Abstract

BackgroundNormal and abnormal processes of pregnancy and childbirth are poorly understood. This second article in a global report explains what is known about the etiologies of preterm births and stillbirths and identifies critical gaps in knowledge. Two important concepts emerge: the continuum of pregnancy, beginning at implantation and ending with uterine involution following birth; and the multifactorial etiologies of preterm birth and stillbirth. Improved tools and data will enable discovery scientists to identify causal pathways and cost-effective interventions.Pregnancy and parturition continuumThe biological process of pregnancy and childbirth begins with implantation and, after birth, ends with the return of the uterus to its previous state. The majority of pregnancy is characterized by rapid uterine and fetal growth without contractions. Yet most research has addressed only uterine stimulation (labor) that accounts for <0.5% of pregnancy.EtiologiesThe etiologies of preterm birth and stillbirth differ by gestational age, genetics, and environmental factors. Approximately 30% of all preterm births are indicated for either maternal or fetal complications, such as maternal illness or fetal growth restriction. Commonly recognized pathways leading to preterm birth occur most often during the gestational ages indicated: (1) inflammation caused by infection (22-32 weeks); (2) decidual hemorrhage caused by uteroplacental thrombosis (early or late preterm birth); (3) stress (32-36 weeks); and (4) uterine overdistention, often caused by multiple fetuses (32-36 weeks). Other contributors include cervical insufficiency, smoking, and systemic infections. Many stillbirths have similar causes and mechanisms. About two-thirds of late fetal deaths occur during the antepartum period; the other third occur during childbirth. Intrapartum asphyxia is a leading cause of stillbirths in low- and middle-income countries.RecommendationsUtilizing new systems biology tools, opportunities now exist for researchers to investigate various pathways important to normal and abnormal pregnancies. Improved access to quality data and biological specimens are critical to advancing discovery science. Phenotypes, standardized definitions, and uniform criteria for assessing preterm birth and stillbirth outcomes are other immediate research needs.ConclusionPreterm birth and stillbirth have multifactorial etiologies. More resources must be directed toward accelerating our understanding of these complex processes, and identifying upstream and cost-effective solutions that will improve these pregnancy outcomes.

Highlights

  • Normal and abnormal processes of pregnancy and childbirth are poorly understood

  • More resources must be directed toward accelerating our understanding of these complex processes, and identifying upstream and cost-effective solutions that will improve these pregnancy outcomes

  • Involution, during which the uterus reduces in size and returns to its non-pregnant state—abnormalities in uterine involution are associated with maternal postpartum hemorrhage, a leading cause of maternal mortality globally

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Summary

Background

As succinctly stated by Romero et al, “Few biological processes as central to the survival of a species as parturition are so incompletely understood” [1]. Experimental animal models for uterine overdistension do not currently exist, and human studies have been entirely observational in nature This is a critical gap in our understanding, given the increasing prevalence of multiple gestations in HICs. Cervical insufficiency Cervical insufficiency has traditionally been associated with second trimester pregnancy losses, but recent evidence suggests that cervical disorders are associated with a wide variety of adverse pregnancy outcomes, including early preterm birth [60,61,62]. Consistent with microarray data, the majority of the SNPs associated with preterm birth are in inflammatory, apoptotic, and tissue remodeling genes [75,76] the application of systems biology, including functional genomics, transcriptomics, and SNP analysis, has contributed to a new paradigm: myometrial activation and the onset of myometrial stimulation is a highly complex genetically-controlled inflammatory process. No evidence of contribution to stillbirth/preterm birth with unknown potential for benefit

Conclusion
Findings
42. Berman SM
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