首页> 外文期刊>Experimental diabetes research >Comparison of Measurements of Autoantibodies to Glutamic Acid Decarboxylase and Islet Antigen-2 in Whole Blood Eluates from Dried Blood Spots Using the RSR-Enzyme Linked Immunosorbent Assay Kits and In-House Radioimmunoassays
【24h】

Comparison of Measurements of Autoantibodies to Glutamic Acid Decarboxylase and Islet Antigen-2 in Whole Blood Eluates from Dried Blood Spots Using the RSR-Enzyme Linked Immunosorbent Assay Kits and In-House Radioimmunoassays

机译:使用RSR酶联免疫吸附测定试剂盒和室内放射免疫测定法测量干血斑全血洗脱液中针对谷氨酸脱羧酶和胰岛抗原2的自身抗体的比较

获取原文
           

摘要

To evaluate the performance of dried blood spots (DBSs) with subsequent analyses of glutamic acid decarboxylase (GADA) and islet antigen-2 (IA-2A) with the RSR-ELISAs, we selected 80 children newly diagnosed with type 1 diabetes and 120 healthy women. DBSs from patients and controls were used for RSR-ELISAs while patients samples were analysed also with in-house RIAs. The RSR-ELISA-GADA performed well with a specificity of 100%, albeit sensitivity (46%) was lower compared to in RIA (56%;P=.008). No prozone effect was observed after dilution of discrepant samples. RSR-ELISA-IA-2A achieved specificity of 69% and sensitivity was lower (59%) compared with RIA (66%;P<.001). Negative or low positive patients and control samples in the RSR-ELISA-IA-2A increased after dilution. Eluates from DBS can readily be used to analyse GADA with the RSR-ELISA, even if low levels of autoantibodies were not detected. Some factor could disturb RSR-ELISA-IA-2A analyses.
机译:为了评估干血斑(DBS)的性能并随后通过RSR-ELISAs分析谷氨酸脱羧酶(GADA)和胰岛抗原2(IA-2A),我们选择了80名新诊断为1型糖尿病的儿童和120名健康的儿童女人。将来自患者和对照组的DBS用于RSR-ELISA,同时还使用内部RIA对患者样品进行分析。尽管RRI-ELISA-GADA的敏感性(46%)低于RIA(56%; P = .008),但特异性为100%,表现良好。稀释不同样品后未观察到前区效应。与RIA(66%; P <.001)相比,RSR-ELISA-IA-2A的特异性达到了69%,灵敏度更低(59%)。稀释后,RSR-ELISA-IA-2A中的阴性或低阳性患者和对照样品增加。即使未检测到低水平的自身抗体,DBS洗脱液也可用于RSR-ELISA分析GADA。某些因素可能会干扰RSR-ELISA-IA-2A分析。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号