prikaz prve stranice dokumenta POLIMORFIZMI GENA ZA PROTEIN VISOKE POKRETLJIVOSTI IZ SKUPINE 1 (HMGB1) U DJECE OBOLJELE OD IgA VASKULITISA (HENOCH-SCHÖNLEINOVE PURPURE (HSP))
  Download
PDF 2.36 MB
doctoral thesis
POLIMORFIZMI GENA ZA PROTEIN VISOKE POKRETLJIVOSTI IZ SKUPINE 1 (HMGB1) U DJECE OBOLJELE OD IgA VASKULITISA (HENOCH-SCHÖNLEINOVE PURPURE (HSP))
2021. urn:nbn:hr:152:084864
Batnožić Varga, Mateja
Josip Juraj Strossmayer University of Osijek
Faculty of Medicine Osijek

Cite this document

Batnožić Varga, M. (2021). POLIMORFIZMI GENA ZA PROTEIN VISOKE POKRETLJIVOSTI IZ SKUPINE 1 (HMGB1) U DJECE OBOLJELE OD IgA VASKULITISA (HENOCH-SCHÖNLEINOVE PURPURE (HSP)) (Doctoral thesis). Osijek: Josip Juraj Strossmayer University of Osijek, Faculty of Medicine Osijek. Retrieved from https://urn.nsk.hr/urn:nbn:hr:152:084864

Batnožić Varga, Mateja. "POLIMORFIZMI GENA ZA PROTEIN VISOKE POKRETLJIVOSTI IZ SKUPINE 1 (HMGB1) U DJECE OBOLJELE OD IgA VASKULITISA (HENOCH-SCHÖNLEINOVE PURPURE (HSP))." Doctoral thesis, Josip Juraj Strossmayer University of Osijek, Faculty of Medicine Osijek, 2021. https://urn.nsk.hr/urn:nbn:hr:152:084864

Batnožić Varga, Mateja. "POLIMORFIZMI GENA ZA PROTEIN VISOKE POKRETLJIVOSTI IZ SKUPINE 1 (HMGB1) U DJECE OBOLJELE OD IgA VASKULITISA (HENOCH-SCHÖNLEINOVE PURPURE (HSP))." Doctoral thesis, Josip Juraj Strossmayer University of Osijek, Faculty of Medicine Osijek, 2021. https://urn.nsk.hr/urn:nbn:hr:152:084864

Batnožić Varga, M. (2021). 'POLIMORFIZMI GENA ZA PROTEIN VISOKE POKRETLJIVOSTI IZ SKUPINE 1 (HMGB1) U DJECE OBOLJELE OD IgA VASKULITISA (HENOCH-SCHÖNLEINOVE PURPURE (HSP))', Doctoral thesis, Josip Juraj Strossmayer University of Osijek, Faculty of Medicine Osijek, accessed 29 March 2024, https://urn.nsk.hr/urn:nbn:hr:152:084864

Batnožić Varga M. POLIMORFIZMI GENA ZA PROTEIN VISOKE POKRETLJIVOSTI IZ SKUPINE 1 (HMGB1) U DJECE OBOLJELE OD IgA VASKULITISA (HENOCH-SCHÖNLEINOVE PURPURE (HSP)) [Doctoral thesis]. Osijek: Josip Juraj Strossmayer University of Osijek, Faculty of Medicine Osijek; 2021 [cited 2024 March 29] Available at: https://urn.nsk.hr/urn:nbn:hr:152:084864

M. Batnožić Varga, "POLIMORFIZMI GENA ZA PROTEIN VISOKE POKRETLJIVOSTI IZ SKUPINE 1 (HMGB1) U DJECE OBOLJELE OD IgA VASKULITISA (HENOCH-SCHÖNLEINOVE PURPURE (HSP))", Doctoral thesis, Josip Juraj Strossmayer University of Osijek, Faculty of Medicine Osijek, Osijek, 2021. Available at: https://urn.nsk.hr/urn:nbn:hr:152:084864

