Omics and Extreme Phenotyping Reveal Longitudinal Association Between Left Atrial Size and Pulmonary Vascular Resistance in Group 2 Pulmonary Hypertension

Background Left heart disease is the most common cause of pulmonary hypertension (PH) and is frequently accompanied by increases in pulmonary vascular resistance. However, the distinction between phenotypes of PH due to left heart disease with a normal or elevated pulmonary vascular resistance—isola...

وصف كامل

التفاصيل البيبلوغرافية
الحاوية / القاعدة:Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
المؤلفون الرئيسيون: Neil J. Kelly, David Newhouse, Himal Chapagain, Ashish Patel, Yicheng Tang, Ato Howard, Anna Kirillova, Hee‐Jung J. Kim, Haris Rahman, Wadih El Khoury, Seyed Mehdi Nouraie, Gavin Hickey, Leyla Elif Sade, Sandeep Jain, Stephen Y. Chan
التنسيق: مقال
اللغة:الإنجليزية
منشور في: Wiley 2023-12-01
الموضوعات:
الوصول للمادة أونلاين:https://www.ahajournals.org/doi/10.1161/JAHA.123.031746
_version_ 1850377267312590848
author Neil J. Kelly
David Newhouse
Himal Chapagain
Ashish Patel
Yicheng Tang
Ato Howard
Anna Kirillova
Hee‐Jung J. Kim
Haris Rahman
Wadih El Khoury
Seyed Mehdi Nouraie
Gavin Hickey
Leyla Elif Sade
Sandeep Jain
Stephen Y. Chan
author_facet Neil J. Kelly
David Newhouse
Himal Chapagain
Ashish Patel
Yicheng Tang
Ato Howard
Anna Kirillova
Hee‐Jung J. Kim
Haris Rahman
Wadih El Khoury
Seyed Mehdi Nouraie
Gavin Hickey
Leyla Elif Sade
Sandeep Jain
Stephen Y. Chan
author_sort Neil J. Kelly
collection DOAJ
container_title Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
description Background Left heart disease is the most common cause of pulmonary hypertension (PH) and is frequently accompanied by increases in pulmonary vascular resistance. However, the distinction between phenotypes of PH due to left heart disease with a normal or elevated pulmonary vascular resistance—isolated postcapillary PH (IpcPH) and combined pre‐ and postcapillary PH (CpcPH), respectively—has been incompletely defined using unbiased methods. Methods and Results Patients with extremes of IpcPH versus CpcPH were identified from a single‐center record of those who underwent right heart catheterization. Individuals with left ventricular ejection fraction <40% or with potential causes of PH beyond left heart disease were excluded. Medication usage in IpcPH and CpcPH was compared across Anatomical Therapeutic Chemical classes and identified vitamin K antagonists as the only medication with pharmacome‐wide significance, being more commonly used in CpcPH and for an indication of atrial fibrillation in ≈90% of instances. Accordingly, atrial fibrillation prevalence was significantly higher in CpcPH in a phenome‐wide analysis. Review of echocardiographic data most proximal to right heart catheterization revealed that left atrial diameter indexed to body surface area—known to be associated with atrial fibrillation—was increased in CpcPH regardless of the presence of atrial fibrillation. An independent cohort with serial right heart catheterizations and PH–left heart disease showed a significant positive correlation between change in left atrial diameter indexed to body surface area and change in pulmonary vascular resistance. Conclusions Guided by pharmacomic and phenomic screens in a rigorously phenotyped cohort, we identify a longitudinal association between left atrial diameter indexed to body surface area and pulmonary vascular resistance with implications for the future development of diagnostic, prognostic, and therapeutic tools.
