Serologic Biomarkers of Progression Toward Diagnosis of Rheumatoid Arthritis in Active Component Military Personnel.


Journal

Arthritis & rheumatology (Hoboken, N.J.)
ISSN: 2326-5205
Titre abrégé: Arthritis Rheumatol
Pays: United States
ID NLM: 101623795

Informations de publication

Date de publication:
11 2022
Historique:
revised: 29 04 2022
received: 03 01 2022
accepted: 02 06 2022
pubmed: 8 6 2022
medline: 2 11 2022
entrez: 7 6 2022
Statut: ppublish

Résumé

To identify a panel of serum biomarkers that could specifically identify imminent cases of rheumatoid arthritis (RA) before diagnosis. Serum samples were collected at 4 time points from active component US military personnel, including 157 anti-citrullinated protein antibody (ACPA)-seropositive and 50 ACPA-seronegative RA subjects, 100 reactive arthritis (ReA) subjects, and 76 healthy controls. The cohorts were split into 2 phases, with samples tested on independent proteomic platforms for each phase. Classification models of RA diagnosis based on samples obtained within 6 months prior to diagnosis were developed both in univariate analyses and by multivariate random forest modeling of training sample sets and testing sample sets from each phase. Increases in serum analytes, including C-reactive protein levels, serum amyloid A, and soluble programmed cell death 1 (PD-1), were observed in seropositive RA subjects at the time point closest to diagnosis, up to several years before diagnosis. Only a small fraction of RA subjects had levels above the 95th percentile of healthy control levels until the time period within 6 months of diagnosis. For classification of RA diagnosis using samples obtained within 6 months prior to diagnosis, soluble PD-1 provided superior specificity compared to ReA cases (>89%), with a sensitivity of 48% for RA classification. An 8-analyte model provided superior sensitivity (69%), with comparable specificity relative to ReA (>82%). Our findings demonstrate that imminent RA diagnosis could be classified with high specificity, relative to healthy controls and ReA cases, using a panel of cytokines measured in serum samples collected within 6 months before actual diagnosis.

Identifiants

pubmed: 35671369
doi: 10.1002/art.42260
doi:

Substances chimiques

Programmed Cell Death 1 Receptor 0
Biomarkers 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1766-1775

Informations de copyright

© 2022 American College of Rheumatology. This article has been contributed to by U.S. Government employees and their work is in the public domain in the USA.

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Auteurs

Matthew J Loza (MJ)

Immunology, Janssen Research & Development, Spring House, Pennsylvania.

Sunil Nagpal (S)

Immunology, Janssen Research & Development, Spring House, Pennsylvania.

Suzanne Cole (S)

Immunology, Janssen Research & Development, Spring House, Pennsylvania.

Renee M Laird (RM)

Henry M. Jackson Foundation for Military Medicine, Bethesda, Maryland.

Ashley Alcala (A)

Henry M. Jackson Foundation for Military Medicine, Bethesda, Maryland.

Navin L Rao (NL)

Immunology, Janssen Research & Development, Spring House, Pennsylvania.

Mark S Riddle (MS)

Enteric Diseases Department, Naval Medical Research Center, Silver Spring, Maryland, Reno-School of Medicine, University of Nevada, and VA Sierra Nevada Health Care System, Reno, Nevada.

Chad K Porter (CK)

Enteric Diseases Department, Naval Medical Research Center, Silver Spring, Maryland.

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