Treatment-related biomarkers in pulmonary hypertension patients on oral therapies

Abstract Background Multiple classes of oral therapy are available for the treatment of pulmonary arterial hypertension (PAH), but there is little to guide clinicians in choosing a specific regimen or therapeutic class. We aimed to investigate whether treatment-relevant blood biomarkers can predict...

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Main Authors: Aparna C. Swaminathan, Hongmei Zhu, Victor Tapson, Yuliya Lokhnygina, Abby Poms, Zach Kelleher, Elijah Gaspard, Karla Kennedy, Brian E. Fee, Terry Fortin, S. Nicholas Mason, Kishan Parikh, Tim J. McMahon
Format: Article
Language:English
Published: BMC 2020-11-01
Series:Respiratory Research
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12931-020-01566-y
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spelling doaj-92fe33bd0f0a4461aeb63464bf07a18e2020-11-25T04:11:30ZengBMCRespiratory Research1465-993X2020-11-0121111110.1186/s12931-020-01566-yTreatment-related biomarkers in pulmonary hypertension patients on oral therapiesAparna C. Swaminathan0Hongmei Zhu1Victor Tapson2Yuliya Lokhnygina3Abby Poms4Zach Kelleher5Elijah Gaspard6Karla Kennedy7Brian E. Fee8Terry Fortin9S. Nicholas Mason10Kishan Parikh11Tim J. McMahon12Department of Medicine, Duke University Medical CenterDepartment of Medicine, Duke University Medical CenterDepartment of Medicine, Cedars-Sinai Medical CenterDepartment of Biostatistics and Bioinformatics, Duke University Medical CenterDepartment of Medicine, Duke University Medical CenterDepartment of Medicine, Duke University Medical CenterDepartment of Medicine, Duke University Medical CenterDepartment of Medicine, Duke University Medical CenterDepartment of Medicine, Duke University Medical CenterDepartment of Medicine, Duke University Medical CenterDepartment of Medicine, Duke University Medical CenterDepartment of Medicine, Duke University Medical CenterDepartment of Medicine, Duke University Medical CenterAbstract Background Multiple classes of oral therapy are available for the treatment of pulmonary arterial hypertension (PAH), but there is little to guide clinicians in choosing a specific regimen or therapeutic class. We aimed to investigate whether treatment-relevant blood biomarkers can predict therapy response in prevalent PAH patients. Methods This prospective cohort study longitudinally assessed biomarkers along the endothelin-1 (ET-1) and nitric oxide (cGMP, ADMA, SDMA, nitrite, and S-nitrosohemoglobin) pathways along with the cGMP/NT-proBNP ratio over 12 months in patients with WHO Group 1 PAH on oral PAH-specific therapies. The relationship between biomarkers and 6MWD at the same and future visits was examined using mixed linear regression models adjusted for age. As cGMP can be elevated when NT-proBNP is elevated, we also tested the relationship between 6MWD and the cGMP/NT-pro BNP ratio. Patients with PAH with concomitant heart or lung disease or chronic thromboembolic pulmonary hypertension (CTEPH) were included in a sensitivity analysis. Results The study cohort included 58 patients with PAH treated with either an endothelin receptor antagonist (27.6%), phosphodiesterase-5 inhibitor (25.9%) or a combination of the two (43.1%). Among biomarkers along the current therapeutic pathways, ET-1 and the cGMP/NT-proBNP ratio associated with same visit 6MWD (p = 0.02 and p = 0.03 respectively), and ET-1 predicted future 6MWD (p = 0.02). ET-1 (p = 0.01) and cGMP/NT-proBNP ratio (p = 0.04) also predicted future 6MWD in the larger cohort (n = 108) of PAH patients with concomitant left heart disease (n = 17), lung disease (n = 20), or CTEPH (n = 13). Finally, in the larger cohort, SDMA associated with 6MWD at the same visit (p = 0.01) in all subgroups and ADMA associated with 6MWD in PAH patients with concomitant lung disease (p = 0.03) and PAH patients on ERA therapy (p = 0.01). Conclusions ET-1, cGMP/NTproBNP ratio, and dimethylarginines ADMA and SDMA are mediators along pathways targeted by oral PAH therapies that associate with or predict 6MWD.http://link.springer.com/article/10.1186/s12931-020-01566-yPulmonary hypertensionBiomarkersNitric oxideEndothelin-1
