Causal relationships between gut microbiota and polycystic ovarian syndrome: A bidirectional Mendelian randomization study
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| Formato: | Artículo Open Access |
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Wiley
2024
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| _version_ | 1867019386602127361 |
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| author | Ruo‐Lin Mao Xiang‐Fei Wang Jue‐Pu Zhou Meng Wang Rui Long Lei Jin Li‐Xia Zhu |
| author_facet | Ruo‐Lin Mao Xiang‐Fei Wang Jue‐Pu Zhou Meng Wang Rui Long Lei Jin Li‐Xia Zhu Ruo‐Lin Mao Xiang‐Fei Wang Jue‐Pu Zhou Meng Wang Rui Long Lei Jin Li‐Xia Zhu |
| collection | Wiley Open Access |
| contents | Causal relationships between gut microbiota and polycystic ovarian syndrome: A bidirectional Mendelian randomization study Ruo‐Lin Mao Xiang‐Fei Wang Jue‐Pu Zhou Meng Wang Rui Long Lei Jin Li‐Xia Zhu Acta Obstetricia et Gynecologica Scandinavica AbstractIntroductionPrevious studies have established a link between gut microbiota and polycystic ovary syndrome (PCOS), but little is known about their precise causal relationship. Therefore, this study aims to explore whether there are precise causal relationships between gut microbiota and PCOS.Material and MethodsWe performed a bidirectional two‐sample Mendelian randomization (MR) analysis. Datasets were from the largest published meta‐analysis on gut microbiota composition and the FinnGen cohort of the IEU Open Genome‐Wide Association Study Project database. Inverse variance weighted (IVW), MR‐Egger, constrained maximum likelihood‐based Mendelian randomization, weighted median, weighted mode, and simple mode were used. Cochran's Q and MR‐Egger intercept tests were employed to measure the heterogeneity.ResultsA total of 211 gut microbiota taxa were identified in MR analysis. Nine taxa of bacteria, including Alphaproteobacteria (0.55, 0.30–0.99, p = 0.04), Bacilli (1.76, 1.07–2.91, p = 0.03), Bilophila (0.42, 0.23–0.77, p < 0.01), Blautia (0.16, 0.03–0.79, p = 0.02), Burkholderiales (2.37, 1.22–4.62, p = 0.01), Candidatus Soleaferrea (0.65, 0.43–0.98, p = 0.04), Cyanobacteria (0.51, 0.31–0.83, p = 0.01), Holdemania (0.53, 0.35–0.81, p < 0.01), and Lachnospiraceae (1.86, 1.04–3.35, p = 0.03), were found to be associated with PCOS in the above MR methods included at least IVW method. Cochran's Q statistics and MR‐Egger intercept test suggested no significant heterogeneity. In addition, 69 taxa were shown significant for at least the IVW method in reverse MR analysis, of these, 25 had a positive correlation, and 37 had a negative correlation. Additionally, Alphaproteobacteria and Lachnospiraceae (0.95, 0.91–0.98, p < 0.01; 0.97, 0.94–0.99, p = 0.02, respectively) were shown a bidirected causally association with PCOS.ConclusionsOur study provides evidence of the bidirectional causal association between gut microbiota and PCOS from a genetic perspective. 10.1111/aogs.14957 http://creativecommons.org/licenses/by-nc-nd/4.0/ |
| doi_str_mv | 10.1111/aogs.14957 |
| format | Artículo Open Access |
| id | wiley_oa_10_1111_aogs_14957 |
| institution | Wiley Open Access |
| license_str_mv | http://creativecommons.org/licenses/by-nc-nd/4.0/ |
| publishDate | 2024 |
| publisher | Wiley |
| record_format | wiley_oa |
| spellingShingle | Causal relationships between gut microbiota and polycystic ovarian syndrome: A bidirectional Mendelian randomization study Ruo‐Lin Mao Xiang‐Fei Wang Jue‐Pu Zhou Meng Wang Rui Long Lei Jin Li‐Xia Zhu Acta Obstetricia et Gynecologica Scandinavica Causal relationships between gut microbiota and polycystic ovarian syndrome: A bidirectional Mendelian randomization study Ruo‐Lin Mao Xiang‐Fei Wang Jue‐Pu Zhou Meng Wang Rui Long Lei Jin Li‐Xia Zhu Acta Obstetricia et Gynecologica Scandinavica AbstractIntroductionPrevious studies have established a link between gut microbiota and polycystic ovary syndrome (PCOS), but little is known about their precise causal relationship. Therefore, this study aims to explore whether there are precise causal relationships between gut microbiota and PCOS.Material and MethodsWe performed a bidirectional two‐sample Mendelian randomization (MR) analysis. Datasets were from the largest published meta‐analysis on gut microbiota composition and the FinnGen cohort of the IEU Open Genome‐Wide Association Study Project database. Inverse variance weighted (IVW), MR‐Egger, constrained maximum likelihood‐based Mendelian randomization, weighted median, weighted mode, and simple mode were used. Cochran's Q and MR‐Egger intercept tests were employed to measure the heterogeneity.ResultsA total of 211 gut microbiota taxa were identified in MR analysis. Nine taxa of bacteria, including Alphaproteobacteria (0.55, 0.30–0.99, p = 0.04), Bacilli (1.76, 1.07–2.91, p = 0.03), Bilophila (0.42, 0.23–0.77, p < 0.01), Blautia (0.16, 0.03–0.79, p = 0.02), Burkholderiales (2.37, 1.22–4.62, p = 0.01), Candidatus Soleaferrea (0.65, 0.43–0.98, p = 0.04), Cyanobacteria (0.51, 0.31–0.83, p = 0.01), Holdemania (0.53, 0.35–0.81, p < 0.01), and Lachnospiraceae (1.86, 1.04–3.35, p = 0.03), were found to be associated with PCOS in the above MR methods included at least IVW method. Cochran's Q statistics and MR‐Egger intercept test suggested no significant heterogeneity. In addition, 69 taxa were shown significant for at least the IVW method in reverse MR analysis, of these, 25 had a positive correlation, and 37 had a negative correlation. Additionally, Alphaproteobacteria and Lachnospiraceae (0.95, 0.91–0.98, p < 0.01; 0.97, 0.94–0.99, p = 0.02, respectively) were shown a bidirected causally association with PCOS.ConclusionsOur study provides evidence of the bidirectional causal association between gut microbiota and PCOS from a genetic perspective. 10.1111/aogs.14957 http://creativecommons.org/licenses/by-nc-nd/4.0/ |
| title | Causal relationships between gut microbiota and polycystic ovarian syndrome: A bidirectional Mendelian randomization study |
| topic | Acta Obstetricia et Gynecologica Scandinavica |
| url | https://obgyn.onlinelibrary.wiley.com/doi/10.1111/aogs.14957 |