The identification of copy number variation of CNV esv27061 among young adults with hypertension: preliminary findings

Introduction: Hypertension related morbidities and mortalities around the world show a gradual increase and early detection and prevention are advocated. The Database of Genomic Variants (DGV) has associated variation in DNA sequences called copy number variation (CNV) with susceptibility...

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Main Authors: Shaik Alaudeen, Siti Radziah, Mohd Shah, Azarisman Shah, A.Talib, Norlelawati, Abdullah, Aszrin
Format: Article
Language:English
Published: Kulliyyah (Faculty) of Medicine, International Islamic University Malaysia. 2017
Subjects:
Online Access:http://irep.iium.edu.my/63474/
http://irep.iium.edu.my/63474/1/Abstract-Book-for-IMJM-final-v2-37.pdf
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author Shaik Alaudeen, Siti Radziah
Mohd Shah, Azarisman Shah
A.Talib, Norlelawati
Abdullah, Aszrin
author_facet Shaik Alaudeen, Siti Radziah
Mohd Shah, Azarisman Shah
A.Talib, Norlelawati
Abdullah, Aszrin
author_sort Shaik Alaudeen, Siti Radziah
building IIUM Repository
collection Online Access
description Introduction: Hypertension related morbidities and mortalities around the world show a gradual increase and early detection and prevention are advocated. The Database of Genomic Variants (DGV) has associated variation in DNA sequences called copy number variation (CNV) with susceptibility to common diseases. However, little is known about CNV role in essential hypertension. Thus, this study aimed to characterize the CNV esv27061 among prehypertensive and hypertensive young adults in Malaysia. Materials and method: In this comparative cross-sectional study, 104 subjects living in Kuantan who gave voluntary consent to participate are recruited and divided into three groups; control (43 subjects), prehypertensive (38 subjects) and mild hypertensive (23 subjects). An optimized droplet digital polymerase chain reaction (ddPCR) was used in the determination of CNV esv27061 in this study. Results: All subjects in the control (n=38; 88.4% gain), prehypertensive (n=33; 86.8% gain) and mild hypertensive (n=21; 91.3% gain) groups had CNV gain (copy number > 2) while 11.6% of control, 13.2% of prehypertensive and 8.7% of mild hypertensive subjects exhibited normal copies (copy number = 2). Conclusion: The present preliminary finding was consistent with the Database of Genomic Variants (DGV) which stated that CNV esv27061 showedmore gain than loss.
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spelling iium-634742018-08-30T03:02:46Z http://irep.iium.edu.my/63474/ The identification of copy number variation of CNV esv27061 among young adults with hypertension: preliminary findings Shaik Alaudeen, Siti Radziah Mohd Shah, Azarisman Shah A.Talib, Norlelawati Abdullah, Aszrin R Medicine (General) RB Pathology Introduction: Hypertension related morbidities and mortalities around the world show a gradual increase and early detection and prevention are advocated. The Database of Genomic Variants (DGV) has associated variation in DNA sequences called copy number variation (CNV) with susceptibility to common diseases. However, little is known about CNV role in essential hypertension. Thus, this study aimed to characterize the CNV esv27061 among prehypertensive and hypertensive young adults in Malaysia. Materials and method: In this comparative cross-sectional study, 104 subjects living in Kuantan who gave voluntary consent to participate are recruited and divided into three groups; control (43 subjects), prehypertensive (38 subjects) and mild hypertensive (23 subjects). An optimized droplet digital polymerase chain reaction (ddPCR) was used in the determination of CNV esv27061 in this study. Results: All subjects in the control (n=38; 88.4% gain), prehypertensive (n=33; 86.8% gain) and mild hypertensive (n=21; 91.3% gain) groups had CNV gain (copy number > 2) while 11.6% of control, 13.2% of prehypertensive and 8.7% of mild hypertensive subjects exhibited normal copies (copy number = 2). Conclusion: The present preliminary finding was consistent with the Database of Genomic Variants (DGV) which stated that CNV esv27061 showedmore gain than loss. Kulliyyah (Faculty) of Medicine, International Islamic University Malaysia. 2017-09-15 Article PeerReviewed application/pdf en http://irep.iium.edu.my/63474/1/Abstract-Book-for-IMJM-final-v2-37.pdf Shaik Alaudeen, Siti Radziah and Mohd Shah, Azarisman Shah and A.Talib, Norlelawati and Abdullah, Aszrin (2017) The identification of copy number variation of CNV esv27061 among young adults with hypertension: preliminary findings. International Medical Journal Malaysia, 16 (Supplementary Issue 1). p. 31. E-ISSN 1823-4631 http://iiumedic.net/imjm/v1/download/Volume%2016%20No%201%20Supp%201/Abstract-Book-for-IMJM-final-v2-37.pdf
spellingShingle R Medicine (General)
RB Pathology
Shaik Alaudeen, Siti Radziah
Mohd Shah, Azarisman Shah
A.Talib, Norlelawati
Abdullah, Aszrin
The identification of copy number variation of CNV esv27061 among young adults with hypertension: preliminary findings
title The identification of copy number variation of CNV esv27061 among young adults with hypertension: preliminary findings
title_full The identification of copy number variation of CNV esv27061 among young adults with hypertension: preliminary findings
title_fullStr The identification of copy number variation of CNV esv27061 among young adults with hypertension: preliminary findings
title_full_unstemmed The identification of copy number variation of CNV esv27061 among young adults with hypertension: preliminary findings
title_short The identification of copy number variation of CNV esv27061 among young adults with hypertension: preliminary findings
title_sort identification of copy number variation of cnv esv27061 among young adults with hypertension: preliminary findings
topic R Medicine (General)
RB Pathology
url http://irep.iium.edu.my/63474/
http://irep.iium.edu.my/63474/
http://irep.iium.edu.my/63474/1/Abstract-Book-for-IMJM-final-v2-37.pdf