STATIN trial: predictive performance of competing-risks model in screening for pre-eclampsia at 35-37 weeks' gestation

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STATIN trial: predictive performance of competing-risks model in screening for pre-eclampsia at 35-37 weeks' gestation. / Döbert, M; Wright, A; Varouxaki, A N; Mu, A C; Syngelaki, A; Rehal, A; Delgado, J L; Akolekar, R; Muscettola, G; Janga, D; Singh, M; Martin-Alonso, R; Dütemeyer, V; De Alvarado, M; Atanasova, V; Wright, D; Nicolaides, K H.

in: ULTRASOUND OBST GYN, Jahrgang 59, Nr. 1, 01.2022, S. 69-75.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Döbert, M, Wright, A, Varouxaki, AN, Mu, AC, Syngelaki, A, Rehal, A, Delgado, JL, Akolekar, R, Muscettola, G, Janga, D, Singh, M, Martin-Alonso, R, Dütemeyer, V, De Alvarado, M, Atanasova, V, Wright, D & Nicolaides, KH 2022, 'STATIN trial: predictive performance of competing-risks model in screening for pre-eclampsia at 35-37 weeks' gestation', ULTRASOUND OBST GYN, Jg. 59, Nr. 1, S. 69-75. https://doi.org/10.1002/uog.24789

APA

Döbert, M., Wright, A., Varouxaki, A. N., Mu, A. C., Syngelaki, A., Rehal, A., Delgado, J. L., Akolekar, R., Muscettola, G., Janga, D., Singh, M., Martin-Alonso, R., Dütemeyer, V., De Alvarado, M., Atanasova, V., Wright, D., & Nicolaides, K. H. (2022). STATIN trial: predictive performance of competing-risks model in screening for pre-eclampsia at 35-37 weeks' gestation. ULTRASOUND OBST GYN, 59(1), 69-75. https://doi.org/10.1002/uog.24789

Vancouver

Bibtex

@article{5e9c7982bb3340e593eeb74ed9566bdf,
title = "STATIN trial: predictive performance of competing-risks model in screening for pre-eclampsia at 35-37 weeks' gestation",
abstract = "OBJECTIVE: To examine the predictive performance of a previously reported competing-risks model of screening for pre-eclampsia (PE) at 35-37 weeks' gestation by combinations of maternal risk factors, mean arterial pressure (MAP), uterine artery pulsatility index (UtA-PI), serum placental growth factor (PlGF) and serum soluble fms-like tyrosine kinase-1 (sFlt-1) in a validation dataset derived from the screened population of the STATIN study.METHODS: This was a prospective third-trimester multicenter study of screening for PE in singleton pregnancies by means of a previously reported algorithm that combines maternal risk factors and biomarkers. Women in the high-risk group were invited to participate in a trial of pravastatin vs placebo, but the trial showed no evidence of an effect of pravastatin in the prevention of PE. Patient-specific risks of delivery with PE were calculated using the competing-risks model, and the performance of screening for PE by maternal risk factors alone and by various combinations of risk factors with MAP, UtA-PI, PlGF and sFlt-1 was assessed. The predictive performance of the model was examined by, first, the ability of the model to discriminate between the PE and no-PE groups using the area under the receiver-operating-characteristics curve (AUC) and the detection rate at a fixed false-positive rate of 10%, and, second, calibration by measurements of calibration slope and calibration-in-the-large.RESULTS: The study population of 29 677 pregnancies contained 653 that developed PE. In screening for PE by a combination of maternal risk factors, MAP, PlGF and sFlt-1 (triple test), the detection rate at a 10% false-positive rate was 79% (95% CI, 76-82%) and the results were consistent with the data used for developing the algorithm. Addition of UtA-PI did not improve the prediction provided by the triple test. The AUC for the triple test was 0.923 (95% CI, 0.913-0.932), demonstrating very high discrimination between affected and unaffected pregnancies. Similarly, the calibration slope was 0.875 (95% CI, 0.831-0.919), demonstrating good agreement between the predicted risk and observed incidence of PE.CONCLUSION: The competing-risks model provides an effective and reproducible method for third-trimester prediction of term PE. {\textcopyright} 2021 International Society of Ultrasound in Obstetrics and Gynecology.",
author = "M D{\"o}bert and A Wright and Varouxaki, {A N} and Mu, {A C} and A Syngelaki and A Rehal and Delgado, {J L} and R Akolekar and G Muscettola and D Janga and M Singh and R Martin-Alonso and V D{\"u}temeyer and {De Alvarado}, M and V Atanasova and D Wright and Nicolaides, {K H}",
note = "{\textcopyright} 2021 International Society of Ultrasound in Obstetrics and Gynecology.",
year = "2022",
month = jan,
doi = "10.1002/uog.24789",
language = "English",
volume = "59",
pages = "69--75",
journal = "ULTRASOUND OBST GYN",
issn = "0960-7692",
publisher = "John Wiley and Sons Ltd",
number = "1",

}

RIS

TY - JOUR

T1 - STATIN trial: predictive performance of competing-risks model in screening for pre-eclampsia at 35-37 weeks' gestation

AU - Döbert, M

AU - Wright, A

AU - Varouxaki, A N

AU - Mu, A C

AU - Syngelaki, A

AU - Rehal, A

AU - Delgado, J L

AU - Akolekar, R

AU - Muscettola, G

AU - Janga, D

AU - Singh, M

AU - Martin-Alonso, R

AU - Dütemeyer, V

AU - De Alvarado, M

AU - Atanasova, V

AU - Wright, D

AU - Nicolaides, K H

N1 - © 2021 International Society of Ultrasound in Obstetrics and Gynecology.