Please login to the repository to save this object to your list.
Metadata
TitlePOLIMORFIZMI GENA ZA PROTEIN VISOKE POKRETLJIVOSTI IZ SKUPINE 1 (HMGB1) U DJECE OBOLJELE OD IgA VASKULITISA (HENOCH-SCHÖNLEINOVE PURPURE (HSP))
Title (english)"High-mobility group box-1 gene (HMGB1) polymorphisms in children with IgA vasculitis (Henoch-Schönlein purpura (HSP))"
AuthorMateja Batnožić Varga
MentorMarija Jelušić (mentor)
Committee memberMario Štefanić (predsjednik povjerenstva)
GranterJosip Juraj Strossmayer University of Osijek
Faculty of Medicine Osijek
Osijek
Defense date and country2021-05-03, Croatia
Scientific / art field,
discipline and subdiscipline		BIOMEDICINE AND HEALTHCARE
Clinical Medical Sciences
Universal decimal classification
(UDC)		61 - Medical sciences
Abstract
IgA vaskultis (IgAV) ili Henoch-Schönleinova purpura najčešći je sistemski vaskulitis malih krvnih žila u dječjoj dobi. Protein visoke pokretljivosti iz skupine 1 (engl. high mobility group box-1 protein, HMGB1) pleiotropni je citokin koji djeluje kao proupalni signal, važan za aktivaciju antigen prezentirajućih stanica i širenje upale. HMGB1 ima ulogu u patofiziologiji različitih upalnih bolesti. Cilj ovog istraživanja bio je istražiti povezanost četiri polimorfizma jednog nukleotida gena za HMGB1 (rs1045411, rs1060348, rs2249825 i rs41369348), s predispozicijom za IgAV i kliničkom slikom bolesnika koji ispunjavaju kriterije za IgAV. DNA je ektstrahirana iz krvnih stanica 81 djeteta s IgAV-om i 151 zdravih kontrola, koji su bili bez poznatih autoimunih bolesti. Klinički podaci i laboratorijski parametri prikupljeni su za sve bolesnike s IgAV-om. Nije utvrđen povećan omjer izgleda za nastanak IgAV-a s obzirom na analizirane polimorfizme gena za HMGB1, niti za pojavu nefritisa ili zglobnih manifestacija bolesti. Nositelji heterozigotnog genotipa C/T polimorfizma rs1045411 gena za HMGB1 čini se da imaju manje izgleda za razvoj GI manifestacija u sklopu IgAV-a. Alel T polimorfizma rs1045411 i alel C polimorfizma rs2249825 gena za HMGB1 čini se da povećavaju izglede za razvoj generaliziranog osipa u sklopu IgAV-a. Nositelji recesivnog homozigotnog genotipa T/T i heterozigotnog genotipa C/T polimorfizma rs1045411 te recesivnog homozigotnog genotipa C/C i heterozigotnog genotipa G/C polimorfizma rs2249825 čini se da imaju manje izgleda za razvoj generaliziranog osipa u sklopu IgAV-a. Zaključno, u ovom istraživanju nije nađena povezanost polimorfizama gena za HMGB1 s predispozicijom za nastanak IgAV-a u djece, ali pojedini genotipovi i aleli polimorfizma rs1045411 i rs2249825 čini se da imaju utjecaj na kliničke manifestacije IgAV-a.
Abstract (english)
IgA vasculitis (IgAV) or Henoch-Schönlein's purpura is the most prevalent systemic small vessel vasculitis in childhood. High mobility group box-1 protein (HMBG1) is a pleiotropic cytokine that functions as a pro-inflammatory signal, important for the activation of antigen-presenting cells (APCs) and propagation of inflammation. HMGB1 is implicated in the pathophysiology of a variety of inflammatory diseases. The aim of this study was to investigate the role of four single nucleotide polymorphism (SNP) for HMGB1 gene (rs1045411, rs1060348, rs2249825 i rs41369348) in the susceptibility and clinical features of patients fulfilling classification criteria for IgAV. DNA was extracted from blood cells of 81 children with IgAV and 151 healthy controls, who were without known autoimmune diseases. Clinical data and laboratory parameters were collected for all IgAV patients. In this study analyzed polymorphisms for HMGB1 gene were not associated with increased susceptibility to childhood IgAV, neither for the occurrence of nephritis or joint involment. Heterozygote C/T carriers of rs1045411 polymorphism might less likely develop gastrointestinal manifestation within IgAV. The T allele of the rs1045411 polymorphism and the C allele of the rs2249825 polymorphism might increase the prospects of developing generalized rash within IgAV. Recessive homozygote T/T and heterozygote C/T carriers of rs1045411 and recessive homozygote C/C and heterozygote G/C carriers of rs2249825 polymorphisms might less likely develop generalized rash within IgAV. In conclusion, in this study no association of HMGB1 gene polymorphisms with a predisposition to IgAV in children was found, but individual genotypes and alleles of the rs1045411 and rs2249825 polymorphisms might affect clinical manifestations of IgAV.
Keywords
Keywords (english)
Languagecroatian
URN:NBNurn:nbn:hr:152:084864
Promotion2021
Study programmeTitle: University Postgraduate Study
Study programme type: university
Study level: postgraduate
Academic / professional title: doktor/doktorica znanosti, područje biomedicine i zdravstvo (doktor/doktorica znanosti, područje biomedicine i zdravstvo)
Type of resourceText
File originBorn digital
Access conditionsOpen access
Terms of useLicence In copyright icon
Created on2021-05-28 12:39:20