Liu Tianhua, Huang Hongman, Liu Xinbing, Yang Yuya, Mei Xiang, Feng Liuliu
Department of Cardiology, Shidong Hospital Shanghai 200000, China.
Int J Clin Exp Pathol. 2020 Nov 1;13(11):2831-2839. eCollection 2020.
To explore the effect of PITX2 gene rs6843082 single nucleotide polymorphism on the efficacy and adverse reactions of warfarin in patients with atrial fibrillation and hypertension, and to provide a theoretical basis for individualized warfarin treatment.
Data on 97 patients with atrial fibrillation and hypertension treated in our hospital were collected from September, 2018 to December, 2019. PCR and SNP genotyping techniques were used to measure the genotype at the rs6843082 locus (pituitary homeobox 2, PITX2) using DNA from the peripheral blood cells of all patients. We compared the efficacy of warfarin and the incidence of adverse reactions in patients of different genotypes.
(1) Among 97 subjects, 58 cases (59.79%), 32 cases (32.99%) and 7 cases (7.22%) of PITX2 (rs6843082) genotypes GG, GA and AA were identified respectively. The G and A allele frequencies were 76.29% and 23.71%, respectively. (2) After all patients took warfarin to achieve the standard, the GA group and AA group's time to achieve the standard was significantly longer than that of the GG group (<0.05). The difference was not statistically significant among groups (>0.05). Compared with the GG group, the maintenance dose of the AA group was increased (<0.05). (3) Compared with the GG and the GA group, the probability of bleeding events was higher in the AA group (<0.05). (4) There was no difference in left ventricular end diastolic volume (LVEDV) and left ventricular end systolic volume (LVESV) group among GG, GA and AA groups (>0.05). Compared with the GG group, left ventricular ejection fraction (LVEF) of the AA group was significantly reduced (<0.05). (5) The mortality rates of the GG, GA, and AA groups were 15.51%, 12.50% and 22.57%, respectively, at the end of 120 d follow-up.
Our findings show that rs6843082 SNP leads to the warfarin dose response differences that were observed in patients with atrial fibrillation and hypertension. Genotyping patients for rs6843082 before initiating warfarin treatment may optimize the treatment response and reduce bleeding incidence.
探讨PITX2基因rs6843082单核苷酸多态性对心房颤动合并高血压患者华法林疗效及不良反应的影响,为华法林个体化治疗提供理论依据。
收集2018年9月至2019年12月在我院治疗的97例心房颤动合并高血压患者的数据。采用聚合酶链反应(PCR)和单核苷酸多态性(SNP)基因分型技术,利用所有患者外周血细胞DNA检测rs6843082位点(垂体同源盒2,PITX2)的基因型。比较不同基因型患者华法林的疗效及不良反应发生率。
(1)97例受试者中,PITX2(rs6843082)基因型GG、GA和AA分别有58例(59.79%)、32例(32.99%)和7例(7.22%)。G和A等位基因频率分别为76.29%和23.71%。(2)所有患者服用华法林达标后,GA组和AA组达标时间显著长于GG组(<0.05)。组间差异无统计学意义(>0.05)。与GG组相比,AA组维持剂量增加(<0.05)。(3)与GG组和GA组相比,AA组出血事件发生率更高(<0.05)。(4)GG、GA和AA组间左心室舒张末期容积(LVEDV)和左心室收缩末期容积(LVESV)差异无统计学意义(>0.05)。与GG组相比,AA组左心室射血分数(LVEF)显著降低(<0.05)。(5)随访120 d结束时,GG、GA和AA组的死亡率分别为15.51%、12.50%和22.57%。
我们的研究结果表明,rs6843082单核苷酸多态性导致心房颤动合并高血压患者出现华法林剂量反应差异。在开始华法林治疗前对患者进行rs6843082基因分型,可能会优化治疗反应并降低出血发生率。