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Biological indicators of the in-utero environment and their association with birth weight for gestational age
N M Talge1, C Holzman1, P K Senagore2
11Department of Epidemiology, Michigan State University, East Lansing, MI, USA.
Insights
Birth weight for gestational age (BW/GA) is linked to health risks. This study found associations between lower BW/GA z-scores and conditions like preeclampsia and placental pathology, offering insights into pregnancy complications.
Area of Science:
- Perinatal Medicine
- Reproductive Biology
- Maternal-Fetal Medicine
Background:
- Birth weight for gestational age (BW/GA) is a critical indicator of infant health, associated with various adverse postnatal outcomes.
- Existing research often examines pregnancy complications, maternal biomarkers, and placental pathology in isolation, limiting understanding of their interplay and relation to the full BW/GA spectrum.
- Elucidating these relationships is crucial for understanding variations in postnatal health across the BW/GA continuum.
Purpose of the Study:
- To investigate the associations between birth weight for gestational age (BW/GA) and a range of biological and clinical indicators of pregnancy complications.
- To explore the overlap between obstetric complications, maternal serum biomarkers, and placental pathology in relation to the entire BW/GA distribution, not just extremes.
- To identify factors that may mediate or mark risk in the association between BW/GA and postnatal health outcomes.
Main Methods:
- Analysis of data from 1371 women in the Pregnancy Outcomes and Community Health Study.
- Examination of BW/GA z-scores in relation to obstetric complications, second-trimester maternal serum screening results (alpha-fetoprotein, unconjugated estriol), and placental histology.
- Inclusion of maternal demographics, anthropometrics, and substance use in adjusted statistical models.
Main Results:
- Adjusted models revealed significant associations between reduced BW/GA z-scores and preeclampsia (β = -0.70), elevated maternal serum alpha-fetoprotein (β = -0.28), elevated unconjugated estriol (β = -0.31), and obstructive vascular pathology in the placenta (β = -0.46).
- These associations remained consistent even when excluding preterm, small-for-gestational age, or large-for-gestational age infants.
- The findings highlight specific biological and pathological markers linked to variations in BW/GA across the continuum.
Conclusions:
- Specific pregnancy complications, maternal serum markers, and placental pathology are associated with lower birth weight for gestational age z-scores.
- These factors may play a role in mediating or marking the risk associated with BW/GA variations.
- Further research is warranted to understand the direct mechanisms linking these factors to BW/GA and subsequent health outcomes.
Abstract:
Birth weight for gestational age (BW/GA) has been associated with a risk of adverse health outcomes. Biological indices of pregnancy complications, maternal mid-pregnancy serum biomarkers and placental pathology may shed light on these associations, but at present, they are most often examined as single entities and offer little insight about overlap. In addition, these indices are typically assessed in relation to the extremes of the BW/GA distribution, leaving open the question of how they relate to the entire BW/GA distribution. Addressing issues such as these may help elucidate why postnatal health outcomes vary across the BW/GA continuum. In this study, we focused on a subset of women who participated in the Pregnancy Outcomes and Community Health Study (n = 1371). We examined BW/GA (i.e. gestational age and sex-referenced z-scores) in relation to obstetric complications, second trimester maternal serum screening results and histologic evidence of placental pathology along with maternal demographics, anthropometrics and substance use. In adjusted models, mean reductions in BW/GA z-scores were associated with preeclampsia (β = -0.70, 95% CI -1.04, -0.36), high maternal serum alpha fetoprotein (β = -0.28, 95% CI -0.43, -0.13), unconjugated estriol (β = -0.31/0.5 multiples of the median decrease, 95% CI -0.41, -0.21) and high levels of maternal obstructive vascular pathology in the placenta (β = -0.46, 95% CI -0.67, -0.25). The findings were similar when preterm infants, small-for-gestational age or large-for-gestational age infants were excluded. More research is needed to examine how the factors studied here might directly mediate or mark risk when evaluating the associations between BW/GA and postnatal health outcomes.
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