Pregled bibliografske jedinice broj: 954809
Maturity onset diabetes of the young due to HNF1A variants in Croatia
Maturity onset diabetes of the young due to HNF1A variants in Croatia // Biochemia medica, 28 (2018), 2; 020703, 11 doi:10.11613/bm.2018.020703 (recenziran, članak, znanstveni)
CROSBI ID: 954809 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Maturity onset diabetes of the young due to HNF1A variants in Croatia
Autori
Pavić, Tamara ; Juszczak, Agata ; Pape Medvidović, Edita ; Burrows, Carla ; Šekerija, Mario ; Bennett, Amanda J ; Ćuća Knežević, Jadranka ; Gloyn, Anna L ; Lauc, Gordan ; McCarthy, Mark I ; Gornik, Olga ; Owen, Katharine R
Izvornik
Biochemia medica (1330-0962) 28
(2018), 2;
020703, 11
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
HNF1A ; maturity onset diabetes of the young (MODY) ; monogenic diabetes ; prevalence study
Sažetak
Introduction: Maturity onset diabetes of the young due to HNF1A mutations (HNF1A-MODY) is the most frequent form of monogenic diabetes in adults. It is often misdiagnosed as type 1 or type 2 diabetes, but establishing genetic diagnosis is important, as treatment differs from the common types of diabetes. HNF1A-MODY has not been investigated in Croatia before due to limited access to genetic testing. In this study we aimed to describe the characteristics of young adults diagnosed with diabetes before the age of 45 years, who have rare HNF1A allele variants, and estimate the prevalence of HNF1A-MODY in Croatia. Materials and methods: We recruited 477 C-peptide positive and beta cell antibody negative subjects through the Croatian Diabetes Registry. HNF1A was sequenced for all participants and systematic assessment of the variants found was performed. The prevalence of HNF1A-MODY was calculated in the study group and results extrapolated to estimate the proportion of diabetic individuals with HNF1A-MODY in Croatia and the population prevalence. Results: Our study identified 13 individuals harbouring rare HNF1A allelic variants. After systematic assessment, 8 were assigned a diagnosis of HNF1A-MODY. Two individuals were able to discontinue insulin treatment following the diagnosis. We estimated that HNF1A-MODY in Croatia has a prevalence of 66 (95% CI 61 - 72) cases per million. Conclusions: The estimated prevalence of HNF1A-MODY in Croatia is similar to that reported in other European countries. Finding cases lead to important treatment changes for patients. This strongly supports the introduction of diagnostic genetic testing for monogenic diabetes in Croatia.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti, Javno zdravstvo i zdravstvena zaštita, Farmacija
POVEZANOST RADA
Ustanove:
Hrvatski zavod za javno zdravstvo,
Farmaceutsko-biokemijski fakultet, Zagreb,
Klinička bolnica "Merkur",
Klinika za dijabetes, endokrinologiju i bolesti metabolizma Vuk Vrhovac,
Medicinski fakultet, Zagreb,
GENOS d.o.o.
Profili:
Mario Šekerija
(autor)
Olga Gornik Kljaić
(autor)
Gordan Lauc
(autor)
Edita Pape-Medvidović
(autor)
Jadranka Knežević-Ćuća
(autor)
Tamara Štambuk
(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