Development and validation of diagnostic and activity-assessing models for relapsing polychondritis based on laboratory parameters.

Front Immunol

Department of Clinical Laboratory, State Key Laboratory of Complex, Severe and Rare Diseases, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing, China.

Published: October 2023

AI Article Synopsis

  • Relapsing polychondritis (RP) is a rare autoimmune disease causing inflammation in cartilage-containing organs, and this study seeks to develop models using laboratory data for better diagnosis and disease activity assessment.
  • Researchers collected clinical data from RP patients and healthy controls over six years, discovering that certain blood parameters could effectively distinguish between RP patients and controls.
  • Key findings indicated that specific blood ratios and counts, like the complement 3 level and C-reactive protein to albumin ratio, are linked to disease activity and can help predict active RP, showing potential as independent risk factors in patient evaluation.

Article Abstract

Background: Relapsing polychondritis (RP) as a rare autoimmune disease is characterized by recurrent inflammation of the organs containing cartilage. Currently, no biomarkers have been integrated into clinical practice. This study aimed to construct and evaluate models based on laboratory parameters to aid in RP diagnosis, assess activity assessment, and explore associations with the pathological process.

Methods: RP patients and healthy controls (HCs) were recruited at the Peking Union Medical College Hospital from July 2017 to July 2023. Clinical data including Relapsing Polychondritis Disease Activity Index (RPDAI) score and laboratory tests were collected. Differences in laboratory data between RP patients and HCs and active and inactive patients were analyzed.

Results: The discovery cohort (cohort 1) consisted of 78 RP patients and 94 HCs. A model based on monocyte counts and neutrophil to lymphocyte ratio (NLR) could effectively distinguish RP patients from HCs with an AUC of 0.845. Active RP patients exhibited increased erythrocyte sedimentation rate, complement 3, platelet to lymphocyte ratio (PLR), NLR, and C-reactive protein to albumin ratio (CAR) compared with stable patients, which were also positively correlated with RPDAI. Notably, CAR emerged as an independent risk factor of disease activity (OR = 4.422) and could identify active patients with an AUC of 0.758. To confirm the reliability and stability of the aforementioned models, a replication cohort (cohort 2) was enrolled, including 79 RP patients and 94 HCs. The monocyte-combined NLR and CAR showed a sensitivity of 0.886 and 0.577 and a specificity of 0.830 and 0.833 in RP diagnosis and activity prediction, respectively. Furthermore, lower natural killer cell levels in RP patients and higher B-cell levels in active patients may contribute to elucidating the pathological mechanisms of disease occurrence and exacerbation.

Conclusions: The utilization of laboratory parameters provides cost-effective and valuable markers that can assist in RP diagnosis, identify disease activity, and elucidate pathogenic mechanisms.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10579920PMC
http://dx.doi.org/10.3389/fimmu.2023.1274677DOI Listing

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