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Updated: Jun 18, 2025

A Murine Model of Fetal Exposure to Maternal Inflammation to Study the Effects of Acute Chorioamnionitis on Newborn Intestinal Development
Published on: June 24, 2020
Maternal inflammatory and microbial drivers of low birthweight in low- and middle-income countries
Jonathan Broad1,2,3, Ruairi C Robertson1,2, Ceri Evans1,2,4
1Maternal and Child Health Research Department, Zvitambo Institute for Maternal and Child Health Research, Harare, Zimbabwe.
Insights
Maternal infections and inflammation contribute to low birthweight (LBW), impacting infant health and development. Addressing these factors during pregnancy may improve birth outcomes.
Area of Science:
- Perinatology
- Maternal-Fetal Medicine
- Infectious Diseases
Background:
- Low birthweight (LBW) affects one in seven infants in low- and middle-income countries, significantly impacting short-term and long-term health.
- Antenatal exposure to microbial and inflammatory factors is a potential contributor to LBW.
Purpose of the Study:
- To evaluate the role of inflammatory, microbial, or infective causes contributing to LBW, small-for-gestational age, intra-uterine growth restriction, and prematurity.
- To synthesize existing literature on the mechanisms linking maternal infections and inflammation to adverse birth outcomes.
Main Methods:
- A comprehensive literature search was conducted in Ovid-Medline, Embase, and Cochrane databases for relevant English-language human studies.
- Inclusion criteria focused on published data, excluding conference abstracts and grey literature.
- A narrative synthesis approach was employed to analyze the findings.
Main Results:
- Local infections (e.g., vaginitis, placental infection) and distal inflammation (e.g., periodontitis, enteric dysfunction) are associated with increased risk of prematurity and reduced intrauterine growth.
- Systemic maternal infections like malaria and HIV are linked to LBW, potentially mediated by chronic inflammation and socio-economic factors.
- Antimicrobial prophylaxis showed minimal impact overall, but some positive effects on birthweight were observed in high infectious disease burden settings.
Conclusions:
- Maternal inflammatory and infective processes are identified as underlying factors for LBW, suggesting potential targets for intervention.
- Further research is crucial to elucidate the complex mechanisms and pathways involved in LBW for improved life-course health outcomes.
Background:
Low birthweight (LBW) is when an infant is born too soon or too small, and it affects one in seven infants in low- and middle-income countries. LBW has a significant impact on short-term morbidity and mortality, and it impairs long-term health and human capital. Antenatal microbial and inflammatory exposure may contribute to LBW.
Methods:
Ovid-Medline, Embase and Cochrane databases were searched for English-language articles evaluating inflammatory, microbial or infective causes of LBW, small-for-gestational age, intra-uterine growth restriction or prematurity. Inclusion criteria were human studies including published data; conference abstracts and grey literature were excluded. A narrative synthesis of the literature was conducted.
Results:
Local infections may drive the underlying causes of LBW: for example, vaginitis and placental infection are associated with a greater risk of prematurity. Distal infection and inflammatory pathways are also associated with LBW, with an association between periodontitis and preterm delivery and environmental enteric dysfunction and reduced intra-uterine growth. Systemic maternal infections such as malaria and HIV are associated with LBW, even when infants are exposed to HIV but not infected. This latter association may be driven by chronic inflammation, co-infections and socio-economic confounders. Antimicrobial prophylaxis against other bacteria in pregnancy has shown minimal impact in most trials, though positive effects on birthweight have been found in some settings with a high infectious disease burden.
Conclusion:
Maternal inflammatory and infective processes underlie LBW, and provide treatable pathways for interventions. However, an improved understanding of the mechanisms and pathways underlying LBW is needed, given the impact of LBW on life-course.
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