Pregled bibliografske jedinice broj: 654055
Concomitant autoantibodies in newly diagnosed diabetic children with transient celiac serology or proven celiac disease
Concomitant autoantibodies in newly diagnosed diabetic children with transient celiac serology or proven celiac disease // Journal of pediatric endocrinology & metabolism, 26 (2013), 11-12; 1099-1104 doi:10.1515/jpem-2013-0035 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 654055 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Concomitant autoantibodies in newly diagnosed diabetic children with transient celiac serology or proven celiac disease
Autori
Hojsak, Iva ; Zevit, N. ; Waisbourd-Zinman, O. ; Rosenbach, Y. ; Mozer-Glassberg, Y. ; Shalitin, S. ; Phillip, M. ; Shamir, R.
Izvornik
Journal of pediatric endocrinology & metabolism (0334-018X) 26
(2013), 11-12;
1099-1104
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
autoantibodies ; celiac disease ; children ; diabetes mellitus type 1 ; tissue transglutaminase
Sažetak
Abstract Background: We previously demonstrated that children with Type 1 Diabetes Mellitus (T1DM) may have transiently elevated tissue transglutaminase antibodies (TTG) on a gluten-containing diet. This study aimed to examine if the presence of autoantibodies in newly diagnosed T1DM differs between patients with celiac disease and those with transient celiac serology. Methods: Forty children were identified who had been diagnosed with T1DM between 2003 and 2009 and who had elevated serum IgA-TTG antibody levels at diagnosis. Blood samples were collected for measurement of insulin (IA-2A) antibodies, islet cell antigen (ICA) antibodies, glutamic acid decarboxylase (GAD) antibodies, thyroglobulin (TgAb) antibodies, and thyroid peroxidase (TPO) antibodies. Children diagnosed with celiac disease (CD ; group 1, n=23) and children in whom TTG antibody levels spontaneously normalized over time (group 2, n=17) were compared. Results: No significant differences in positivity rates between groups 1 and 2 were found for any of the autoantibodies tested. The respective findings were as follows: IA-2A 50% and 47.1% (p=0.855) ; ICA 77.3% and 76.5% (p=0.953) ; GAD 27.3% and 52.9% (p=0.102). Thyroid antibodies were found positive in a limited number of patients: TgAb 4.5% and 11.8% ; TPO 4.5% and 11.8%. In addition, antibody titer levels did not differ significantly for all autoantibodies. Difference in occurrence of clinical or subclinical thyroid disease did not reach significance (4.3% vs. 29.4% ; p=0.07). Age was positively correlated with the presence of thyroglobulin and thyroid peroxidase antibodies, and negatively correlated with the presence of insulin antibody. Conclusion: Neither the number of concomitant autoantibodies nor their titers in newly diagnosed T1DM differed between patients with proven CD and those with transient TTG serology.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti
POVEZANOST RADA
Projekti:
072-1083107-2054 - Celijakija u djece: primarna prevencija i patogeneza kromosomske nestabilnosti (Kolaček, Sanja, MZOS ) ( CroRIS)
Ustanove:
Klinika za dječje bolesti Medicinskog fakulteta
Profili:
Iva Hojsak
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE