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July 22, 2014Circulation Heart Failure62 citationsOpen Access

Pulmonary Hypertension Is Related to Peripheral Endothelial Dysfunction in Heart Failure With Preserved Ejection Fraction

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MFMarta FarreroIBIsabel BlancoMBMontserrat Batlle

Key Points

  • This research aims to determine the association between pulmonary hypertension and peripheral endothelial dysfunction in patients with heart failure with preserved ejection fraction (HFpEF).
  • Evaluated flow-mediated dilation and biomarkers in 28 patients with HFpEF and 42 hypertensive controls.

Structured PICO

Is pulmonary hypertension associated with peripheral endothelial dysfunction and impaired collagen metabolism in patients with HFpEF?

P
Population
28 patients with heart failure with preserved ejection fraction (HFpEF) and 42 hypertensive controls
C
Comparator
Hypertensive controls
O
Outcome
Flow-mediated dilation of the brachial artery, matrix metalloproteinase-2, matrix metalloproteinase-9, tissue metalloproteinase inhibitor 1, and C-terminal propeptide of type I procollagensurrogate

In patients with HFpEF, peripheral endothelial dysfunction and impaired collagen metabolism are significantly correlated with pulmonary vascular resistance, suggesting their potential utility in identifying patients at risk for pulmonary hypertension.

Abstract

BACKGROUND: Pulmonary hypertension (PH) and collagen metabolism abnormalities are prevalent in patients with heart failure with preserved ejection fraction (HFpEF). Peripheral endothelial dysfunction (PED) has been described in HF and in pulmonary arterial hypertension. Our aim is to determine whether PH is associated with PED and impaired collagen metabolism in patients with HFpEF.; METHODS AND RESULTS: Flow-mediated dilation of the brachial artery, matrix metalloproteinase-2 and matrix metalloproteinase-9, tissue metalloproteinase inhibitor 1, and C-terminal propeptide of type I procollagen were determined in 28 patients with HFpEF and 42 hypertensive controls. Patients with systolic pulmonary artery pressure >35 mm Hg on echocardiogram underwent a right heart catheterization. Patients with HFpEF had more severe PED than controls: flow-mediated dilation 1.95% (-0.81 to 4.92) versus 5.02% (3.90 to 10.12), P=0.002. Twenty patients with PH underwent right heart catheterization: mean pulmonary artery pressure 38 (27-52) mm Hg, wedge capillary pressure 18 (16-22) mm Hg, pulmonary vascular resistance 362 (235-603) dyn s cm(-5). There was a significant inverse correlation between flow-mediated dilation and pulmonary vascular resistance in patients with HFpEF and PH (r=-0.679; P=0.002). Patients with HFpEF showed higher matrix metalloproteinase-2 and C-terminal propeptide of type I procollagen values than hypertensive controls. Patients with HFpEF and higher C-terminal propeptide of type I procollagen values also had higher mean pulmonary artery pressure (r=0.553; P=0.014), transpulmonary gradient (r=0.560; P=0.013), and pulmonary vascular resistance (r=0.626; P=0.004). CONCLUSIONS: In patients with HFpEF, there is a significant correlation between PED and pulmonary vascular resistance. Collagen metabolism was more impaired in patients with HFpEF and PH. PED and collagen metabolism assessment could be useful tools to identify patients with HFpEF at risk of developing PH.

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Cite This Study

Farrero et al. (2014) studied this question.

synapsesocial.com/papers/69fe7a26d8476229fea35b5dhttps://doi.org/10.1161/circheartfailure.113.000942
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