format Article
id doaj-art-a4fced695e4c486aaf6fe8ebe1aa57df
institution Directory of Open Access Journals
issn 2047-9980
language English
publishDate 2023-12-01
publisher Wiley
record_format Article
spelling doaj-art-a4fced695e4c486aaf6fe8ebe1aa57df2025-08-19T22:58:50ZengWileyJournal of the American Heart Association: Cardiovascular and Cerebrovascular Disease2047-99802023-12-01122310.1161/JAHA.123.031746Omics and Extreme Phenotyping Reveal Longitudinal Association Between Left Atrial Size and Pulmonary Vascular Resistance in Group 2 Pulmonary HypertensionNeil J. Kelly0David Newhouse1Himal Chapagain2Ashish Patel3Yicheng Tang4Ato Howard5Anna Kirillova6Hee‐Jung J. Kim7Haris Rahman8Wadih El Khoury9Seyed Mehdi Nouraie10Gavin Hickey11Leyla Elif Sade12Sandeep Jain13Stephen Y. Chan14Center for Pulmonary Vascular Biology and Medicine, Pittsburgh Heart, Lung, and Blood Vascular Medicine Institute Pittsburgh PACenter for Pulmonary Vascular Biology and Medicine, Pittsburgh Heart, Lung, and Blood Vascular Medicine Institute Pittsburgh PADepartment of Medicine UPMC McKeesport McKeesport PAHeart and Vascular Institute Pittsburgh PACenter for Pulmonary Vascular Biology and Medicine, Pittsburgh Heart, Lung, and Blood Vascular Medicine Institute Pittsburgh PADivision of Pulmonary, Allergy, and Critical Care Medicine, Department of Medicine University of Pittsburgh School of Medicine and University of Pittsburgh Medical Center Pittsburgh PACenter for Pulmonary Vascular Biology and Medicine, Pittsburgh Heart, Lung, and Blood Vascular Medicine Institute Pittsburgh PACenter for Pulmonary Vascular Biology and Medicine, Pittsburgh Heart, Lung, and Blood Vascular Medicine Institute Pittsburgh PACenter for Pulmonary Vascular Biology and Medicine, Pittsburgh Heart, Lung, and Blood Vascular Medicine Institute Pittsburgh PACenter for Pulmonary Vascular Biology and Medicine, Pittsburgh Heart, Lung, and Blood Vascular Medicine Institute Pittsburgh PADivision of Pulmonary, Allergy, and Critical Care Medicine, Department of Medicine University of Pittsburgh School of Medicine and University of Pittsburgh Medical Center Pittsburgh PAHeart and Vascular Institute Pittsburgh PAHeart and Vascular Institute Pittsburgh PAHeart and Vascular Institute Pittsburgh PACenter for Pulmonary Vascular Biology and Medicine, Pittsburgh Heart, Lung, and Blood Vascular Medicine Institute Pittsburgh PABackground Left heart disease is the most common cause of pulmonary hypertension (PH) and is frequently accompanied by increases in pulmonary vascular resistance. However, the distinction between phenotypes of PH due to left heart disease with a normal or elevated pulmonary vascular resistance—isolated postcapillary PH (IpcPH) and combined pre‐ and postcapillary PH (CpcPH), respectively—has been incompletely defined using unbiased methods. Methods and Results Patients with extremes of IpcPH versus CpcPH were identified from a single‐center record of those who underwent right heart catheterization. Individuals with left ventricular ejection fraction <40% or with potential causes of PH beyond left heart disease were excluded. Medication usage in IpcPH and CpcPH was compared across Anatomical Therapeutic Chemical classes and identified vitamin K antagonists as the only medication with pharmacome‐wide significance, being more commonly used in CpcPH and for an indication of atrial fibrillation in ≈90% of instances. Accordingly, atrial fibrillation prevalence was significantly higher in CpcPH in a phenome‐wide analysis. Review of echocardiographic data most proximal to right heart catheterization revealed that left atrial diameter indexed to body surface area—known to be associated with atrial fibrillation—was increased in CpcPH regardless of the presence of atrial fibrillation. An independent cohort with serial right heart catheterizations and PH–left heart disease showed a significant positive correlation between change in left atrial diameter indexed to body surface area and change in pulmonary vascular resistance. Conclusions Guided by pharmacomic and phenomic screens in a rigorously phenotyped cohort, we identify a longitudinal association between left atrial diameter indexed to body surface area and pulmonary vascular resistance with implications for the future development of diagnostic, prognostic, and therapeutic tools.https://www.ahajournals.org/doi/10.1161/JAHA.123.031746atrial fibrillationleft atriumpulmonary hypertensionpulmonary vascular resistance
