Impact of PCSK9, WDR12, CDKN2A, and CXCL12 Polymorphisms in Jordanian Cardiovascular Patients on Warfarin Responsiveness and Sensitivity

The main objective of this study is sought to determine the impacts of PCSK9, WDR12, CDKN2A, and CXCL12 polymorphisms on warfarin sensitivity and responsiveness in Jordanian cardiovascular patients during the initiation and stabilization phases of therapy. This study took place at the anticoagulatio...

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Bibliographic Details
Published in:International journal of general medicine 2021-01, Vol.14, p.103-118
Main Authors: Ibdah, Rasheed K, Al-Eitan, Laith N, Alrabadi, Nasr N, Almasri, Ayah Y, Alnaamneh, Adan H, Khasawneh, Rame H, Alghamdi, Mansour A
Format: Article
Language:English
Subjects:
Anticoagulants
Cardiovascular disease
cdkn2a
Cell cycle
Cell division
cxcl1
Cyclin-dependent kinases
Genes
Genomics
Metabolism
Original Research
Patients
pcsk9
Proteins
Thrombosis
warfarin
wdr12
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Summary:The main objective of this study is sought to determine the impacts of PCSK9, WDR12, CDKN2A, and CXCL12 polymorphisms on warfarin sensitivity and responsiveness in Jordanian cardiovascular patients during the initiation and stabilization phases of therapy. This study took place at the anticoagulation clinic at Queen Alia Heart Institute (QAHI) in Jordan. DNA samples were collected from 212 cardiovascular patients and 213 healthy controls. Genomic SNPs genotyping was conducted using the MassARRAY System at the Australian Genome Research Facility. This study assessed 10 polymorphisms (rs11206510 within the gene, rs6725887 and rs7582720 within the gene, rs4977574, rs10757278, and rs1333049 within the gene, rs2862116, rs7906426, rs1746048, and rs268322 within the gene) in 212 Jordanian cardiovascular patients. Carriers of CDKN2A rs1333049, rs10757278, and PCSK9 rs11206510 polymorphisms had an increased risk of resistance during the initiation phase of warfarin therapy compared to those who do not carry it, or those who are carrying one polymorphism only (P < 0.05), while carriers of CXCL12 rs7906426 polymorphism had similar increased risk but during the stabilization phase of warfarin therapy (P < 0.05). Carriers of CXCL12 rs2862116 polymorphism had an increased risk to be warfarin extensive responders compared to those with no or only one polymorphism (P = 0.01). However, the presence of PCSK9 rs11206510 polymorphism affects the warfarin maintenance doses (P ˃ 0.0001).
ISSN:1178-7074
1178-7074
DOI:10.2147/IJGM.S287238