Gene microarray analysis of peripheral blood cells in pulmonary arterial hypertension.

Am J Respir Crit Care Med

Division of Pulmonary Sciences and Critical Care Medicine, 4200 East 9th Avenue, Denver, CO 80262, USA.

Published: October 2004

AI Article Synopsis

  • The study emphasizes the role of genetic factors, inflammation, and autoimmune mechanisms in pulmonary arterial hypertension (PAH) development.
  • Researchers analyzed gene expression profiles from blood cells of 15 PAH patients and 6 healthy volunteers to distinguish between them.
  • A specific set of 106 genes was identified that accurately differentiated PAH patients from normal individuals, suggesting potential improvements in diagnosis and understanding of the disease's causes.

Article Abstract

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 < or = 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.

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http://dx.doi.org/10.1164/rccm.200312-1686OCDOI Listing

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