主持海报会议II:流行病学和公共卫生

K. Ueshima, K. Oba, A. Fujimoto, T. Ogihara, T. Saruta, K. Nakao, F. Farahati
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引用次数: 0

摘要

高敏感性c -反应蛋白(hsCRP)是炎症的标志物,被发现是心血管疾病(CVD)的重要预测因子。代谢综合征和腹部肥胖与动脉粥样硬化的早期和更严重的表现有关。目的:评价10岁以下儿童hsCRP水平与超重/肥胖状况、心血管参数及其他危险因素的关系。研究对象和方法:168名平均年龄8.1 - 1.2岁的健康儿童(男78名,女90名),根据体重指数(BMI)、国际参考(Cole, 2000)和腰围(WC)分为正常(NW, 31.5%)、超重(OW, 27.4%)和肥胖(OB, 41.1%) 3组。测量他们的血压(BP)和心率(HR),并进行空腹血糖(BG)、免疫反应性胰岛素(IRI)、血脂、肝酶、hsCRP和其他促炎和激素标志物的血液检测。HOMA-IR按标准公式计算。由于分布偏倚,在适当的地方对hsCRP、BMI和其他变量的数据进行对数变换。结果:OB组儿童的hsCRP为7.53 0.91(平均SE), OW组为4.11 0.9 (p1⁄40.029),NW组为3.17 0.88 mg/l (p1⁄40.001),差异无统计学意义。炎症指标随BMI和wc呈显著的线性增加。hsCRP与IRI (r1⁄40.237,p1⁄4 0.004)、HOMAIR (r1⁄40.279,p1⁄40.001)、收缩压(r1⁄40.396,p<0.0001)和舒张压(r1⁄40.299,p<0.0001)呈正相关,与hdl -胆固醇(r1⁄4-0.202,p1⁄40.013)呈负相关。在多变量线性回归模型中,调整年龄、性别、BMI、出生体重、BG、HOMA-IR后,hsCRP每WC四分位数增加1.84 mg/l (95%CI1 / 41.5 -2.26, p<0.0001)。对于BMI,在单因素分析中存在的与hsCRP关系的显著性在多因素模型中调整WC后消失。结论:健康超重和肥胖儿童在青春期前hsCRP升高。它与高血压和其他心血管疾病的重要危险因素相关。在这个年龄段,腰围比BMI更能预测hsCRP水平。通过控制体重来预防心血管疾病必须在生命早期就开始。
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Moderated Poster Session II: Epidemiology and public health
P22 C-reactive protein in prepubertal children with abdominal obesity as a marker of cardiovascular and metabolic risk S Galcheva, Y Yotov, V Iotova Medical University, Varna, Bulgaria Topic: Risk factors and risk prediction High sensitivity C-reactive protein (hsCRP) is a marker of inflammation and is found to be a significant predictor of cardiovascular diseases (CVD). Metabolic syndrome and abdominal obesity are associated with earlier and more severe presentation of atherosclerosis. Aim: To evaluate the level of hsCRP in children aged below 10 years according to overweight/ obesity status and in relation to cardiovascular parameters and other risk factors. Participants and methods:We evaluated 168 healthy children (78 boys and 90 girls) at the mean age 8.1 1.2 years divided in three groups normal (NW, 31.5%), overweight (OW, 27.4%) or obese (OB, 41.1%) according to bodymass index (BMI) international reference (Cole, 2000) and waist circumference (WC). Their blood pressure (BP) and heart rate (HR) were measured and blood tests for fasting blood glucose (BG), immunoreactive insulin (IRI), lipids, liver enzymes, hsCRP, and other proinflammatory and hormonal markers were drawn. HOMA-IR was calculated according to the standard formula. Log transformation of data for the hsCRP, BMI and other variables was performed where appropriate because of skewed distribution. Results: The hsCRP was significantly higher in the OB 7.53 0.91 (mean SE) compared with the OW 4.11 0.9 (p1⁄40.029) and NW 3.17 0.88 mg/l (p1⁄40.001) children, without important gender differences. The inflammation marker displayed significant linear increase with both BMI andWC. The hsCRP was positively correlated with IRI (r1⁄40.237, p1⁄4 0.004), with HOMAIR (r1⁄40.279, p1⁄40.001), with systolic BP (r1⁄40.396, p<0.0001) and diastolic BP (r1⁄40.299, p <0.0001), and negatively with HDL-cholesterol (r1⁄4-0.202, p1⁄40.013). In multivariable linear regression model, the hsCRP increased with 1.84 mg/l (95%CI1⁄41.50-2.26, p<0.0001) per WC quartile after adjustment for age, gender, BMI, birth weight, BG, HOMA-IR. For BMI, the significance of the relation with hsCRP which was present in the univariate analysis disappeared after adjusting for WC in the multivariate model. Conclusions: The hsCRP is elevated in healthy overweight and obese children already in prepuberty. It correlates with higher BP and other important risk factors for CVD. At this age, waist circumference is a better predictor of the hsCRP levels than is BMI. The prevention of CVD through weight control has to start early in life.
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