Gliadin, endomysial and thyroid antibodies in patients with latent autoimmune diabetes of adults (LADA)
Jazyk angličtina Země Anglie, Velká Británie Médium print
Typ dokumentu srovnávací studie, časopisecké články, práce podpořená grantem
PubMed
12823288
PubMed Central
PMC1808742
DOI
10.1046/j.1365-2249.2003.02205.x
PII: 2205
Knihovny.cz E-zdroje
- MeSH
- autoprotilátky analýza MeSH
- diabetes mellitus 1. typu imunologie MeSH
- diabetes mellitus 2. typu imunologie MeSH
- diabetes mellitus imunologie MeSH
- gliadin imunologie MeSH
- imunoglobulin A imunologie MeSH
- imunoglobulin G imunologie MeSH
- jodidperoxidasa imunologie MeSH
- lidé středního věku MeSH
- lidé MeSH
- protilátky anti-idiotypické analýza MeSH
- rozdělení chí kvadrát MeSH
- senioři MeSH
- studie případů a kontrol MeSH
- thyreoglobulin imunologie MeSH
- věk při počátku nemoci MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- srovnávací studie MeSH
- Názvy látek
- autoprotilátky MeSH
- gliadin MeSH
- imunoglobulin A MeSH
- imunoglobulin G MeSH
- jodidperoxidasa MeSH
- protilátky anti-idiotypické MeSH
- thyreoglobulin MeSH
Latent autoimmune diabetes of adults (LADA) manifested after the age of 35 is characterized by the presence of disease-specific autoantibodies (anti-glutamate decarboxylase GADAb, anti-IA2Ab). However, autoimmunity in Type 1 diabetes mellitus is not targeted only to pancreatic beta-cells. No data have so far been published concerning the antibodies associated with other autoimmune disease in LADA patients. The presence of anti-thyroglobulin (TGAb), anti-thyroid peroxidase (TPOAb), anti-gliadin IgA (AGAAb) and IgG (AGGAb) and endomysial antibodies (EMAb) in sera of 68 diabetics typed as LADA was compared with the antibody presence in sera of 85 patients with Type 2 diabetes. We found a significantly higher occurrence of gliadin antibodies in LADA patients: the rate of AGGAb was 19.1% in comparison with 3.5% in the T2DM group (P = 0.0026), the rate of AGAAb was 13.2% in comparison with 3.5% (P = 0.035). The prevalence of EMAb was very low in both groups (1.5% and 0). The two groups differed significantly in the TPOAb rate: 22.1% in LADA compared to 9.4% in T2DM (P = 0.04), whereas no significant difference was found in the presence of TGAb (8.8% and 3.5%, P = 0.187). In comparison with T2DM patients, LADA patients were found to express higher antibody activity against gluten-related antigens and against TPO.
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