Inflammation and Obesity Correlate in Pulmonary Hypertension but Associate with Diverging Outcomes.
Year: 2025
Type: article
Study design: Observational Study
Abstract: RATIONALE & OBJECTIVES: Inflammation is associated with all types of Pulmonary Hypertension (PH) both as a known cause and/or 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 informed clinical endotyping and outcomes. Methods & Measurements: Time-series clustering of longitudinal CRP levels was employed. Clinical differences between clusters were validated in three independent UK/international cohorts using clinical cut off values (n=10,301; UK-cohort, ASPIRE and FDA cohort). Associations were analysed with functional and mortality outcomes by linear and Cox regression models including all-causes of PH (groups 1-5). To add mechanistic insight, multi-omics were interrogated from associated previously published arrays. MAIN RESULTS: Patients segregated into two stable CRP clusters (median CRP 2 versus 6.5 mg/l), with the high cluster exhibiting significantly higher BMI (difference between medians DBM=5.4 kg/m2), higher RAP (DBM=2mmHg) and reduced 6-minute walk distance (6MWD (DBM=55m)). Inflammation was associated with worse survival, comorbidities, higher pulmonary vascular resistance (PVR), and smoking status. CRP and BMI were associated with differing inflammatory profiles in proteomic and transcriptomic analyses. Despite the relationship with CRP, higher BMI associated with improved survival, lower PVR and did not negatively affect 6MWD treatment-related functional responses. CONCLUSIONS: We establish a relationship between CRP and BMI across all-cause PH, though CRP and BMI associate 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.
Source: Apollo (University of Cambridge)
DOI: 10.17863/cam.122938
Authors: De Bie, Eckart, Correa-Jaque, Priscilla, Jones, Rowena, Bogaard, Harm J, Chan, Justine, Church, Colin, Coghlan, John G, Gaur, Akshay, Ghio, Stefano, Ghofrani, Hossein-Ardeschir, Goh, Ze Ming, Howard, Luke S, Humbert, Marc, Kovacs, Gabor, Lawrie, Allan, Lordan, James, Lin, Wei-Yu, Neelam-Naganathan, Dharshan, Newman, Joseph, Rhodes, Christopher J, Sheares, Karen, Sitbon, Olivier, Willis, Thomas W, Wort, Stephen J, Gräf, Stefan, Kiely, David G, Benza, Raymond L, Rothman, Alex, Wallace, Chris, Toshner, Mark
Language: English
Subfield: Pulmonary and Respiratory Medicine
Field: Medicine
Domain: Health Sciences
Open Access status: green
Funders: Wellcome Trust, National Institute for Health and Care Research, British Heart Foundation, Department of Health and Social Care, ZonMw, Nederlandse Organisatie voor Wetenschappelijk Onderzoek, Cambridge Trust, Gates Cambridge Trust, Nederlandse Federatie van Universitair Medische Centra, National Institutes of Health, U.S. Food and Drug Administration, NIHR BioResource, Medical Research Council, NIHR Sheffield Biomedical Research Centre
Awards: G1690597291, G174330183, G2128552377, G2322700648, G2524323436, Mechanisms underlying the development of pulmonary arterial hypertension, G339059223, G3566717051, G393167863, G3935550431, G4948928463, Novel decentralised and digital endpoints for use in clinical trials in pulmonary hypertension, G5327194790, G5799002165, G5969533927, G6787457574, National Cohort Study of Heritable Pulmonary Arterial Hypertension, Engineering genomic features to better understand the molecular basis of immune mediated diseases and their treatment, Determining Novel SMURF1 Signalling Pathways and Precision Medicine Strategies in Patients with Pulmonary Arterial Hypertension, G9000119691
OpenAlex ID: W7105171508
FWCI:
Cites:
Cited by:
Related to: