Royal Brompton Hospital, London, United Kingdom (A.G., S.R., B.P.H., N.A.I., K.M., J.K., C.S., P.R.K., J.G.F.C., M.R.C., R.G.A., D.J.P., S.K.P.).
Edinburgh Heart Centre, United Kingdom (A.G.J., N.S.).
Circ Cardiovasc Imaging. 2018 Sep;11(9):e007722. doi: 10.1161/CIRCIMAGING.118.007722.
Myocardial fibrosis, identified by late gadolinium enhancement cardiovascular magnetic resonance, predicts outcomes in chronic heart failure (HF). Its prognostic significance in new-onset HF and reduced left ventricular ejection fraction (LVEF) is unclear. We investigated whether the pattern and extent of fibrosis predict survival in new-onset HF and reduced LVEF of initially uncertain pathogenesis.
Of 120 consecutive patients with new-onset (<6 months) HF and reduced LVEF, 31 (26%) had infarct fibrosis, 25 (21%) had midwall fibrosis, and 64 (53%) had no fibrosis. During median follow-up of 8.9 years, 33 (28%) patients died. Patients with infarct fibrosis (hazard ratios [HR], 3.32; 95% CI, 1.46-7.58; P=0.004) or midwall fibrosis (HR, 2.99; 95% CI, 1.24-7.19; P=0.014) were more likely to die compared with those without fibrosis. On multivariable analysis, the pattern and extent of fibrosis were both associated with all-cause mortality (by fibrosis pattern: infarct: HR, 2.60; 95% CI, 1.08-6.27; P=0.033; midwall: HR, 2.64; 95% CI, 1.08-6.47; P=0.034; by fibrosis extent per 1%: HR, 1.07; 95% CI, 1.03-1.12; P<0.001). Fibrosis pattern also predicted composites of cardiovascular mortality or aborted sudden cardiac death (infarct: HR, 3.45; 95% CI, 1.20-9.90; P=0.022; midwall: HR, 6.59; 95% CI, 2.26-19.22; P<0.001), and all-cause mortality, HF hospitalization, or aborted sudden cardiac death (infarct: HR, 2.69; 95% CI, 1.26-5.76; P=0.011; midwall fibrosis: HR, 2.97; 95% CI, 1.37-6.45; P=0.006). Addition of fibrosis pattern to LVEF improved risk prediction for all-cause mortality (LVEF versus LVEF+fibrosis C statistic: 0.66 versus 0.71; P=0.033). Importantly, the absence of fibrosis heralded a favorable prognosis with an 85% survival rate over the duration of follow-up.
The pattern and extent of myocardial fibrosis predict adverse outcomes in new-onset HF and reduced LVEF. In contrast, the absence of fibrosis portends a durable warranty period with a low incidence of adverse events. These findings support a role for late gadolinium enhancement cardiovascular magnetic resonance in the early risk stratification of patients with HF of uncertain pathogenesis.
通过晚期钆增强心血管磁共振成像(cardiovascular magnetic resonance,CMR)检测到的心肌纤维化可预测慢性心力衰竭(HF)的结局。其在新发 HF 和射血分数降低(left ventricular ejection fraction,LVEF)中的预后意义尚不清楚。我们研究了纤维化的模式和程度是否可预测新发 HF 和最初病因不明的 LVEF 降低患者的生存情况。
在 120 例新发(<6 个月)HF 和 LVEF 降低的连续患者中,31 例(26%)存在梗死性纤维化,25 例(21%)存在中壁纤维化,64 例(53%)不存在纤维化。在中位 8.9 年的随访期间,33 例(28%)患者死亡。与无纤维化患者相比,存在梗死性纤维化(风险比[hazard ratios,HR],3.32;95%置信区间[confidence intervals,CI],1.46-7.58;P=0.004)或中壁纤维化(HR,2.99;95%CI,1.24-7.19;P=0.014)的患者更有可能死亡。多变量分析显示,纤维化的模式和程度均与全因死亡率相关(按纤维化模式:梗死性:HR,2.60;95%CI,1.08-6.27;P=0.033;中壁性:HR,2.64;95%CI,1.08-6.47;P=0.034;按纤维化程度每增加 1%:HR,1.07;95%CI,1.03-1.12;P<0.001)。纤维化模式也预测心血管死亡或心源性猝死(sudden cardiac death,SCD)未遂的复合终点(梗死性:HR,3.45;95%CI,1.20-9.90;P=0.022;中壁性:HR,6.59;95%CI,2.26-19.22;P<0.001)以及全因死亡、HF 住院或心源性猝死未遂(梗死性:HR,2.69;95%CI,1.26-5.76;P=0.011;中壁纤维化:HR,2.97;95%CI,1.37-6.45;P=0.006)。与 LVEF 相比,将纤维化模式加入 LVEF 可改善全因死亡率的风险预测(LVEF 与 LVEF+纤维化 C 统计量:0.66 与 0.71;P=0.033)。重要的是,无纤维化预示着预后良好,随访期间的不良事件发生率为 85%。这些发现支持晚期钆增强 CMR 在病因不明的 HF 患者早期风险分层中的作用。