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Updated: Jul 31, 2026

Isolation of Leukocytes from the Human Maternal-fetal Interface
Published on: May 21, 2015
Amniotic fluid granulocyte colony stimulating factor levels: a rapid marker for diagnosing chorioamnionitis
I A Hoskins1, P Zandieh, F Schatz
1Department of Obstetrics and Gynecology, New York University Medical Center, NY 10016, USA.
Amniotic fluid granulocyte colony-stimulating factor (G-CSF) levels are elevated in chorioamnionitis (CAM). Elevated AF G-CSF is a reliable predictor of CAM, outperforming other diagnostic tests.
Area of Science:
- Obstetrics and Gynecology
- Neonatal Medicine
- Infectious Diseases
Background:
- Chorioamnionitis (CAM) is an infection of the amniotic fluid and membranes.
- Accurate and rapid diagnosis of CAM is crucial for maternal and fetal outcomes.
- Current diagnostic methods for CAM have limitations in sensitivity and specificity.
Purpose of the Study:
- To evaluate the diagnostic utility of amniotic fluid (AF) granulocyte colony-stimulating factor (G-CSF) levels for chorioamnionitis (CAM).
- To compare the effectiveness of AF G-CSF with existing clinical and laboratory markers for CAM diagnosis.
Main Methods:
- AF samples were collected from term and preterm patients with and without CAM.
- Patients with other infections were excluded.
- AF G-CSF levels were measured and compared with maternal fever, leukocytosis, AF glucose, white blood cell count, Gram stain, and cultures.
Main Results:
- AF G-CSF levels were significantly higher in patients with CAM (1600-14,000 pg/ml) compared to uninfected controls (400-1600 pg/ml).
- Using a cutoff of 2000 pg/ml, AF G-CSF demonstrated 67% sensitivity, 100% specificity, and 100% positive predictive value for CAM.
- AF G-CSF showed high sensitivity, specificity, and predictive values, outperforming other individual diagnostic parameters.
Conclusions:
- Elevated amniotic fluid G-CSF levels are indicative of chorioamnionitis.
- An AF G-CSF level exceeding 2000 pg/ml is a strong positive predictor of CAM.
- AF G-CSF appears to be a more reliable marker for predicting CAM than currently used single clinical or laboratory tests.
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