Trambas Christina, Lu Zhong, Yen Tina, Sikaris Ken
1 Melbourne Pathology, Collingwood, Australia.
2 Department of Medicine, Monash University, Clayton, Australia.
Ann Clin Biochem. 2018 Mar;55(2):205-215. doi: 10.1177/0004563217701777. Epub 2017 Sep 6.
Background Biotin interference is a significant problem to which at-risk laboratories must now be attuned. We sought to systematically characterize the nature of this interference in Roche immunoassays. Methods Known concentrations of biotin were titrated into serum samples and the effects on competitive and sandwich immunoassays were analysed. The maximum and minimum concentrations examined reflect those likely to be achieved in individuals on 5 to 10 mg supplements at the lower end, and 100 to 300 mg biotin at the high end. Results A high variability in biotin tolerance was observed. Some assays, such as troponin T, TSH and antithyroid antibodies, were extremely sensitive to the lower concentrations of biotin (15.6 and 31.3 ng/mL), whereas the majority of assays were relatively resistant. At concentrations ≥500 ng/mL, all assays showed significant interference from biotin but, again, the magnitude of the interference was variable. The more sensitive assays showed profound analytical bias at biotin concentrations that occur with high-dose therapy. Conclusion Our data demonstrate high variability in biotin tolerance across Roche immunoassays. The shape of the dose-response curves provides more detailed information than the single manufacturer-quoted figure for biotin tolerance. Accordingly, these data may be used by laboratories for more accurate risk assessment in predicting the effects of biotin. Our data may also be extrapolated to guide timing of blood tests in patients on high-dose biotin therapy: it demonstrates the number of half-lives required to withhold biotin in order to decrease its concentration to below a given assay tolerance.
背景 生物素干扰是一个重要问题,现在有风险的实验室必须对此有所关注。我们试图系统地描述罗氏免疫测定中这种干扰的性质。方法 将已知浓度的生物素滴定到血清样本中,并分析其对竞争性和夹心免疫测定的影响。所检测的最大和最小浓度反映了个体在低剂量时服用5至10毫克补充剂以及高剂量时服用100至300毫克生物素可能达到的浓度。结果 观察到生物素耐受性存在高度变异性。一些检测方法,如肌钙蛋白T、促甲状腺激素和抗甲状腺抗体,对较低浓度的生物素(15.6和31.3纳克/毫升)极为敏感,而大多数检测方法则相对耐药。在浓度≥500纳克/毫升时,所有检测方法均显示出生物素的显著干扰,但干扰程度同样存在差异。更敏感的检测方法在高剂量治疗时出现的生物素浓度下显示出严重的分析偏差。结论 我们的数据表明罗氏免疫测定中生物素耐受性存在高度变异性。剂量反应曲线的形状比单一制造商引用的生物素耐受性数值提供了更详细的信息。因此,实验室可以使用这些数据进行更准确的风险评估,以预测生物素的影响。我们的数据还可以外推,以指导高剂量生物素治疗患者的血液检测时间:它显示了为将生物素浓度降至给定检测耐受性以下而需要停用生物素的半衰期数量。