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Circulating miR-125a but not miR-125b is decreased in active disease status and negatively correlates with disease severity as well as inflammatory cytokines in patients with Crohn’s disease

World Journal of Gastroenterology Dec 05, 2017

Sun CM, et al. - Researchers carried out this study to ascertain the association of circulating miR-125a/b expression with the risk and disease severity of Crohn’s disease (CD), and with inflammatory cytokines. In patients with active disease status, circulating miR-125a was decreased. However, this was not observed with miR-125b. In patients with CD, circulating miR-125a was negatively correlated with disease severity and inflammatory cytokines.

Methods

  • The researchers collected plasma samples from patients with active CD (A-CD), or CD in remission (R-CD) and from healthy controls (HCs).
  • They measured the levels of the inflammatory cytokines interleukin-17 (IL-17), tumour necrosis factor-α (TNF-α), and interferon-γ (IFN-γ) by enzyme-linked immunosorbent assay.
  • They evaluated the expression of miR-125a/b by quantitative polymerase chain reaction (qPCR).

Results

  • The researchers included 29 A-CD patients, 37 R-CD patients, and 37 HCs in the study.
  • In A-CD patients, plasma miR-125a expression was decreased compared with that in R-CD patients (P < 0.001) and HCs (P < 0.001).
  • The differentiation of A-CD from R-CD patients [area under curve (AUC) = 0.854] and from HCs (AUC = 0.780) was enabled by miR-125a expression, while this was not noted with miR-125b expression.
  • In A-CD patients, miR-125a was negatively associated with C-reaction protein (CRP) (P=0.017), erythrocyte sedimentation rate (ESR) (P=0.026), Crohn’s disease activity index (CDAI) (P=0.003), IL-17 (P=0.015), and TNF-α (P=0.004).
  • Furthermore, in R-CD patients, miR-125a was negatively correlated with CRP (P=0.038) and CDAI (P=0.021).
  • No association with CRP, CDAI, IL-17, TNF-α, or IFN-γ was found in A-CD or in R-CD patients regarding miR-125b.
  • In A-CD patients who achieved clinical remission (P=0.009) after 3-mo treatment, miR-125a levels gradually increased, while they remained unchanged among patients who failed to achieve remission.
  • In remission or non-remission patients, no changes in miR-125b expression were detected after treatment.

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