ArticleJAMA network open2026
Maternal Circulating sFlt-1:PlGF Ratio and Stillbirth.
Article in JAMA network open, 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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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
1 citing paper in PubMed.
- Independent Predictors of Major Adverse Cardiac and Hepatic Outcomes Following Acute Liver Complications of Pregnancy; A Retrospective Cohort Study.Archives of academic emergency medicine · 2026Article
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3 authors.
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Abstract
Importance: Stillbirth remains a major global health challenge, particularly in low- and middle-income countries. Angiogenic imbalance, characterized by elevated soluble fms-like tyrosine kinase-1 (sFlt-1) and reduced placental growth factor (PlGF), is implicated in placental dysfunction, yet few studies have examined the association between the sFlt-1:PlGF ratio and stillbirth. Objective: To investigate the association between maternal circulating sFlt-1:PlGF ratio, using clinically relevant cutoffs, and risk of stillbirth. Design, Setting, and Participants: This case-control study included participants from 2 health clinics operated by the Dhaka Community Hospital Trust in rural Bangladesh. Pregnant women aged 18 years or older with ultrasonography-confirmed singleton pregnancies were enrolled before or at 16 weeks' gestation between March 1, 2008, and July 30, 2011. Those delivering stillborn infants (cases) were matched 1:2 with participants in the same cohort who delivered full-term live-born infants (controls). Data were analyzed between September 1, 2025, and January 1, 2026. Exposure: Maternal serum sFlt-1:PlGF ratio. Main Outcomes and Measures: The main outcome was stillbirth, defined as fetal death at 28 weeks' gestation or more. The association between sFlt-1:PlGF ratio cutoffs of greater than 38 and greater than 85 and stillbirth were estimated using Firth penalized logistic regression, with models adjusted using a propensity score incorporating maternal factors. Results: The analytic sample included 125 participants (mean [SD] age, 22.3 [3.8] years), of whom 39 were included in the stillbirth group and 86 in the live birth control group. After adjusting for propensity score, an sFlt-1:PlGF ratio greater than 38 was significantly associated with an increased odds of stillbirth (odds ratio [OR], 13.44; 95% CI, 2.03-88.89). Similar results were observed using the cutoff of 85 (OR, 12.95; 95% CI, 1.57-106.64). Elevated sFlt-1:PlGF ratios showed high positive predictive value for stillbirth at the cutoff of 38 (88.9%; 95% CI, 51.8%-99.7%) and 85 (85.7%; 95% CI, 42.1%-99.6%). Negative predictive values were moderate at 73.3% (95% CI, 64.3%-81.1%) and 72.0% (95% CI, 63.0%-79.9%), respectively, indicating that low ratios had a limited ability to rule out stillbirth. Conclusions and Relevance: This case-control study found that a high sFlt-1:PlGF ratio using clinically relevant thresholds was associated with stillbirth and corresponded to an estimated 13-fold increased risk. These findings suggest that angiogenic imbalance may contribute to stillbirth and highlight the potential utility of angiogenic markers as indicators of pregnancy complications in low-resource settings.
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