Hypertensive disorders in pregnancy: combined screening by uterine artery Doppler, blood pressure and serum PAPP-A at 11-13 weeks

Objective To explore if the addition of pregnancy‐associated plasma protein‐A (PAPP‐A) to maternal factors and biophysical markers yields a significant improvement in the detection of hypertensive disorders before the clinical onset of disease. Methods Prospective screening study for early preeclamp...

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Veröffentlicht in:Prenatal diagnosis 2010-03, Vol.30 (3), p.216-223
Hauptverfasser: Poon, Leona C. Y., Stratieva, Violeta, Piras, Silvia, Piri, Solmaz, Nicolaides, Kypros H.
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container_end_page 223
container_issue 3
container_start_page 216
container_title Prenatal diagnosis
container_volume 30
creator Poon, Leona C. Y.
Stratieva, Violeta
Piras, Silvia
Piri, Solmaz
Nicolaides, Kypros H.
description Objective To explore if the addition of pregnancy‐associated plasma protein‐A (PAPP‐A) to maternal factors and biophysical markers yields a significant improvement in the detection of hypertensive disorders before the clinical onset of disease. Methods Prospective screening study for early preeclampsia (PE), late PE and gestational hypertension (GH) in women attending their first hospital visit at 11+0–13+6 weeks of gestation. The performance of screening for PE and GH by combinations of maternal factors, uterine artery with the lowest pulsatility index (L‐PI), mean arterial pressure (MAP) and serum PAPP‐A was determined. Results There were 8061 unaffected controls, 37 of whom developed early PE, 128 with late PE and 140 with GH. Compared to the controls, in early PE and late PE MAP and uterine artery L‐PI were increased and PAPP‐A was decreased. In GH PAPP‐A was not significantly different from controls. In screening for a combination of maternal factors, uterine artery L‐PI, MAP and PAPP‐A the detection rate of early PE was 83.8%, at a 5% false‐positive rate. In the prediction of late PE and GH there was no significant improvement from the addition of PAPP‐A to the combination of maternal factors, MAP and uterine artery L‐PI. Conclusion Measurement of PAPP‐A improves the performance of screening for early PE provided by a combination of maternal factors and biophysical tests at 11–13 weeks. Copyright © 2010 John Wiley & Sons, Ltd.
doi_str_mv 10.1002/pd.2440
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Y. ; Stratieva, Violeta ; Piras, Silvia ; Piri, Solmaz ; Nicolaides, Kypros H.</creator><creatorcontrib>Poon, Leona C. Y. ; Stratieva, Violeta ; Piras, Silvia ; Piri, Solmaz ; Nicolaides, Kypros H.</creatorcontrib><description>Objective To explore if the addition of pregnancy‐associated plasma protein‐A (PAPP‐A) to maternal factors and biophysical markers yields a significant improvement in the detection of hypertensive disorders before the clinical onset of disease. Methods Prospective screening study for early preeclampsia (PE), late PE and gestational hypertension (GH) in women attending their first hospital visit at 11+0–13+6 weeks of gestation. The performance of screening for PE and GH by combinations of maternal factors, uterine artery with the lowest pulsatility index (L‐PI), mean arterial pressure (MAP) and serum PAPP‐A was determined. Results There were 8061 unaffected controls, 37 of whom developed early PE, 128 with late PE and 140 with GH. Compared to the controls, in early PE and late PE MAP and uterine artery L‐PI were increased and PAPP‐A was decreased. In GH PAPP‐A was not significantly different from controls. In screening for a combination of maternal factors, uterine artery L‐PI, MAP and PAPP‐A the detection rate of early PE was 83.8%, at a 5% false‐positive rate. In the prediction of late PE and GH there was no significant improvement from the addition of PAPP‐A to the combination of maternal factors, MAP and uterine artery L‐PI. Conclusion Measurement of PAPP‐A improves the performance of screening for early PE provided by a combination of maternal factors and biophysical tests at 11–13 weeks. Copyright © 2010 John Wiley &amp; Sons, Ltd.