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首页> 外文期刊>European journal of pharmaceutical sciences >How ineffective hypertension control in subjects treated with angiotensin-converting enzyme inhibitors is related to polymorphisms in the renin-angiotensin-aldosterone system.
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How ineffective hypertension control in subjects treated with angiotensin-converting enzyme inhibitors is related to polymorphisms in the renin-angiotensin-aldosterone system.

机译:在用血管紧张素转换酶抑制剂治疗的受试者中无效的高血压控制如何与肾素-血管紧张素-醛固酮系统中的多态性相关。

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PURPOSE: To investigate how genetic polymorphisms of the renin-angiotensin-aldosterone system (RAAS) influence hypertension (HT) control with angiotensin-converting enzyme inhibitor drugs (ACEI). METHODS: A case-control, cross-sectional population-based nested study (n=1514) included hypertensive patients treated with ACEI drugs, either alone or with other antihypertensive drugs. We differentiated between those who did not control their HT (cases) with those who did (controls). Each group's characteristics were compared to determine the risk of non-controlled HT associated with RAAS polymorphisms by adjusting for different variables. RESULTS: rs11571074 obtained an ORa of 5.26 for T/T (1.25-20). rs5945377 obtained an ORa 16.16 (1.61-162.62) for genotypes G/G-G/C. rs909383, rs275649 and rs4681444 obtained an ORa of 4.00 (1.19-14.28), 5.89 (1.53-25) and 3.89 (1.53-25) when genotypes C/C and A/A were expressed for the first and for the other two, respectively. For rs2272089, rs13117325 and rs11099680, a higher non-control risk was seen in A/G-G/G carriers (ORa: 4.9 (1.3-18.3); ORa: 3.7 (1.0-13.4); ORa: 6.5 (1.7-24.7). Finally, rs6535598 obtained an ORa of 10.4 (1.2-92.9) in T/T carriers. CONCLUSIONS: Although this study shows a possible association of polymorphisms of RAAS genes with the risk of non-control of HT in ACEI-treated patients and indicates the importance of all this system's components in regulating HT, it needs to be replicated in other data sources.
机译:目的:探讨肾素-血管紧张素-醛固酮系统(RAAS)的遗传多态性如何通过血管紧张素转换酶抑制剂药物(ACEI)影响高血压(HT)控制。方法:一项病例对照,基于人群的横断面嵌套研究(n = 1514)包括接受ACEI药物治疗的高血压患者,单独或与其他降压药一起使用。我们区分了那些没有控制他们的HT(病例)的人和那些没有控制他们的HT(病例)的人。比较各组的特征,以通过调整不同变量来确定与RAAS多态性相关的不受控制的HT的风险。结果:rs11571074获得的T / T(1.25-20)的ORa为5.26。 rs5945377获得了基因型G / G-G / C的ORa 16.16(1.61-162.62)。当分别针对第一个基因型和其他两个基因型分别表达C / C和A / A基因型时,rs909383,rs275649和rs4681444获得的ORa为4.00(1.19-14.28),5.89(1.53-25)和3.89(1.53-25)。 。对于rs2272089,rs13117325和rs11099680,在A / GG / G携带者中观察到更高的非控制风险(ORa:4.9(1.3-18.3); ORa:3.7(1.0-13.4); ORa:6.5(1.7-24.7)。最后,rs6535598在T / T携带者中获得了10.4(1.2-92.9)的ORa结论:尽管本研究表明RAEI基因多态性与ACEI治疗的患者无法控制HT的风险有关,并指出该系统所有组件在调节HT方面的重要性,需要在其他数据源中进行复制。

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