Prediction of preterm birth in symptomatic women using decision tree modeling for biomarkers

被引:32
作者
Hill, Jacquelyn L. [1 ]
Campbell, Karen [1 ,2 ]
Zou, Guang Yong [1 ]
Challis, John R. G. [6 ,7 ]
Reid, Gregor [3 ,4 ,5 ]
Chisaka, Hiroshi [6 ,7 ,8 ]
Bocking, Alan D. [6 ,7 ]
机构
[1] Univ Western Ontario, Dept Epidemiol & Biostat, London, ON N6A 3K7, Canada
[2] Univ Western Ontario, Dept Obstet & Gynaecol, London, ON N6A 3K7, Canada
[3] Univ Western Ontario, Dept Surg, London, ON N6A 3K7, Canada
[4] Univ Western Ontario, Dept Immunol & Microbiol, London, ON N6A 3K7, Canada
[5] Univ Western Ontario, Canadian R&D Ctr Probiot, Lawson Hlth Res Inst, London, ON N6A 3K7, Canada
[6] Univ Toronto, Dept Physiol, Toronto, ON, Canada
[7] Univ Toronto, Dept Obstet & Gynaecol, Toronto, ON, Canada
[8] Tohoku Univ, Grad Sch Med, Sendai, Miyagi 980, Japan
基金
加拿大健康研究院;
关键词
corticotrophin-releasing hormone; infection; preterm labor; recursive partitioning;
D O I
10.1016/j.ajog.2008.01.007
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
OBJECTIVE: The objective of the study was to use recursive partitioning (RP) to identify gestational age-specific and threshold values for infectious and endocrine biomarkers of imminent delivery. STUDY DESIGN: RP was developed using a previously collected data set and then applied to a prospectively collected cohort of women in threatened preterm labor. Predictors of preterm birth were considered, including white blood cell count (WBC), corticotrophin-releasing hormone (CRH), cortisol, and maternal age. RESULTS: At 22-27 weeks' gestation, WBC of greater than 12,000/mL was the most accurate predictor of delivery within 48 hours; at 28-31 weeks' gestation, CRH of greater than 684 pg/mL was the most accurate predictor; and at 32-26 weeks' gestation, CRH and maternal age were the most important variables. CONCLUSIONS: These results indicate that maternal WBC greater than 12,000/mL prior to 28 weeks' gestation and CRH beyond 28 weeks are the most accurate biomarkers in predicting preterm birth within 48 hours. RP assists in establishing clinically relevant and gestational age-specific threshold levels for these variables.
引用
收藏
页码:468.e1 / 468.e9
页数:7
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