Autoantibodies against ZnT8 are rare in Central-European LADA patients and absent in MODY patients, including those positive for other autoantibodies
Language English Country United States Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
30377089
DOI
10.1016/j.jdiacomp.2018.10.004
PII: S1056-8727(18)30518-X
Knihovny.cz E-resources
- Keywords
- Adult-onset autoimmune diabetes, BMI, LADA, LYP, PTPRN, Zinc transporter ZnT8,
- MeSH
- Autoantibodies blood immunology MeSH
- Biomarkers blood MeSH
- Diabetes Mellitus, Type 1 blood drug therapy genetics immunology MeSH
- Diabetes Mellitus, Type 2 blood drug therapy genetics immunology MeSH
- Phenotype MeSH
- Genotype MeSH
- Hypoglycemic Agents therapeutic use MeSH
- Insulin therapeutic use MeSH
- Middle Aged MeSH
- Humans MeSH
- Disease Progression MeSH
- Protein Tyrosine Phosphatase, Non-Receptor Type 22 genetics MeSH
- Zinc Transporter 8 blood immunology MeSH
- Check Tag
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Geographicals
- Czech Republic MeSH
- Names of Substances
- Autoantibodies MeSH
- Biomarkers MeSH
- Hypoglycemic Agents MeSH
- Insulin MeSH
- PTPN22 protein, human MeSH Browser
- SLC30A8 protein, human MeSH Browser
- Protein Tyrosine Phosphatase, Non-Receptor Type 22 MeSH
- Zinc Transporter 8 MeSH
BACKGROUND: Testing for autoantibodies against the zinc transporter ZnT8 (ZnTA) is becoming routine in pediatric diabetes. However, available data are inconclusive when focusing on adult-onset diabetes, including autoimmune diabetes, which does not require insulin at diagnosis (LADA). BASIC PROCEDURES: We examined the ZnTA prevalence and titers and matched them with the clinical phenotype and PTPN22 genotypes of Czech LADA patients who were positive for GADA and/or IA2A and had a fasting C-peptide level >200 pmol/L at diagnosis as well as HNF4A-, GCK- or HNF1A-MODY patients and healthy controls. MAIN FINDINGS: Most LADA patients were negative for ZnTA, and the sensitivity of the assay was only 18-20% for patients with LADA-like progression to insulinotherapy compared to healthy controls. In LADA patients, there was no association between the ZnTA and PTPN22 risk genotypes. LADA patients positive for ZnTA had a lower BMI than those positive for other autoantibodies alone. Importantly, MODY patients were completely negative for ZnTA, and the levels of ZnTA in MODY patients were similar to those in healthy controls. CONCLUSIONS: ZnTA quantification did not improve LADA diagnosis. However, positivity for ZnTA can be used as a negative MODY pre-diagnostic criterion even in the region of Central and East Europe, where other islet cell autoantibodies are common in MODY patients.
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