A Helicobacter pylori-associated insulin resistance in asymptomatic sedentary young men does not correlate with inflammatory markers and urine levels of 8-iso-PGF2-α or 1, 4-dihydroxynonane mercapturic acid. (27th May 2018)

• Record Type: Journal Article
• Authors: Cherkas, Andriy; Golota, Sergii; Guéraud, Françoise; Abrahamovych, Orest; Pichler, Christoph; Nersesyan, Armen; Krupak, Volodymyr; Bugiichyk, Vira; Yatskevych, Ostap; Pliatsko, Mykhaylo; Eckl, Peter; Knasmüller, Siegfried
• Is Part Of: Archives of physiology and biochemistry. Volume 124:Number 3(2018)
• Page Start: 275
• Page End: 285
• Publication Date: 2018-05-27
• Subjects: Helicobacter pylori -- sedentary lifestyle -- insulin resistance -- oxidative stress -- inflammation; Physiology -- Periodicals; Biochemistry -- Periodicals; Biophysics -- Periodicals; Biochemistry; Physiology; 571
• DOI: 10.1080/13813455.2017.1396346
• Languages: English
• ISSNs: 1381-3455

Abstract

Abstract: A potential contribution of H. pylori contamination to low-grade inflammation, oxidative stress (OS) and insulin resistance as well as correlations between these parameters in asymptomatic sedentary males was analysed. We enrolled 30 apparently healthy asymptomatic young subjects (18 H. pylori negative and 12 positive) and measured whole blood glucose, glycated haemoglobin, insulin, C-peptide, cortisol, aldosterone, testosterone, thyroid stimulating hormone, C-reactive protein, interleukins 6 and 10, TNF-alpha and comet assay. As markers of OS, we used urine levels of iso-PGF2 -α and 1, 4-dihydroxynonane mercapturic acid (DHN-MA). Twofold elevation of fasting insulin level and HOMA index in H. pylori –positive subjects ( p < .05) was shown. Inflammatory parameters and monocyte DNA damage, urine levels of DHN-MA and iso-PGF2-α did not show significant differences between the groups. The early stage of H. pylori -triggered metabolic derangements in sedentary subjects include development of insulin resistance in H. pylori -positive subjects; however, there is no evidence of systemic inflammatory and OS-related changes.