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Published on: August 7, 2017
Progression of C-reactive protein from birth through preadolescence varies by mode of delivery
Alexandra R Sitarik1, Christine C Johnson1, Albert M Levin1
1Department of Public Health Sciences, Henry Ford Health, Detroit, MI, United States.
Insights
Planned C-sections are linked to higher childhood inflammation and BMI, unlike emergency C-sections. Experiencing labor may reduce long-term chronic disease risk by lowering systemic inflammation.
Area of Science:
- Pediatric chronic disease
- Inflammation markers
- Birth outcomes
Background:
- Caesarean section (C-section) delivery is associated with increased childhood chronic disease risk, potentially due to systemic inflammation.
- Specific C-section types may have differential impacts, with emergency C-sections often involving labor or membrane rupture.
Purpose of the Study:
- To investigate the association between delivery mode and longitudinal high-sensitivity C-reactive protein (hs-CRP) profiles from birth to preadolescence.
- To determine if hs-CRP mediates the relationship between delivery mode and preadolescent body mass index (BMI).
Main Methods:
- Analysis of data from the WHEALS birth cohort (N=564).
- Longitudinal plasma hs-CRP levels measured from birth through 10 years of age.
- Growth mixture models (GMMs) used to identify hs-CRP trajectories; Poisson regression for risk ratios.
Main Results:
- Two hs-CRP trajectories identified: low (76%) and high/increasing (24%).
- Planned C-section delivery increased the risk of high hs-CRP trajectory (RR=1.15, p=0.028) compared to vaginal delivery.
- No association found for unplanned C-section; hs-CRP class mediated 43.4% of the planned C-section effect on BMI z-score at age 10.
Conclusions:
- Experiencing labor may lead to lower childhood systemic inflammation and reduced preadolescent BMI.
- Findings suggest potential benefits of labor for mitigating long-term chronic disease development.
- Mode of delivery and labor experience may influence inflammatory pathways impacting childhood health outcomes.
Introduction:
Delivery via caesarean section (C-section) has been associated with an increased risk of childhood chronic diseases such as obesity and asthma, which may be due to underlying systemic inflammation. However, the impact of specific C-section types may be differential, as emergency C-sections typically involve partial labor and/or membrane rupture. Our objectives were to determine if mode of delivery associates with longitudinal profiles of high sensitivity CRP (hs-CRP) -a marker of systemic inflammation-from birth through preadolescence, and to examine if CRP mediates the association between mode of delivery and preadolescent body mass index (BMI).
Methods:
Data from the WHEALS birth cohort (N = 1,258) were analyzed; 564 of the 1,258 children in the cohort had data available for analysis. Longitudinal plasma samples (birth through 10-years of age) from 564 children from were assayed for hs-CRP levels. Maternal medical records were abstracted to obtain mode of delivery. Growth mixture models (GMMs) were used to determine classes of hs-CRP trajectories. Poisson regression with robust error variance was used to calculate risk ratios (RRs).
Results:
Two hs-CRP trajectory classes were identified: class 1 (76% of children) was characterized by low hs-CRP, while class 2 (24% of children) was characterized by high and steadily increasing hs-CRP. In multivariable models, children delivered via planned C-section had 1.15 times higher risk of being in hs-CRP class 2, compared to vaginal deliveries (p = 0.028), while no association was found for unplanned C-section deliveries [RR (95% CI) = 0.96 (0.84, 1.09); p = 0.49]. Further, the effect of planned C-section on BMI z-score at age 10 was significantly mediated by hs-CRP class (percent mediated = 43.4%).
Conclusions:
These findings suggest potentially beneficial effects of experiencing partial or full labor, leading to a lower trajectory of systemic inflammation throughout childhood and decreased BMI during preadolescence. These findings may have implications for chronic disease development later in life.
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