</description><identifier>ISSN: 0197-3851</identifier><identifier>EISSN: 1097-0223</identifier><identifier>DOI: 10.1002/pd.2440</identifier><identifier>PMID: 20108221</identifier><identifier>CODEN: PRDIDM</identifier><language>eng</language><publisher>Chichester, UK: John Wiley &amp; Sons, Ltd</publisher><subject>Adult ; Biological and medical sciences ; Blood Pressure - physiology ; Delivery. Postpartum. Lactation ; False Positive Reactions ; Female ; Fundamental and applied biological sciences. Psychology ; Genetics of eukaryotes. Biological and molecular evolution ; Gestational Age ; gestational hypertension ; Gynecology. Andrology. Obstetrics ; Humans ; Mass Screening - methods ; mean arterial pressure ; Medical sciences ; Molecular and cellular biology ; PAPP-A ; Pre-Eclampsia - blood ; Pre-Eclampsia - diagnosis ; Pre-Eclampsia - diagnostic imaging ; preeclampsia ; Pregnancy ; Pregnancy Trimester, First - blood ; Pregnancy-Associated Plasma Protein-A - analysis ; Prospective Studies ; Pulsatile Flow - physiology ; screening ; Ultrasonography, Doppler ; United Kingdom - epidemiology ; Uterine Artery - diagnostic imaging ; uterine artery Doppler</subject><ispartof>Prenatal diagnosis, 2010-03, Vol.30 (3), p.216-223</ispartof><rights>Copyright © 2010 John Wiley &amp; Sons, Ltd.</rights><rights>2015 INIST-CNRS</rights><rights>Copyright (c) 2010 John Wiley &amp; Sons, Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4830-566f102dc153d1fc3b5a2012c5e9a8e37cb16d700ae000017324c001e6522ae13</citedby><cites>FETCH-LOGICAL-c4830-566f102dc153d1fc3b5a2012c5e9a8e37cb16d700ae000017324c001e6522ae13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fpd.2440$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fpd.2440$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=22432773$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20108221$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Poon, Leona C. Y.</creatorcontrib><creatorcontrib>Stratieva, Violeta</creatorcontrib><creatorcontrib>Piras, Silvia</creatorcontrib><creatorcontrib>Piri, Solmaz</creatorcontrib><creatorcontrib>Nicolaides, Kypros H.</creatorcontrib><title>Hypertensive disorders in pregnancy: combined screening by uterine artery Doppler, blood pressure and serum PAPP-A at 11-13 weeks</title><title>Prenatal diagnosis</title><addtitle>Prenat. Diagn</addtitle><description>Objective To explore if the addition of pregnancy‐associated plasma protein‐A (PAPP‐A) to maternal factors and biophysical markers yields a significant improvement in the detection of hypertensive disorders before the clinical onset of disease. Methods Prospective screening study for early preeclampsia (PE), late PE and gestational hypertension (GH) in women attending their first hospital visit at 11+0–13+6 weeks of gestation. The performance of screening for PE and GH by combinations of maternal factors, uterine artery with the lowest pulsatility index (L‐PI), mean arterial pressure (MAP) and serum PAPP‐A was determined. Results There were 8061 unaffected controls, 37 of whom developed early PE, 128 with late PE and 140 with GH. Compared to the controls, in early PE and late PE MAP and uterine artery L‐PI were increased and PAPP‐A was decreased. In GH PAPP‐A was not significantly different from controls. In screening for a combination of maternal factors, uterine artery L‐PI, MAP and PAPP‐A the detection rate of early PE was 83.8%, at a 5% false‐positive rate. In the prediction of late PE and GH there was no significant improvement from the addition of PAPP‐A to the combination of maternal factors, MAP and uterine artery L‐PI. Conclusion Measurement of PAPP‐A improves the performance of screening for early PE provided by a combination of maternal factors and biophysical tests at 11–13 weeks. 