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Inflammation and Obesity Correlate in Pulmonary Hypertension but Are Associated with Diverging Outcomes

Lookup NU author(s): Dr James Lordan

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This work is licensed under a Creative Commons Attribution 4.0 International License (CC BY 4.0).


Abstract

Copyright © 2025 by the American Thoracic Society. RATIONALE AND OBJECTIVES: Inflammation is associated with all types of pulmonary hypertension (PH), both as a known cause and as a putative confounder. The most common marker of inflammation, C-reactive protein (CRP), has not been widely studied in PH. This study set out to clarify if CRP informs clinical endotyping and outcomes. METHODS: Time-series clustering of longitudinal CRP concentrations was employed. Clinical differences between clusters were validated in three independent U.K./international cohorts using clinical cutoff values (n = 10,301; U.K. cohort, ASPIRE and FDA cohort). Associations were analyzed with functional and mortality outcomes by linear and Cox regression models including all causes of PH (groups 1-5). To add mechanistic insight, multiomics were interrogated from associated previously published arrays. MEASUREMENTS AND MAIN RESULTS: Patients were segregated into two stable CRP clusters (median CRP, 2 vs. 6.5 mg/L), with the high cluster exhibiting significantly higher body mass index (BMI) (difference between medians [DBM], 5.4 kg/m2), higher right atrial pressure (DBM, 2 mm Hg), and reduced 6-minute-walk distance (DBM, 55 m). Inflammation was associated with worse survival and comorbidities, higher pulmonary vascular resistance, and smoking status. CRP and BMI were associated with differing inflammatory profiles in proteomic and transcriptomic analyses. Despite the relationship with CRP, higher BMI was associated with improved survival and lower pulmonary vascular resistance and did not negatively affect 6-minute-walk distance treatment-related functional responses. CONCLUSIONS: We establish a relationship between CRP and BMI across all-cause PH, although CRP and BMI are associated with diverging clinical outcomes. Inflammation and obesity are relevant phenotypes for consideration in clinical trial design. Understanding their impacts on outcomes is important for clinical practice.


Publication metadata

Author(s): De Bie E, Correa-Jaque P, Jones R, Bogaard HJ, Chan J, Church C, Coghlan JG, Gaur A, Ghio S, Ghofrani H-A, Goh ZM, Howard LS, Humbert M, Kovacs G, Lawrie A, Lordan J, Lin W-Y, Neelam-Naganathan D, Newman J, Rhodes CJ, Sheares K, Sitbon O, Willis TW, Wort SJ, Graf S, Kiely DG, Benza RL, Rothman A, Wallace C, Toshner M

Publication type: Article

Publication status: Published

Journal: American Journal of Respiratory and Critical Care Medicine

Year: 2026

Volume: 212

Issue: 1

Pages: 117-128

Print publication date: 01/01/2026

Online publication date: 11/08/2025

Acceptance date: 06/08/2025

Date deposited: 09/03/2026

ISSN (print): 1073-449X

ISSN (electronic): 1535-4970

Publisher: Oxford University Press

URL: https://doi.org/10.1164/rccm.202412-2393OC

DOI: 10.1164/rccm.202412-2393OC

ePrints DOI: 10.57711/rqct-y853

PubMed id: 40788756


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Funding

Funder referenceFunder name
BHF Basic Science Research fellowship (FS/SBSRF/21/31025)
British Heart Foundation Clinical Research Training Fellowship (FS/CRTF/22/24390)
Dutch Federation of University Medical Centres
Dutch Heart Foundation
MRC (MC_UU_00040/01)
National Institutes of Health (R01 HL164906-05)
National Institute for Health Research BioResource and National Institute for Health Research Cardiorespiratory Biomedical Research Centre, Gates Cambridge Trust (grant number OPP1144)
Netherlands Organisation for Health Research and Development
Netherlands Organization for Scientific Research (NWO-VICI: 918.16.610, NWO-VIDI: 917.18.338)
NIHR Sheffield Biomedical Research Centre (NIHR203321)
Royal Netherlands Academy of Sciences (CVON-2017-10 Dolphin-Genesis)
Royal Netherlands Academy of Sciences (CVON-2012-08 PHAEDRA & CVON-2018-29 PHAEDRA-IMPACT)
Wellcome Trust (WT220788)
Wellcome Trust Clinical Research Development Fellowship (206632/Z/17/Z)

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