Creating a placental inflammatory composite index that has a high prognostic relevance to child morbidity

J Obstet Gynaecol Res. 2017 Jul;43(7):1169-1179. doi: 10.1111/jog.13328. Epub 2017 May 31.

Abstract

Aim: Selecting pathologic measures of placental inflammation that affect pregnancy and childhood health is largely empirical. We aimed to systematically select several core inflammation-related placental measures to construct a novel placental inflammatory evaluation criterion with a high prognostic relevance to child morbidity.

Methods: We used data from the US Collaborative Perinatal Project (1959-1976), a longitudinal birth cohort study that recruited women during pregnancy and followed the children until 7 years of age. Bootstrap resampling, least absolute shrinkage and selection operator, and receiver-operator curve were used to select placental pathologic measures that were closely related to child morbidity to form a placental inflammatory composite index.

Results: Twenty-six candidate placental inflammation-related measures were ranked based on their close association with adverse neonatal outcomes. The top five placental measures were: (i) neutrophilic infiltration in umbilical artery; (ii) placental weight-birthweight ratio; (iii) necrosis in decidua capsularis; (iv) bacterial colony in epithelium of amnion; and (v) opacity of membranes and fetal surface. Several composite indexes were constructed. A five-measure composite index that had the highest prognostic relevance was chosen. Compared with subjects without any of the five abnormal measures, those with any lesion ranging from 1 to 5 had a 1.2- to 4.6-fold risk of adverse child outcomes, respectively.

Conclusion: Our composite index is simple, evidence-based, and has predictive value for child morbidity. It may be used as a novel placental inflammatory evaluation criterion.

Keywords: child morbidity; composite index; placental inflammation-related measure; prognostic relevance.

MeSH terms

  • Child
  • Child Development*
  • Cohort Studies
  • Female
  • Humans
  • Infant
  • Infant, Newborn
  • Infant, Newborn, Diseases*
  • Inflammation / diagnosis*
  • Placenta Diseases / diagnosis*
  • Pregnancy
  • Prenatal Exposure Delayed Effects*
  • Prognosis
  • Severity of Illness Index*