defects and Down Syndrome at Maternal Serum Screening: Gestational Outcome
Objective: To evaluate the gestational outcome of pregnancies screen-positive for both neural tube defects (NTD) and Down syndrome (DS) (‘dual positivity’). Methods: Among 10,667 mid-trimester women screened for DS and NTD with α-fetoprotein (AFP), unconjugated estriol (uE 3 ), and human chorionic g...
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creator | Zanini, Roberto Tarantini, Michele Cerri, Valeria Jacobello, Carmelo Bellotti, Daniela Lancetti, Sara Scalchi, Sabrina Groli, Caterina Bianchi, Umberto A. |
description | Objective: To evaluate the gestational outcome of pregnancies screen-positive for both neural tube defects (NTD) and Down syndrome (DS) (‘dual positivity’). Methods: Among 10,667 mid-trimester women screened for DS and NTD with α-fetoprotein (AFP), unconjugated estriol (uE 3 ), and human chorionic gonadotropin (hCG), delivered up to July 1996, we have selected cases with both an unexplained AFP value ≥2.5 multiples of median (MoM) and a DS risk ≥1:250. All these pregnant women were managed with amniocentesis and/or CVS, ultrasound scans, and Doppler velocimetry. We have collected all data about the gestations with ‘dual positivity’ and no obvious explanation for these findings (cases with fetal malformations related to raised AFP). Results: Twelve women (1.1:1,000) showed unexplained ‘dual positivity’. Abnormal karyotypes were found in 3 fetuses, and pregnancies were terminated: there were 2 triploidies with partial hydatiform mola, and 1 DS. In 9 cases the fetal karyotype was normal, but a confined placental trisomy 16 was found in 4. Of the 9 continuing gestations, 8 displayed fetal growth retardation (FGR). One gestation ended with fetal death at 27 weeks. All 9 fetuses were morphologically normal, and 8 were small for gestational age. Conclusions: ‘Dual positivity’ at NTD/DS screening may anticipate pregnancy complications. The finding of trisomy 16 confined to the placenta and FGR in 4 cases suggests that at least some fetuses with growth restriction may suffer from a distinct placental disease. Maternal serum screening may have implications different from DS and NTD, as demonstrated by the 2 cases with triploidy and incomplete hydatiform mola, the 4 cases with placental trisomy 16, and the 4 cases of FGR of the 5 fetuses without chromosome abnormalities. As the pathologic outcome of these pregnancies is more important than the mere serum screening results, we feel that these cases need a strict work-up, including CVS, amniocentesis and ultrasound studies to better address the obstetrical management. |
doi_str_mv | 10.1159/000020816 |
format | Article |
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Methods: Among 10,667 mid-trimester women screened for DS and NTD with α-fetoprotein (AFP), unconjugated estriol (uE 3 ), and human chorionic gonadotropin (hCG), delivered up to July 1996, we have selected cases with both an unexplained AFP value ≥2.5 multiples of median (MoM) and a DS risk ≥1:250. All these pregnant women were managed with amniocentesis and/or CVS, ultrasound scans, and Doppler velocimetry. We have collected all data about the gestations with ‘dual positivity’ and no obvious explanation for these findings (cases with fetal malformations related to raised AFP). Results: Twelve women (1.1:1,000) showed unexplained ‘dual positivity’. Abnormal karyotypes were found in 3 fetuses, and pregnancies were terminated: there were 2 triploidies with partial hydatiform mola, and 1 DS. In 9 cases the fetal karyotype was normal, but a confined placental trisomy 16 was found in 4. Of the 9 continuing gestations, 8 displayed fetal growth retardation (FGR). One gestation ended with fetal death at 27 weeks. All 9 fetuses were morphologically normal, and 8 were small for gestational age. Conclusions: ‘Dual positivity’ at NTD/DS screening may anticipate pregnancy complications. The finding of trisomy 16 confined to the placenta and FGR in 4 cases suggests that at least some fetuses with growth restriction may suffer from a distinct placental disease. Maternal serum screening may have implications different from DS and NTD, as demonstrated by the 2 cases with triploidy and incomplete hydatiform mola, the 4 cases with placental trisomy 16, and the 4 cases of FGR of the 5 fetuses without chromosome abnormalities. As the pathologic outcome of these pregnancies is more important than the mere serum screening results, we feel that these cases need a strict work-up, including CVS, amniocentesis and ultrasound studies to better address the obstetrical management.</description><identifier>ISSN: 1015-3837</identifier><identifier>EISSN: 1421-9964</identifier><identifier>DOI: 10.1159/000020816</identifier><identifier>PMID: 9650657</identifier><language>eng</language><publisher>Basel, Switzerland: Karger</publisher><subject>Adult ; alpha-Fetoproteins - analysis ; Amniocentesis ; Biological and medical sciences ; Chorionic Gonadotropin - blood ; Chorionic Villi Sampling ; Down Syndrome - diagnosis ; Estriol - blood ; Female ; Fetal Growth Retardation - diagnosis ; Gestational Age ; Gynecology. Andrology. Obstetrics ; Humans ; Hydatidiform Mole - diagnosis ; Karyotyping ; Management. Prenatal diagnosis ; Medical sciences ; Middle Aged ; Mola ; Neural Tube Defects - diagnosis ; Pregnancy ; Pregnancy Outcome ; Pregnancy. Fetus. Placenta ; Prenatal Diagnosis ; Ultrasonography, Prenatal</subject><ispartof>Fetal diagnosis and therapy, 1998-03, Vol.13 (2), p.106-110</ispartof><rights>1998 S. Karger AG, Basel</rights><rights>1998 INIST-CNRS</rights><rights>Copyright (c) 1998 S. Karger AG, Basel</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c414t-574c3034c03ae5d40f85996f35f6c86c5b4313fab2330a7625912d738e996d303</citedby><cites>FETCH-LOGICAL-c414t-574c3034c03ae5d40f85996f35f6c86c5b4313fab2330a7625912d738e996d303</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,2423,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2252290$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9650657$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zanini, Roberto</creatorcontrib><creatorcontrib>Tarantini, Michele</creatorcontrib><creatorcontrib>Cerri, Valeria</creatorcontrib><creatorcontrib>Jacobello, Carmelo</creatorcontrib><creatorcontrib>Bellotti, Daniela</creatorcontrib><creatorcontrib>Lancetti, Sara</creatorcontrib><creatorcontrib>Scalchi, Sabrina</creatorcontrib><creatorcontrib>Groli, Caterina</creatorcontrib><creatorcontrib>Bianchi, Umberto A.</creatorcontrib><title>‘Dual Positivity’ for Neural Tube Defects and Down Syndrome at Maternal Serum Screening: Gestational Outcome</title><title>Fetal diagnosis and therapy</title><addtitle>Fetal Diagn Ther</addtitle><description>Objective: To evaluate the gestational outcome of pregnancies screen-positive for both neural tube defects (NTD) and Down syndrome (DS) (‘dual positivity’). Methods: Among 10,667 mid-trimester women screened for DS and NTD with α-fetoprotein (AFP), unconjugated estriol (uE 3 ), and human chorionic gonadotropin (hCG), delivered up to July 1996, we have selected cases with both an unexplained AFP value ≥2.5 multiples of median (MoM) and a DS risk ≥1:250. All these pregnant women were managed with amniocentesis and/or CVS, ultrasound scans, and Doppler velocimetry. We have collected all data about the gestations with ‘dual positivity’ and no obvious explanation for these findings (cases with fetal malformations related to raised AFP). Results: Twelve women (1.1:1,000) showed unexplained ‘dual positivity’. Abnormal karyotypes were found in 3 fetuses, and pregnancies were terminated: there were 2 triploidies with partial hydatiform mola, and 1 DS. In 