Utility of factor D and other alternative complement factors as biomarkers in systemic sclerosis-associated pulmonary arterial hypertension (SSc-PAH).

Complement Pulmonary arterial hypertension Systemic sclerosis

Journal

Seminars in arthritis and rheumatism
ISSN: 1532-866X
Titre abrégé: Semin Arthritis Rheum
Pays: United States
ID NLM: 1306053

Informations de publication

Date de publication:
13 Sep 2024
Historique:
received: 07 03 2024
revised: 22 08 2024
accepted: 23 08 2024
medline: 20 9 2024
pubmed: 20 9 2024
entrez: 19 9 2024
Statut: aheadofprint

Résumé

Activation of the complement cascade is thought to play a role in scleroderma vasculopathy. We previously showed that complement factor D was elevated in patients with limited cutaneous SSc and pulmonary arterial hypertension (PAH). In this study, we sought to assess multiple relevant components of the complement cascade to determine if they are altered in SSc-PAH, as well as their potential utility as biomarkers of disease severity and progression. Complement components (n = 14) were measured using multiplex assays in 156 patients with SSc-PAH from a multi-site repository and were compared to 33 patients with SSc without PAH, and 40 healthy controls. Data were evaluated for correlations between complement levels, right heart catheterization measures, and clinical endpoints including 6-minute walk distance. To assess complement longitudinally, serum complement levels were assayed at 0, 4, 12, 24, 36 and 48 weeks in 52 SSc-PAH patients who participated in a prior clinical trial. We found that factor D was significantly elevated in SSc-PAH compared to SSc without PAH (p < 0.0001) and was highly sensitive and specific for SSc-PAH (AUC=0.82, p < 0.001). In SSc-PAH patients, alterations in factor H, C4, and factor D were associated with measures of PAH disease severity including right heart catheterization measurements (cardiac output, right atrial pressure, and VO2 max), survival, and 6-minute walk distance. No significant changes in complement levels or clinical associations were seen over time or associated with treatment in the longitudinal clinical trial study. Our work confirms prior studies demonstrating a role for complement activation in SSc vascular disease and elevations of factor D in a large SSc-PAH population. Further, factor H and other complement factors are associated with severity of PAH including mortality. Taken together, these findings suggest that the alternative complement pathway plays a role in SSc-PAH pathogenesis and may serve as a biomarker to inform diagnosis and prognosis.

Sections du résumé

BACKGROUND BACKGROUND
Activation of the complement cascade is thought to play a role in scleroderma vasculopathy. We previously showed that complement factor D was elevated in patients with limited cutaneous SSc and pulmonary arterial hypertension (PAH). In this study, we sought to assess multiple relevant components of the complement cascade to determine if they are altered in SSc-PAH, as well as their potential utility as biomarkers of disease severity and progression.
METHODS METHODS
Complement components (n = 14) were measured using multiplex assays in 156 patients with SSc-PAH from a multi-site repository and were compared to 33 patients with SSc without PAH, and 40 healthy controls. Data were evaluated for correlations between complement levels, right heart catheterization measures, and clinical endpoints including 6-minute walk distance. To assess complement longitudinally, serum complement levels were assayed at 0, 4, 12, 24, 36 and 48 weeks in 52 SSc-PAH patients who participated in a prior clinical trial.
RESULTS RESULTS
We found that factor D was significantly elevated in SSc-PAH compared to SSc without PAH (p < 0.0001) and was highly sensitive and specific for SSc-PAH (AUC=0.82, p < 0.001). In SSc-PAH patients, alterations in factor H, C4, and factor D were associated with measures of PAH disease severity including right heart catheterization measurements (cardiac output, right atrial pressure, and VO2 max), survival, and 6-minute walk distance. No significant changes in complement levels or clinical associations were seen over time or associated with treatment in the longitudinal clinical trial study.
CONCLUSION CONCLUSIONS
Our work confirms prior studies demonstrating a role for complement activation in SSc vascular disease and elevations of factor D in a large SSc-PAH population. Further, factor H and other complement factors are associated with severity of PAH including mortality. Taken together, these findings suggest that the alternative complement pathway plays a role in SSc-PAH pathogenesis and may serve as a biomarker to inform diagnosis and prognosis.

Identifiants

pubmed: 39298973
pii: S0049-0172(24)00194-X
doi: 10.1016/j.semarthrit.2024.152554
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

152554

Informations de copyright

Copyright © 2024 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: VMH is a co-founder of Q32 Bio, has stock and has previously received sponsored research support

Auteurs

Eva Petrow (E)

Department of Medicine, Division of Allergy, Immunology and Rheumatology, University of Rochester Medical Center, 601 Elmwood Ave, Box 695, Rochester, NY 14642, United States. Electronic address: epetrow1@bu.edu.

Changyong Feng (C)

Department of Biostatistics and Computational Biology, University of Rochester, Saunders Research Building, 265 Crittenden Boulevard, Box 630, Rochester, NY 14642, United States. Electronic address: changyong_feng@urmc.rochester.edu.

Ashley Frazer-Abel (A)

Exsera BioLabs, University of Colorado School of Medicine, 1775 Aurora Court, Mail Stop B115, Aurora, CO 80045, United States. Electronic address: ashley.frazer-abel@cuanschutz.edu.

Roberta Goncalves Marangoni (RG)

Department of Medicine, Division of Allergy, Immunology and Rheumatology, University of Rochester Medical Center, 601 Elmwood Ave, Box 695, Rochester, NY 14642, United States. Electronic address: roberta_goncalvesmarangoni@urmc.rochester.edu.

Katie Lutz (K)

Division of Human Genetics, Cincinnati Children's Medical Center and Department of Pediatrics, University of Cincinnati College of Medicine, 3333 Burnet Ave, ML7016, Cincinnati, OH 45229, United States. Electronic address: katie.lutz@cchmc.org.

William C Nichols (WC)

Division of Human Genetics, Cincinnati Children's Medical Center and Department of Pediatrics, University of Cincinnati College of Medicine, 3333 Burnet Ave, ML7016, Cincinnati, OH 45229, United States. Electronic address: bill.nichols@cchmc.org.

V Michael Holers (VM)

Departments of Medicine and Immunology, Division of Rheumatology, University of Colorado School of Medicine, 1775 North Aurora Court, 3102, Aurora, CO 80045, United States. Electronic address: michael.holers@ucdenver.edu.

Christopher Ritchlin (C)

Department of Medicine, Division of Allergy, Immunology and Rheumatology, University of Rochester Medical Center, 601 Elmwood Ave, Box 695, Rochester, NY 14642, United States. Electronic address: christopher_ritchlin@urmc.rochester.edu.

R James White (RJ)

Department of Medicine, Division of Pulmonary & Critical Care Medicine, University of Rochester Medical Center, 601 Elmwood Ave, Box 692, Rochester NY 14642, United States. Electronic address: jim_white@urmc.rochester.edu.

Benjamin D Korman (BD)

Department of Medicine, Division of Allergy, Immunology and Rheumatology, University of Rochester Medical Center, 601 Elmwood Ave, Box 695, Rochester, NY 14642, United States. Electronic address: benjamin_korman@urmc.rochester.edu.

Classifications MeSH