4.6 Article

Right Ventricular Dysfunction in Systemic Sclerosis-Associated Pulmonary Arterial Hypertension

Journal

CIRCULATION-HEART FAILURE
Volume 6, Issue 5, Pages 953-963

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1161/CIRCHEARTFAILURE.112.000008

Keywords

hypertension; pulmonary; scleroderma; systemic; vascular capacitance; vascular resistance; ventricular function; right

Funding

  1. National Heart, Lung, and Blood Institute [5P50HL084946-05, 1R01HL114910-01]
  2. National Institutes of Health [K23-HL086714, KL2-RR024156, K23-AR061439]
  3. Robert Wood Johnson Physician Faculty Scholars Program
  4. Catherine Keilty Memorial Fund for Scleroderma Research
  5. Scleroderma Research Foundation
  6. Herbert and Florence Irving Scholar Award

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Background Systemic sclerosis-associated pulmonary artery hypertension (SScPAH) has a worse prognosis compared with idiopathic pulmonary arterial hypertension (IPAH), with a median survival of 3 years after diagnosis often caused by right ventricular (RV) failure. We tested whether SScPAH or systemic sclerosis-related pulmonary hypertension with interstitial lung disease imposes a greater pulmonary vascular load than IPAH and leads to worse RV contractile function. Methods and Results We analyzed pulmonary artery pressures and mean flow in 282 patients with pulmonary hypertension (166 SScPAH, 49 systemic sclerosis-related pulmonary hypertension with interstitial lung disease, and 67 IPAH). An inverse relation between pulmonary resistance and compliance was similar for all 3 groups, with a near constant resistancexcompliance product. RV pressure-volume loops were measured in a subset, IPAH (n=5) and SScPAH (n=7), as well as SSc without PH (n=7) to derive contractile indexes (end-systolic elastance [E-es] and preload recruitable stroke work [M-sw]), measures of RV load (arterial elastance [E-a]), and RV pulmonary artery coupling (E-es/E-a). RV afterload was similar in SScPAH and IPAH (pulmonary vascular resistance=7.04.5 versus 7.9 +/- 4.3 Wood units; E-a=0.9 +/- 0.4 versus 1.2 +/- 0.5 mm Hg/mL; pulmonary arterial compliance=2.4 +/- 1.5 versus 1.7 +/- 1.1 mL/mm Hg; P>0.3 for each). Although SScPAH did not have greater vascular stiffening compared with IPAH, RV contractility was more depressed (E-es=0.8 +/- 0.3 versus 2.3 +/- 1.1, P<0.01; M-sw=21 +/- 11 versus 45 +/- 16, P=0.01), with differential RV-PA uncoupling (E-es/E-a=1.0 +/- 0.5 versus 2.1 +/- 1.0; P=0.03). This ratio was higher in SSc without PH (E-es/E-a=2.3 +/- 1.2; P=0.02 versus SScPAH). Conclusions RV dysfunction is worse in SScPAH compared with IPAH at similar afterload, and may be because of intrinsic systolic function rather than enhanced pulmonary vascular resistive and pulsatile loading.

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