Pregled bibliografske jedinice broj: 671559
TLR-4 GENE POLYMORPHISM IN RENAL TRANSPLANT PATIENTS
TLR-4 GENE POLYMORPHISM IN RENAL TRANSPLANT PATIENTS // The Eighth ISABS Conference in Forensic, Anthropologic and Medical Genetics and Mayo Clinic Lectures in Translational Medicine
Split, Hrvatska, 2013. str. 309-309 (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 671559 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
TLR-4 GENE POLYMORPHISM IN RENAL TRANSPLANT PATIENTS
Autori
Glavaš, Josipa ; Sesar, Sanda ; Alkhamis, Tamara ; Kralik, Kristina ; Prlić, Damir ; Barbić, Jerko
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
The Eighth ISABS Conference in Forensic, Anthropologic and Medical Genetics and Mayo Clinic Lectures in Translational Medicine
/ - , 2013, 309-309
ISBN
978-953-57695-0-7
Skup
The Eighth ISABS Conference in Forensic, Anthropologic and Medical Genetics and Mayo Clinic Lectures in Translational Medicine
Mjesto i datum
Split, Hrvatska, 24.06.2013. - 28.06.2013
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
kidney transplantation; graft function; TLR4
Sažetak
The study included 70 patients with a transplanted kidney and 50 healthy volunteers representing a control group. Median age of the transplanted patients was 53 years (48-58 years). Transplanted patients had been receiving an adjuvant kidney therapy for an average of 4 years (2-6 years). Median time lapse from receiving kidney transplant was 3 years (ranging from 2-5years). The most common chronic kidney disease diagnosis was chronic glomerulonephritis (21 patient ; 32, 8%), followed by a polycystic kidney disease in 7 patients (10, 9%). Detection of gene polymorphism for tlr4 rs4986790 (A896G, D299G) i tlr4 rs4986791 (C1196T, T399I) was conducted using multiplex real-time PCR. Polymorphism detection was performed using LightCycler. Detection of the TLR4 rs4986790 polymorphism revealed a great predominance in the AA-wild type (104 patients, 86.7%), 44 (88%) out of which were from the control group and 60 (85.7%) from the transplanted group. When analysing rs4986791 polymorphism, the largest proportion of patients (99 ; 82.5%) displays a CC-wild type, followed by a CT-heterozygous group (19 ; 15, 8%), while only 2 patients from the tranplanted group (2.9%) showed a TT-mutation. A significant decrease in erythrocytes (Kruskal Wallis test, p=0.037), creatinine clearence (p=0.019) and hemoglobin levels (p=0.009) was observed in the AA-wild type rs4984790 group, while the AG-heterozygous group showed the highest levels of blood glucose. CC-wild type group type rs4986791 shows significantly lower erythrocyte values (p=0.027), creatinine clearance (p=0.030) and hemoglobin levels (p=0.049).
Izvorni jezik
Engleski
POVEZANOST RADA
Projekti:
219-0000000-3362 - Genski polimorfizam i funkcija bubrežnog presatka (Barbić, Jerko, MZOS ) ( CroRIS)
Ustanove:
Medicinski fakultet, Osijek