Kelly Jacalyn, Raizman Joshua E, Bevilacqua Victoria, Chan Man Khun, Chen Yunqi, Quinn Frank, Shodin Beth, Armbruster David, Adeli Khosrow
CALIPER Program, Pediatric Laboratory Medicine, The Hospital for Sick Children, University of Toronto, Toronto, ON, Canada.
Abbott Diagnostics, Abbott Park, IL, USA.
Clin Chim Acta. 2015 Oct 23;450:196-202. doi: 10.1016/j.cca.2015.08.020. Epub 2015 Aug 24.
The CALIPER program has previously reported a comprehensive database of pediatric reference intervals for 63 biochemical and immunochemical markers. Here, covariate-stratified reference intervals were determined for a number of special assays not previously reported.
A total of 1917 healthy children and adolescents were recruited and serum concentrations of 14 biochemical markers were measured using the Abbott Architect ci4100 system. Age and gender partitions were statistically determined, outliers removed and reference intervals calculated using CSLI C28-A3 guidelines.
Many analytes showed dynamic changes in concentration requiring at least 3 age partitions. Unique intervals were required within the first year of life for: pancreatic amylase, C-peptide, ceruloplasmin, insulin, β-2-microglobulin, cystatin C, dehydroepiandrosterone sulfate (DHEA-S), and α-1-glycoprotein. Cholinesterase, cholinesterase-dibucaine number, and immunoglobulin E required only 2 age partitions and α-1-antitrypsin required only one. Anti-CCP and anti-TPO levels were below the detection limit of the assay. Some analytes including insulin and DHEA-S required additional gender partitions for specific age groups.
Complex profiles were observed for endocrine and special chemistry markers, requiring establishment of age- and gender-specific reference intervals. These updated reference intervals will allow improved laboratory assessment of pediatric patients but should be validated for each analytical platform and local population as recommended by CLSI.
CALIPER项目此前报告了一个包含63种生化和免疫化学标志物的儿科参考区间综合数据库。在此,我们确定了一些此前未报告的特殊检测项目的协变量分层参考区间。
共招募了1917名健康儿童和青少年,使用雅培Architect ci4100系统测量了14种生化标志物的血清浓度。通过统计学方法确定年龄和性别分区,去除异常值,并根据临床和实验室标准协会(CSLI)C28 - A3指南计算参考区间。
许多分析物的浓度呈现动态变化,需要至少3个年龄分区。在生命的第一年,胰腺淀粉酶、C肽、铜蓝蛋白、胰岛素、β - 2微球蛋白、胱抑素C、硫酸脱氢表雄酮(DHEA - S)和α - 1糖蛋白需要独特的区间。胆碱酯酶、胆碱酯酶 - 丁卡因值和免疫球蛋白E仅需2个年龄分区,而α - 1抗胰蛋白酶仅需1个年龄分区。抗环瓜氨酸肽(anti - CCP)和抗甲状腺过氧化物酶(anti - TPO)水平低于检测限。包括胰岛素和DHEA - S在内的一些分析物在特定年龄组需要额外的性别分区。
观察到内分泌和特殊化学标志物的复杂谱型,需要建立年龄和性别特异性参考区间。这些更新的参考区间将有助于改善对儿科患者的实验室评估,但应按照CLSI的建议在每个分析平台和当地人群中进行验证。