Right Atrial Function in Pulmonary Arterial Hypertension.
Right Atrial Function in Pulmonary Arterial Hypertension.
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DOI:
10.1161/circimaging.115.003521
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发表时间:
2015-11
期刊:
影响因子:
--
通讯作者:
Shah AM
中科院分区:
文献类型:
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作者:
Querejeta Roca G;Campbell P;Claggett B;Solomon SD;Shah AM
Elevated right atrial (RA) pressure is an established prognostic measure in pulmonary arterial hypertension (PAH). However, little is known about perturbations in RA function in PAH. Reservoir (RA longitudinal strain [RA LS]), conduit (RA early longitudinal strain rate [LSR]), and active (RA late LSR) phases were assessed by 2D speckle tracking in 65 patients with PAH, 6-minute walk distance ≤ 450 meters, and a PVR >800 dynes·sec·cm−5 despite therapy with at least two PAH-specific medications enrolled in the Imatinib in Pulmonary arterial hypertension, a Randomized Efficacy Study (IMPRES) trial, and were compared to 30 healthy controls of similar age and sex. We studied the association of RA functional measures with invasive pulmonary hemodynamics, cardiac structure and function, and NT-proBNP. RA LS and early LSR were reduced in PAH patients compared to controls (27.1±11.6 vs 56.9±12.7, adjusted p<0.001 and −0.6±0.5 vs −1.5±0.5, adjusted p<0.001, respectively) even after adjusting for RA area and invasive RA pressure, while RA late SR was similar between groups (−1.4±0.7 vs −1.5±0.4, p=0.42). Among PAH patients, worse RA LS correlated with greater RA size (r=−0.50, p<0.0001) and pressure (r=−0.37, p=0.002), but not pulmonary artery pressure (r=−0.07, p=0.58). Worse RA LS was also associated with right ventricular enlargement and dysfunction and higher NT-proBNP independent of RA size and pressure. RA reservoir and passive conduit functions are impaired in PAH, independent of RA size and pressure, and likely reflect RV failure and overload. URL: http://www.clinicaltrials.gov. Unique identifier: NCT00902174.