Department of Laboratory Medicine & Pathobiology, University of Toronto, Canada.
Department of Laboratory Medicine & Pathobiology, University of Toronto, Canada; CALIPER Program, The Hospital for Sick Children, Toronto, ON, Canada.
Clin Biochem. 2023 Oct;120:110644. doi: 10.1016/j.clinbiochem.2023.110644. Epub 2023 Sep 4.
Prominent physiological changes occurring throughout childhood and adolescence necessitate the consideration of age and sex in biomarker interpretation. Critical gaps exist in pediatric reference intervals (RIs) for specialized endocrine markers, despite expected influence of growth and development. The current study aimed to establish and/or verify RIs for six specialized endocrine markers on a specialized immunoassay system.
Samples were collected from healthy children and adolescents (5 to <19 years) and apparently healthy outpatients (0 to <5 years) as part of the Canadian Laboratory Initiative on Pediatric Reference Intervals (CALIPER). Serum samples were analysed for aldosterone, renin (plasma), thyroglobulin, anti-thyroglobulin, growth hormone, and insulin-like growth factor-1 (IGF-1) on the Liaison XL (DiaSorin) immunoassay platform. RIs (2.5th and 97.5th percentiles) were established for aldosterone, renin, thyroglobulin, anti-thyroglobulin, and growth hormone. Manufacturer-recommended pediatric RIs for IGF-1 were verified.
Age-specific RIs were established for aldosterone, renin, and thyroglobulin, while no age-specific differences were observed for anti-thyroglobulin or growth hormone. IGF-1 was the only endocrine marker studied that demonstrated significant sex-specific differences. Manufacturer-recommended IGF-1 RIs were verified for children aged 6 to <19 years, while those for children aged 0 to <6 years did not verify.
This study marks the first time that pediatric RIs for aldosterone and renin were established in the CALIPER cohort and highlights the dynamic changes that occur in water and sodium homeostasis during the first years of life. Overall, these data will assist pediatric clinical laboratories in test result interpretation and improve clinical decision-making for patients tested using Liaison immunoassays.
儿童和青少年期会发生显著的生理变化,因此在解读生物标志物时必须考虑年龄和性别因素。尽管生长和发育会对其产生影响,但专门的内分泌标志物在儿科参考区间(RI)方面仍存在很大空白。本研究旨在建立和/或验证特定免疫分析系统上的六种专门内分泌标志物的 RI。
作为加拿大儿科参考区间实验室倡议(CALIPER)的一部分,从健康儿童和青少年(5 岁至<19 岁)以及明显健康的门诊患者(0 岁至<5 岁)中采集样本。使用 Liaison XL(DiaSorin)免疫分析平台对血清样本进行醛固酮、肾素(血浆)、甲状腺球蛋白、抗甲状腺球蛋白、生长激素和胰岛素样生长因子-1(IGF-1)分析。建立了醛固酮、肾素、甲状腺球蛋白、抗甲状腺球蛋白和生长激素的 RI(2.5 百分位和 97.5 百分位)。验证了 IGF-1 的制造商推荐的儿科 RI。
建立了年龄特异性的醛固酮、肾素和甲状腺球蛋白 RI,而抗甲状腺球蛋白或生长激素则没有观察到年龄特异性差异。在所研究的内分泌标志物中,只有 IGF-1 表现出显著的性别特异性差异。制造商推荐的 6 至<19 岁儿童的 IGF-1 RI 得到验证,而 0 至<6 岁儿童的 IGF-1 RI 则没有得到验证。
本研究首次在 CALIPER 队列中建立了儿童醛固酮和肾素的儿科 RI,并强调了生命最初几年水和钠平衡中发生的动态变化。总体而言,这些数据将有助于儿科临床实验室对检验结果进行解读,并为使用 Liaison 免疫分析法进行检测的患者改善临床决策。