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Please use this identifier to cite or link to this item: http://142.54.178.187:9060/xmlui/handle/123456789/12794
Title: Relationship of oxidative stress with elevated level of DNA damage and homocysteine in cardiovascular disease patients
Authors: Qasim, Muhammad
Bukhari, Shazia Anwer
Ghani, Madiha Javeed
Masoud, Muhammad Shareef
Huma, Tayyabah
Arshad, Muhammad
Haque, Asma
Ibrahim, Zubair
Javed, Sadia
Rajoka, Muhammad Ibrahim
Keywords: Antioxidants
heart disease
CVD
homocysteine
TOS
DNA damage
malondialdehyde
8-Hydroxy2’deoxyguanosine
Issue Date: 16-Nov-2016
Publisher: Karachi: Faculty of Pharmacy & Pharmaceutical Sciecnes, University of Karachi
Abstract: Amounts of DNA damage and homocysteine (Hcy) in heart patients blood may have strong function in the causation of cardiovascular disease (CVD). The main objective of this work was to know experimentally the role of total oxidants (produced by Reactive Oxygen species (ROS), clinical biochemical indices, their oxidized products and total antioxidant status (TAS) among such patients to find the association of homocysteine, total oxidation status (TOS) and oxidative DNA damage with other clinical parameters in sixty positive CVD patients compared with those of 60 normal subjects. As compared to healthy individuals, CVD patients had significantly higher concentrations of homocysteine (p<0.0001), total oxidants stress (TOS) (p<0.0001), serum total lipids (p<0.04), malondialdehyde (MDA) (p<0.001), high density lipoprotein-cholesterol (HDL-C) (p<0.0001), and low density lipoprotein cholesterol (LDL-C) (p<0.01), than those of healthy individuals. Plasma Hcy content, TOS and amount of DNA were positively and significantly associated with cholesterol, triglycerides, systolic blood pressure, urea, and albumin (p values<0.01). TOS, Hcy and oxidative DNA damage were negatively correlated with HDL-c, TAS and proteins. It is suggested that these parameters have pivotal role in diagnostic process of determining severity in CAD patients. Oxidized products of macromolecules in blood of CVD patients impart major functions in causing CVD disease.
URI: http://142.54.178.187:9060/xmlui/handle/123456789/12794
ISSN: 1011-601X
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