Sosenko Jay M, Yu Liping, Skyler Jay S, Krischer Jeffrey P, Gottlieb Peter A, Boulware David, Miao Dongmei, Palmer Jerry P, Steck Andrea K
1 Division of Endocrinology, University of Miami , Miller School of Medicine, Miami, Florida.
2 Barbara Davis Center for Childhood Diabetes, University of Colorado School of Medicine , Aurora, Colorado.
Diabetes Technol Ther. 2017 Mar;19(3):183-187. doi: 10.1089/dia.2016.0243. Epub 2017 Feb 8.
Electrochemiluminescence (ECL) assays have shown promise for enhancing the prediction of type 1 diabetes (T1D) with autoantibodies. We thus studied relatives of T1D patients to determine whether ECL assays can be used to refine risk assessments for T1D among individuals either positive for single GADA or single mIAA autoantibodies.
TrialNet Pathway to Prevention (PTP) study participants with either GADA or mIAA single autoantibodies were tested for ECL positivity during their participation in the TrialNet PTP study. Those ECL positive (ECL) were compared with those ECL negative (ECL) for conversion to multiple autoantibodies, 6-month glycemic progression (PS6M), and the progression to T1D.
The progression to multiple autoantibodies was significantly higher for those GADA/ECL (n = 107) than those GADA/ECL (n = 78) (P = 0.001) and for those mIAA/ECL (n = 24) than those mIAA/ECL (n = 63) (P < 0.001). The hazard ratios with 95% confidence intervals were 3.42 (1.58-7.39; P < 0.01) for GADA and 8.15 (3.02-22.00; P < 0.001) for mIAA. GADA/ECL and mIAA/ECL participants had significantly higher PS6M values than their ECL counterparts (P = 0.001 for GADA and P = 0.009 for mIAA). Of those GADA/ECL, 14% progressed to T1D; of those mIAA/ECL, 17% progressed to T1D. Only 1 individual (positive for GADA) of the 141 who was ECL progressed to T1D (median follow-up: 5 years).
ECL measurements appear to have utility for natural history studies and prevention trials of individuals with single autoantibodies. Those ECL are at appreciable risk for developing multiple autoantibodies and for glycemic progression toward T1D, whereas those ECL are at very low risk.
电化学发光(ECL)检测在增强利用自身抗体预测1型糖尿病(T1D)方面已显示出前景。因此,我们对T1D患者的亲属进行了研究,以确定ECL检测是否可用于完善对单一谷氨酸脱羧酶自身抗体(GADA)或单一胰岛细胞自身抗体(mIAA)阳性个体的T1D风险评估。
参与预防糖尿病前期试验网(PTP)研究且携带GADA或mIAA单一自身抗体的受试者,在参与试验网PTP研究期间接受了ECL阳性检测。将那些ECL阳性(ECL⁺)者与ECL阴性(ECL⁻)者在转化为多种自身抗体、6个月血糖进展(PS6M)以及进展为T1D方面进行比较。
GADA/ECL⁺组(n = 107)转化为多种自身抗体的比例显著高于GADA/ECL⁻组(n = 78)(P = 0.001),mIAA/ECL⁺组(n = 24)转化为多种自身抗体的比例显著高于mIAA/ECL⁻组(n = 63)(P < 0.001)。GADA的95%置信区间的风险比为3.42(1.58 - 7.39;P < 0.01),mIAA的风险比为8.15(3.02 - 22.00;P < 0.001)。GADA/ECL⁺和mIAA/ECL⁺参与者的PS6M值显著高于其ECL⁻对应者(GADA为P = 0.001,mIAA为P = 0.009)。在GADA/ECL⁺者中,14%进展为T1D;在mIAA/ECL⁺者中,17%进展为T1D。在141名ECL⁻者中,只有1名(GADA阳性)进展为T1D(中位随访时间:5年)。
ECL检测似乎对单一自身抗体个体的自然史研究和预防试验有用。那些ECL⁺者发生多种自身抗体以及血糖向T1D进展的风险相当高,而那些ECL⁻者风险极低。