Abstract | AIMS: METHODS: A total of 80 patients with alcoholic cirrhosis (AC), 80 patients with alcoholic non- cirrhosis (ANC), 80 with viral hepatitis B-related cirrhosis (VC), and 165 healthy controls (HC) were enrolled into this study. A polymerase chain reaction was used to genotype their SOD2 47T>C (rs4880). RESULTS: There was no statistical difference in the frequency distribution of the three SOD2 47T>C genotypes among groups. However, if individuals with C variant were grouped together, the AC group had higher frequency of SOD2 C/C or C/T genotype than ANC, VC and HC groups had (38.7% vs. 21.3%, 26.3% and 21.8%, respectively, P = 0.010). After adjustment for confounders, the SOD2 C/C and C/T genotypes remained associated with the risk of AC (adjusted OR: 2.79 and 3.50, respectively, P < 0.03, compared with ANC and HC groups). In contrast, there was no significant difference of SOD2 genetic variation between VC and HC groups. CONCLUSIONS: Anti-oxidative enzyme SOD2 47T>C genetic variant may increase the susceptibility to AC. This suggests that oxidative stress plays a role in the development of AC.
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Authors | Yi-Shin Huang, Li Yueh Wang, Chih-Hao Chang, Chin-Lin Perng, Han-Chieh Lin |
Journal | Alcohol and alcoholism (Oxford, Oxfordshire)
(Alcohol Alcohol)
Vol. 51
Issue 6
Pg. 633-637
(Nov 2016)
ISSN: 1464-3502 [Electronic] England |
PMID | 26873981
(Publication Type: Journal Article)
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Copyright | © The Author 2016. Medical Council on Alcohol and Oxford University Press. All rights reserved. |
Chemical References |
- Superoxide Dismutase
- superoxide dismutase 2
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Topics |
- Case-Control Studies
- Female
- Genetic Predisposition to Disease
(genetics)
- Hepatitis B
(genetics)
- Humans
- Liver Cirrhosis
(genetics, virology)
- Liver Cirrhosis, Alcoholic
(genetics)
- Male
- Middle Aged
- Polymorphism, Single Nucleotide
(genetics)
- Risk Factors
- Superoxide Dismutase
(genetics, physiology)
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