Right ventricular and pulmonary vascular reserve in asymptomatic BMPR2 mutation carriers
- PMID: 27475894
- DOI: 10.1016/j.healun.2016.06.018
Right ventricular and pulmonary vascular reserve in asymptomatic BMPR2 mutation carriers
Abstract
Background: Non-invasive estimates have suggested that asymptomatic BMPR2 mutation carriers may have an abnormal pulmonary vascular response to exercise and hypoxia. However, this has not been assessed with "gold standard" invasive measures.
Methods: Eight controls and 8 asymptomatic BMPR2 mutation carriers underwent cardiac magnetic resonance imaging with simultaneous invasive pressure recording during bicycle exercise in normoxia, hypoxia and after sildenafil administration. Abnormal pulmonary vascular reserve was defined as an increase in mean pulmonary artery pressure relative to cardiac output (P/Q slope) >3 mm Hg/liter/min.
Results: During normoxic exercise, BMPR2 mutation carriers had a similar P/Q slope when compared with healthy subjects. Only 1 of 8 BMPR2 mutation carriers had a P/Q slope >3 mm Hg/liter/min. During exercise in hypoxia, 3 of 8 BMPR2 mutation carriers had P/Q slopes >3 mm Hg/liter/min compared with none of the controls. Sildenafil decreased the P/Q slope both in controls and BMPR2 mutation carriers. The exercise-induced increase in right ventricular ejection fraction was similar between groups. None of the BMPR2 mutation carriers developed pulmonary arterial hypertension within 2 (range 1.3 to 2.8) years.
Conclusions: The presence of a BMPR2 mutation, per se, is not associated with an abnormal pulmonary vascular and right ventricular functional response to exercise in asymptomatic individuals. Longer follow-up will be required to determine whether a P/Q slope of >3 mm Hg/liter/min during exercise in normoxia or hypoxia is a sign of pre-clinical disease expression.
Keywords: BMPR2; cardiac magnetic resonance imaging; exercise physiology; hypoxia; pulmonary vascular function; right ventricular function.
Copyright © 2016 International Society for Heart and Lung Transplantation. Published by Elsevier Inc. All rights reserved.
Comment in
-
From bone morphogenic protein receptor II mutations to heritable pulmonary arterial hypertension-the long and winding road.J Heart Lung Transplant. 2017 Feb;36(2):134-135. doi: 10.1016/j.healun.2016.08.002. Epub 2016 Aug 17. J Heart Lung Transplant. 2017. PMID: 27646063 No abstract available.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Miscellaneous
