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Genetic association study of ABCB1 gene polymorphisms with hypertension in Han Chinese population

机译:汉族人群ABCB1基因多态性与高血压的遗传关联研究

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OBJECTIVE: Hypertension is a common disorder related to cardiovascular diseases and stroke. Identification of genetic variations related to hypertension may advance our knowledge of the molecular mechanism underlying blood pressure regulation. Here, we aimed to investigate the associations between ABCB1 gene polymorphisms and hypertension-related traits in 1154 Han Chinese subjects. PATIENTS AND METHODS: A total of 13 SNPs in ABCB1 were genotyped. RESULTS: Three SNPs were significantly associated with systolic blood pressure (SBP), including rs17327624 (p = 6.167 × 10-4, beta = 5.650), rs3789243 (p = 4.331 × 10-3, beta = 2.800), and rs4148734 (p = 3.514 × 10-3, beta = 3.692). Rs17327624 (p = 2.818 × 10-4, beta = 2.753) and rs3789243 (p = 6.345 × 10-3, beta = 1.497) were significantly associated with diastolic blood pressure (DBP) and rs17327624 was significantly associated with hypertension (p = 1.746 × 10-4, OR = 1.605). These three SNPs (rs17327624, rs3789243 and rs4148734) were also associated with hypertension in female subjects but no significant signal was detected in males. CONCLUSIONS: Our results suggest that ABCB1 polymorphisms may contribute to the blood pressure variation in Han Chinese population and the effect may be specific in females. Further studies performed in other populations are needed to confirm our findings and elucidate the underlying molecular mechanism.
机译:目的:高血压是与心血管疾病和中风有关的常见疾病。鉴定与高血压有关的遗传变异可能会提高我们对血压调节的分子机制的认识。在这里,我们旨在调查1154名汉族人群中ABCB1基因多态性与高血压相关性状之间的关联。患者与方法:对ABCB1中的13个SNP进行基因分型。结果:三个SNP与收缩压(SBP)显着相关,包括rs17327624(p = 6.167×10-4,β= 5.650),rs3789243(p = 4.331×10-3,β= 2.800)和rs4148734(p = 3.514×10-3,β= 3.692)。 Rs17327624(p = 2.818×10-4,beta = 2.753)和rs3789243(p = 6.345×10-3,beta = 1.497)与舒张压(DBP)显着相关,而rs17327624与高血压(p = 1.746)显着相关×10-4,或= 1.605)。这三个SNP(rs17327624,rs3789243和rs4148734)在女性受试者中也与高血压相关,但在男性中未检测到明显的信号。结论:我们的结果表明,ABCB1基因多态性可能是导致汉族人群血压变化的原因,其影响可能在女性中是特定的。需要在其他人群中进行进一步的研究以证实我们的发现并阐明潜在的分子机制。

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