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Obstetrics</subject><subject>Humans</subject><subject>Mass Screening - methods</subject><subject>mean arterial pressure</subject><subject>Medical sciences</subject><subject>Molecular and cellular biology</subject><subject>PAPP-A</subject><subject>Pre-Eclampsia - blood</subject><subject>Pre-Eclampsia - diagnosis</subject><subject>Pre-Eclampsia - diagnostic imaging</subject><subject>preeclampsia</subject><subject>Pregnancy</subject><subject>Pregnancy Trimester, First - blood</subject><subject>Pregnancy-Associated Plasma Protein-A - analysis</subject><subject>Prospective Studies</subject><subject>Pulsatile Flow - physiology</subject><subject>screening</subject><subject>Ultrasonography, Doppler</subject><subject>United Kingdom - epidemiology</subject><subject>Uterine Artery - diagnostic imaging</subject><subject>uterine artery Doppler</subject><issn>0197-3851</issn><issn>1097-0223</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kEFv1DAQhS0EosuC-AfIF8QBUjx2Eme5rbqlRWphJYp6tBx7UpkmTrAT2hz553i1S-HCXGY0_t48-RHyEtgxMMbfD_aY5zl7RBbAVjJjnIvHZMEgzaIq4Ig8i_F7Aiu-kk_JEWfAKs5hQX6dzwOGEX10P5FaF_tgMUTqPB0C3njtzfyBmr6rnUdLowmI3vkbWs90GjGkLdVJH2a66YehxfCO1m3f2508ximkZ590GKaObtfbbbameqQAGQh6h3gbn5MnjW4jvjj0Jfn28fTq5Dy7-HL26WR9kZm8EiwryrIBxq2BQlhojKgLnb7BTYErXaGQpobSSsY0slQgBc9N6lgWnGsEsSRv9neH0P-YMI6qc9Fg22qP_RSVFAKqnFX_kCb0MQZs1BBcp8OsgKld3Gqwahd3Il8dbk51h_aB-5NvAl4fAB2NbpuQ8nTxL8dzwWVyXpK3e-7OtTj_z09tNwfbbE-7OOL9A63DrSqlkIW6_nymNtfsEq4uv6pc_AZi26Lh</recordid><startdate>201003</startdate><enddate>201003</enddate><creator>Poon, Leona C. Y.</creator><creator>Stratieva, Violeta</creator><creator>Piras, Silvia</creator><creator>Piri, Solmaz</creator><creator>Nicolaides, Kypros H.</creator><general>John Wiley &amp; Sons, Ltd</general><general>Wiley</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>201003</creationdate><title>Hypertensive disorders in pregnancy: combined screening by uterine artery Doppler, blood pressure and serum PAPP-A at 11-13 weeks</title><author>Poon, Leona C. Y. ; Stratieva, Violeta ; Piras, Silvia ; Piri, Solmaz ; Nicolaides, Kypros H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4830-566f102dc153d1fc3b5a2012c5e9a8e37cb16d700ae000017324c001e6522ae13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Adult</topic><topic>Biological and medical sciences</topic><topic>Blood Pressure - physiology</topic><topic>Delivery. Postpartum. Lactation</topic><topic>False Positive Reactions</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Genetics of eukaryotes. Biological and molecular evolution</topic><topic>Gestational Age</topic><topic>gestational hypertension</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>Humans</topic><topic>Mass Screening - methods</topic><topic>mean arterial pressure</topic><topic>Medical sciences</topic><topic>Molecular and cellular biology</topic><topic>PAPP-A</topic><topic>Pre-Eclampsia - blood</topic><topic>Pre-Eclampsia - diagnosis</topic><topic>Pre-Eclampsia - diagnostic imaging</topic><topic>preeclampsia</topic><topic>Pregnancy</topic><topic>Pregnancy Trimester, First - blood</topic><topic>Pregnancy-Associated Plasma Protein-A - analysis</topic><topic>Prospective Studies</topic><topic>Pulsatile Flow - physiology</topic><topic>screening</topic><topic>Ultrasonography, Doppler</topic><topic>United Kingdom - epidemiology</topic><topic>Uterine Artery - diagnostic imaging</topic><topic>uterine artery Doppler</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Poon, Leona C. Y.