Objective: This study explores the causal relationship between endometriosis and pelvic inflammatory diseases (PID).
Methods: The study utilized genome-wide association study (GWAS) datasets for endometriosis ("finn-b-N14_ENDOMETRIOSIS") and PID ("finn-b-N14_OTHFEMPELINF"). Subsequently, two-sample Mendelian randomization (MR) analyses were conducted using inverse variance weighting (IVW), Egger regression (MR-Egger), and weighted median (WM) methods. Heterogeneity was evaluated using Cochran's Q test, and in case of detected outliers, they were removed for re-evaluation of MR causality.
Results: From the endometriosis GWAS dataset, 33 single nucleotide polymorphisms (SNPs) were selected as instrumental variables. All three methods, IVW (OR = 1.39, P < 1×10), MR-Egger (OR = 1.41, P = 0.003), and WM (OR = 1.37, P = 1.16×10) confirmed a causal relationship between endometriosis and PID. The association between endometriosis and pelvic inflammation remained unaffected by the exclusion of individual SNPs. Lastly, Cochran's Q test and funnel plots showed no evidence of SNP asymmetry.
Conclusion: The results of the MR analysis support a potential causal relationship between endometriosis and an increased risk of PID.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11063464 | PMC |
http://dx.doi.org/10.2147/IJWH.S440110 | DOI Listing |
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