Department of Medical Biochemistry and Immunology, University Hospital of Wales, Heath Park, Cardiff CF14 4XW, UK.
Ann Clin Biochem. 2011 Sep;48(Pt 5):438-40. doi: 10.1258/acb.2011.011061. Epub 2011 Jul 27.
Falsely decreased serum alphafetoprotein (AFP) concentrations are reported in the autoDELFIA(®) hAFP immunoassay due to interference by complement. AFP is measured, using this assay, as part of second-trimester and integrated Down's syndrome screening tests. Decreased AFP concentrations increase the calculated risk of Down's syndrome; therefore falsely low AFP, due to assay interference, may artificially increase a patient's risk, and have the potential to cause false screen positive results. It was our aim to assess whether negative interference in the autoDELFIA(®) hAFP assay was a cause of very low AFP concentrations, and to examine the effect of falsely decreased concentrations on the calculated risk of Down's syndrome.
Three hundred and twenty-three sequential Down's screening serum samples with very low serum AFP concentration (<15 KU/L) using the autoDELFIA(®) hAFP immunoassay were selected and AFP re-measured using the E170 AFP immunoassay.
Interference was detected in nine samples (from eight patients) on the basis of discordant AFP concentrations. The interference decreased following storage of samples at 4°C to deplete complement. Use of the falsely low AFP concentrations to calculate risk of Down's syndrome resulted in significantly increased calculated risk compared with complement depleted results.
Laboratories should be aware that falsely low AFP concentrations due to complement interference may be obtained using the autoDELFIA(®) hAFP immunoassay. We have shown that falsely low AFP concentrations increase the calculated risk of Down's syndrome. This is a potential cause of false Down's syndrome screen positive results.
由于补体的干扰,在 autoDELFIA(®) hAFP 免疫分析中报告了血清甲胎蛋白(AFP)浓度的假性降低。该检测方法用于测定 AFP,作为中期和综合唐氏综合征筛查试验的一部分。AFP 浓度的降低会增加唐氏综合征的计算风险;因此,由于检测干扰而导致的假性低 AFP 可能会人为地增加患者的风险,并有可能导致假阳性筛查结果。我们的目的是评估 autoDELFIA(®) hAFP 测定中是否存在阴性干扰是导致 AFP 浓度非常低的原因,并检查假性降低的浓度对唐氏综合征计算风险的影响。
选择了 323 例唐氏筛查血清样本,这些样本的 AFP 浓度非常低(<15KU/L),使用 autoDELFIA(®) hAFP 免疫分析法,并使用 E170 AFP 免疫分析法重新测量 AFP。
根据 AFP 浓度的不一致性,在 9 个样本(来自 8 个患者)中检测到干扰。在 4°C 下储存样本以耗尽补体后,干扰降低。使用假性低 AFP 浓度来计算唐氏综合征的风险,与耗尽补体的结果相比,计算风险显著增加。
实验室应注意,使用 autoDELFIA(®) hAFP 免疫分析法可能会获得由于补体干扰而导致的假性低 AFP 浓度。我们已经表明,假性低 AFP 浓度会增加唐氏综合征的计算风险。这是假唐氏综合征筛查阳性结果的潜在原因。