AI Article Synopsis

  • The study investigates the relationship between liver fibrosis and reactive oxygen species (ROS) levels produced by neutrophils, focusing on how this varies with age and sex in the general population.
  • It involved 1,000 participants categorized into four groups based on sex and age, using various indices to assess liver fibrosis.
  • Findings indicated positive correlations between liver fibrosis scores and basal ROS levels in younger participants, while in females, higher liver fibrosis scores were associated with lower stimulated ROS levels, suggesting that enhancing neutrophil function could help prevent liver-related diseases.

Article Abstract

Fibrosis, induced by reactive oxygen species (ROS) production in neutrophils, has harmful effects on the liver and various other organs. However, little is known about the association between liver fibrosis and ROS levels in neutrophils in the general population. This large-scale epidemiological study aimed to determine the association between liver fibrosis and neutrophil-generated ROS levels according to age and sex in the general population. This cross-sectional study included 1,000 participants from a district health promotion project. Participants were grouped based on sex (male; female) and age (young, <65 years; old, ≥65 years). The four groups were as follows: male, young ( = 289); male, old ( = 100); female, young ( = 425); and female, old ( = 186). Liver fibrosis was assessed using the fibrosis 4 (FIB-4) index, aspartate aminotransferase-to-platelet ratio index (APRI), and non-alcoholic fatty liver disease (NAFLD) fibrosis score (NFS). Basal and stimulated ROS were considered in the analysis. Multiple linear analyses showed (1) significant positive correlations between all liver fibrosis scores and basal ROS in the young groups, and (2) significant negative correlations between NFS and stimulated ROS in females. Preventing liver fibrosis through neutrophil-related immune system enhancement may avert the development of lifestyle-related diseases and infections.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10636577PMC
http://dx.doi.org/10.3164/jcbn.23-46DOI Listing

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