
Honors Theses
Date of Award
5-2025
Document Type
Undergraduate Thesis
Degree Name
BS
Department
Biomedical Sciences
Faculty Mentor
Nancy A. Rice
Advisor(s)
Padmamalini Thulasiraman, Robin J. Mockett
Abstract
Accounting for the majority of deaths worldwide, non-communicable diseases (NCDs) present the greatest health challenge of the twenty-first century. Specifically, cardiovascular diseases (CVDs) exceed all other NCDs in annual deaths and especially affect low- and middle-income countries (LMICs). Hypertension, being the primary risk factor for CVD, affects over 75% of adults in LMICs due to inadequate health care and preventative measures. Additionally, epigenetic modifications of DNA are important mechanisms that regulate gene expression; DNA methylation, in particular, affects cytosine residues in cytosine-phosphate-guanine (CpG) islands on regulatory sequences. Previous research in our laboratory analyzed percent methylation at 8 different CpG islands in intron 1 of the NF-κB1 gene. As a result, this study further investigates the hypothesis that hypomethylated regulatory sequences of the NF-κB1 gene allows for greater transcriptional activity, resulting in a sustained inflammatory response and ultimately leading to hypertension. Results from this study showed that there may be increased percent methylation in normotensive/elevated versus hypertensive Kenyans (3.09% ± 0.47% and 2.43% ± 0.43%, respectively) when eight CpG sites of intron 1 were analyzed (n=20). In addition, Pearson's correlation showed that 23 pairs of CpG sites in the target sequence were positively associated with percent methylation. Moreover, results depicted statistical significance in predictive ability in 5 CpG sites for systolic blood pressure (SBP) and 6 CpG sites for diastolic blood pressure (DBP).
Recommended Citation
Piracha, Aaryan Barlas, "A Comparative Analysis of NF-κB1 Gene Regulatory Sequence Methylation in Normotensive and Hypertensive Kenyans" (2025). Honors Theses. 99.
https://jagworks.southalabama.edu/honors_college_theses/99
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