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June 2018 Vol. 6 No.6
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Merit Research Journal of Medicine and Medical
Sciences (ISSN: 2354-323X) Vol. 6(6) pp. 219-227,
June, 2018
Copyright © 2018 Merit Research Journals |
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Original Research Article
Comparison of the
prevalence of four coding polymorphisms of KCNH2 in
healthy Kurds and Malays |
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1Muslih Abdulkarim Ibrahim,
1,3Zalina Zahari, 2Zawiyah Derani, 2Nurfadhlina
Musa and 4Khoo Boon Yin |
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1Department
of Pharmacology and Toxicology, College of Pharmacy, Hawler
Medical University, Hawler, Iraq
2Pharmacogenetics and Novel Therapeutics Cluster,
Institute for Research in Molecular Medicine (INFORMM),
Universiti Sains Malaysia (USM), Kelantan, Malaysia
3Faculty of Pharmacy, Universiti Sultan Zainal Abidin
(UniSZA), Besut Campus, Terengganu, Malaysia
4Institute for Research in Molecular Medicine (INFORMM),
Universiti Sains Malaysia (USM), Penang, Malaysia
*Corresponding Authors’ E-mail: boonyin@usm.my/zalinazahari@unisza.edu.my
Accepted June 21, 2018 |
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Abstract |
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KCNH2
polymorphisms appear to be associated with arrhythmia
susceptibility, drug-associated acquired long-QT syndrome and
variability in drug responses. To date, little is known about
the prevalence of KCNH2 polymorphisms among Kurds and
Malays. As such, there is clearly a need to explore the genetic
polymorphisms of KCNH2 among Kurds and Malays in order to
understand the ethnic variation in KCNH2 polymorphisms.
DNA was extracted from whole blood and then subjected to
genotyping for KCNH2 polymorphisms, including 1539C>T
(rs1805120), 1956T>C (rs1137617), 2350C>T (rs12720441) and
2690A>C (rs1805123) using nested allele-specific PCR. The 2350T
allele for the 2350C>T polymorphism was absent in 487 unrelated
healthy Kurds and 117 Malays. The most frequent mutant allele in
Kurds was 1956C (63.9%), followed by 1539T (26.6%) and 2690C
(22.4%). Frequencies of the1956C, 1539T and 2690C alleles in
Malays were 80.8%, 52.6% and 8.1%, respectively. The relative
commonness of mutant alleles of KCNH2 polymorphisms in
our study calls attention to KCNH2 polymorphisms, which
should be incorporated into future association studies in Kurds
and Malays for the development of effective QT-prolonging
medications.
Keywords: Genetic polymorphisms, nested allele-specific
PCR, KCNH2; Kurds; Malays
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