Please use this identifier to cite or link to this item:
10.2478/s11535-013-0249-y
Title: | Impact of the genes UGT1A1, GSTT1, GSTM1, GSTA1, GSTP1 and NAT2 on acute alcohol-toxic hepatitis |
Authors: | Piekuse, Linda Lace, Baiba Kreile, Madara Sadovska, Lilite Kempa, Inga Daneberga, Zanda Mičule, Ieva Sondore, Valentina Keiss, Jazeps Krumina, Astrida Scientific Laboratory of Molecular Genetics |
Keywords: | Alcoholic;Hepatitis;Oxidative stress;Pharmacogenetics;1.6 Biological sciences;3.2 Clinical medicine;1.1. Scientific article indexed in Web of Science and/or Scopus database;General Neuroscience;General Biochemistry,Genetics and Molecular Biology;General Immunology and Microbiology;General Agricultural and Biological Sciences;SDG 3 - Good Health and Well-being |
Issue Date: | Feb-2014 |
Citation: | Piekuse , L , Lace , B , Kreile , M , Sadovska , L , Kempa , I , Daneberga , Z , Mičule , I , Sondore , V , Keiss , J & Krumina , A 2014 , ' Impact of the genes UGT1A1, GSTT1, GSTM1, GSTA1, GSTP1 and NAT2 on acute alcohol-toxic hepatitis ' , Central European Journal of Biology , vol. 9 , no. 2 , pp. 125-130 . https://doi.org/10.2478/s11535-013-0249-y |
Abstract: | Alcohol metabolism causes cellular damage by changing the redox status of cells. In this study, we investigated the relationship between genetic markers in genes coding for enzymes involved in cellular redox stabilization and their potential role in the clinical outcome of acute alcohol-induced hepatitis. Study subjects comprised 60 patients with acute alcohol-induced hepatitis. The control group consisted of 122 healthy non-related individuals. Eight genetic markers of the genes UGT1A1, GSTA1, GSTP1, NAT2, GSTT1 and GSTM1 were genotyped. GSTT1 null genotype was identified as a risk allele for alcohol-toxic hepatitis progression (OR 2.146, P=0.013). It was also found to correlate negatively with the level of prothrombin (β= -11.05, P=0.037) and positively with hyaluronic acid (β=170.4, P=0.014). NAT2 gene alleles rs1799929 and rs1799930 showed opposing associations with the activity of the biochemical markers γ-glutamyltransferase and alkaline phosphatase; rs1799929 was negatively correlated with γ-glutamyltransferase (β=-261.3, P=0.018) and alkaline phosphatase (β= -270.5, P=0.032), whereas rs1799930 was positively correlated with Γ-glutamyltransferase (β=325.8, P=0.011) and alkaline phosphatase (β=374.8, P=0.011). Enzymes of the glutathione S-transferase family and NAT2 enzyme play an important role in the detoxification process in the liver and demonstrate an impact on the clinical outcome of acute alcohol-induced hepatitis. |
Description: | Funding Information: This study was supported by grants from the Latvian Science Council grant Nos. 09.1384 and 10.0010.02. and the European Social Fund project, which supports the doctoral study program and PhD degree qualification in Riga Stradins University. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. |
DOI: | 10.2478/s11535-013-0249-y |
ISSN: | 1895-104X |
Appears in Collections: | Research outputs from Pure / Zinātniskās darbības rezultāti no ZDIS Pure |
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