Associations between placental pathology and poor intrauterine growth among a cohort of mother–infant singleton pairs in Leyte, the Philippines

Author:

Colt Susannah12,Barry Christopher V.1,Sagliba Marianne J.3,Amoylen Amabelle J.3,Tallo Veronica3,Friedman Jennifer F.12,Gundogan Fusun4,McDonald Emily A.12

Affiliation:

1. Center for International Health Research, Rhode Island Hospital The Warren Alpert Medical School of Brown University Providence Rhode Island USA

2. Department of Pediatrics The Warren Alpert Medical School of Brown University Providence Rhode Island USA

3. Research Institute of Tropical Medicine Manila Philippines

4. Department of Pathology and Laboratory Medicine The Warren Alpert Medical School of Brown University Providence Rhode Island USA

Abstract

AbstractObjectivePoor intrauterine growth has negative impacts for child growth and development and disproportionately affects children living in low‐resource settings. In the present study, we investigated relationships between placental pathologies and indicators of poor intrauterine growth.MethodsWe enrolled a longitudinal cohort of 279 mother–infant pairs from Leyte, the Philippines. Placental measures included characteristics, pathological findings, and immunohistochemistry. At birth, intrauterine growth was assessed using anthropometric measures, weight‐for‐gestational age, and the clinical assessment of nutritional status score (CANSCORE) for determining fetal malnutrition. Multivariate linear regression and log‐binomial regression models were applied, controlling for potential confounding factors.ResultsMaternal vascular malperfusion (MVM) was related to reduced birthweight (P < 0.0001), birth length (P = 0.002), head circumference (P = 0.001), and weight‐to‐length ratio (P = 0.016). MVM increased the risk for preterm delivery (P = 0.0005) and small for gestational age (SGA) (P = 0.016). Acute chorioamnionitis (P = 0.013) and MVM (P = 0.021) both led to an increased risk for fetal malnutrition defined by CANSORE<25. Villous tissue activated caspase‐3 was associated with lower birth length (P = 0.0006), higher weight‐to‐length ratio (P = 0.004), reduced risks for SGA (P = 0.011) and low weight‐to‐length ratio for gestational age (P = 0.004).ConclusionThe present study applied comprehensive measures for intrauterine growth and demonstrates that low placental weight and placental pathology, chiefly MVM, contribute to poor intrauterine growth. A better understanding of the mechanistic role of specific placental pathologies on adverse newborn outcomes will provide opportunities for reducing incidence of poor intrauterine growth and associated long‐term morbidities.

Funder

Division of Microbiology and Infectious Diseases, National Institute of Allergy and Infectious Diseases

Publisher

Wiley

Subject

Obstetrics and Gynecology,General Medicine

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