Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/318728
Title: Somatic DNA Damages in Modifiable and Non modifiable risk factors in Coronary Artery Disease
Researcher: Jiju JS
Guide(s): Vijikrishnan
Keywords: Biochemistry and Molecular Biology
Biology and Biochemistry
Life Sciences
University: Meenakshi Academy of Higher Education and Research
Completed Date: 2019
Abstract: ABSTRACT newlineThe present study was undertaken to evaluate the somatic DNA damages associated with modifiable and non-modifiable risk factors among Coronary Artery Disease (CAD) patients and to identify new biomarkers for the early detection of CAD. The study subjects comprised of 200 clinically proven CAD patients and One hundred age and sex matched healthy subjects were selected as controls where all subjects were taken within the age group of 31 to 55 years. The present study frankly proved the clinical utility of emerging risk markers such as ADMA, CerK and Lp-PLA2 for the early prediction of CAD and showed a positive correlation with the mean CBMN frequency. The extent of somatic DNA damages was expressed as mean CBMN frequency and it showed inter-individual variation. The increased mean CBMN frequency among the study subjects with 95% of confidence interval revealed its predictability for CAD. The present study concluded that modifiable risk factors contribute more somatic DNA damages in CAD patients than non-modifiable risk factors. Overall, the study recorded a broader understanding of genetic and molecular events that predisposing to CAD. In short, CAD is multi-faceted disease process with several different well-defined risk factors. Although traditional risk factors remain important, the application of genetic approach has pointed out a substantial role in predicting CAD. newline newline
Pagination: xix 306
URI: http://hdl.handle.net/10603/318728
Appears in Departments:Department of Biochemistry

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02_certificate.pdf335.05 kBAdobe PDFView/Open
03_declaration.pdf130.57 kBAdobe PDFView/Open
04_chapter 1.pdf372.78 kBAdobe PDFView/Open
05_chapter 2.pdf662.9 kBAdobe PDFView/Open
06_chapter 3.pdf731.04 kBAdobe PDFView/Open
07_chapter 4.pdf1.27 MBAdobe PDFView/Open
08_chapter 5.pdf308.88 kBAdobe PDFView/Open
09_chapter6.pdf129.17 kBAdobe PDFView/Open
10_bibliography.pdf914.5 kBAdobe PDFView/Open
11_annexure.pdf2.92 MBAdobe PDFView/Open
12_contents.pdf83.89 kBAdobe PDFView/Open
13_list of table and figures.pdf97.67 kBAdobe PDFView/Open
80_recommendation.pdf163.73 kBAdobe PDFView/Open
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