4.2 Article

Evaluation of Atherosclerotic Risk by Oxidative Contributors in Alcohol Use Disorder

Journal

CLINICAL PSYCHOPHARMACOLOGY AND NEUROSCIENCE
Volume 21, Issue 3, Pages 526-533

Publisher

KOREAN COLL NEUROPSYCHOPHARMACOLOGY
DOI: 10.9758/cpn.22.1010

Keywords

Alcohol use disorder; Atherosclerosis; Lipid hydroperoxide; Myeloperoxidase; Oxidative stress

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This study aimed to evaluate oxidative contributors of atherosclerotic risk factors in patients with Alcohol Use Disorder (AUD). The results showed significantly elevated oxidative markers in AUD patients and decreased antioxidant capacity. Atherosclerotic markers were also higher and correlated with alcohol intake. Thus, oxidative markers may serve as indicators for atherosclerotic risk and therapeutic interventions targeting oxidative load may help prevent clinical manifestation of atherosclerotic diseases.
Objective: Alcohol Use Disorder (AUD) is a condition described as the inability to control or stop alcohol consumption. The patients with AUD have an increased risk of developing atherosclerosis-related diseases. The present study aimed to evaluate oxidative contributors of atherosclerotic risk factors in patients with AUD.Methods: The male subjects diagnosed with AUD (n = 45) and the male subjects as control (n = 35) were enrolled in this study. All participants were undergone psychiatric evaluation and sociodemographic tests. Also, serum oxidative contributors of atherosclerosis including myeloperoxidase (MPO), ferroxidase, catalase (CAT), and lipid hydroperoxides (LOOH) were measured. Additionally, serum lipid profile tests and atherogenic indicators including atherogenic index of plasma (AIP) and non-high-density lipoprotein (HDL) cholesterol were also analyzed.Results: The AUD subject had significantly elevated MPO activity and LOOH levels with decreased antioxidant capacity. AIP and non-HDL cholesterol levels, the atherogenic indicators, were also higher in AUD group compared to the control group. We found the MPO activity and LOOH levels were positively correlated with AIP, non-HDL cholesterol levels, and amount of alcohol consumption. Additionally, CAT activity was negatively correlated with duration of alcohol consumption. Conclusion: Our results revealed that MPO and LOOH levels were elevated by severe alcohol intake and the athero-genic indicators, AIP and non-HDL cholesterol, were significantly correlated alcohol induced elevated oxidative risk factors. Therefore, it can be suggested that MPO activity and LOOH levels may be useful to determine jeopardy of atherosclerotic and the therapeutic interventions that reduce oxidative load could be taken into account to prevent atherosclerotic diseases before clinical manifestation.

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