• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

自动 DELFIA(R) hAFP 免疫分析的干扰及其对中期唐氏综合征筛查的影响。

Interference in the autoDELFIA(R) hAFP immunoassay and effect on second-trimester Down's syndrome screening.

机构信息

Department of Medical Biochemistry and Immunology, University Hospital of Wales, Heath Park, Cardiff CF14 4XW, UK.

出版信息

Ann Clin Biochem. 2011 Sep;48(Pt 5):438-40. doi: 10.1258/acb.2011.011061. Epub 2011 Jul 27.

DOI:10.1258/acb.2011.011061
PMID:21795408
Abstract

BACKGROUND

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.

METHODS

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.

RESULTS

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.

CONCLUSIONS

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.

摘要

背景

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。

方法

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。

结果

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。

结论

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。

相似文献

1
Interference in the autoDELFIA(R) hAFP immunoassay and effect on second-trimester Down's syndrome screening.自动 DELFIA(R) hAFP 免疫分析的干扰及其对中期唐氏综合征筛查的影响。
Ann Clin Biochem. 2011 Sep;48(Pt 5):438-40. doi: 10.1258/acb.2011.011061. Epub 2011 Jul 27.
2
[Evaluation of Down's syndrome screening methods using maternal serum biochemistry in the second trimester pregnancy].[孕中期使用母体血清生化指标进行唐氏综合征筛查方法的评估]
Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011 Jun;28(3):332-5. doi: 10.3760/cma.j.issn.1003-9406.2011.03.021.
3
First-trimester or second-trimester screening, or both, for Down's syndrome.孕早期或孕中期唐氏综合征筛查,或两者皆做。
N Engl J Med. 2005 Nov 10;353(19):2001-11. doi: 10.1056/NEJMoa043693.
4
Prenatal screening using maternal serum alpha-fetoprotein, human chorionic gonadotropin, and unconjugated estriol: two-year experience in a health maintenance organization.使用母体血清甲胎蛋白、人绒毛膜促性腺激素和未结合雌三醇进行产前筛查:在一家健康维护组织中的两年经验。
J Matern Fetal Med. 1996 Mar-Apr;5(2):70-3. doi: 10.1002/(SICI)1520-6661(199603/04)5:2<70::AID-MFM4>3.0.CO;2-N.
5
[Second trimester maternal serum screening for Down's syndrome in mainland China: a multi-center prospective study].[中国大陆孕中期唐氏综合征血清学筛查:一项多中心前瞻性研究]
Zhonghua Fu Chan Ke Za Zhi. 2008 Nov;43(11):805-9.
6
Comparison of Down's syndrome screening strategies in Asians combining serum free beta-hCG and alpha-fetoprotein with maternal age.亚洲人结合血清游离β-人绒毛膜促性腺激素和甲胎蛋白与孕妇年龄进行唐氏综合征筛查策略的比较。
Prenat Diagn. 1997 Aug;17(8):707-16.
7
Dimeric inhibin A as a marker for Down's syndrome in early pregnancy.二聚体抑制素A作为孕早期唐氏综合征的标志物。
N Engl J Med. 1996 May 9;334(19):1231-6. doi: 10.1056/NEJM199605093341904.
8
Second-trimester maternal serum alpha-fetoprotein and human chorionic gonadotrophin screening for Down's syndrome in Hong Kong.香港孕中期孕妇血清甲胎蛋白和人绒毛膜促性腺激素筛查唐氏综合征
Prenat Diagn. 1998 Jun;18(6):585-89.
9
First trimester maternal serum screening for Down's syndrome: an evaluation of the DPC Immulite 2000 free beta-hCG and pregnancy-associated plasma protein-A assays.孕早期唐氏综合征的母体血清筛查:DPC Immulite 2000游离β-人绒毛膜促性腺激素和妊娠相关血浆蛋白A检测方法的评估
Ann Clin Biochem. 2005 Jan;42(Pt 1):30-40. doi: 10.1258/0004563053026880.
10
Down's syndrome risk estimates demonstrate considerable heterogeneity despite homogeneity of input.唐氏综合征风险评估结果显示,尽管输入数据具有同质性,但仍存在相当大的异质性。
Ann Clin Biochem. 2004 Nov;41(Pt 6):464-8. doi: 10.1258/0004563042466901.

引用本文的文献

1
External Quality Assessment of Maternal Serum Levels of Alpha-Fetoprotein, Free Beta-Human Chorionic Gonadotropin, and Unconjugated Estriol in Detecting Down Syndrome and Neural Tube Defects in the Second Trimester of 87 Maternal Serum Samples, Based on 105-139 Days.基于 105-139 天的 87 例母血清样本,对甲胎蛋白、游离β-人绒毛膜促性腺激素和未结合雌三醇进行检测,以评估其在检测唐氏综合征和神经管缺陷中的外部质量。
Med Sci Monit. 2022 Apr 13;28:e935573. doi: 10.12659/MSM.935573.
2
Evaluation of chemiluminescent immunoassay quantitative detection for pro-gastrin-releasing peptide (ProGRP) in serum and plasma.血清和血浆中胃泌素释放肽前体(ProGRP)化学发光免疫分析定量检测的评估
J Int Med Res. 2020 Apr;48(4):300060519882802. doi: 10.1177/0300060519882802. Epub 2019 Dec 19.