Relationship of BMPR2 mutations to vasoreactivity in pulmonary arterial hypertension

C. Gregory Elliott*, Eric W. Glissmeyer, Gregory T. Havlena, John Carlquist, Jason T. McKinney, Stuart Rich, Michael D. McGoon, Mary Beth Scholand, Miryoung Kim, Robert L. Jensen, Jon W. Schmidt, Kenneth Ward

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

116 Scopus citations

Abstract

BACKGROUND - Vasoreactivity tests are fundamental in evaluating pulmonary arterial hypertension (PAH). Mutations of the transforming growth factor-β type II receptor gene, BMPR2, predispose to the development of pulmonary hypertension and may alter the response to vasodilators. Previous investigations have not examined the relationship of BMPR2 mutations to vasoreactivity. METHODS AND RESULTS - We identified 133 consecutive unrelated patients with either idiopathic or familial PAH. Sixty-six patients were excluded because we lacked either DNA samples (n=18) or complete data from a vasoreactivity test (n=48). The remaining 67 patients were screened for BMPR2 DNA sequence variations, and specific variations were confirmed by gene sequencing. The vasoreactivity of patients with nonsynonymous BMPR2 variations was compared with that of patients without nonsynonymous BMPR2 variations. We found nonsynonymous BMPR2 variations in 27 of 67 patients with idiopathic (n=16 of 52) or familial (n=11 of 15) PAH. Vasoreactivity was identified in 3.7% of 27 patients with nonsynonymous BMPR2 variations and in 35% of 40 patients without nonsynonymous BMPR2 variations (P=0.003). Five of the 27 nonsynonymous variations occur commonly in healthy individuals. None of the remaining 22 patients with BMPR2 variations demonstrated vasoreactivity, and the analysis remained unchanged when we assumed that nonsynonymous BMPR2 variations were present in all 15 patients with familial PAH. CONCLUSIONS - Patients with familial or idiopathic PAH and nonsynonymous BMPR2 variations are unlikely to demonstrate vasoreactivity. Further trials are required to determine whether long-term therapy can be directed by tests for BMPR2 variations.

Original languageEnglish (US)
Pages (from-to)2509-2515
Number of pages7
JournalCirculation
Volume113
Issue number21
DOIs
StatePublished - May 2006

Keywords

  • Genetics
  • Molecular biology
  • Pulmonary arterial hypertension
  • Vasoconstriction
  • Vasodilation

ASJC Scopus subject areas

  • Cardiology and Cardiovascular Medicine
  • Physiology (medical)

Fingerprint

Dive into the research topics of 'Relationship of BMPR2 mutations to vasoreactivity in pulmonary arterial hypertension'. Together they form a unique fingerprint.

Cite this