Evaluating of Red Blood Cell Distribution Width, Comorbidities and Electrocardiographic Ratios as Predictors of Prognosis in Patients with Pulmonary Hypertension
Mario E. Baltazares-Lipp,
Alberto Aguilera-Velasco,
Arnoldo Aquino-Gálvez,
Rafael Velázquez-Cruz,
Rafael J. Hernández-Zenteno,
Noé Alvarado-Vásquez,
Angel Camarena,
M. Patricia Sierra-Vargas,
Juan L. Chávez-Pacheco,
Víctor Ruiz,
Citlaltepetl Salinas-Lara,
Martha L. Tena-Suck,
Yair Romero,
Luz M. Torres-Espíndola,
Manuel Castillejos-López
Affiliations
Mario E. Baltazares-Lipp
Department of Hemodynamics and Echocardiography, National Institute of Respiratory Diseases Ismael Cosio Villegas, Mexico City 14080, Mexico
Alberto Aguilera-Velasco
Epidemiology and Statistics Department, National Institute of Respiratory Diseases Ismael Cosio Villegas, Mexico City 14080, Mexico
Arnoldo Aquino-Gálvez
Laboratory of Molecular Biology, Pulmonary Fibrosis Research Department, National Institute of Respiratory Diseases Ismael Cosio Villegas, Mexico City 14080, Mexico
Rafael Velázquez-Cruz
Genomics of Bone Metabolism Laboratory, National Institute of Genomic Medicine (INMEGEN), Mexico City 14610, Mexico
Rafael J. Hernández-Zenteno
Clinical Service of Chronic Obstructive Pulmonary Disease, National Institute of Respiratory Diseases Ismael Cosio Villegas, Mexico City 14080, Mexico
Noé Alvarado-Vásquez
Biochemistry Department, National Institute of Respiratory Diseases Ismael Cosio Villegas, Mexico City 14080, Mexico
Angel Camarena
Laboratory of HLA, National Institute of Respiratory Diseases Ismael Cosio Villegas, Mexico City 14080, Mexico
M. Patricia Sierra-Vargas
Toxicology and Environmental Medicine Research Department, National Institute of Respiratory Diseases Ismael Cosio Villegas, Mexico City 14080, Mexico
Juan L. Chávez-Pacheco
Laboratory of Pharmacology, National Institute of Paediatrics, Mexico City 04530, Mexico
Víctor Ruiz
Laboratory of Molecular Biology, Pulmonary Fibrosis Research Department, National Institute of Respiratory Diseases Ismael Cosio Villegas, Mexico City 14080, Mexico
Citlaltepetl Salinas-Lara
Laboratory of Neuropathology, National Institute of Neurology and Neurosurgery, Mexico City 14269, Mexico
Martha L. Tena-Suck
Laboratory of Neuropathology, National Institute of Neurology and Neurosurgery, Mexico City 14269, Mexico
Yair Romero
Faculty of Sciences, National Autonomous University of Mexico, Mexico City 04510, Mexico
Luz M. Torres-Espíndola
Laboratory of Pharmacology, National Institute of Paediatrics, Mexico City 04530, Mexico
Manuel Castillejos-López
Epidemiology and Statistics Department, National Institute of Respiratory Diseases Ismael Cosio Villegas, Mexico City 14080, Mexico
Pulmonary hypertension is a rare condition that impairs patients’ quality of life and life expectancy. The development of noninvasive instruments may help elucidate the prognosis of this cardiorespiratory disease. We aimed to evaluate the utility of routinely performed noninvasive test results as prognostic markers in patients with pulmonary hypertension. We enrolled 198 patients with mean pulmonary artery pressure >25 mmHg measured at cardiac catheterisation or echocardiographic pulmonary artery systolic pressure > 40 mmHg and tricuspid regurgitation Vmax >2.9 m/s, and clinical information regarding management and follow-up studies from the date of diagnosis. Multivariate analysis revealed that female sex [HR: 0.21, (95% CI: 0.07–0.64); p = 0.006], the presence of collagenopathies [HR: 8.63, (95% CI: 2.38–31.32); p = 0.001], an increased red blood cell distribution width [HR: 1.25, (95% CI: 1.04–1.49); p = 0.017] and an increased electrocardiographic P axis (P°)/T axis (T°) ratio [HR: 0.93, (95% CI: 0.88–0.98); p = 0.009] were severity-associated factors, while older age [HR: 1.57, (95% CI: 1.04–1.28); p = 0.006], an increased QRS axis (QRS°)/T° ratio [HR: 1.21, (95% CI: 1.09–1.34); p p = 0.01] and haematocrit [HR: 0.93, (95% CI: 0.87–0.99); p = 0.04] were mortality-associated factors. Our results support the importance of red blood cell distribution width, electrocardiographic ratios and collagenopathies for assessing pulmonary hypertension prognosis.