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Circular RNA expression profiles and identification of hsa_circ_0028381 as a potential biomarker of anti-neutrophil cytoplasmic antibody-associated vasculitis


1, 2, 3, 4, 5, 6

 

  1. Department of Rheumatology, Zhongshan Hospital, Fudan University, Shanghai, China.
  2. Department of Rheumatology, Zhongshan Hospital, Fudan University, Shanghai, China.
  3. Department of Rheumatology, Zhongshan Hospital, Fudan University, Shanghai, China.
  4. Department of Rheumatology, Zhongshan Hospital, Fudan University, Shanghai, China.
  5. Department of Rheumatology, Zhongshan Hospital, Fudan University, Shanghai, China.
  6. Department of Rheumatology, Zhongshan Hospital, Fudan University, Shanghai, and Centre of Clinical Epidemiology and Evidence-based Medicine, Fudan University, Shanghai, China. zsh-rheum@hotmail.com

CER15802
2023 Vol.41, N°4
PI 0837, PF 0847
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PMID: 36441649 [PubMed]

Received: 26/04/2022
Accepted : 29/09/2022
In Press: 16/11/2022
Published: 18/04/2023

Abstract

OBJECTIVES:
Accumulating evidence indicates the role of dysregulated circRNAs in autoimmune diseases. In this study, we investigated their role in anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) by analysing the expression profiles of circRNA in plasma of AAV patients and exploring their potential as biomarkers of AAV.
METHODS:
RNA-sequencing (RNA-seq) was performed to identify the plasma circRNA and mRNA expression profiles from five AAV patients and five healthy controls (HCs). Quantitative reverse-transcription (qRT)-PCR confirmed that hsa_circ_0028381 was confirmed to be significantly upregulated in a validation cohort of 51 AAV patients and 30 HCs and was further verified in other connective tissue diseases (CTDs). The diagnostic value of hsa_circ_0028381 was assessed by receiver operating characteristic (ROC) curve analysis.
RESULTS:
RNA expression profiles revealed aberrant expression of 143 circRNAs (62 upregulated and 81 downregulated) and 304 mRNAs (151 upregulated and 153 downregulated) in AAV patients compared to HCs. qRT-PCR verification suggested that hsa_circ_0028381 levels were significantly increased in plasma from AAV patients compared to those in HCs and other CTDs. ROC curve analysis showed has_circ_0028381 had good diagnostic value for distinguishing AAV patients from controls (HCs and other CTDs) with an area under the curve (AUC) of 0.81. In addition, hsa_circ_0028381 was associated with renal involvement. Most importantly, increased baseline levels of hsa_circ_0028381 had predictive value for progression to end-stage renal disease (ESRD).
CONCLUSIONS:
RNA-seq revealed that circRNAs are aberrantly expressed in the plasma of AAV patients. Hsa_circ_0028381 was implicated as a potential biomarker for AAV diagnosis and renal prognosis.

DOI: https://doi.org/10.55563/clinexprheumatol/1z9lsh

Rheumatology Article