9 cases the fetal karyotype was normal, but a confined placental trisomy 16 was found in 4. Of the 9 continuing gestations, 8 displayed fetal growth retardation (FGR). One gestation ended with fetal death at 27 weeks. All 9 fetuses were morphologically normal, and 8 were small for gestational age. Conclusions: ‘Dual positivity’ at NTD/DS screening may anticipate pregnancy complications. The finding of trisomy 16 confined to the placenta and FGR in 4 cases suggests that at least some fetuses with growth restriction may suffer from a distinct placental disease. Maternal serum screening may have implications different from DS and NTD, as demonstrated by the 2 cases with triploidy and incomplete hydatiform mola, the 4 cases with placental trisomy 16, and the 4 cases of FGR of the 5 fetuses without chromosome abnormalities. As the pathologic outcome of these pregnancies is more important than the mere serum screening results, we feel that these cases need a strict work-up, including CVS, amniocentesis and ultrasound studies to better address the obstetrical management.</description><subject>Adult</subject><subject>alpha-Fetoproteins - analysis</subject><subject>Amniocentesis</subject><subject>Biological and medical sciences</subject><subject>Chorionic Gonadotropin - blood</subject><subject>Chorionic Villi Sampling</subject><subject>Down Syndrome - diagnosis</subject><subject>Estriol - blood</subject><subject>Female</subject><subject>Fetal Growth Retardation - diagnosis</subject><subject>Gestational Age</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Humans</subject><subject>Hydatidiform Mole - diagnosis</subject><subject>Karyotyping</subject><subject>Management. Prenatal diagnosis</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Mola</subject><subject>Neural Tube Defects - diagnosis</subject><subject>Pregnancy</subject><subject>Pregnancy Outcome</subject><subject>Pregnancy. Fetus. Placenta</subject><subject>Prenatal Diagnosis</subject><subject>Ultrasonography, Prenatal</subject><issn>1015-3837</issn><issn>1421-9964</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqFkV1rFDEYhYMota1eeC1CkCJ4MZrPycQ76doqVCvsej1kM2_K1JnJNh_K3vVn6N_rLzHrLiuIYG4SOM97cl4OQk8oeUWp1K9JOYw0tL6HDqlgtNK6FvfLm1BZ8Yarh-goxutCNYrXB-hA15LUUh2i1d3tj1k2A_7sY5_6b31a393-xM4H_AlyKMIiLwHPwIFNEZupwzP_fcLz9dQFPwI2CX80CcJU0DmEPOK5DQBTP129wecQk0m934iXOdky8Ag9cGaI8Hh3H6MvZ-8Wp--ri8vzD6dvLyorqEiVVMJywoUl3IDsBHGNLEs5Ll1tm9rKpeCUO7NknBOjaiY1ZZ3iDRSqK5PH6MXWdxX8TS452rGPFobBTOBzbJXWSgjN_wsyoomQQhbw-V_gtc-bvQvDGFeCNRu3l1vIBh9jANeuQj-asG4paTddtfuuCvtsZ5iXI3R7cldO0U92uonWDC6YyfZxjzEmGdPkT66vJlxB2Otns8Xvf9pV5wr09J_QNskvkcSvRw</recordid><startdate>19980301</startdate><enddate>19980301</enddate><creator>Zanini, Roberto</creator><creator>Tarantini, Michele</creator><creator>Cerri, Valeria</creator><creator>Jacobello, Carmelo</creator><creator>Bellotti, Daniela</creator><creator>Lancetti, Sara</creator><creator>Scalchi, Sabrina</creator><creator>Groli, Caterina</creator><creator>Bianchi, Umberto A.</creator><general>Karger</general><general>S. 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Andrology. Obstetrics</topic><topic>Humans</topic><topic>Hydatidiform Mole - diagnosis</topic><topic>Karyotyping</topic><topic>Management. Prenatal diagnosis</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Mola</topic><topic>Neural Tube Defects - diagnosis</topic><topic>Pregnancy</topic><topic>Pregnancy Outcome</topic><topic>Pregnancy. Fetus. Placenta</topic><topic>Prenatal Diagnosis</topic><topic>Ultrasonography, Prenatal</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zanini, Roberto</creatorcontrib><creatorcontrib>Tarantini, Michele</creatorcontrib><creatorcontrib>Cerri, Valeria</creatorcontrib><creatorcontrib>Jacobello, Carmelo</creatorcontrib><creatorcontrib>Bellotti, Daniela</creatorcontrib><creatorcontrib>Lancetti, Sara</creatorcontrib><creatorcontrib>Scalchi, Sabrina</creatorcontrib><creatorcontrib>Groli, Caterina</creatorcontrib><creatorcontrib>Bianchi, Umberto A.