Inserm, U915, Nantes, France.
J Cell Mol Med. 2010 Jun;14(6B):1443-52. doi: 10.1111/j.1582-4934.2009.00913.x. Epub 2009 Sep 30.
Risk stratification in advanced heart failure (HF) is crucial for the individualization of therapeutic strategy, in particular for heart transplantation and ventricular assist device implantation. We tested the hypothesis that cardiac gene expression profiling can distinguish between HF patients with different disease severity. We obtained tissue samples from both left (LV) and right (RV) ventricle of explanted hearts of 44 patients undergoing cardiac transplantation or ventricular assist device placement. Gene expression profiles were obtained using an in-house microarray containing 4217 muscular organ-relevant genes. Based on their clinical status, patients were classified into three HF-severity groups: deteriorating (n= 12), intermediate (n= 19) and stable (n= 13). Two-class statistical analysis of gene expression profiles of deteriorating and stable patients identified a 170-gene and a 129-gene predictor for LV and RV samples, respectively. The LV molecular predictor identified patients with stable and deteriorating status with a sensitivity of 88% and 92%, and a specificity of 100% and 96%, respectively. The RV molecular predictor identified patients with stable and deteriorating status with a sensitivity of 100% and 96%, and a specificity of 100% and 100%, respectively. The molecular prediction was reproducible across biological replicates in LV and RV samples. Gene expression profiling has the potential to reproducibly detect HF patients with highest HF severity with high sensitivity and specificity. In addition, not only LV but also RV samples could be used for molecular risk stratification with similar predictive power.
在晚期心力衰竭 (HF) 中进行风险分层对于治疗策略的个体化至关重要,特别是对于心脏移植和心室辅助装置植入。我们测试了这样一个假设,即心脏基因表达谱可以区分不同疾病严重程度的 HF 患者。我们从接受心脏移植或心室辅助装置植入的 44 名患者的心脏移植心脏中获取了左心室 (LV) 和右心室 (RV) 的组织样本。使用包含 4217 个肌肉器官相关基因的内部微阵列获得基因表达谱。根据他们的临床状况,患者被分为三组 HF 严重程度组:恶化组 (n=12)、中间组 (n=19) 和稳定组 (n=13)。对恶化和稳定患者的基因表达谱进行的两分类统计分析,分别确定了 LV 和 RV 样本的 170 个基因和 129 个基因预测因子。LV 分子预测因子可识别出稳定和恶化状态的患者,其敏感性分别为 88%和 92%,特异性分别为 100%和 96%。RV 分子预测因子可识别出稳定和恶化状态的患者,其敏感性分别为 100%和 96%,特异性分别为 100%和 100%。LV 和 RV 样本中的分子预测具有可重复性。基因表达谱具有高灵敏度和特异性,有潜力可重复检测 HF 严重程度最高的 HF 患者。此外,不仅 LV 而且 RV 样本都可以用于具有相似预测能力的分子风险分层。