AI Article Synopsis

  • Type 2 diabetes is a key factor contributing to non-alcoholic fatty liver disease (NAFLD), leading to increased fasting blood sugar, insulin levels, and insulin resistance in affected patients.
  • This meta-umbrella study analyzed existing research on how gut microbial treatments (probiotics, prebiotics, and synbiotics) influence glycemic indices in NAFLD patients.
  • Results indicated that these treatments significantly lowered insulin resistance and fasting insulin levels, but had no notable impact on fasting blood sugar levels.

Article Abstract

Background: Type 2 diabetes mellitus (T2DM) is a significant risk factor for non-alcoholic fatty liver disease (NAFLD). Increased fasting blood sugar (FBS), fasting insulin (FI), and insulin resistance (HOMA-IR) are observed in patients with NAFLD. Gut microbial modulation using prebiotics, probiotics, and synbiotics has shown promise in NAFLD treatment. This meta-umbrella study aimed to investigate the effects of gut microbial modulation on glycemic indices in patients with NAFLD and discuss potential mechanisms of action.

Methods: A systematic search was conducted in PubMed, Web of Science, Scopus, and Cochrane Library until March 2023 for meta-analyses evaluating the effects of probiotics, prebiotics, and synbiotics on patients with NAFLD. Random-effect models, sensitivity analysis, and subgroup analysis were employed.

Results: Gut microbial therapy significantly decreased HOMA-IR (ES: -0.41; 95%CI: -0.52, -0.31; P < 0.001) and FI (ES: -0.59; 95%CI: -0.77, -0.41; P < 0.001). However, no significant effect was observed on FBS (ES: -0.17; 95%CI: -0.36, 0.02; P = 0.082). Subgroup analysis revealed prebiotics had the most potent effect on HOMA-IR, followed by probiotics and synbiotics. For FI, synbiotics had the most substantial effect, followed by prebiotics and probiotics.

Conclusion: Probiotics, prebiotics, and synbiotics administration significantly reduced FI and HOMA-IR, but no significant effect was observed on FBS.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11087547PMC
http://dx.doi.org/10.1038/s41387-024-00281-7DOI Listing

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