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首页> 外文期刊>Journal of developmental origins of health and disease >Caesarean delivery, immune function and inflammation in early life among Ecuadorian infants and young children
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Caesarean delivery, immune function and inflammation in early life among Ecuadorian infants and young children

机译:厄瓜多尔婴儿和幼儿早期生活中的剖腹产,免疫功能和炎症

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Caesarean delivery has been linked to a number of inflammatory conditions in childhood and adolescence. Yet the mechanisms underlying these associations and their generalizability across contexts with different postnatal feeding and pathogenic exposures remain unclear. This study tests the association between delivery type and three measures of immune function, inflammation, morbidity and leukocyte proportions, in Ecuadorian infants and children aged 6 months to 2 years. Data were collected from mother–child pairs participating in a nationally representative health and nutrition survey Encuesta Nacional de Salud y Nutricion (ENSANUT-ECU) conducted in 2012. The analytic sample includes 828 mothers and infants with delivery information and measured biomarkers. Poisson regression models were used to examine the association between delivery type and markers of immune function, controlling for maternal and infant characteristics, including age, sex, sociodemographic characteristics and medical indications. 40.8% (n=338) of sample infants and children were delivered by caesarean. Compared to those born vaginally, infants born by caesarean were less likely to have elevated C-reactive protein (CRP) [CRP>2 mg/l; risk ratio (RR): 0.76, 95% confidence interval (CI): 0.58–1.00] and more likely to have illness symptoms (RR: 1.22, 95% CI: 1.01–1.46) and elevated basophils (RR: 1.83, 95% CI: 1.03–3.25). No other immune cell proportions differed by delivery type. The results suggest that differences in the perinatal exposures accompanying caesarean delivery may alter immune development and function, particularly in the inflammatory response to infection and in cells involved in the allergic response, across infancy and early childhood. Understanding the pathways linking perinatal exposures to immune development is important for preventing the development of inflammatory conditions.
机译:剖腹产有关儿童及青春期的许多炎症病症。然而,这些关联的机制及其在不同出生后饲养和致病曝光的上下文的概括性仍然不清楚。该研究测试了厄瓜多尔婴儿和6个月达到2年的厄瓜多尔婴儿和儿童免疫功能,炎症,发病率和白细胞比例的三种免疫功能,发病,发病率和白细胞比例之间的关联。从参与2012年进行的国家代表性健康和营养调查的母婴对中收集的数据收集了2012年进行的Nacional De Salud Y Natricion(Ensanut-ECU)。分析样品包括828名母亲和婴儿,具有递送信息和测量的生物标志物。泊松回归模型用于检查递送类型和免疫功能标志物之间的关联,控制妇幼的母婴特征,包括年龄,性别,社会渗目特征和医学适应症。剖腹产递送40.8%(n = 338)样品婴儿和儿童。与阴道出生的那些相比,由剖腹产出生的婴儿不太可能具有升高的C-反应蛋白(CRP)[CRP> 2 mg / L;风险比(RR):0.76,95%置信区间(CI):0.58-1.00]和更可能具有疾病症状(RR:1.22,95%CI:1.01-1.46)和嗜碱性粒细胞(RR:1.83,95%) CI:1.03-3.25)。没有其他免疫细胞比例通过递送类型不同。结果表明,伴随剖享物的围产期暴露的差异可能会改变免疫发育和功能,特别是在婴儿和幼儿期涉及过敏反应的炎症反应和参与过敏反应的细胞中。了解将围产期暴露的途径与免疫发育联系起来对防止炎症病症的发展是重要的。

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