AI Article Synopsis

  • The study investigates the relationship between inflammation and the regression of low-grade squamous intraepithelial lesions (LSIL) in women, focusing on a biomarker called high-sensitivity C-reactive protein (hs-CRP).
  • Conducted from 2006 to 2015, it followed 520 women aged 22-64 with annual or biannual cervical screenings to track the natural progression of LSIL.
  • Results indicated that higher hs-CRP levels are linked to a lower rate of LSIL regression, suggesting that host inflammatory status may play a role in the development of cervical cancer.

Article Abstract

Background: Inflammation is emerging as a potential mechanism of cervical carcinogenesis. However, few studies have investigated the association between host inflammatory status and the natural course of cervical precursor lesion. The aim of this study was to assess the probability of LSIL regression, associated with an inflammatory biomarker, high-sensitivity C-reactive protein (hs-CRP).

Methods: In a longitudinal cohort study, female participants were examined annually or biannually using cervical cytology between 2006 and 2015. Incident LSIL cases were included in the analysis, with regression defined as at least one consecutive normal cytologic result. A total of 520 women aged 22-64 years were followed up for LSIL regression. The multivariable-adjusted hazard ratios (HRs) for LSIL regression were estimated using a parametric proportional hazards model.

Results: During 827.5 person-years of follow-up, 486 out of 520 subjects (93.5%) showed LSIL regression. After adjusting several important potential confounders, a higher quartile of hs-CRP levels was significantly associated with a lower rate of regression (for quartile 4 vs quartile 1, inverse HR 1.33; 95% CI, 1.04-1.69; P for trend = 0.028).

Conclusions: The low rate of spontaneous regression recorded in women with higher hs-CRP lends support to the role of the perturbated host inflammatory status in cervical carcinogenesis, and suggests that hs-CRP level could help monitor LSIL.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8593578PMC
http://dx.doi.org/10.2188/jea.JE20200142DOI Listing

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