The Value of 8-iso Prostaglandin F2 Alpha and Superoxide Dismutase Activity as a Clinical Indicator of Oxidative Stress in Type II Diabetes Mellitus
Introduction: Type II Diabetes Mellitus (T2DM) is a serious metabolic disorder in which Oxidative Stress (OS) is responsible for tissue damage and complications. An 8-iso prostaglandin F2 alpha (8-iso-PGF2α) is a stable and abundant active product of oxidative stress that could promote complications...
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Veröffentlicht in: | Journal of clinical and diagnostic research 2018-11, Vol.12 (11), p.BC10-BC14 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Introduction: Type II Diabetes Mellitus (T2DM) is a serious metabolic disorder in which Oxidative Stress (OS) is responsible for tissue damage and complications. An 8-iso prostaglandin F2 alpha (8-iso-PGF2α) is a stable and abundant active product of oxidative stress that could promote complications in DM and could be used as a biomarker for the detection of oxidative injury and lipid peroxidation. Aim: The study was designed to evaluate the accuracy of 8-iso prostaglandin F2 alpha (8-iso-PGF2α) and Superoxide Dismutase (SOD) activity as a biomarker of OS in T2DM and to verify their relation with the glycaemic control and lipid profile. Materials and Methods: This is a cross-sectional case control study that included 58 (20 good glycaemic control and 38 poor glycaemic control) T2DM patients from Al-Noor Specialist Hospital, Holly Makkah and 20 healthy volunteers. 8-iso-PGF2α was measured by quantitative ELISA and SOD enzyme activity assayed by colorimetric technique. Data were analysed using SPSS version 20. All numerical data were represented as mean±SD. ANOVA test was used for comparisons between the different groups. Receiver Operating Characteristic (ROC) curve was conducted to calculate sensitivity and specificity. Results: There was a highly significant increase in 8-iso-PGF2α level in the uncontrolled DM cases compared to both the control and controlled DM groups (p |
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ISSN: | 2249-782X 0973-709X |
DOI: | 10.7860/JCDR/2018/35505.12255 |