Autoantibodies against ZnT8 are rare in Central-European LADA patients and absent in MODY patients, including those positive for other autoantibodies
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
30377089
DOI
10.1016/j.jdiacomp.2018.10.004
PII: S1056-8727(18)30518-X
Knihovny.cz E-zdroje
- Klíčová slova
- Adult-onset autoimmune diabetes, BMI, LADA, LYP, PTPRN, Zinc transporter ZnT8,
- MeSH
- autoprotilátky krev imunologie MeSH
- biologické markery krev MeSH
- diabetes mellitus 1. typu krev farmakoterapie genetika imunologie MeSH
- diabetes mellitus 2. typu krev farmakoterapie genetika imunologie MeSH
- fenotyp MeSH
- genotyp MeSH
- hypoglykemika terapeutické užití MeSH
- inzulin terapeutické užití MeSH
- lidé středního věku MeSH
- lidé MeSH
- progrese nemoci MeSH
- tyrosinfosfatasa nereceptorového typu 22 genetika MeSH
- zinkový transportér 8 krev imunologie MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Geografické názvy
- Česká republika MeSH
- Názvy látek
- autoprotilátky MeSH
- biologické markery MeSH
- hypoglykemika MeSH
- inzulin MeSH
- PTPN22 protein, human MeSH Prohlížeč
- SLC30A8 protein, human MeSH Prohlížeč
- tyrosinfosfatasa nereceptorového typu 22 MeSH
- zinkový transportér 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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