spellingShingle Neil J. Kelly
David Newhouse
Himal Chapagain
Ashish Patel
Yicheng Tang
Ato Howard
Anna Kirillova
Hee‐Jung J. Kim
Haris Rahman
Wadih El Khoury
Seyed Mehdi Nouraie
Gavin Hickey
Leyla Elif Sade
Sandeep Jain
Stephen Y. Chan
Omics and Extreme Phenotyping Reveal Longitudinal Association Between Left Atrial Size and Pulmonary Vascular Resistance in Group 2 Pulmonary Hypertension
atrial fibrillation
left atrium
pulmonary hypertension
pulmonary vascular resistance
title Omics and Extreme Phenotyping Reveal Longitudinal Association Between Left Atrial Size and Pulmonary Vascular Resistance in Group 2 Pulmonary Hypertension
title_full Omics and Extreme Phenotyping Reveal Longitudinal Association Between Left Atrial Size and Pulmonary Vascular Resistance in Group 2 Pulmonary Hypertension
title_fullStr Omics and Extreme Phenotyping Reveal Longitudinal Association Between Left Atrial Size and Pulmonary Vascular Resistance in Group 2 Pulmonary Hypertension
title_full_unstemmed Omics and Extreme Phenotyping Reveal Longitudinal Association Between Left Atrial Size and Pulmonary Vascular Resistance in Group 2 Pulmonary Hypertension
title_short Omics and Extreme Phenotyping Reveal Longitudinal Association Between Left Atrial Size and Pulmonary Vascular Resistance in Group 2 Pulmonary Hypertension
title_sort omics and extreme phenotyping reveal longitudinal association between left atrial size and pulmonary vascular resistance in group 2 pulmonary hypertension
topic atrial fibrillation
left atrium
pulmonary hypertension
pulmonary vascular resistance
url https://www.ahajournals.org/doi/10.1161/JAHA.123.031746
work_keys_str_mv AT neiljkelly omicsandextremephenotypingreveallongitudinalassociationbetweenleftatrialsizeandpulmonaryvascularresistanceingroup2pulmonaryhypertension
AT davidnewhouse omicsandextremephenotypingreveallongitudinalassociationbetweenleftatrialsizeandpulmonaryvascularresistanceingroup2pulmonaryhypertension
AT himalchapagain omicsandextremephenotypingreveallongitudinalassociationbetweenleftatrialsizeandpulmonaryvascularresistanceingroup2pulmonaryhypertension
AT ashishpatel omicsandextremephenotypingreveallongitudinalassociationbetweenleftatrialsizeandpulmonaryvascularresistanceingroup2pulmonaryhypertension
AT yichengtang omicsandextremephenotypingreveallongitudinalassociationbetweenleftatrialsizeandpulmonaryvascularresistanceingroup2pulmonaryhypertension
AT atohoward omicsandextremephenotypingreveallongitudinalassociationbetweenleftatrialsizeandpulmonaryvascularresistanceingroup2pulmonaryhypertension
AT annakirillova omicsandextremephenotypingreveallongitudinalassociationbetweenleftatrialsizeandpulmonaryvascularresistanceingroup2pulmonaryhypertension
AT heejungjkim omicsandextremephenotypingreveallongitudinalassociationbetweenleftatrialsizeandpulmonaryvascularresistanceingroup2pulmonaryhypertension
AT harisrahman omicsandextremephenotypingreveallongitudinalassociationbetweenleftatrialsizeandpulmonaryvascularresistanceingroup2pulmonaryhypertension
AT wadihelkhoury omicsandextremephenotypingreveallongitudinalassociationbetweenleftatrialsizeandpulmonaryvascularresistanceingroup2pulmonaryhypertension
AT seyedmehdinouraie omicsandextremephenotypingreveallongitudinalassociationbetweenleftatrialsizeandpulmonaryvascularresistanceingroup2pulmonaryhypertension
AT gavinhickey omicsandextremephenotypingreveallongitudinalassociationbetweenleftatrialsizeandpulmonaryvascularresistanceingroup2pulmonaryhypertension
AT leylaelifsade omicsandextremephenotypingreveallongitudinalassociationbetweenleftatrialsizeandpulmonaryvascularresistanceingroup2pulmonaryhypertension
AT sandeepjain omicsandextremephenotypingreveallongitudinalassociationbetweenleftatrialsizeandpulmonaryvascularresistanceingroup2pulmonaryhypertension
AT stephenychan omicsandextremephenotypingreveallongitudinalassociationbetweenleftatrialsizeandpulmonaryvascularresistanceingroup2pulmonaryhypertension