Gene microarray analysis of peripheral blood cells in pulmonary arterial hypertension

Todd M. Bull, Christopher D. Coldren, Mark Moore, Sylk M. Sotto-Santiago, David V. Pham, S. Patrick Nana-Sinkam, Norbert F. Voelkel, Mark W. Geraci

Research output: Contribution to journalArticlepeer-review

115 Scopus citations


The importance of genetic predisposition, inflammation, and autoimmune mechanisms in the development of pulmonary arterial hypertension (PAH) is becoming increasingly clear. We hypothesized that the analysis of gene expression profiles from peripheral blood mononuclear cells would distinguish patients with PAH from normal volunteers. We also hypothesized that a subset of genes would discriminate between patients with idiopathic PAH and pulmonary hypertension related to secondary causes. Mononuclear cells were isolated from 15 patients diagnosed with PAH and 6 normal control subjects. Microarray expression was performed, and the expression profiles were analyzed for consistent and predictive differences in gene expression. We identified a signature set of 106 genes that discriminated with high certainty (p ≤ 0.002) between patients with PAH and normal individuals. The results of the microarray analysis were retrospectively and prospectively confirmed by quantitative polymerase chain reaction for 2 of the 106 genes. Supervised clustering analysis generated a list of differentially expressed genes between patients with idiopathic and secondary causes of pulmonary hypertension. Microarray expression profiling of peripheral blood cells can discriminate between patients with PAH and normal volunteers. These findings may have important implications toward diagnosis, screening, and pathogenesis of this disease.

Original languageEnglish (US)
Pages (from-to)911-919
Number of pages9
JournalAmerican journal of respiratory and critical care medicine
Issue number8
StatePublished - Oct 15 2004


  • Biomarker
  • Gene microarray
  • Inflammation
  • Mononuclear cells
  • Pulmonary arterial hypertension

ASJC Scopus subject areas

  • Pulmonary and Respiratory Medicine
  • Critical Care and Intensive Care Medicine

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