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首页> 外文期刊>European Journal of Inflammation >Association of IL-1β polymorphisms and plasma levels with chronic heart failure: A case-control study in Chinese patients:
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Association of IL-1β polymorphisms and plasma levels with chronic heart failure: A case-control study in Chinese patients:

机译:IL-1β基因多态性和血浆水平与慢性心力衰竭的关系:中国患者的病例对照研究:

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Heart failure (HF) has been major health concern affecting 1%–2% of world adult population. Role of various cytokines in chronic heart failure (CHF) have been demonstrated in different populations; however, association of an important cytokine, interleukin-1β (IL-β), is poorly documented. Furthermore, polymorphism in promoter region is shown to be linked with cytokines levels. In this study, we explored plasma levels of IL-1β in healthy controls (HCs) and different clinical categories of CHF and association of common IL-1β promoter variants with susceptibility to development of HF. In all, 354 CHF patients admitted to Department of Cardiology at the first affiliated hospital of Soochow University were enrolled in this study. These patients were further clinically sub-categorized into New York Heart Association (NYHA)-I to IV based on NYHA criteria. A total of 77 HCs were included in the current investigation. Plasma levels of IL-1β were quantified by enzyme-linked immunosorbent assay (ELISA) and common promoter gene polymorphisms in IL-1β gene were genotyped by polymerase chain reaction (PCR)-restriction fragment length polymorphism (RFLP). CHF patients displayed higher plasma IL-1β compared to HCs. Interestingly, plasma levels of IL-1β were associated with severity of HF patients: NYHA-IV had highest levels, and least quantity was noticed in NYHA-I cases. Prevalence of heterozygous and homozygous mutant for C-511T polymorphisms were significantly higher in CHF patients when compared to HCs. Importantly, these observations remained valid for NYHA-III and IV sub-groups in comparison to controls. Elevated plasma levels of IL-1β were observed in 511 mutants (CT and TT) than wild type (CC), indicating important function variants determining plasma levels of cytokine in both controls and patients. In conclusion, IL-1β (C-511T) variants are associated with elevated plasma IL-1β and predisposed to severe chronic HF in Chinese.
机译:心力衰竭(HF)是主要的健康问题,影响了全世界1%–2%的成年人口。在不同人群中已经证明了各种细胞因子在慢性心力衰竭(CHF)中的作用。然而,关于重要的细胞因子白介素-1β(IL-β)的相关文献报道却很少。此外,显示启动子区域的多态性与细胞因子水平有关。在这项研究中,我们探讨了健康对照(HCs)和CHF的不同临床类别中血浆IL-1β的水平,以及常见的IL-1β启动子变体与HF易感性的关系。总共纳入了苏州大学第一附属医院心血管内科的354名CHF患者。根据NYHA标准,将这些患者进一步临床分类为纽约心脏协会(NYHA)-I至IV。本次调查共纳入了77种HC。通过酶联免疫吸附测定(ELISA)定量测定IL-1β的血浆水平,并通过聚合酶链反应(PCR)-限制性片段长度多态性(RFLP)对IL-1β基因中常见的启动子基因多态性进行基因分型。与HCs相比,CHF患者的血浆IL-1β更高。有趣的是,IL-1β的血浆水平与HF患者的病情相关:NYHA-IV的水平最高,而在NYHA-I的病例中发现的量最少。与HCs相比,CHF患者中C-511T多态性杂合和纯合突变的患病率显着更高。重要的是,与对照相比,这些观察结果对于NYHA-III和IV子组仍然有效。与野生型(CC)相比,在511个突变体(CT和TT)中观察到IL-1β的血浆水平升高,表明在对照组和患者中确定细胞因子血浆水平的重要功能变异。总之,IL-1β(C-511T)变异与血浆IL-1β升高有关,易患重度慢性HF。

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