AI Article Synopsis

  • Various studies show significant links between obstructive sleep apnea (OSA), gut microbiota, and related metabolites, but establishing causation is still ongoing.
  • Multiple Mendelian randomization analyses were conducted to explore the genetic impact of 196 gut microbiota and 83 metabolites on OSA, using methods like two-sample MR and multivariable MR for deeper insights.
  • The study found certain gut microbiota and metabolites that either increase or decrease OSA risk, suggesting the gut microbiome plays a crucial role in OSA development, which could lead to new prevention strategies.

Article Abstract

Various studies have highlighted the important associations between obstructive sleep apnea (OSA) and gut microbiota and related metabolites. Nevertheless, the establishment of causal relationships between these associations remains to be determined. Multiple mendelian randomization (MR) analyses were performed to genetically predict the causative impact of 196 gut microbiota and 83 metabolites on OSA. Two-sample MR was used to assess the potential association, and causality was evaluated using inverse variance weighted (IVW), MR-Egger, and weighted median (WM) methods. Multivariable MR (MVMR) was employed to ascertain the causal independence between gut microbiota and the metabolites linked to OSA. Additionally, Cochran's Q test, the MR Egger intercept test and the MR Steiger test were used for the sensitivity analyses. The analysis of the 196 gut microbiota revealed that _ () (P = 0.010) and _ (P = 0.041) were associated with an increased risk of OSA onset. Conversely, _ (P = 0.030), _ (P = 0.025), _ (P = 0.011), and _ (_) (P = 0.001) were negatively related to the risk of OSA. Among the 83 metabolites evaluated, 3-dehydrocarnitine, epiandrosterone sulfate, and leucine were determined to be potential independent risk factors associated with OSA. Moreover, the reverse MR analysis demonstrated a suggestive association between OSA exposure and six microbiota taxa. This study offers compelling evidence regarding the potential beneficial or detrimental causative impact of the gut microbiota and its associated metabolites on OSA risk, thereby providing new insights into the mechanisms of gut microbiome-mediated OSA development.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10648878PMC
http://dx.doi.org/10.3390/nu15214544DOI Listing

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