Severity: Warning
Message: file_get_contents(https://...@gmail.com&api_key=61f08fa0b96a73de8c900d749fcb997acc09&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 197
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 197
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 271
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3165
Function: getPubMedXML
File: /var/www/html/application/controllers/Detail.php
Line: 597
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 511
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 317
Function: require_once
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This study aimed to explore the bidirectional causal relationship between inflammatory bowel disease (IBD) and Hashimoto thyroiditis (HT) using Mendelian randomization (MR) analysis. While both conditions are characterized by persistent inflammation and immune dysregulation, the direction of causality remains unclear. We performed a 2-sample bidirectional MR analysis using summary statistics from genome-wide association studies for IBD and HT. Genetic variants strongly associated with IBD and HT were selected as instrumental variables for forward and reverse MR analyses, respectively. Various MR methods, including inverse-variance weighted (IVW), MR-Egger regression, weighted median, and weighted mode, were employed to assess causal relationships. Sensitivity analyses were conducted to evaluate the reliability of results, including tests for pleiotropy and heterogeneity. Data were sourced from individuals of European descent to minimize population stratification bias. In the forward MR analysis, no strong evidence of a causal effect of IBD on HT was found, with the IVW method yielding an odds ratio (OR) of 0.9617 (95% CI: 0.7549-1.2251; P = .7519) Similarly, in the reverse MR analysis, no significant causal effect of HT on IBD was observed, with the IVW method showing an OR of 0.9991 (95% CI: 0.9693-1.0298, P = .9527). Sensitivity analyses confirmed the absence of heterogeneity or pleiotropic effects that could influence the results. The MR-PRESSO analysis did not detect any outlier SNPs. This bidirectional MR analysis provides no evidence for a causal relationship between IBD and HT in either direction.
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Source |
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12401396 | PMC |
http://dx.doi.org/10.1097/MD.0000000000044049 | DOI Listing |