Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, United States.
Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, United States.
Clin Biochem. 2021 Jan;87:93-99. doi: 10.1016/j.clinbiochem.2020.11.007. Epub 2020 Nov 12.
Bovine alkaline phosphatase (BALP) mediated interference is a potential issue in the Beckman Access unconjugated estriol (uE3) assay. As the uE3 assay is a component of second trimester maternal serum screening characterizing this interference is essential for delivering accurate trisomy 18 and trisomy 21 risks.
Residual serum samples (n = 517) were measured by two different lots of uE3 assay. Scavenger BALP (sBALP) was added to all samples to remove potential BALP dependent interference and assessed using both lots of uE3 reagent.
BALP mediated interference was observed in similar frequency in both lots of reagent (~3%), although the patterns of positive and negative interference differed between the lots. Pretreatment with sBALP improved lot-to-lot comparison. The presence of BALP related interference was not related to the concentration of endogenous human alkaline phosphatase. The use of polyethylene glycol and sBALP treatment appeared to mitigate BALP mediated interference equally well, and resulted in concordance in measured uE3 concentrations between reagent lots. Additionally, heterophile antibody interference was observed in two samples affected with BALP interference, and the heterophile antibody interference was resolved by both PEG and heterophile antibody blocking reagent treatment, but not sBALP treatment. While the maternal screen numeric risk for affected samples changed, the risk classification changed from a negative to positive screen in two samples.
Interference in the uE3 assay has the potential to affect maternal serum risk calculations in different reagent lots, and pretreatment of samples with scavenger BALP or PEG should be considered in cases of unexplained uE3 concentrations.
牛碱性磷酸酶(BALP)介导的干扰是贝克曼 Access 未结合雌三醇(uE3)测定法的一个潜在问题。由于 uE3 测定法是中期母体血清筛查的一个组成部分,因此描述这种干扰对于提供准确的 18 三体和 21 三体风险至关重要。
使用两种不同批次的 uE3 测定法测量了 517 份残留血清样本。向所有样本中添加了 scavenger BALP(sBALP)以去除潜在的 BALP 依赖性干扰,并使用两种 uE3 试剂评估。
两种试剂的 BALP 介导的干扰频率相似(约 3%),尽管两种试剂之间的阳性和阴性干扰模式不同。sBALP 预处理改善了批次间的比较。BALP 相关干扰的存在与内源性人碱性磷酸酶的浓度无关。聚乙二醇和 sBALP 处理的使用似乎同样可以减轻 BALP 介导的干扰,并导致试剂批次之间测量的 uE3 浓度一致。此外,在受 BALP 干扰影响的两个样本中观察到异嗜性抗体干扰,并且异嗜性抗体干扰通过 PEG 和异嗜性抗体阻断试剂处理得到解决,但不能通过 sBALP 处理解决。虽然受影响样本的母体筛查数字风险发生了变化,但在两个样本中,风险分类从阴性筛查变为阳性筛查。
uE3 测定法中的干扰有可能影响不同试剂批次的母体血清风险计算,并且在解释不明的 uE3 浓度的情况下,应考虑对样本进行 scavenger BALP 或 PEG 预处理。