Population Health and Immunity Division, Walter and Eliza Hall Institute, Parkville, Australia.
Department of Medical Biology, University of Melbourne, Parkville, Australia.
Diabetes Technol Ther. 2024 Feb;26(2):87-94. doi: 10.1089/dia.2023.0345. Epub 2024 Jan 16.
Self-collection of a blood sample for autoantibody testing has potential to facilitate screening for type 1 diabetes risk. We sought to determine the feasibility and acceptability of this approach and the performance of downstream antibody assays. People living with type 1 diabetes and their family members ( = 97) provided paired capillary blood spot and serum samples collected, respectively, by themselves and a health worker. They provided feedback on the ease, convenience, and painfulness of blood spot collection. Islet antibodies were measured in blood spots by antibody detection by agglutination PCR (ADAP) or multiplex enzyme-linked immunoassay (ELISA), and in serum by radioimmunoassay (RIA) or ELISA. Using serum RIA and ELISA to define antibody status, 50 antibody-negative (Ab) and 47 antibody-positive (Ab) participants enrolled, of whom 43 and 47, respectively, returned testable blood spot samples. The majority indicated that self-collection was easier, more convenient, and less painful than formal venesection. The sensitivity and specificity for detection of Ab by blood spot were, respectively, 85% and 98% for ADAP and 87% and 100% for multiplex ELISA. The specificities by ADAP for each of the four antigen specificities ranged from 98% to 100% and areas under the receiver operator curve from 0.841 to 0.986. Self-collected blood spot sampling is preferred over venesection by research participants. ADAP and multiplex ELISA are highly specific assays for islet antibodies in blood spots with acceptable performance for use alone or in combination to facilitate screening for type 1 diabetes risk. Clinical Trial Registration number: ACTRN12620000510943.
自我采集血样进行自身抗体检测有可能促进 1 型糖尿病风险筛查。我们旨在确定这种方法的可行性和可接受性,以及下游抗体检测的性能。97 名 1 型糖尿病患者及其家庭成员分别自行和医务人员采集毛细血管血斑和血清样本。他们对血斑采集的简便性、便利性和疼痛程度提供了反馈。通过抗体凝集 PCR(ADAP)或多重酶联免疫吸附测定(ELISA)在血斑中测量胰岛抗体,通过放射免疫测定(RIA)或 ELISA 在血清中测量。使用血清 RIA 和 ELISA 定义抗体状态,纳入 50 名抗体阴性(Ab)和 47 名抗体阳性(Ab)参与者,其中分别有 43 名和 47 名参与者返回可检测的血斑样本。大多数人表示,自我采集比正规静脉采血更容易、更方便、疼痛更少。ADAP 和多重 ELISA 检测 Ab 的敏感性和特异性分别为 85%和 98%,87%和 100%。ADAP 对每种四种抗原特异性的特异性分别为 98%至 100%,接收器操作曲线下面积为 0.841 至 0.986。研究参与者更喜欢自我采集血斑采样,而不是静脉采血。ADAP 和多重 ELISA 是血斑中胰岛抗体的高度特异性检测方法,具有良好的性能,可单独或联合使用,以促进 1 型糖尿病风险筛查。临床试验注册号:ACTRN12620000510943。