Literature DB >> 25584813

Determining oxidant and antioxidant status in patients with genital warts.

Erdem Cokluk, Mehmet Ramazan Sekeroglu, Mehmet Aslan, Ragip Balahoroglu, Serap Gunes Bilgili, Zubeyir Huyut.   

Abstract

OBJECTIVES: Warts are abnormal skin growths caused by human papilloma virus (HPV) infections within the skin of patients. Genital warts usually appear in the perianal and perigenital regions. Asymptomatic warts may be activated after years and may damage natural immunity. The inflammation that occurs during this process may lead to an imbalance between the prooxidant and the antioxidant systems. The aim of this study was to investigate erythrocyte glutathione peroxidase (GSH-Px) activity, serum paraoxonase enzyme levels, and oxidative stress levels in patients with genital warts. PATIENTS AND METHODS: In total, 32 patients with genital warts and 35 healthy subjects were included in this study. Erythrocyte GSH-Px activity, serum catalase activity, and paraoxonase enzyme, and malondialdehyde (MDA) levels were determined.
RESULTS: Erythrocyte GSH-Px activity, serum MDA levels, and catalase activity were significantly higher in patients with genital warts than in controls (P < 0.01, P < 0.05, and P < 0.05, respectively). However, serum paraoxonase enzyme levels were not significantly different between groups (P > 0.05). Serum triglyceride levels were significantly lower in patients with genital warts than in controls (P < 0.01). However, there were no statistically significant differences between groups with respect to total cholesterol, high-density lipoprotein cholesterol, or low-density lipoprotein cholesterol levels (all P > 0.05).
CONCLUSIONS: Our data suggest that oxidative stress is increased in genital warts. Increased oxidative stress levels may contribute to the pathogenesis of genital warts, and prolonged HPV infection due to chronic inflammation could also affect oxidative stress.

Entities:  

Keywords:  Catalase activity; Genital warts; Glutathione peroxidase activity; Lipid parameters; Malondialdehyde; Paraoxonase-1

Mesh:

Substances:

Year:  2015        PMID: 25584813      PMCID: PMC6837376          DOI: 10.1179/1351000215Y.0000000002

Source DB:  PubMed          Journal:  Redox Rep        ISSN: 1351-0002            Impact factor:   4.412


  33 in total

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  5 in total

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