Evidence map›Paper›PMID 42670368›Full record

ArticleCureus2026

Predictive Value of the Soluble fms-Like Tyrosine Kinase-1/Placental Growth Factor Ratio in Preeclampsia and Placenta Accreta Spectrum: A Prospective Observational Study.

Ashima Taneja, Guntas Kaur, Surbhi Handa, Sukriti Gupta

Abstract read
In one paragraph

Article in Cureus, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Ashima TanejaDepartment of Obstetrics and Gynaecology, Dayanand Medical College and Hospital, Ludhiana, IND.
Guntas KaurDepartment of Obstetrics and Gynaecology, Dayanand Medical College and Hospital, Ludhiana, IND.
Surbhi HandaDepartment of Obstetrics and Gynaecology, Dayanand Medical College and Hospital, Ludhiana, IND.
Sukriti GuptaDepartment of Obstetrics and Gynaecology, Dayanand Medical College and Hospital, Ludhiana, IND.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCertain placentation disorders, such as preeclampsia and placenta accreta spectrum (PAS), are prevalent causes of maternal and fetal morbidity. Angiogenic biomarkers, including soluble fms-like tyrosine kinase-1 (sFlt-1), placental growth factor (PlGF), and the sFlt-1/PlGF ratio, are increasingly used in the evaluation of preeclampsia; however, their relevance in PAS remains unclear.

objectiveTo evaluate the diagnostic performance of sFlt-1, PlGF, and the sFlt-1/PlGF ratio for preeclampsia and explore their potential diagnostic utility in PAS. METHODOLOGY: This prospective observational study was conducted at a tertiary care hospital in North India from June 2024 to June 2025. A total of 200 antenatal women at 20-37 weeks of gestation were recruited and divided into three groups: preeclampsia, PAS, and a comparison group without preeclampsia or PAS. Serum levels of sFlt-1 and PlGF were determined by electrochemiluminescence immunoassay (ECL), and the ratio sFlt-1/PlGF was calculated. The optimum cutoff values were determined by the receiver operating characteristic curve, and the diagnostic performance was evaluated.

resultsOf the 200 participants, 57 (28.5%) had preeclampsia, 16 (8.0%) had PAS, and 127 (63.5%) had neither condition. At a cutoff of 77.65, the sFlt-1/PlGF ratio performed the best, with an area under the curve of 0.902 for preeclampsia, an accuracy of 88.0%, a positive predictive value (PPV) of 80.7%, a negative predictive value (NPV) of 91.3%, and a sensitivity of 80.7%. PAS had a high NPV of 97.1%, a low PPV of 18.7%, a high sensitivity of 87.5%, a low specificity of 52.0%, an accuracy of 55.9%, and an area under the curve (AUC) of 0.678.

conclusionsThe sFlt-1/PlGF ratio was an excellent discriminator of preeclampsia and could be used to help identify and stratify at-risk individuals. It is not very specific and has a low PPV in PAS, meaning that it should not be used as a surrogate for imaging-based diagnosis and clinical risk assessment in PAS.

Indexed as

angiogenic biomarkersplacenta accreta spectrumplacental growth factorpreeclampsiasoluble fms-like tyrosine kinase-1

Identifiers

PMID42670368
PMCPMC13526203

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