Prediction of Preeclampsia Using the Soluble fms-Like Tyrosine Kinase 1 to Placental Growth Factor Ratio
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- Ulla Sovio
- From the Department of Obstetrics and Gynaecology, University of Cambridge, United Kingdom (U.S., F.G., E.C., D.S.C.-J., G.C.S.S.); NIHR (National Institute for Health Research) Cambridge Comprehensive Biomedical Research Centre, United Kingdom (U.S., F.G., E.C., D.S.C.-J., G.C.S.S.); and Roche Diagnostics International, Rotkreuz, Switzerland (M.H.).
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- Francesca Gaccioli
- From the Department of Obstetrics and Gynaecology, University of Cambridge, United Kingdom (U.S., F.G., E.C., D.S.C.-J., G.C.S.S.); NIHR (National Institute for Health Research) Cambridge Comprehensive Biomedical Research Centre, United Kingdom (U.S., F.G., E.C., D.S.C.-J., G.C.S.S.); and Roche Diagnostics International, Rotkreuz, Switzerland (M.H.).
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- Emma Cook
- From the Department of Obstetrics and Gynaecology, University of Cambridge, United Kingdom (U.S., F.G., E.C., D.S.C.-J., G.C.S.S.); NIHR (National Institute for Health Research) Cambridge Comprehensive Biomedical Research Centre, United Kingdom (U.S., F.G., E.C., D.S.C.-J., G.C.S.S.); and Roche Diagnostics International, Rotkreuz, Switzerland (M.H.).
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- Martin Hund
- From the Department of Obstetrics and Gynaecology, University of Cambridge, United Kingdom (U.S., F.G., E.C., D.S.C.-J., G.C.S.S.); NIHR (National Institute for Health Research) Cambridge Comprehensive Biomedical Research Centre, United Kingdom (U.S., F.G., E.C., D.S.C.-J., G.C.S.S.); and Roche Diagnostics International, Rotkreuz, Switzerland (M.H.).
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- D. Stephen Charnock-Jones
- From the Department of Obstetrics and Gynaecology, University of Cambridge, United Kingdom (U.S., F.G., E.C., D.S.C.-J., G.C.S.S.); NIHR (National Institute for Health Research) Cambridge Comprehensive Biomedical Research Centre, United Kingdom (U.S., F.G., E.C., D.S.C.-J., G.C.S.S.); and Roche Diagnostics International, Rotkreuz, Switzerland (M.H.).
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- Gordon C.S. Smith
- From the Department of Obstetrics and Gynaecology, University of Cambridge, United Kingdom (U.S., F.G., E.C., D.S.C.-J., G.C.S.S.); NIHR (National Institute for Health Research) Cambridge Comprehensive Biomedical Research Centre, United Kingdom (U.S., F.G., E.C., D.S.C.-J., G.C.S.S.); and Roche Diagnostics International, Rotkreuz, Switzerland (M.H.).
書誌事項
- タイトル別名
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- A Prospective Cohort Study of Unselected Nulliparous Women
説明
<jats:p>We sought to assess the ratio of sFlt-1 (soluble fms-like tyrosine kinase 1) to PlGF (placental growth factor) in maternal serum as a screening test for preeclampsia in unselected nulliparous women with a singleton pregnancy. We studied 4099 women recruited to the POP study (Pregnancy Outcome Prediction) (Cambridge, United Kingdom). The sFlt-1:PlGF ratio was measured using the Roche Cobas e411 platform at ≈20, ≈28, and ≈36 weeks of gestational age (wkGA). Screen positive was defined as an sFlt-1:PlGF ratio >38, but higher thresholds were also studied. At 28 wkGA, an sFlt-1:PlGF ratio >38 had a positive predictive value (PPV) of 32% for preeclampsia and preterm birth, and the PPV was similar comparing women with low and high prior risk of disease. At 36 wkGA, an sFlt-1:PlGF ratio >38 had a PPV for severe preeclampsia of 20% in high-risk women and 6.4% in low-risk women. At 36 wkGA, an sFlt-1:PlGF ratio >110 had a PPV of 30% for severe preeclampsia, and the PPV was similar comparing low- and high-risk women. Overall, at 36 wkGA, 195 (5.2%) women either had an sFlt-1:PlGF ratio of >110 or an sFlt-1:PlGF ratio >38 plus maternal risk factors: 43% of these women developed preeclampsia, about half with severe features. Among low-risk women at 36 wkGA, an sFlt-1:PlGF ratio ≤38 had a negative predictive value for severe preeclampsia of 99.2%. The sFlt-1:PlGF ratio provided clinically useful prediction of the risk of the most important manifestations of preeclampsia in a cohort of unselected nulliparous women.</jats:p>
収録刊行物
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- Hypertension
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Hypertension 69 (4), 731-738, 2017-04
Ovid Technologies (Wolters Kluwer Health)