: Systemic Lupus Erythematous (SLE) is a chronic systemic autoimmune disorder whose diagnosis depends on combination of multiple factors. Circulating lncRNAs could serve as diagnostic non-invasive biomarkers for SLE. We hypothesised that serum FAS-AS1 and PVT1 are new biomarkers for SLE that relate to clinical features and laboratory markers. : Measurement of serum FAS-AS1 & PVT1 by qRT-PCR, analysis of the association between two RNAs and the clinical data, activity index and laboratory markers by standard routine methods. : There was a significant relative increased serum FAS-AS1 (median (IQR) 2.19 (0.13-8.62) and a significant reduced PVT1 (median (IQR) 0.52 (0.01-7.55) in SLE patients compared to controls ( < 0.0001 for FAS-AS1 and = 0.007 for PVT1). Serum FAS-AS1 and PVT1 were positively correlated (= 0.37, = 0.001). Higher FAS-AS1 was significantly linked with nephritis ( = 0.011), positive anti-dsDNA (= 0.01) and lower serum PVT1 was significantly associated with oral ulcers (= 0.023), photosensitivity (= 0.017), and neurological manifestations (= 0.041). Serum PVT1 negatively correlated with age (= -0.52, < 0.0001) and ESR level (= -0.29, = 0.011) in SLE patients. No correlation between disease activity and serum FAS-AS1 or PVT1 was detected. : Our study provides evidence that serum FAS-AS1 and PVT1 are new biomarkers for SLE.

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http://dx.doi.org/10.1080/09674845.2020.1765459DOI Listing

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