Pregled bibliografske jedinice broj: 869641
Interleukin-1beta gene promoter polymorphism is associated with higher liver fibrosis progression rate in Croatian patients with biochemically active chronic hepatitis C
Interleukin-1beta gene promoter polymorphism is associated with higher liver fibrosis progression rate in Croatian patients with biochemically active chronic hepatitis C // Medica Jadertina, 47 (2017), 1-2; 13-21 (međunarodna recenzija, članak, znanstveni)
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Naslov
Interleukin-1beta gene promoter polymorphism is associated with higher liver fibrosis progression rate in Croatian patients with biochemically active chronic hepatitis C
Autori
Ivica Grgurević, Sanja Kozić Dokmanović, Mira Šćukanec-Špoljar, Ivan Kurelac, Zdenko Sonicki, Marijan Kirin, Nikola Štoković, Snježana Židovec Lepej, Adriana Vince
Izvornik
Medica Jadertina (0351-0093) 47
(2017), 1-2;
13-21
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
Hepatitis C, interleukin -1beta, gene polymorphism
Sažetak
Background and aims: Genetic polymorphisms of immune mediators have been associated with differences in the natural course of chronic hepatitis C (CHC). The aim of this study was to analyze the association of IL-1β gene polymorphism with the stage of liver fibrosis (LF), grade of necroinflammatory activity (NIA) and fibrosis progression rate (FPR) in CHC patients. Patients and methods: The study included 50 treatment-naive Croatian CHC patients (36 male and 14 female ; age median 37.5 years) with elevated ALT. Diallele polymorphism (C/T) at locus -31 in the IL-1β gene promoter region was determined by restriction fragment length polymorphism (RFLP). Stage of LF and NIA were assessed from liver biopsy sample according to Ishak classification. Results: There was no difference in the stage of LF and NIA level between particular patient genotypes. However, patients with at least 1 C allele at locus -31showed significantly faster FPR than those with no C allele (0.4 vs. 0.258 Ishak's units/year ; p = 0.043). Higher stages of fibrosis were observed in older patients (p = 0.001) and those infected at an older age (p = 0.017). Conclusion: Our study demonstrated that the carriage of at least 1 C allele at -31 locus of IL-1β gene led to faster progression of LF in CHC patients with a biochemically active disease, but did not determine the final stage of fibrosis development. Combined with other risk factors, this finding may serve as a genetic marker to identify patients that require earlier introduction of therapy, since delay could hamper therapeutic success due to rapid disease progression
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti
POVEZANOST RADA
Ustanove:
Klinička bolnica "Merkur",
Klinika za infektivne bolesti "Dr Fran Mihaljević",
Klinička bolnica "Dubrava"
Profili:
Zdenko Sonicki
(autor)
Adriana Vince
(autor)
Mira Šćukanec-Špoljar
(autor)
Ivan Kurelac
(autor)
Sanja Kozić Dokmanović
(autor)
Ivica Grgurević
(autor)
Marijan Kirin
(autor)
Snježana Židovec-Lepej
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Scopus
Uključenost u ostale bibliografske baze podataka::
- EMBASE (Excerpta Medica)
- Scopus