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Mendelian randomization study of gastroesophageal reflux disease and major depression
This study systematically investigated the causal relationship between gastroesophageal reflux disease (GERD) and major depression (MD). Single-nucleotide polymorphisms (SNPs) associated with disorders of interest were screened via the genome-wide association study (GWAS) enrolling individuals of Eu...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10538746/ https://www.ncbi.nlm.nih.gov/pubmed/37768900 http://dx.doi.org/10.1371/journal.pone.0291086 |
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author | Zheng, Xiaofei Zhou, Xin Tong, Li Gu, Wang Wang, Siyu Yuang, Wenkang Zhang, Chong Zhang, Chaoyang Zhang, Chao Wan, Bangbei |
author_facet | Zheng, Xiaofei Zhou, Xin Tong, Li Gu, Wang Wang, Siyu Yuang, Wenkang Zhang, Chong Zhang, Chaoyang Zhang, Chao Wan, Bangbei |
author_sort | Zheng, Xiaofei |
collection | PubMed |
description | This study systematically investigated the causal relationship between gastroesophageal reflux disease (GERD) and major depression (MD). Single-nucleotide polymorphisms (SNPs) associated with disorders of interest were screened via the genome-wide association study (GWAS) enrolling individuals of European descent. Summary-level data for GERD and MD were extracted from the UK Biobank. The inverse-variance-weighted (IVW) method was utilized as the primary analysis. Sensitivity analyses were performed using the MR-Egger method, the Maximum likelihood method, the MR-pleiotropy residual sum outlier (MR-PRESSO) method, and MR-robust adjusted profile score (MR-RAPS) method. MR-Egger regression, heterogeneity tests, pleiotropy tests, and leave-one-out tests were also performed to analyze sensitivity. The MR Steiger test was used to verify the directionality of the exposure to the outcome. An available website tool (https://shiny.cnsgenomics.com/mRnd/) was used to calculate the statistical power of MR analysis. Meta-analysis was applied to test MD’s average genetically predicted effect on GERD. Our MR study showed a bidirectional causal association between MD and GERD. Regarding MD to GERD, there was a positive association between them; the ORs were 1.500 (95% CI = 1.320–1.704; P = 4.91E-10) and 2.058 (95% CI = 1.868–2.267; P = 2.20E-48) in the IVW method, respectively. In addition, the meta-analysis also showed a strong positive causal association between MD and GERD. When exposure and outcome were reversed, genetic predisposition to GERD was significantly associated with the overall Risk of advanced MD (ieu-a-1187, OR = 1.982, 95% CI = 1.694–2.319, P = 1.41E-17; ieu-b-102, OR = 1.612, 95% CI = 1.530–2.700, P = 1.15E-70). Our study provides 100% power to detect the causal effect of MD on GERD and vice versa. Genetically predicted MD was positively associated with higher GERD risk, and vice versa. Our study reminds clinicians to pay attention to screening for GERD when diagnosing and treating MD and vice versa. Moreover, there may be positive feedback between MD and GERD when treating and preventing one disorder may benefit the treatment and prevention of the other. |
format | Online Article Text |
id | pubmed-10538746 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-105387462023-09-29 Mendelian randomization study of gastroesophageal reflux disease and major depression Zheng, Xiaofei Zhou, Xin Tong, Li Gu, Wang Wang, Siyu Yuang, Wenkang Zhang, Chong Zhang, Chaoyang Zhang, Chao Wan, Bangbei PLoS One Research Article This study systematically investigated the causal relationship between gastroesophageal reflux disease (GERD) and major depression (MD). Single-nucleotide polymorphisms (SNPs) associated with disorders of interest were screened via the genome-wide association study (GWAS) enrolling individuals of European descent. Summary-level data for GERD and MD were extracted from the UK Biobank. The inverse-variance-weighted (IVW) method was utilized as the primary analysis. Sensitivity analyses were performed using the MR-Egger method, the Maximum likelihood method, the MR-pleiotropy residual sum outlier (MR-PRESSO) method, and MR-robust adjusted profile score (MR-RAPS) method. MR-Egger regression, heterogeneity tests, pleiotropy tests, and leave-one-out tests were also performed to analyze sensitivity. The MR Steiger test was used to verify the directionality of the exposure to the outcome. An available website tool (https://shiny.cnsgenomics.com/mRnd/) was used to calculate the statistical power of MR analysis. Meta-analysis was applied to test MD’s average genetically predicted effect on GERD. Our MR study showed a bidirectional causal association between MD and GERD. Regarding MD to GERD, there was a positive association between them; the ORs were 1.500 (95% CI = 1.320–1.704; P = 4.91E-10) and 2.058 (95% CI = 1.868–2.267; P = 2.20E-48) in the IVW method, respectively. In addition, the meta-analysis also showed a strong positive causal association between MD and GERD. When exposure and outcome were reversed, genetic predisposition to GERD was significantly associated with the overall Risk of advanced MD (ieu-a-1187, OR = 1.982, 95% CI = 1.694–2.319, P = 1.41E-17; ieu-b-102, OR = 1.612, 95% CI = 1.530–2.700, P = 1.15E-70). Our study provides 100% power to detect the causal effect of MD on GERD and vice versa. Genetically predicted MD was positively associated with higher GERD risk, and vice versa. Our study reminds clinicians to pay attention to screening for GERD when diagnosing and treating MD and vice versa. Moreover, there may be positive feedback between MD and GERD when treating and preventing one disorder may benefit the treatment and prevention of the other. Public Library of Science 2023-09-28 /pmc/articles/PMC10538746/ /pubmed/37768900 http://dx.doi.org/10.1371/journal.pone.0291086 Text en © 2023 Zheng et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Zheng, Xiaofei Zhou, Xin Tong, Li Gu, Wang Wang, Siyu Yuang, Wenkang Zhang, Chong Zhang, Chaoyang Zhang, Chao Wan, Bangbei Mendelian randomization study of gastroesophageal reflux disease and major depression |
title | Mendelian randomization study of gastroesophageal reflux disease and major depression |
title_full | Mendelian randomization study of gastroesophageal reflux disease and major depression |
title_fullStr | Mendelian randomization study of gastroesophageal reflux disease and major depression |
title_full_unstemmed | Mendelian randomization study of gastroesophageal reflux disease and major depression |
title_short | Mendelian randomization study of gastroesophageal reflux disease and major depression |
title_sort | mendelian randomization study of gastroesophageal reflux disease and major depression |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10538746/ https://www.ncbi.nlm.nih.gov/pubmed/37768900 http://dx.doi.org/10.1371/journal.pone.0291086 |
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