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Early Right Ventricular Apical Pacing-Induced Gene Expression Alterations Are Associated with Deterioration of Left Ventricular Systolic Function

机译:早期右心室心尖起搏诱导的基因表达改变与左心室收缩功能恶化相关

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摘要

The chronic high-dose right ventricular apical (RVA) pacing may have deleterious effects on left ventricular (LV) systolic function. We hypothesized that the expression changes of genes regulating cardiomyocyte energy metabolism and contractility were associated with deterioration of LV function in patients who underwent chronic RVA pacing. Sixty patients with complete atrioventricular block and preserved ejection fraction (EF) who underwent pacemaker implantation were randomly assigned to either RVA pacing (n = 30) group or right ventricular outflow tract (RVOT) pacing (n = 30) group. The mRNA levels of OPA1 and SERCA2a were significantly lower in the RVA pacing group at 1 month's follow-up (both p < 0.001). Early changes in the expression of selected genes OPA1 and SERCA2a were associated with deterioration in global longitudinal strain (GLS) that became apparent months later (p = 0.002 and p = 0.026, resp.) The altered expressions of genes that regulate cardiomyocyte energy metabolism and contractility measured in the peripheral blood at one month following pacemaker implantation were associated with subsequent deterioration in LV dyssynchrony and function in patients with preserved LVEF, who underwent RVA pacing.
机译:慢性大剂量右心室顶端(RVA)起搏可能会对左心室(LV)收缩功能产生有害影响。我们假设,接受慢性RVA起搏的患者中调节心肌能量代谢和收缩力的基因的表达变化与LV功能的恶化有关。将60例完全房室传导阻滞且射血分数保留(EF)的患者接受了起搏器植入,随机分为RVA起搏(n = 30)组或右室流出道(RVOT)起搏(n = 30)组。在RVA起搏组中,在随访1个月时,OPA1和SERCA2a的mRNA水平显着降低(均为p <0.001)。所选基因OPA1和SERCA2a表达的早期变化与几个月后出现的全局纵向应变(GLS)恶化有关(p = 0.002和p​​ = 0.026,分别)。调节心肌能量代谢和调节的基因表达改变。接受起搏器起搏的LVEF保留患者在起搏器植入后一个月的外周血中测得的收缩力与LV不同步和功能的恶化有关。

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