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Fetal diagnosis and therapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zanini, Roberto</au><au>Tarantini, Michele</au><au>Cerri, Valeria</au><au>Jacobello, Carmelo</au><au>Bellotti, Daniela</au><au>Lancetti, Sara</au><au>Scalchi, Sabrina</au><au>Groli, Caterina</au><au>Bianchi, Umberto A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>‘Dual Positivity’ for Neural Tube Defects and Down Syndrome at Maternal Serum Screening: Gestational Outcome</atitle><jtitle>Fetal diagnosis and therapy</jtitle><addtitle>Fetal Diagn Ther</addtitle><date>1998-03-01</date><risdate>1998</risdate><volume>13</volume><issue>2</issue><spage>106</spage><epage>110</epage><pages>106-110</pages><issn>1015-3837</issn><eissn>1421-9964</eissn><abstract>Objective: To evaluate the gestational outcome of pregnancies screen-positive for both neural tube defects (NTD) and Down syndrome (DS) (‘dual positivity’). Methods: Among 10,667 mid-trimester women screened for DS and NTD with α-fetoprotein (AFP), unconjugated estriol (uE 3 ), and human chorionic gonadotropin (hCG), delivered up to July 1996, we have selected cases with both an unexplained AFP value ≥2.5 multiples of median (MoM) and a DS risk ≥1:250. All these pregnant women were managed with amniocentesis and/or CVS, ultrasound scans, and Doppler velocimetry. We have collected all data about the gestations with ‘dual positivity’ and no obvious explanation for these findings (cases with fetal malformations related to raised AFP). Results: Twelve women (1.1:1,000) showed unexplained ‘dual positivity’. Abnormal karyotypes were found in 3 fetuses, and pregnancies were terminated: there were 2 triploidies with partial hydatiform mola, and 1 DS. In 9 cases the fetal karyotype was normal, but a confined placental trisomy 16 was found in 4. Of the 9 continuing gestations, 8 displayed fetal growth retardation (FGR). One gestation ended with fetal death at 27 weeks. All 9 fetuses were morphologically normal, and 8 were small for gestational age. Conclusions: ‘Dual positivity’ at NTD/DS screening may anticipate pregnancy complications. The finding of trisomy 16 confined to the placenta and FGR in 4 cases suggests that at least some fetuses with growth restriction may suffer from a distinct placental disease. Maternal serum screening may have implications different from DS and NTD, as demonstrated by the 2 cases with triploidy and incomplete hydatiform mola, the 4 cases with placental trisomy 16, and the 4 cases of FGR of the 5 fetuses without chromosome abnormalities. As the pathologic outcome of these pregnancies is more important than the mere serum screening results, we feel that these cases need a strict work-up, including CVS, amniocentesis and ultrasound studies to better address the obstetrical management.</abstract><cop>Basel, Switzerland</cop><pub>Karger</pub><pmid>9650657</pmid><doi>10.1159/000020816</doi><tpages>5</tpages></addata></record> |
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subjects | Adult alpha-Fetoproteins - analysis Amniocentesis Biological and medical sciences Chorionic Gonadotropin - blood Chorionic Villi Sampling Down Syndrome - diagnosis Estriol - blood Female Fetal Growth Retardation - diagnosis Gestational Age Gynecology. Andrology. Obstetrics Humans Hydatidiform Mole - diagnosis Karyotyping Management. Prenatal diagnosis Medical sciences Middle Aged Mola Neural Tube Defects - diagnosis Pregnancy Pregnancy Outcome Pregnancy. Fetus. Placenta Prenatal Diagnosis Ultrasonography, Prenatal |
title | ‘Dual Positivity’ for Neural Tube Defects and Down Syndrome at Maternal Serum Screening: Gestational Outcome |
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