PY - 2022/1

Y1 - 2022/1

N2 - OBJECTIVE: To examine the predictive performance of a previously reported competing-risks model of screening for pre-eclampsia (PE) at 35-37 weeks' gestation by combinations of maternal risk factors, mean arterial pressure (MAP), uterine artery pulsatility index (UtA-PI), serum placental growth factor (PlGF) and serum soluble fms-like tyrosine kinase-1 (sFlt-1) in a validation dataset derived from the screened population of the STATIN study.METHODS: This was a prospective third-trimester multicenter study of screening for PE in singleton pregnancies by means of a previously reported algorithm that combines maternal risk factors and biomarkers. Women in the high-risk group were invited to participate in a trial of pravastatin vs placebo, but the trial showed no evidence of an effect of pravastatin in the prevention of PE. Patient-specific risks of delivery with PE were calculated using the competing-risks model, and the performance of screening for PE by maternal risk factors alone and by various combinations of risk factors with MAP, UtA-PI, PlGF and sFlt-1 was assessed. The predictive performance of the model was examined by, first, the ability of the model to discriminate between the PE and no-PE groups using the area under the receiver-operating-characteristics curve (AUC) and the detection rate at a fixed false-positive rate of 10%, and, second, calibration by measurements of calibration slope and calibration-in-the-large.RESULTS: The study population of 29 677 pregnancies contained 653 that developed PE. In screening for PE by a combination of maternal risk factors, MAP, PlGF and sFlt-1 (triple test), the detection rate at a 10% false-positive rate was 79% (95% CI, 76-82%) and the results were consistent with the data used for developing the algorithm. Addition of UtA-PI did not improve the prediction provided by the triple test. The AUC for the triple test was 0.923 (95% CI, 0.913-0.932), demonstrating very high discrimination between affected and unaffected pregnancies. Similarly, the calibration slope was 0.875 (95% CI, 0.831-0.919), demonstrating good agreement between the predicted risk and observed incidence of PE.CONCLUSION: The competing-risks model provides an effective and reproducible method for third-trimester prediction of term PE. © 2021 International Society of Ultrasound in Obstetrics and Gynecology.

AB - OBJECTIVE: To examine the predictive performance of a previously reported competing-risks model of screening for pre-eclampsia (PE) at 35-37 weeks' gestation by combinations of maternal risk factors, mean arterial pressure (MAP), uterine artery pulsatility index (UtA-PI), serum placental growth factor (PlGF) and serum soluble fms-like tyrosine kinase-1 (sFlt-1) in a validation dataset derived from the screened population of the STATIN study.METHODS: This was a prospective third-trimester multicenter study of screening for PE in singleton pregnancies by means of a previously reported algorithm that combines maternal risk factors and biomarkers. Women in the high-risk group were invited to participate in a trial of pravastatin vs placebo, but the trial showed no evidence of an effect of pravastatin in the prevention of PE. Patient-specific risks of delivery with PE were calculated using the competing-risks model, and the performance of screening for PE by maternal risk factors alone and by various combinations of risk factors with MAP, UtA-PI, PlGF and sFlt-1 was assessed. The predictive performance of the model was examined by, first, the ability of the model to discriminate between the PE and no-PE groups using the area under the receiver-operating-characteristics curve (AUC) and the detection rate at a fixed false-positive rate of 10%, and, second, calibration by measurements of calibration slope and calibration-in-the-large.RESULTS: The study population of 29 677 pregnancies contained 653 that developed PE. In screening for PE by a combination of maternal risk factors, MAP, PlGF and sFlt-1 (triple test), the detection rate at a 10% false-positive rate was 79% (95% CI, 76-82%) and the results were consistent with the data used for developing the algorithm. Addition of UtA-PI did not improve the prediction provided by the triple test. The AUC for the triple test was 0.923 (95% CI, 0.913-0.932), demonstrating very high discrimination between affected and unaffected pregnancies. Similarly, the calibration slope was 0.875 (95% CI, 0.831-0.919), demonstrating good agreement between the predicted risk and observed incidence of PE.CONCLUSION: The competing-risks model provides an effective and reproducible method for third-trimester prediction of term PE. © 2021 International Society of Ultrasound in Obstetrics and Gynecology.

U2 - 10.1002/uog.24789

DO - 10.1002/uog.24789

M3 - SCORING: Journal article

C2 - 34580947

VL - 59

SP - 69

EP - 75

JO - ULTRASOUND OBST GYN

JF - ULTRASOUND OBST GYN

SN - 0960-7692

IS - 1

ER -