首页> 外文期刊>Clinical and experimental hypertension: CEH >Association analysis about HLA-DRB1, -DQB1 polymorphism and auto-antibodies against alpha(1)-adrenergic receptors in Chinese patients with essential hypertension.
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Association analysis about HLA-DRB1, -DQB1 polymorphism and auto-antibodies against alpha(1)-adrenergic receptors in Chinese patients with essential hypertension.

机译:中国原发性高血压患者HLA-DRB1,-DQB1多态性与抗α(1)-肾上腺素能受体自身抗体的关联分析。

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The auto-antibodies against alpha(1)-adrenergic receptors (alpha(1)-AAs) with agonist activity likes norepinephrine have been discovered in patients with essential hypertension but the mechanism of alpha(1)-AA production remains unclear. We supposed the alpha(1)-AAs be correlated to the HLA-DQB1 and DRB1 alleles. Three hundred ninety-six patients with essential hypertension (EH) and 224 normotensives were enrolled, and DNA typing was detected by protein coupled receptor (PCR) amplification with sequence-specific primers. Analysis was performed by alpha(2) and logistic regression. There were the significant associations of the haplotype HLA-DQB1*0301-DRB1*04 with the prevalence of alpha(1)-AAs in hypertensive patients and it obviously added to the risk for the alpha(1)-AA production (adjusted P = 0.019, OR 4.037, 95% CI 1.259-12.947). In normotensives, the haplotype HLA-DQB1*05-DRB1*04 provided a strong predisposition in alpha (1)-AAs production (adjusted P = 0.024, OR 3.922, 95% CI 1.200-12.817). These results suggest the HLA-DRB1*04 might be the primary risk alleles associated with alpha(1)-AA production on the haplotypes HLA-DQB1*0301-DRB1*04 and HLA-DQB1*05-DRB1*04 and increased the risk for alpha (1)-AA production.
机译:在患有原发性高血压的患者中发现了具有激动剂活性(如去甲肾上腺素)的抗α(1)-肾上腺素受体(α(1)-AAs)的自身抗体,但尚不清楚α(1)-AA产生的机制。我们假设alpha(1)-AA与HLA-DQB1和DRB1等位基因相关。纳入396例原发性高血压(EH)和224血压正常的患者,并通过使用序列特异性引物的蛋白质偶联受体(PCR)扩增检测DNA分型。通过alpha(2)和逻辑回归进行分析。在高血压患者中,单倍型HLA-DQB1 * 0301-DRB1 * 04与α(1)-AA的患病率之间存在显着关联,并且显然增加了α(1)-AA产生的风险(校正后的P = 0.019,或4.037,95%CI 1.259-12.947)。在血压正常的人群中,单倍型HLA-DQB1 * 05-DRB1 * 04在α(1)-AAs的产生中具有很强的易感性(调整后的P = 0.024,或3.922,95%CI 1.200-12.817)。这些结果表明,HLA-DRB1 * 04可能是与单体型HLA-DQB1 * 0301-DRB1 * 04和HLA-DQB1 * 05-DRB1 * 04的alpha(1)-AA产生相关的主要风险等位基因,并增加了风险用于生产alpha(1)-AA。

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