collection DOAJ
language English
format Article
sources DOAJ
author Aparna C. Swaminathan
Hongmei Zhu
Victor Tapson
Yuliya Lokhnygina
Abby Poms
Zach Kelleher
Elijah Gaspard
Karla Kennedy
Brian E. Fee
Terry Fortin
S. Nicholas Mason
Kishan Parikh
Tim J. McMahon
spellingShingle Aparna C. Swaminathan
Hongmei Zhu
Victor Tapson
Yuliya Lokhnygina
Abby Poms
Zach Kelleher
Elijah Gaspard
Karla Kennedy
Brian E. Fee
Terry Fortin
S. Nicholas Mason
Kishan Parikh
Tim J. McMahon
Treatment-related biomarkers in pulmonary hypertension patients on oral therapies
Respiratory Research
Pulmonary hypertension
Biomarkers
Nitric oxide
Endothelin-1
author_facet Aparna C. Swaminathan
Hongmei Zhu
Victor Tapson
Yuliya Lokhnygina
Abby Poms
Zach Kelleher
Elijah Gaspard
Karla Kennedy
Brian E. Fee
Terry Fortin
S. Nicholas Mason
Kishan Parikh
Tim J. McMahon
author_sort Aparna C. Swaminathan
title Treatment-related biomarkers in pulmonary hypertension patients on oral therapies
title_short Treatment-related biomarkers in pulmonary hypertension patients on oral therapies
title_full Treatment-related biomarkers in pulmonary hypertension patients on oral therapies
title_fullStr Treatment-related biomarkers in pulmonary hypertension patients on oral therapies
title_full_unstemmed Treatment-related biomarkers in pulmonary hypertension patients on oral therapies
title_sort treatment-related biomarkers in pulmonary hypertension patients on oral therapies
publisher BMC
series Respiratory Research
issn 1465-993X
publishDate 2020-11-01
description Abstract Background Multiple classes of oral therapy are available for the treatment of pulmonary arterial hypertension (PAH), but there is little to guide clinicians in choosing a specific regimen or therapeutic class. We aimed to investigate whether treatment-relevant blood biomarkers can predict therapy response in prevalent PAH patients. Methods This prospective cohort study longitudinally assessed biomarkers along the endothelin-1 (ET-1) and nitric oxide (cGMP, ADMA, SDMA, nitrite, and S-nitrosohemoglobin) pathways along with the cGMP/NT-proBNP ratio over 12 months in patients with WHO Group 1 PAH on oral PAH-specific therapies. The relationship between biomarkers and 6MWD at the same and future visits was examined using mixed linear regression models adjusted for age. As cGMP can be elevated when NT-proBNP is elevated, we also tested the relationship between 6MWD and the cGMP/NT-pro BNP ratio. Patients with PAH with concomitant heart or lung disease or chronic thromboembolic pulmonary hypertension (CTEPH) were included in a sensitivity analysis. Results The study cohort included 58 patients with PAH treated with either an endothelin receptor antagonist (27.6%), phosphodiesterase-5 inhibitor (25.9%) or a combination of the two (43.1%). Among biomarkers along the current therapeutic pathways, ET-1 and the cGMP/NT-proBNP ratio associated with same visit 6MWD (p = 0.02 and p = 0.03 respectively), and ET-1 predicted future 6MWD (p = 0.02). ET-1 (p = 0.01) and cGMP/NT-proBNP ratio (p = 0.04) also predicted future 6MWD in the larger cohort (n = 108) of PAH patients with concomitant left heart disease (n = 17), lung disease (n = 20), or CTEPH (n = 13). Finally, in the larger cohort, SDMA associated with 6MWD at the same visit (p = 0.01) in all subgroups and ADMA associated with 6MWD in PAH patients with concomitant lung disease (p = 0.03) and PAH patients on ERA therapy (p = 0.01). Conclusions ET-1, cGMP/NTproBNP ratio, and dimethylarginines ADMA and SDMA are mediators along pathways targeted by oral PAH therapies that associate with or predict 6MWD.
topic Pulmonary hypertension
Biomarkers
Nitric oxide
Endothelin-1
url http://link.springer.com/article/10.1186/s12931-020-01566-y
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