Haddad Georges E, Saunders Lori J, Crosby Seth D, Carles Maria, del Monte Federica, King Kindra, Bristow Michael R, Spinale Francis G, Macgillivray Thomas E, Semigran Marc J, Dec G William, Williams Steven A, Hajjar Roger J, Gwathmey Judith K
Department of Physiology and Biophysics, College of Medicine, Howard University, Washington, District of Columbia, USA.
Physiol Genomics. 2008 Apr 22;33(2):267-77. doi: 10.1152/physiolgenomics.00265.2007. Epub 2008 Feb 26.
Idiopathic dilated cardiomyopathy (IDCM) constitutes a large portion of patients with heart failure of unknown etiology. Up to 50% of all transplant recipients carry this clinical diagnosis. Female-specific gene expression in IDCM has not been explored. We report sex-related differences in the gene expression profile of ventricular myocardium from patients undergoing cardiac transplantation. We produced and sequenced subtractive cDNA libraries, using human left ventricular myocardium obtained from male transplant recipients with IDCM and nonfailing human heart donors. With the resulting sequence data, we generated a custom human heart failure microarray for IDCM containing 1,145 cardiac-specific oligonucleotide probes. This array was used to characterize RNA samples from female IDCM transplant recipients. We identified a female gene expression pattern that consists of 37 upregulated genes and 18 downregulated genes associated with IDCM. Upon functional analysis of the gene expression pattern, deregulated genes unique to female IDCM were those that are involved in energy metabolism and regulation of transcription and translation. For male patients we found deregulation of genes related to muscular contraction. These data suggest that 1) the gene expression pattern we have detected for IDCM may be specific for this disease and 2) there is a sex-specific profile to IDCM. Our observations further suggest for the first time ever novel targets for treatment of IDCM in women and men.
特发性扩张型心肌病(IDCM)在病因不明的心力衰竭患者中占很大比例。所有心脏移植受者中高达50%患有这种临床诊断疾病。IDCM中女性特异性基因表达尚未得到探索。我们报告了心脏移植患者心室心肌基因表达谱中的性别差异。我们使用从患有IDCM的男性移植受者和无心力衰竭的人类心脏供体获得的人类左心室心肌,构建并测序了消减cDNA文库。利用所得序列数据,我们生成了一个针对IDCM的定制人类心力衰竭微阵列,其中包含1145个心脏特异性寡核苷酸探针。该阵列用于表征女性IDCM移植受者的RNA样本。我们鉴定出一种女性基因表达模式,其由37个上调基因和18个与IDCM相关的下调基因组成。对该基因表达模式进行功能分析时,女性IDCM特有的失调基因是那些参与能量代谢以及转录和翻译调控的基因。对于男性患者,我们发现与肌肉收缩相关的基因失调。这些数据表明:1)我们检测到的IDCM基因表达模式可能是该疾病特有的;2)IDCM存在性别特异性特征。我们的观察结果首次进一步表明了针对男性和女性IDCM治疗的新靶点。