Identifying high risk clinical phenogroups of pulmonary hypertension through a clustering analysis

Author:

Rambarat PaulaORCID,Zern Emily K.,Wang Dongyu,Roshandelpoor Athar,Zarbafian Shahrooz,Liu Elizabeth E.,Wang Jessica K.,McNeill Jenna N.,Andrews Carl T.,Pomerantsev Eugene V.,Diamant Nathaniel,Batra PuneetORCID,Lubitz Steven A.,Picard Michael H.,Ho Jennifer E.ORCID

Abstract

Introduction The classification and management of pulmonary hypertension (PH) is challenging due to clinical heterogeneity of patients. We sought to identify distinct multimorbid phenogroups of patients with PH that are at particularly high-risk for adverse events. Methods A hospital-based cohort of patients referred for right heart catheterization between 2005–2016 with PH were included. Key exclusion criteria were shock, cardiac arrest, cardiac transplant, or valvular surgery. K-prototypes was used to cluster patients into phenogroups based on 12 clinical covariates. Results Among 5208 patients with mean age 64±12 years, 39% women, we identified 5 distinct multimorbid PH phenogroups with similar hemodynamic measures yet differing clinical outcomes: (1) “young men with obesity”, (2) “women with hypertension”, (3) “men with overweight”, (4) “men with cardiometabolic and cardiovascular disease”, and (5) “men with structural heart disease and atrial fibrillation.” Over a median follow-up of 6.3 years, we observed 2182 deaths and 2002 major cardiovascular events (MACE). In age- and sex-adjusted analyses, phenogroups 4 and 5 had higher risk of MACE (HR 1.68, 95% CI 1.41–2.00 and HR 1.52, 95% CI 1.24–1.87, respectively, compared to the lowest risk phenogroup 1). Phenogroup 4 had the highest risk of mortality (HR 1.26, 95% CI 1.04–1.52, relative to phenogroup 1). Conclusions Cluster-based analyses identify patients with PH and specific comorbid cardiometabolic and cardiovascular disease burden that are at highest risk for adverse clinical outcomes. Interestingly, cardiopulmonary hemodynamics were similar across phenogroups, highlighting the importance of multimorbidity on clinical trajectory. Further studies are needed to better understand comorbid heterogeneity among patients with PH.

Funder

NIH

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

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