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Breastfeeding in infancy is not associated with inflammatory status in healthy adolescents
Caroline M P Vérier1, Alain Duhamel, Laurent Béghin
1Inserm U995, IFR114, Department of Paediatrics, Faculty of Medicine, University of Lille 2, Lille 59037, France.
Insights
Breast-feeding (BF) was not associated with reduced inflammation markers in healthy adolescents. Potential cardiovascular benefits of BF may involve other mechanisms or manifest later in life.
Area of Science:
- Pediatrics
- Cardiovascular Health
- Immunology
Background:
- Breast-feeding (BF) may reduce adult cardiovascular disease (CVD) risk.
- Low-grade inflammation is linked to increased CVD risk, even in children.
- Adolescent inflammatory status may predict future cardiovascular health.
Purpose of the Study:
- To investigate the effect of breast-feeding (BF) on inflammatory markers in healthy adolescents.
- To determine if BF influences the low-grade inflammation associated with CVD risk.
Main Methods:
- Study included 484 healthy European adolescents from the Healthy Lifestyle in Europe by Nutrition and Adolescence study.
- BF duration data collected from parental records.
- Measured serum inflammatory markers: hs-CRP, complement factors, ceruloplasmin, adhesion molecules, cytokines, TGFβ1, WBC.
- Propensity score analysis adjusted for confounding factors.
Main Results:
- No significant association found between breast-feeding (BF) and measured inflammatory markers.
- Inflammatory status in healthy adolescents was not modulated by BF duration.
- Results suggest BF's cardiovascular benefits may not be mediated by inflammation in adolescence.
Conclusions:
- Breast-feeding (BF) does not appear to impact low-grade inflammation in healthy adolescents.
- Cardiovascular benefits of BF may operate through non-inflammatory pathways or at different life stages.
- Further research should focus on high-risk groups for BF's long-term cardiovascular effects.
Abstract:
It has been suggested that breast-feeding (BF) may be associated with a decreased risk of cardiovascular disease in adulthood. A low-grade inflammation is associated with an increased risk of cardiovascular disease, even in apparently healthy children. The objective of this study was to assess the potential modulating effect of BF on the inflammatory status of healthy adolescents. Information on BF (duration) was obtained from parental records in 484 of 1040 healthy European urban adolescents (56.4% females) that had a blood sample obtained as part of the Healthy Lifestyle in Europe by Nutrition and Adolescence study. Blood serum inflammatory markers were measured, including high sensitivity C-reactive protein, complement factors 3 and 4, ceruloplasmin, adhesion molecules (L-selectin and soluble endothelial selectin, soluble vascular cell adhesion molecule 1, and intercellular adhesion molecule 1), cytokines, TGFβ1, and white blood cells. After univariate analysis, a propensity score, including the potential confounding factors, was computed and used to assess the association between BF and selected inflammatory markers. BF was not significantly associated with any of the selected inflammatory markers after adjustment for gender and propensity score. In our study, BF was not associated with low-grade inflammatory status in healthy adolescents, suggesting that the potential cardiovascular benefits of BF are related to other mechanisms than modulation of inflammation or might become relevant at a later age. Groups at high risk for cardiovascular disease should be a target for further research concerning the effects of BF.
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