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CD163+ macrophage density in perimysial connective tissue associated with prognosis in IMNM

Authors :
Hui Sun
Zi‐Yi Wang
Ye Han
Xiao‐Jing Wei
Yong‐Chun Wang
Xue‐Fan Yu
Source :
Annals of Clinical and Translational Neurology, Vol 11, Iss 5, Pp 1267-1279 (2024)
Publication Year :
2024
Publisher :
Wiley, 2024.

Abstract

Abstract Objective The pathological features of immune‐mediated necrotizing myopathy (IMNM) are dominated by the infiltration of macrophages. We aimed to perform a histopathologic semiquantitative analysis to investigate the relationship between macrophage markers and prognosis. Methods Semiquantitative analysis of histologic features was performed in 62 samples of IMNM. Independent risk factors were identified through univariate and multivariate regression analysis. Cluster analysis was performed using the partitioning around the medoids (PAM) method. Decision tree modeling was utilized to efficiently determine cluster labels for IMNM patients. The validity of the developmental cohort was assessed by accuracy in comparison with the validation cohort. Results The most enriched groups in patients with IMNM were macrophages expressing CD206 and CD163. In the multivariate logistic regression model, the high density of CD163+ macrophages in perimysial connective tissue increased the risk of unfavorable prognosis (p = 0.025, OR = 1.463, 95% CI: 1.049–2.041). In cluster analysis, patients in Cluster 1, with lower CD163+ macrophage density and inflammatory burden, had a more favorable prognosis. Conversely, patients in Cluster 3, which were enriched for CD163+ macrophages in the perimysial connective tissue, had the most severe clinical features and the worst prognosis. Correlations were found between the density of CD163+ macrophages in connective tissue and symptom duration (R2 = 0.166, p

Details

Language :
English
ISSN :
23289503
Volume :
11
Issue :
5
Database :
Directory of Open Access Journals
Journal :
Annals of Clinical and Translational Neurology
Publication Type :
Academic Journal
Accession number :
edsdoj.95497e58cb44b76b9a911de26a45aa0
Document Type :
article
Full Text :
https://doi.org/10.1002/acn3.52065