AI Article Synopsis

  • Recent studies suggest that long-term exposure to air pollution (AP) increases the risk of metabolic dysfunction-associated fatty liver disease (MAFLD), with blood lipids potentially playing a key mediating role.
  • An analysis of 6,350 participants from the China Multi-Ethnic Cohort revealed new diagnoses of MAFLD and established associations between specific air pollutants and MAFLD risk, supported by causal mediation analysis.
  • Findings indicated that changes in blood lipids, especially cholesterol types, mediate 5% to 30% of the relationship between air pollution and the onset of MAFLD, highlighting a significant health impact from environmental pollution.

Article Abstract

Background & Aims: Recent cross-sectional studies found that exposure to ambient air pollution (AP) was associated with an increased risk of metabolic dysfunction-associated fatty liver disease (MAFLD). The alternation of blood lipids may explain the association, but epidemiological evidence is lacking. We aimed to examine whether and to what extent the association between long-term exposure to AP and incident MAFLD is mediated by blood lipids and dyslipidemia in a prospective cohort.

Methods: We included 6350 participants from the China Multi-Ethnic Cohort (CMEC, baseline 2018-2019, follow-up 2020-2021). Three-year average (2016-2018) of AP (PM, PM, PM, NO), blood lipids (TC, LDL-C, HDL-C, TG with their combinations) and incident MAFLD for each individual were assessed chronologically. Linear and logistic regression was used to assess the associations among AP, blood lipids, and MAFLD, and the potential mediation effects of blood lipids were evaluated using causal mediation analysis.

Results: A total of 744 participants were newly diagnosed with MAFLD at follow-up. The odds ratios of MAFLD associated with a 10 μm increase in PM, PM, and NO were 1.35 (95 % CI: 1.14, 1.58), 1.34 (1.10, 1.65) and 1.28 (1.14, 1.44), respectively. Blood lipids are important mediators between AP and incident MAFLD. LDL-C (Proportion Mediated: 6.9 %), non-HDL (13.4 %), HDL-C (20.7 %), LDL/HDL (30.1 %), and dyslipidemia (6.5 %) significantly mediated the association between PM and MAFLD. For PM, the indirect effects were similar to those for PM, with a larger value for the direct effect, and the mediation proportion by blood lipids was less for NO.

Conclusion: Blood lipids are important mediators between AP and MAFLD, and can explain 5 %-30 % of the association between AP and incident MAFLD, particularly cholesterol-related variables, indicating that AP could lead to MAFLD through the alternation of blood lipids. These findings provided mechanical evidence of AP leading to MAFLD in epidemiological studies.

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Source
http://dx.doi.org/10.1016/j.scitotenv.2023.166347DOI Listing

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