| Literature DB >> 28025044 |
Zhong Zhang1, Xiaozhu Liu2, Yinfeng Li2, Ruolan Huang3, Ling Wang3, Laiqing Li4, Cuicui Chen4, Lijun Ou5, Xiao Chang3, Qiujie Qiao3, Mingtai Chen3.
Abstract
Atherosclerosis is the underlying cause of most coronary events. The conventional method for coronary atherosclerosis detection is morphological examination or coronary arterionyraphy. These methods are complex and time-consuming. In this study a two-step dual-label TRFIA was developed for the simultaneous detection of Lp-PLA2 and hsCRP in a single run. The performance of this assay was first evaluated using clinical serum samples, and then compared with commercialized kits. The sensitivity of this assay for Lp-PLA2 detection was 1ng/mL (dynamic range, 0-1000U/L), and the sensitivity for hsCRP detection was 1mg/L (dynamic range, 1-1000mg/L). High correlation coefficients (R) were obtained between the present dual-label TRFIA and commercially available kits(R=0.99 for LP-PLA2 and hsCRP). The present dual-label TRFIA has high sensitivity, specificity, and accuracy in clinical sample analysis. It is a good alternative to the single-label diagnostic methods.Entities:
Keywords: Coronary atherosclerosis; Dual-label TRFIA; LP-PLA2; hsCRP
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Year: 2016 PMID: 28025044 DOI: 10.1016/j.imlet.2016.12.004
Source DB: PubMed Journal: Immunol Lett ISSN: 0165-2478 Impact factor: 3.685