Anti-zinc transporter protein 8 autoantibodies significantly improve the diagnostic approach to type 1 diabetes: an Italian multicentre study on paediatric patients
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  • 作者:Martina Fabris ; Silvia Zago ; Marco Liguori…
  • 关键词:Autoimmune diabetes ; Autoantibodies ; Anti ; ZnT8 antibodies ; Paediatrics ; Sensitivity
  • 刊名:Autoimmunity Highlights
  • 出版年:2015
  • 出版时间:August 2015
  • 年:2015
  • 卷:6
  • 期:1-2
  • 页码:17-22
  • 全文大小:473 KB
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  • 作者单位:Martina Fabris (1) (2)
    Silvia Zago (2)
    Marco Liguori (3)
    Maria Teresa Trevisan (4)
    Manuela Zanatta (5)
    Alberto Comici (6)
    Giorgio Zanette (7)
    Eva Carlin (8)
    Francesco Curcio (1) (2)
    Elio Tonutti (9)

    1. Institute of Clinical Pathology, University Hospital of Udine, Piazzale S. Maria Misericordia 15, 33100, Udine, Italy
    2. Department of Medical and Biological Sciences, University of Udine, Udine, Italy
    3. Laboratory of Clinical Pathology, Brotzu Hospital, Cagliari, Italy
    4. Unit of Laboratory Medicine, G. Fracastoro Hospital, San Bonifacio, Verona, Italy
    5. Clinic of Pediatrics, University Hospital of Udine, Udine, Italy
    6. Unit of Pediatrics, San Daniele del Friuli Hospital, Udine, Italy
    7. Unit of Diabetology, Santa Maria degli Angeli Hospital, Pordenone, Italy
    8. Unit of Pediatrics, Latisana Hospital, Udine, Italy
    9. Laboratory of Immune Pathology and Allergy, University Hospital of Udine, Udine, Italy
  • 刊物主题:Immunology;
  • 出版者:Springer Milan
  • ISSN:2038-3274
文摘
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 4years 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.

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