Individualized diagnosis of rheumatoid arthritis: A rank-based qualitative T cell-related signature
Hang Su, Xingyi Li, Yawei Li, Wan-Tien Chiang, Wan-Tien Chiang, Wan-Tien Chiang, Wan-Tien Chiang

TL;DR
This paper introduces a new diagnostic signature for rheumatoid arthritis based on two genes, which helps distinguish RA from healthy individuals with high accuracy.
Contribution
The study proposes a novel rank-based gene signature (IOS) for individualized RA diagnosis with high sensitivity and specificity.
Findings
The ICAM2-OSTF1 signature (IOS) achieved 87.39% sensitivity and 86.79% specificity in the training dataset.
IOS demonstrated 91.07% accuracy in an independent validation dataset with 280 samples.
Transcriptome analysis showed RA-related pathways are enriched in immune microenvironment processes like T cell activation.
Abstract
Rheumatoid arthritis (RA) is a systemic autoimmune disease with persistent synovitis and joint destruction, leading to a huge economic and physical burden on patients. The detection of RA is important for the individual’s guiding therapeutic. However, current signatures lacked enough effects for the diagnosis of RA. Here, a pariwise signature, including genes ICAM2 and OSTF1, was derived based on a rank-based method, which was called ICAM2-OSTF1 signature (IOS). The sensitivity and specificity of IOS in the training dataset were 87.39% and 86.79%, respectively. The accuracy of IOS was 91.07% in the validation dataset that contained a total of 280 samples from two independent datasets. Besides, when using eight methods, such as ssGSEA, xCell and TIMER, to quantitate the immune infiltration characteristics in RA. We found that RA presented elevated pro-inflammation immune infiltration and…
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Taxonomy
TopicsSystemic Lupus Erythematosus Research · Rheumatoid Arthritis Research and Therapies · interferon and immune responses
