Association of Klotho gene polymorphism with hypertension and coronary artery disease in an Iranian population |
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Authors: | Hamed Akbari Gholamreza Asadikaram Hamid Aria Saba Fooladi Sina Vakili Mohammad Masoumi |
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Affiliation: | 1.Neuroscience Research Center, Institute of Neuropharmacology,Kerman University of Medical Sciences,Kerman,Iran;2.Endocrinology and Metabolism Research Center, Institute of Basic and Clinical Physiology Sciences,Kerman University of Medical Sciences,Kerman,Iran;3.Department of Biochemistry, School of Medicine,Kerman University of Medical Sciences,Kerman,Iran;4.Department of Immunology, School of Medicine,Shiraz University of Medical Sciences,Shiraz,Iran;5.Bioinformatics and Computational Biology Research Center,Shiraz University of Medical Sciences,Shiraz,Iran;6.Student Research Committee, School of Medicine,Kerman University of Medical Sciences,Kerman,Iran;7.Biochemistry Department, School of Medicine,Shiraz University of Medical Sciences,Shiraz,Iran;8.Cardiovascular Research Center, Institute of Basic and Clinical Physiology Sciences,Kerman University of Medical Sciences,Kerman,Iran |
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Abstract: | BackgroundKlotho, possibly an age-regulating protein, is considered an important factor contributing to the lifespan and pathophysiology of hypertension and coronary artery disease (CAD). The present study was carried out aiming to investigate the association of Klotho-rs564481 (C1818T) gene polymorphism with hypertension and CAD.MethodsA total of 286 CAD-suspicious subjects were entered into this case-control study. The polymorphism was investigated in hypertensive patients with no CAD (H-Tens, n?=?60); hypertensive patients with CAD (CAD?+?H-Tens, n?=?95); CAD patients with no hypertension (CAD, n?=?61); and non-hypertensive non-CAD subjects, which were regarded as the control group (Ctrl, n?=?70). Genotype and allele frequencies were assessed using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method.ResultsA significant difference was found in allele frequency of Klotho C1818T among the four research groups (P?=?0.03). It was also found that wild-type homozygote subjects were negatively associated with hypertension as compared to heterozygote ones (OR?=?0.07 [95% CI: 0.008–0.69] P?=?0.02). Moreover, in the subgroups older than 57?years old, dominant genetic model demonstrated a negative association with CAD combined with hypertension (OR?=?0.31 [95% CI: 0.10–0.95] P?=?0.04).ConclusionsIn conclusion, Klotho C1818T variant may be associated with a decreased risk of hypertension. Moreover, aging enhanced positive effects of the Klotho polymorphism on CAD combined with hypertension, indicating the possibility that the KLOTHO gene might play a part in the age-related occurrence of CAD combined with hypertension. |
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