Background: Inflammation contributed to myopia. Scarce evidence explored the relationship between systemic inflammation and high myopia. Thus, we aim to elucidate this issue via the “Gut-retina axis”.
Methods: Patients with age-related cataracts (ARC) and high myopic cataracts (HMC) were included in the study. After comprehensive ophthalmic examinations, feces, plasma, and aqueous humor (AH) specimenswere collected from each patient.Detecting the V3-V4 region of 16S rDNA to obtain information on gut taxa and distinct gut taxa was obtained. LC-MS/MS systems were used to explore the metabolites of plasma and AH specimens. Using the “Dr. Tom” platform to find distinct metabolites. Then “corrplot” package and “pROC” package in R studio were conducted to find the relationship between gut taxa, metabolites, and axial lengths (AL).
Results: Class Bacilli (P=0.008), Order Lactobacillales (P=0.013) and Burkholderiales (P=0.047), and Family Lactobacillaceae (P=0.003) were increased in the HMC group. Genus Roseburia in the HMC group was decreased (P=0.012). 79 and 197 distinct metabolites were found in the plasma and AH specimensrespectively. From KEGG analysis, the distinct plasma metabolites of HMC were enriched in “ABC transporters”, “Steroid hormone biosynthesis”, and “PPAR signaling pathway”, whilst “Protein digestion and absorption”, “Aminoacyl-tRNA biosynthesis”, and “D-Amino acid metabolism” pathways enriched in AH specimens. Finally, we identified the 4-Phenolsulfonic acid in plasma and 5'-N-Ethylcarboxamidoadenosine in AH may be potential biomarkers of high myopia.
Conclusions: High myopic patients have distinct gut taxa and significantly different metabolites. Using multi-omics integrative analysis, new insights and biomarkers of high myopia will help us explore the pathogenesis of myopia.
Trial registration: www.chictr.org.cn identifier is ChiCTR2300071397.