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. 2020 Sep;34(9):e23360.
doi: 10.1002/jcla.23360. Epub 2020 Jul 22.

Long non-coding RNA CRNDE and toll-like receptor 3 correlate with disease severity, inflammation, and mortality in sepsis

Affiliations

Long non-coding RNA CRNDE and toll-like receptor 3 correlate with disease severity, inflammation, and mortality in sepsis

Junhui Yang et al. J Clin Lab Anal. 2020 Sep.

Abstract

Objective: This study aimed to assess the interaction between long non-coding RNA colorectal neoplasia differentially expressed (lncRNA CRNDE) and toll-like receptor 3 (TLR3), and assess their correlations with disease severity, inflammation, and 28-days mortality in sepsis patients.

Methods: We consecutively enrolled 146 sepsis patients and 146 healthy controls (HCs), and collected their peripheral blood mononuclear cells to detect lncRNA CRNDE and TLR3 expressions using reverse transcription quantitative polymerase chain reaction. LncRNA CRNDE and TLR3 in sepsis patients were classified into four clusters according to quantile expressions (Quantile 1 (0%-24%), Quantile 2 (25%-50%), Quantile 3 (50%-74%), and Quantile 4 (75%-100%)) for correlation analysis.

Results: LncRNA CRNDE was upregulated in sepsis patients compared with HCs, and it showed good value in differentiating sepsis patients form HCs by receiver operating characteristic curve analysis. In sepsis patients, lncRNA CRNDE positively correlated with acute pathologic and chronic health evaluation II (APACHE II) score and sequential organ failure assessment (SOFA) score, as well as serum creatinine (Scr). As for inflammation, lncRNA CRNDE positively correlated with C-reactive protein (CRP), tumor necrosis factor-α (TNF-α), interleukin (IL)-1β, IL-6, and IL-8. Regarding mortality, lncRNA CRNDE positively correlated with 28-days mortality. Furthermore, lncRNA CRNDE positively correlated with TLR3, and TLR3 positively associated with APACHE II score, SOFA score, Scr, albumin, CRP, TNF-α, IL-1β, IL-6, IL-8, and 28-days mortality in sepsis patients.

Conclusion: LncRNA CRNDE interacts with TLR3, both of which correlate with advanced disease severity, inflammation, and higher 28-days mortality in sepsis patients.

Keywords: LncRNA CRNDE; TLR3; inflammation; mortality; sepsis.

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Conflict of interest statement

No potential conflict of interest was reported by the authors.

Figures

FIGURE 1
FIGURE 1
The expression of lncRNA CRNDE in sepsis and its value in predicting sepsis vulnerability. Comparison of lncRNA CRNDE expression between sepsis patients and HCs (A). The performance of lncRNA CRNDE in distinguishing sepsis patients from HCs (B). The triangles represented healthy controls, dots represented sepsis patients, the upper/lower line represented 25%/75% quantile, and the middle line represented median of lncRNA CRNDE relative expression. HCs, healthy controls; lncRNA CRNDE, long non‐coding RNA colorectal neoplasia differentially expressed
FIGURE 2
FIGURE 2
Positive correlation of lncRNA CRNDE with APACHE II score and SOFA score in sepsis patients. The correlation of lncRNA CRNDE quantile with APACHE II score (A). The correlation of lncRNA CRNDE quantiles with SOFA score (B). LncRNA CRNDE, long non‐coding RNA colorectal neoplasia differentially expressed; APACHE II, acute pathologic and chronic health evaluation II; and SOFA, sequential organ failure assessment
FIGURE 3
FIGURE 3
Positive correlation of lncRNA CRNDE with 28‐days mortality in sepsis patients. Correlation of lncRNA CRNDE quantile with 28‐days mortality. LncRNA CRNDE, long non‐coding RNA colorectal neoplasia differentially expressed
FIGURE 4
FIGURE 4
Positive correlation of lncRNA CRNDE with TLR3 in sepsis patients and HCs. The correlation of lncRNA CRNDE with TLR3 in sepsis patients (A). The correlation of lncRNA CRNDE with TLR3 in HCs (B). LncRNA CRNDE, long non‐coding RNA colorectal neoplasia differentially expressed; TLR3, toll‐like receptor 3; and HCs, healthy controls

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