CALIPER program, Department of Pediatric Laboratory Medicine, The Hospital for Sick Children, Toronto, Ontario, Canada;
Clin Chem. 2014 Mar;60(3):518-29. doi: 10.1373/clinchem.2013.214312. Epub 2013 Dec 23.
Studies of biological variation provide insight into the physiological changes that occur within and between study participants. Values obtained from such investigations are important for patient monitoring and for establishing quality specifications. In this study we evaluated the short-term biological variation of 38 chemistry, lipid, enzyme, and protein analytes in a pediatric population, assessed the effect of age partitions on interindividual variation, and compared the findings to adult values.
Four plasma samples each were obtained within 8 h from 29 healthy children (45% males), age 4-18 years. Samples were stored at -80 °C and analyzed in 3 batches, with samples from 9-10 study participants per batch. Within-person and between-person biological variation values were established using nested ANOVA after exclusion of outliers by use of the Tukey outlier test. Analytical quality specifications were established with the Fraser method.
Biological variation coefficients and analytical goals were established for 38 analytes. Age partitioning was required for 6 analytes. Biological variation characteristics of 14 assays (37%) were distinct from adult values found in the Westgard database on biological variation. Biological variation characteristics were established for 2 previously unreported analytes, unconjugated bilirubin and soluble transferrin receptor.
This study is the first to examine biological variation and to establish analytical quality specifications on the basis of biological variation for common assays in a pediatric population. These results provide insight into pediatric physiology, are of use for reference change value calculations, clarify the appropriateness of reference interval use, and aid in the development of quality management strategies specific to pediatric laboratories.
生物学变异研究提供了对研究参与者体内和个体间发生的生理变化的深入了解。此类研究获得的值对于患者监测和建立质量规范非常重要。在这项研究中,我们评估了儿童人群中 38 种化学、脂质、酶和蛋白质分析物的短期生物学变异,评估了年龄分区对个体间变异的影响,并将研究结果与成人值进行了比较。
从 29 名健康儿童(45%为男性)中在 8 小时内采集了 4 份血浆样本,年龄为 4-18 岁。将样本储存在-80°C 下,并分 3 批进行分析,每批有 9-10 名研究参与者的样本。通过 Tukey 异常值检验排除离群值后,使用嵌套 ANOVA 确定个体内和个体间生物学变异值。使用 Fraser 方法建立分析质量规范。
为 38 种分析物建立了生物学变异系数和分析目标。需要对 6 种分析物进行年龄分区。14 种测定法(37%)的生物学变异特征与 Westgard 数据库中关于生物学变异的成人值不同。为 2 种以前未报告的分析物,即未结合胆红素和可溶性转铁蛋白受体,建立了生物学变异特征。
这是第一项针对儿童人群中常见测定法基于生物学变异进行生物学变异研究和建立分析质量规范的研究。这些结果深入了解了儿科生理学,有助于参考变化值的计算,阐明了参考区间使用的适当性,并有助于制定针对儿科实验室的质量管理策略。