</creatorcontrib><creatorcontrib>Stratieva, Violeta</creatorcontrib><creatorcontrib>Piras, Silvia</creatorcontrib><creatorcontrib>Piri, Solmaz</creatorcontrib><creatorcontrib>Nicolaides, Kypros H.</creatorcontrib><collection>Istex</collection><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>MEDLINE - Academic</collection><jtitle>Prenatal diagnosis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Poon, Leona C. Y.</au><au>Stratieva, Violeta</au><au>Piras, Silvia</au><au>Piri, Solmaz</au><au>Nicolaides, Kypros H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hypertensive disorders in pregnancy: combined screening by uterine artery Doppler, blood pressure and serum PAPP-A at 11-13 weeks</atitle><jtitle>Prenatal diagnosis</jtitle><addtitle>Prenat. Diagn</addtitle><date>2010-03</date><risdate>2010</risdate><volume>30</volume><issue>3</issue><spage>216</spage><epage>223</epage><pages>216-223</pages><issn>0197-3851</issn><eissn>1097-0223</eissn><coden>PRDIDM</coden><abstract>Objective To explore if the addition of pregnancy‐associated plasma protein‐A (PAPP‐A) to maternal factors and biophysical markers yields a significant improvement in the detection of hypertensive disorders before the clinical onset of disease. Methods Prospective screening study for early preeclampsia (PE), late PE and gestational hypertension (GH) in women attending their first hospital visit at 11+0–13+6 weeks of gestation. The performance of screening for PE and GH by combinations of maternal factors, uterine artery with the lowest pulsatility index (L‐PI), mean arterial pressure (MAP) and serum PAPP‐A was determined. Results There were 8061 unaffected controls, 37 of whom developed early PE, 128 with late PE and 140 with GH. Compared to the controls, in early PE and late PE MAP and uterine artery L‐PI were increased and PAPP‐A was decreased. In GH PAPP‐A was not significantly different from controls. In screening for a combination of maternal factors, uterine artery L‐PI, MAP and PAPP‐A the detection rate of early PE was 83.8%, at a 5% false‐positive rate. In the prediction of late PE and GH there was no significant improvement from the addition of PAPP‐A to the combination of maternal factors, MAP and uterine artery L‐PI. Conclusion Measurement of PAPP‐A improves the performance of screening for early PE provided by a combination of maternal factors and biophysical tests at 11–13 weeks. Copyright © 2010 John Wiley &amp; Sons, Ltd.</abstract><cop>Chichester, UK</cop><pub>John Wiley &amp; Sons, Ltd</pub><pmid>20108221</pmid><doi>10.1002/pd.2440</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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subjects Adult
Biological and medical sciences
Blood Pressure - physiology
Delivery. Postpartum. Lactation
False Positive Reactions
Female
Fundamental and applied biological sciences. Psychology
Genetics of eukaryotes. Biological and molecular evolution
Gestational Age
gestational hypertension
Gynecology. Andrology. Obstetrics
Humans
Mass Screening - methods
mean arterial pressure
Medical sciences
Molecular and cellular biology
PAPP-A
Pre-Eclampsia - blood
Pre-Eclampsia - diagnosis
Pre-Eclampsia - diagnostic imaging
preeclampsia
Pregnancy
Pregnancy Trimester, First - blood
Pregnancy-Associated Plasma Protein-A - analysis
Prospective Studies
Pulsatile Flow - physiology
screening
Ultrasonography, Doppler
United Kingdom - epidemiology
Uterine Artery - diagnostic imaging
uterine artery Doppler
title Hypertensive disorders in pregnancy: combined screening by uterine artery Doppler, blood pressure and serum PAPP-A at 11-13 weeks
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