Abstract
Objectives: Presepsin (PSEP: soluble CD14 subtype) is produced from bacteria-stimulated monocytes or neutrophils, thus recognized as a biomarker of sepsis. Aberrant functions in monocyte or neutrophils are increasingly recognized in systemic lupus erythematosus (SLE). We investigated whether plasma PSEP reflects disease activity in patients with SLE. Methods: This retrospective study comprised 35 patients with SLE and 72 with non-SLE autoimmune diseases who visited our facility during the period from August 2012 to September 2015. Plasma PSEP levels and laboratory data were compared between SLE and non-SLE. Clinical markers of SLE disease activity, including SLE disease activity index 2000 (SLEDAI-2K), serum complement concentrations and serum anti-ds-DNA antibodies were assessed in correlation with plasma PSEP levels. Results: Plasma PSEP levels in SLE were higher than those in non-SLE. This phenomenon holds true when comparing SLE and non-SLE patients in the absence of infection (p =.0008). Plasma PSEP levels in SLE patients negatively correlated with C3 (r = –0.4454, p =.0430), CH50 (r = –0.4502, p =.0406) and positively with SLEDAI-2K (r = 0.4801, p =.0237). Conclusion: Elevated plasma PSEP levels were correlated with disease activity of SLE, suggesting inappropriate monocyte or neutrophil activation in the pathophysiology of SLE exacerbation.
Original language | English |
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Pages (from-to) | 865-871 |
Number of pages | 7 |
Journal | Modern Rheumatology |
Volume | 28 |
Issue number | 5 |
DOIs | |
State | Published - 2018/09/03 |
Keywords
- CD14
- monocyte
- presepsin (PSEP)
- soluble CD14-ST
- systemic lupus erythematosus (SLE)
ASJC Scopus subject areas
- General Medicine