Serum soluble-fms-like tyrosine kinase 1-to-placental growth factor ratio on Elecsys immunoassay platform predicts preeclampsia with severe features in hospitalized women with hypertensive disorders of pregnancy
Year: 2025
Type: article
Abstract: BACKGROUND: Previous single-center studies conducted in the United States in women with suspected preeclampsia indicated that serum soluble fms-like tyrosine kinase 1-to-placental growth factor ratio values of >38 measured on a widely available Elecsys immunoassay platform during the third trimester of pregnancy predicted the development of preeclampsia with severe features and adverse outcomes within 2 weeks of testing. OBJECTIVE: This study aimed to validate the Elecsys soluble fms-like tyrosine kinase 1-to-placental growth factor ratio test for the prediction of preeclampsia with severe features in a United States population using the prospective Preeclampsia Risk Assessment: Evaluation of Cut-offs to Improve Stratification cohort that recruited women with a hypertensive disorder of pregnancy (gestational hypertension, chronic hypertension, de novo and superimposed preeclampsia) across 18 tertiary and community hospitals throughout the United States. STUDY DESIGN: We measured soluble fms-like tyrosine kinase 1-to-placental growth factor ratios using the Elecsys platform in archived serum samples from the Preeclampsia Risk Assessment: Evaluation of Cut-offs to Improve Stratification study that recruited hospitalized women with a hypertensive disorder of pregnancy between 23 0/7 and 34 6/7 weeks of gestation. The primary study outcome was prediction of preeclampsia with severe features within 2 weeks after testing. The secondary outcomes included a composite of adverse maternal and fetal/neonatal outcomes and prediction of delivery within 2 weeks. RESULTS: In the validation cohort of the Preeclampsia Risk Assessment: Evaluation of Cut-offs to Improve Stratification study (556 enrollments), the serum soluble fms-like tyrosine kinase 1-to-placental growth factor ratio at a cutoff value of >38 demonstrated a 67% positive predictive value (95% confidence interval, 61-73) and a 95% negative predictive value (95% confidence interval, 92-97) for the progression to preeclampsia with severe features within 2 weeks. Among women at <30 weeks of gestation (n=188), serum soluble fms-like tyrosine kinase 1-to-placental growth factor ratio at a cutoff value of >38 demonstrated a 78% positive predictive value (95% confidence interval, 68-86) and a 100% negative predictive value (95% confidence interval, 96-100) for the progression to preeclampsia with severe features within 2 weeks. The Elecsys soluble fms-like tyrosine kinase 1-to-placental growth factor ratio test performed better than standard-of-care clinical measures, with an area under the receiver operating characteristic curve of 0.92 (95% confidence interval, 0.89-0.90) for soluble fms-like tyrosine kinase 1-to-placental growth factor ratio vs <0.70 for standard-of-care tests, such as liver enzymes, platelet count, and serum creatinine (P<.001). Compared with women with a ratio of ≤38, those with a ratio of >38 had a higher risk of developing adverse maternal (relative risk, 4.9 [95% confidence interval, 2.6-9.9]; P<.001) and fetal/neonatal (relative risk, 3.2 [95% confidence interval, 2.6-4.0]; P<.001) outcomes and were more likely to deliver within 2 weeks (adjusted hazard ratio, 3.3 [95% confidence interval, 2.7-4.0]; P<.001). CONCLUSION: The soluble fms-like tyrosine kinase 1-to-placental growth factor ratio of >38 measured on the Elecsys platform predicted the development of preeclampsia with severe features, delivery, and adverse maternal and fetal/neonatal outcomes within 2 weeks of testing among preterm pregnant women hospitalized with a hypertensive disorder of pregnancy.
Authors: Anders H. Berg, Vinicius F. Calsavara, Martin Hund, Ge Guo, Sarosh Rana, Maged M. Costantine, Jimmy Espinoza, Kim Boggess, Blair J. Wylie, Tiffany A. Moore Simas, Judette M. Louis, Stephanie L. Gaw, Amy Murtha, Samantha Wiegand, Yvonne Gollin, Deepjot Singh, Robert M. Silver, Danielle E. Durie, Britta Panda, Errol R. Norwitz, Irina Burd, Beth Plunkett, Rachel K. Scott, Martha Bautista, Elizabeth Lemoine, Sarah Kilpatrick, Ravi Thadhani, S. Ananth Karumanchi
Institutions: Cedars-Sinai Medical Center, Roche (Switzerland), Roche Diagnostics International AG (Switzerland), University of Chicago Medical Center, The Ohio State University Wexner Medical Center, The University of Texas Health Science Center at Houston, University of North Carolina at Chapel Hill, Beth Israel Deaconess Medical Center, Columbia University, University of Massachusetts Chan Medical School, UMass Memorial Medical Center, University of South Florida, University of California, San Francisco, Rutgers, The State University of New Jersey, Miami Valley Hospital, Sharp Mary Birch Hospital for Women & Newborns, Torrance Memorial Medical Center, University of Utah, Lehigh Valley Health Network, Tufts Medical Center, Newton Wellesley Hospital, University of Maryland, Baltimore, Endeavor Health, Wake Forest University Health Sciences, Wake Forest University, Emory University
Language: English
Subfield: Obstetrics and Gynecology
Field: Medicine
Domain: Health Sciences
Open Access status: hybrid
Estimated APC paid: $5,410
Funders: Roche, Roche Diagnostics
OpenAlex ID: W4416239357
