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首页> 外文期刊>Clinica chimica acta: International journal of clinical chemistry and applied molecular biology >Additive effect of interleukin-6 and C-reactive protein (CRP) single nucleotide polymorphism on serum CRP concentration and other cardiovascular risk factors.
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Additive effect of interleukin-6 and C-reactive protein (CRP) single nucleotide polymorphism on serum CRP concentration and other cardiovascular risk factors.

机译:白细胞介素6和C反应蛋白(CRP)单核苷酸多态性对血清CRP浓度和其他心血管危险因素的累加作用。

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BACKGROUND: Serum C-reactive protein (CRP) levels, closely associated with cardiovascular disease (CVD) risk are influenced by CRP or interleukin-6 (IL-6) single nucleotide polymorphism (SNPs). However, it is still controversial. Therefore, we investigated the association of IL-6/CRP SNPs and serum CRP levels or other CVD risk factors in healthy adult Korean men. METHODS: In healthy adult men (age>/=20 years, n=677), we genotyped IL-6-572C>G and CRP SNPs (-717G>A, 1444C>T, 2147A>G) and measured anthropometric parameters, lipid profile, serum levels of CRP and IL-6 and insulin resistance. RESULTS: At IL-6-572C>G (n=677), subjects with G/G genotype (n=42) showed higher concentrations of CRP (P=0.027) and IL-6 (P=0.028) as compared with C allele carriers after age-adjustment (C/C: n=371, C/G: n=264). Fasting insulin and homeostatis model assessment insulin resistance (HOMA-IR) were also higher in G/G genotype. However, there were no significant differences in other metabolic biomarkers. Among 677 study subjects, 676 were genotyped at CRP-717G>A (G/G: n=513, G/A: n=150, A/A: n=13), 672 at CRP+1444C>T (C/C: n=580, C/T: n=85, T/T: n=7), and 668 at CRP+2147A>G (A/A: n=273, A/G: n=296, G/G: n=99). There were no significant differences in CRP concentrations and other markers related to CVD risk according to each CRP SNP genotype. However, we could find the additive gene-gene interaction between IL-6-572C>G and CRP SNPs on CRP concentration; subjects with the 'G/G' at IL-6-572 showed the highest CRP levels when they have variant allele at CRP SNPs after adjusted for age, body mass index, cigarette smoking and alcohol drinking (-717G>A: F=7.806, P=0.005; CRP+1444C>T: F=8.398, P=0.004; and CRP+2147A>G: F=7.564, P=0.006, respectively) Particularly, G allele carriers at CRP+2147A>G in subjects with IL-6-572G/G showed highest HOMA-IR (F=9.092, P=0.003). CONCLUSION: The present data showed that serum CRP levels and other CVD risk factors appeared more influenced by IL-6-572C>G rather than CRP SNPs (-717G>A, 1444C>T, and2147A>G), however CRP levels and insulin resistance may be additively affected by IL-6-572 and CRP SNP, particularly when subjects with G/G genotype at IL-6-572 have allele variant at CRP SNPs.
机译:背景:与心血管疾病(CVD)风险密切相关的血清C反应蛋白(CRP)水平受CRP或白介素6(IL-6)单核苷酸多态性(SNP)的影响。但是,它仍然是有争议的。因此,我们调查了健康成年韩国男性中IL-6 / CRP SNP与血清CRP水平或其他CVD危险因素的关系。方法:在健康的成年男性(年龄> / = 20岁,n = 677)中,我们对IL-6-572C> G和CRP SNP(-717G> A,1444C> T,2147A> G)进行了基因分型,并测量了人体测量学参数,血脂,血清CRP和IL-6水平以及胰岛素抵抗。结果:在IL-6-572C> G(n = 677)时,与C相比,G / G基因型(n = 42)的受试者表现出较高的CRP浓度(P = 0.027)和IL-6(P = 0.028)。年龄调整后的等位基因携带者(C / C:n = 371,C / G:n = 264)。空腹胰岛素和稳态模型评估的胰岛素抵抗(HOMA-IR)在G / G基因型中也较高。但是,其他代谢生物标志物无显着差异。在677个研究对象中,有676个在CRP-717G> A(G / G:n = 513,G / A:n = 150,A / A:n = 13)和CRP + 1444C> T(C / C:n = 580,C / T:n = 85,T / T:n = 7),CRP + 2147A> G时为668(A / A:n = 273,A / G:n = 296,G / G:n = 99)。根据每种CRP SNP基因型,CRP浓度和与CVD风险相关的其他标志物无显着差异。然而,我们发现IL-6-572C> G与CRP SNPs在CRP浓度上存在加性基因-基因相互作用。在对年龄,体重指数,吸烟和饮酒进行调整后,IL-6-572的“ G / G”值为“ G / G”的受试者在CRP SNP处具有等位基因时显示最高的CRP水平(-717G> A:F = 7.806 ,P = 0.005; CRP + 1444C> T:F = 8.398,P = 0.004;以及CRP + 2147A> G:F = 7.564,P = 0.006)特别是,在患有以下疾病的受试者中,CRP + 2147A> G的G等位基因携带者IL-6-572G / G显示最高的HOMA-IR(F = 9.092,P = 0.003)。结论:现有数据表明,血清CRP水平和其他CVD危险因素似乎受IL-6-572C> G而不是CRP SNPs影响更大(-717G> A,1444C> T和2147A> G),但是CRP水平和胰岛素IL-6-572和CRP SNP可能会进一步增加耐药性,特别是当IL-6-572具有G / G基因型的受试者在CRP SNPs具有等位基因变异时。

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