Comparison of Whole-Blood Sirolimus Concentrations Measured by EMIT-based Siemens Viva-ProE® System and LC-MS/MS in Chinese Transplant Patients

化学 线性回归 色谱法 治疗药物监测 组内相关 相关系数 液相色谱-质谱法 威尔科克森符号秩检验 药代动力学 质谱法 再现性 药理学 内科学 医学 统计 曼惠特尼U检验 数学
作者
Rongqi Lin,Yipeng Cai,Yingbin Huang,Xueyong Li,Yi‐Ying Chen,Bo Chen,Kaixian Lai,Junnan Wu,Yu Cheng,Maobai Liu,Yisheng Chen,Hongqiang Qiu
出处
期刊:Journal of Pharmaceutical and Biomedical Analysis [Elsevier]
卷期号:247: 116271-116271
标识
DOI:10.1016/j.jpba.2024.116271
摘要

Sirolimus (SRL) is commonly used in transplant patients to prevent organ transplant rejection. The current guidelines recommend to perform SRL therapeutic drug monitoring regularly to improve treatment outcomes and avoid adverse effects. Consequently, a precise and accurate method for determining SRL is crucial in clinical practice. Currently, liquid chromatography-tandem mass spectrometry (LC-MS/MS) and immunoassays have been widely adopted for determining SRL concentrations. However, previous studies have shown that immunoassays exhibit a positive bias compared to LC-MS/MS. As the new updated version of the EMIT-based Viva-E® System (SVPS), this study aims to compare SRL blood concentrations measured by the SVPS and LC-MS/MS. The residual whole-blood samples obtained from transplant patients were simultaneously analyzed using the SVPS and LC-MS/MS, respectively. The correlation between the two assays was analyzed using the linear regression analysis and Deming linear regression. The Pearson correlation coefficient and Intraclass correlation coefficient (ICC) analysis were executed. The Paired Wilcoxon test and Bland-Altman analysis were performed to assess the concordance between the two methods. The SVPS considerably increased SRL concentration value by 46.62 % as compared to the LC-MS/MS method. When SRL concentrations measured by the SVPS were above 4.0 ng/mL, there was no significant difference between the corrected SVPS concentrations after using the Deming linear regression equation, indicating their interchangeability. Given the significant disparities observed between EMIT and LC-MS/MS, it is crucial to indicate the methodology and instruments in both TDM reports and future clinical guidelines. Our study also provides the conversion formulas between the SVPS and LC-MS/MS, which can be applied as a reference for different clinical centers.

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