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Association of long-chain non-coding RNA MHRT gene single nucleotide polymorphism with risk and prognosis of chronic heart failure

机译:长链非编码RNA MHRT基因单核苷酸多态性与慢性心力衰竭风险和预后的关联

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Long-chain non-coding RNA (lncRNA) Myosin Heavy Chain Associated RNA Transcripts (MHRT) are newly identified cardioprotective lncRNAs. In this study, we investigated the association of MHRT gene single nucleotide polymorphisms with risk and prognosis of chronic heart failure (CHF). Sanger sequencing was performed to detect the genotypes of rs3729830, rs7140721, rs76614781, rs3729829, rs3729828, rs3729825, and rs3729822 loci in the non-coding region of the MHRT gene from 240 patients with CHF and 240 control subjects. After 3 years of follow-up, progression-free survival was recorded in patients with CHF. The risk of CHF in subjects carrying A allele of the MHRT gene rs7140721 locus was 1.43 times higher than that of C allele carriers (95% CI: 1.23–1.62, P .001). The risk of CHF in subjects carrying A allele of the rs3729829 locus was 1.41 times higher than that of G allele carriers (95% CI: 1.20–1.61, P .01). The risk of CHF in the carriers of T allele of the rs3729825 locus was 1.89 times higher than that of C allele carriers (adjusted OR = 1.89, 95% CI: 1.66–2.04, P .01). Further, the level of lncRNA MHRT in the plasma of subjects carrying CA/AA genotype of the rs7140721 locus was significantly higher than that of subjects carrying the CC genotype. The level of lncRNA MHRT in the plasma of subjects carrying GA/AA genotype of the rs3729829 locus was significantly higher than that of subjects carrying the GG genotype. In addition, the level of lncRNA MHRT in subjects with CT/TT genotype of the rs3729825 locus carriers was significantly higher than that in subjects with the CC genotype ( P .05). In addition, significant differences in the mortality of patients with CHF were observed between different genotypes of rs7140721, rs3729829, and rs3729825 loci ( P .001). The single nucleotide polymorphisms of MHRT gene rs7140721, rs3729829, and rs3729825 loci were associated with the risk of CHF and prognosis.
机译:长链非编码RNA(LNCRNA)肌苷重链相关的RNA转录物(MHRT)是新鉴定的心脏保护剂LNCRNA。在这项研究中,我们研究了MHRT基因单核苷酸多态性与慢性心力衰竭(CHF)的风险和预后的关联。进行Sanger测序以检测来自240例CHF和240个对照组的MHRT基因的非编码区的RS3729830,RS7140721,RS7614781,RS3729829,RS3729828,RS3729825和RS3729822的基因座。 3年后随访后,CHF患者记录了无进展的存活。携带MHRT基因RS7140721基因座等位基因的受试者中CHF的风险比C等位基因载体高1.43倍(95%CI:1.23-1.62,P <.001)。携带RS3729829基因座等位基因的受试者中CHF的风险比G等位基因载体高1.41倍(95%CI:1.20-1.61,P <.01)。 RS3729825轨迹的T等位基因载体中CHF的风险比C等位基因载体高1.89倍(调节或= 1.89,95%CI:1.66-2.04,P <.01)。此外,携带RS7140721基因座的CA / AA基因型的受试者的血浆中LNCRNA MHRT的水平显着高于携带CC基因型的受试者。携带RS3729829基因座的GA / AA基因型的受试者的血浆中LNCRNA MHRT的水平显着高于携带GG基因型的受试者。此外,RS3729825基因座的CT / TT基因型的受试者中LNCRNA MHRT的水平明显高于CC基因型的受试者(P <.05)。此外,在RS7140721,RS3729829和RS3729825基因座的不同基因型之间观察到CHF患者死亡率的显着差异(P <.001)。 MHRT基因RS7140721,RS3729829和RS3729825基因座的单核苷酸多态性与CHF和预后的风险有关。

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