Biological variations of seven tumor markers

烯醇化酶 癌胚抗原 置信区间 内科学 肿瘤标志物 变异系数 胃肠病学 医学 病理 肿瘤科 化学 免疫组织化学 癌症 色谱法
作者
Zhihong Qi,Lin Zhang,Yu Chen,Xin‐Ming Ma,Xuehui Gao,Juan Du,Fang Zhang,Xinqi Cheng,Wei Cui
出处
期刊:Clinica Chimica Acta [Elsevier BV]
卷期号:450: 233-236 被引量:22
标识
DOI:10.1016/j.cca.2015.08.026
摘要

We sought to identify biological variations in the following tumor markers: pepsinogen I (PGI), pepsinogen II (PGII), carbohydrate antigen 724 (CA724), neuron-specific enolase (NSE), pro-gastrin-releasing peptide (ProGRP), carcinoembryonic antigen (CEA), and carbohydrate antigen 199 (CA199). Serum samples were collected from 20 healthy Chinese individuals over 5 days. Samples were then screened for the presence of the seven aforementioned tumor markers. Within-individual coefficient of variation (CVI), between-individual coefficient of variation (CVG), confidence interval (CI) of biological variations, index of individuality (II), and the reference change value (RCV) of the seven tumor markers were calculated. Of the 7 tumor markers, index of individuality was all < 1.0. ProGRP showed the lowest CVI and CVG, at 4.75% (CI: 3.96%–5.94%) and 16.42% (CI: 12.32%‐24.61%), respectively. The 95% and 99% RCVs for ProGRP were 14.68 and 19.32, respectively, and were the lowest of the markers. In contrast, the CVI and CVG for CA724 were the highest, at 16.06% (CI: 13.83%–19.17%) and 96.95% (CI: 73.73%–141.59%), respectively. The 95% and 99% RCVs for CA724 were the highest, at 45.89 and 60.41, respectively. Our findings provide additional information regarding the biological variation of tumor markers, and could be applied in a clinical setting.
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