Anti-zinc transporter protein 8 autoantibodies significantly improve the diagnostic approach to type 1 diabetes: an Italian multicentre study on paediatric patients

被引:27
|
作者
Fabris, Martina [1 ,2 ]
Zago, Silvia [2 ]
Liguori, Marco [3 ]
Trevisan, Maria Teresa [4 ]
Zanatta, Manuela [5 ]
Comici, Alberto [6 ]
Zanette, Giorgio [7 ]
Carlin, Eva [8 ]
Curcio, Francesco [1 ,2 ]
Tonutti, Elio [9 ]
机构
[1] Univ Hosp Udine, Inst Clin Pathol, I-33100 Udine, Italy
[2] Univ Udine, Dept Med & Biol Sci, I-33100 Udine, Italy
[3] Brotzu Hosp, Clin Pathol Lab, Cagliari, Italy
[4] G Fracastoro Hosp, Unit Lab Med, Verona, Italy
[5] Univ Hosp Udine, Pediat Clin, I-33100 Udine, Italy
[6] San Daniele del Friuli Hosp, Pediat Unit, Udine, Italy
[7] Santa Maria degli Angeli Hosp, Unit Diabetol, Pordenone, Italy
[8] Latisana Hosp, Pediat Unit, Udine, Italy
[9] Univ Hosp Udine, Lab Immune Pathol & Allergy, I-33100 Udine, Italy
关键词
Autoimmune diabetes; Autoantibodies; Anti-ZnT8; antibodies; Paediatrics; Sensitivity;
D O I
10.1007/s13317-015-0068-4
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background and aim Anti-ZnT8 antibodies (ZnT8A) were recently proposed as a new independent serological marker in Type 1 diabetes (T1D), leading to a significant improvement of the positive predictive value of autoantibody measurement in this setting. The aim of this retrospective multicentre study was to investigate ZnT8A as a complement to the current T1D autoantibody assays in a large cohort of paediatric Italian patients. Methods ZnT8A were assessed by ELISA in 213 T1DM paediatric patients referred to six different centres in North-East Italy. Fifty-four were analysed at disease onset, 79 within 4 years from diagnosis and 80 after 5 or more years from diagnosis. Retrospective data about islet cell autoantibodies (ICA), anti-insulin (IAA), anti-glutamate decarboxylase (GADA) and anti-protein tyrosine phosphatase IA-2 (IA-2A) antibodies were collected and compared. Results Overall, ZnT8A showed positive results in 106/213 (49.8 %) T1D patients and were found in 10 (4.7 %) subjects previously classified as autoantibody negative based on the existing markers (GADA, IA-2A, IAA and ICA), increasing the overall diagnostic sensitivity from 85.9 to 90.6 %. ZnT8A disclosed the same sensitivity (61.1 %) at disease onset as GADA (61.1 %) and higher than IA-2A (53.7 %), with only GADA showing much persistence in the long-term follow-up. Focusing on patients at disease onset, all the ICA positive were associated with at least one positive autoantibody among GADA, IA-2A and ZnT8A, 16.7 % of whom presenting only anti-ZnT8-positive antibodies. Conclusion This study confirms ZnT8A as an important additional and independent diagnostic marker of T1D and supports its introduction in the routine diagnostic process to replace less sensitive methods and improve the overall autoantibody sensitivity.
引用
收藏
页码:17 / 22
页数:6
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