Exercise physiology in pulmonary hypertension patients with and without congenital heart disease

Eur J Prev Cardiol. 2019 Jan;26(1):86-93. doi: 10.1177/2047487318809479. Epub 2018 Oct 24.

Abstract

Background: Cardiopulmonary exercise testing allows the assessment of integrative cardiopulmonary response to exercise.

Aims: The aim of the study was to better understand the exercise physiology in pulmonary arterial hypertension related to adult congenital heart disease compared to non-adult congenital heart disease patients by means of cardiopulmonary exercise testing parameters.

Methods: The present is a multicentre retrospective study which includes pulmonary hypertension group 1 and group 4 patients. All subjects underwent full clinical and instrumental evaluation, including cardiopulmonary exercise testing and right heart catheterization.

Results: One hundred and sixty-seven pulmonary hypertension patients (93 women and 74 men, 57 adult congenital heart disease and 110 non-adult congenital heart disease) were enrolled. Adult congenital heart disease patients had higher pulmonary pressure (mean pulmonary arterial pressure: 59.8 ± 19.5 mmHg vs 44.6 ± 16.5 mmHg, p < 0.001) and lower pulmonary blood flow (pulmonary blood flow: 3.3 (2.1-4.3) l/min vs 4.5 (3.8-5.4) l/min, p < 0.001). At cardiopulmonary exercise testing they had lower peak oxygen uptake/kg (12.8 ± 3.8 ml/kg/min vs 15.5 ± 4.2 ml/kg/min, p < 0.001) and higher ventilation/carbon dioxide elimination slope (53.2 (43.3-64.8) vs 44.0 (34.6-51.6), p < 0.001). When patients were paired for gender and peak oxygen uptake ( ± 1 ml/kg/min), obtaining 44 pairs, adult congenital heart disease patients had higher pulmonary pressure (mean pulmonary arterial pressure: 58.4 ± 20.2 mmHg vs 42.8 ± 16.8 mmHg, p < 0.001) and ventilation/carbon dioxide elimination slope (51.2 (43.4-63.6) vs 44.9 (35.4-55.1), p = 0.033).

Conclusions: In pulmonary arterial hypertension-adult congenital heart disease patients, pulmonary pressure and ventilation/carbon dioxide elimination slope are higher compared to non-adult congenital heart disease pulmonary hypertension patients, while pulmonary blood flow and peak oxygen uptake are lower. After matching patients for gender and peak oxygen uptake, pulmonary pressure and ventilation/carbon dioxide elimination remain higher in adult congenital heart disease patients suggesting that the long-term adaptation to high pulmonary pressure, hypoxia and low pulmonary blood flow, as well as a persisting shunt has, at least partially, preserved exercise performance of pulmonary arterial hypertension-adult congenital heart disease patients.

Keywords: Cardiopulmonary exercise testing; adult congenital heart disease; pulmonary arterial hypertension; oxygen uptake.

Publication types

  • Comparative Study
  • Meta-Analysis

MeSH terms

  • Adaptation, Physiological
  • Adult
  • Aged
  • Arterial Pressure
  • Cardiac Catheterization
  • Exercise Test
  • Exercise Tolerance*
  • Female
  • Germany
  • Heart Defects, Congenital / complications
  • Heart Defects, Congenital / diagnosis
  • Heart Defects, Congenital / physiopathology*
  • Humans
  • Italy
  • Male
  • Middle Aged
  • Oxygen Consumption*
  • Pulmonary Arterial Hypertension / diagnosis
  • Pulmonary Arterial Hypertension / etiology
  • Pulmonary Arterial Hypertension / physiopathology*
  • Pulmonary Artery / physiopathology
  • Retrospective Studies