STUDY OF BIOCHEMICAL MARKERS OF OXIDATIVE AND NITROSATIVE STRESS PATHWAYS IN MAJOR DEPRESSION

被引:2
|
作者
Rangaswamy, R. [1 ]
Swathi, K. [2 ]
机构
[1] Kannur Med Coll, Dept Biochem, Kannur, India
[2] CSI Holdsworth Hosp, Dept Biochem, Mysore, Karnataka, India
关键词
Malondialdehyde; Superoxide Dismutase; Nitric oxide; 21- item Hamilton Rating Scale for Major Depression;
D O I
10.14260/jemds/2014/3360
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND: Several investigators have implicated that major depression is characterized by decreased antioxidant status, an induction of the oxidative and nitrosative pathways. Abnormal levels of antioxidant enzymes and lipid peroxidation in major depression further substantiate the role of free radical in major depression. The objective of this study is to evaluate & compare serum levels of oxidative stress markers and peroxidation marker and nitrosative stress pathway markers (SOD, uric acid, MDA and NO levels). METHODOLOGY: The study included 100 subjects consisting of 50 healthy controls and 50 newly diagnosed patients of Major Depressive Disorder (MDD). Informed consent and institutional ethics committee approval was taken. Serum MDA levels was compared with parameters like SOD, Uric acid, NO. Clinical severity was diagnosed by trained psychiatrist using 21-items Hamilton Rating Scale for Depression (HRSD). RESULTS: Serum MDA, NO levels were significantly (p < 0.05) increased and SOD, Uric acid were significantly decreased in MDD patients as compared to healthy controls. There was moderate positive correlation between MDA levels and clinical severity of depression as measured by 21-items Hamilton Rating Scale for Depression (HRSD) score which was found to be statistically significant (r = 0.317, p value = 0.025). There was poor negative correlation between clinical severity and Uric acid levels. CONCLUSION: The study concluded that serum MDA, SOD, Uric acid and NO combined together provided fairly useful index of oxidative stress and nitrosative stress pathways in MDD. Evaluation of such critical biomarkers would certainly be useful and supportive for early diagnosis and treatment response.
引用
收藏
页码:10448 / 10453
页数:6
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