Division of General Pediatrics and Adolescent Medicine, Department of Pediatrics, University of North Carolina School of Medicine, Chapel Hill, NC 27599, USA.
Pediatrics. 2010 Apr;125(4):e801-9. doi: 10.1542/peds.2009-2182. Epub 2010 Mar 1.
Inflammatory markers such as C-reactive protein (CRP) are related to obesity in adults, but the association is less clear in children. Our objective was to examine relationships between multiple markers of inflammation and children's weight status; we hypothesized that the prevalence of inflammatory markers would increase as weight status increased.
We conducted a cross-sectional analysis of children in the United States aged 1 to 17 years in the National Health and Nutrition Examination Survey, 1999-2006. Children were categorized using weight-for-length when age <2 years and BMI for > or =2 years, as very obese (> or =99th percentile), obese (<99th and > or =95th percentile), overweight (<95th and > or =85th percentile), and healthy weight (>5th to < or =85th percentile) according to expert consensus. Our main outcome measures were high-sensitivity CRP and absolute neutrophil count, in addition to a novel third measure: ferritin controlled for iron status using a ferritin/transferrin ratio. We used Cox proportional hazards models to examine risk of abnormal values of inflammatory markers according to weight.
Increased risk of a CRP level of >1.0 mg/L was evident among very obese children from ages 3 to 5 years (hazard ratio [HR]: 2.29; P < .01) through 15 to 17 years (HR: 4.73; P < .01). Increased risk of abnormal neutrophil count among very obese children began at 6 to 8 years (HR: 2.00; P = .049), and increased prevalence of abnormal ferritin/transferrin ratio began at 9 to 11 years (HR: 7.06; P < .001).
Multiple inflammatory markers are strongly and positively associated with increasing weight status in children, and this relationship starts as young as age 3. Elevated inflammatory markers in very young obese children are particularly concerning, because inflammation may cause long-term, cumulative vascular damage. This deserves additional research via longitudinal design.
C 反应蛋白(CRP)等炎症标志物与成年人肥胖有关,但在儿童中其关联尚不清楚。我们的目的是研究多种炎症标志物与儿童体重状况之间的关系;我们假设随着体重状况的增加,炎症标志物的患病率将会增加。
我们对美国年龄在 1 至 17 岁的儿童进行了横断面分析,这些儿童来自于 1999 年至 2006 年的国家健康和营养检查调查。当年龄<2 岁时,根据身长体重进行分类,当年龄>2 岁时,根据 BMI 进行分类,分为极度肥胖(>或=99 百分位)、肥胖(<99 百分位且>或=95 百分位)、超重(<95 百分位且>或=85 百分位)和健康体重(>5 百分位至<或=85 百分位)。我们的主要观察指标包括高敏 CRP 和绝对中性粒细胞计数,以及一种新的第三个指标:铁蛋白,该指标使用铁蛋白/转铁蛋白比值来控制铁状态。我们使用 Cox 比例风险模型来根据体重检查炎症标志物异常值的风险。
在 3 至 5 岁(风险比[HR]:2.29;P<.01)到 15 至 17 岁(HR:4.73;P<.01)的极度肥胖儿童中,CRP 水平>1.0mg/L 的风险明显增加。在极度肥胖儿童中,异常中性粒细胞计数的风险从 6 至 8 岁开始增加(HR:2.00;P=0.049),异常铁蛋白/转铁蛋白比值的患病率从 9 至 11 岁开始增加(HR:7.06;P<.001)。
在儿童中,多种炎症标志物与体重状况呈强烈的正相关,这种关系从 3 岁就开始了。非常年幼的肥胖儿童中升高的炎症标志物尤其令人担忧,因为炎症可能导致长期的、累积性的血管损伤。这需要通过纵向设计进行更多的研究。