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Insights into modifiable risk factors of cholelithiasis: A Mendelian randomization study
BACKGROUND AND AIMS: The risk factors of cholelithiasis have not been clearly identified, especially for total cholesterol. Here, we try to identify these causal risk factors. APPROACH AND RESULTS: We obtained genetic variants associated with the exposures at the genome‐wide significance (p < 5 ×...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9300195/ https://www.ncbi.nlm.nih.gov/pubmed/34624136 http://dx.doi.org/10.1002/hep.32183 |
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author | Chen, Lanlan Yang, Hongqun Li, Haitao He, Chang Yang, Liu Lv, Guoyue |
author_facet | Chen, Lanlan Yang, Hongqun Li, Haitao He, Chang Yang, Liu Lv, Guoyue |
author_sort | Chen, Lanlan |
collection | PubMed |
description | BACKGROUND AND AIMS: The risk factors of cholelithiasis have not been clearly identified, especially for total cholesterol. Here, we try to identify these causal risk factors. APPROACH AND RESULTS: We obtained genetic variants associated with the exposures at the genome‐wide significance (p < 5 × 10(−8)) level from corresponding genome‐wide association studies. Summary‐level statistical data for cholelithiasis were obtained from FinnGen and UK Biobank (UKB) consortia. Both univariable and multivariable Mendelian randomization (MR) analyses were conducted to identify causal risk factors of cholelithiasis. Results from FinnGen and UKB were combined using the fixed‐effect model. In FinnGen, the odds of cholelithiasis increased per 1‐SD increase of body mass index (BMI) (OR = 1.631, p = 2.16 × 10(−7)), together with body fat percentage (OR = 2.108, p = 4.56 × 10(−3)) and fasting insulin (OR = 2.340, p = 9.09 × 10(−3)). The odds of cholelithiasis would also increase with lowering of total cholesterol (OR = 0.789, p = 8.34 × 10(−5)) and low‐density lipoprotein–cholesterol (LDL‐C) (OR = 0.792, p = 2.45 × 10(−4)). However, LDL‐C was not significant in multivariable MR. In UKB, the results of BMI, body fat percentage, total cholesterol, and LDL‐C were replicated. In meta‐analysis, the liability to type 2 diabetes mellitus and smoking could also increase the risk of cholelithiasis. Moreover, there were no associations with other predominant risk factors. CONCLUSIONS: Our MR study corroborated the risk factors of cholelithiasis from previous MR studies. Furthermore, lower total cholesterol level could be an independent risk factor. |
format | Online Article Text |
id | pubmed-9300195 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93001952022-07-21 Insights into modifiable risk factors of cholelithiasis: A Mendelian randomization study Chen, Lanlan Yang, Hongqun Li, Haitao He, Chang Yang, Liu Lv, Guoyue Hepatology Original Articles BACKGROUND AND AIMS: The risk factors of cholelithiasis have not been clearly identified, especially for total cholesterol. Here, we try to identify these causal risk factors. APPROACH AND RESULTS: We obtained genetic variants associated with the exposures at the genome‐wide significance (p < 5 × 10(−8)) level from corresponding genome‐wide association studies. Summary‐level statistical data for cholelithiasis were obtained from FinnGen and UK Biobank (UKB) consortia. Both univariable and multivariable Mendelian randomization (MR) analyses were conducted to identify causal risk factors of cholelithiasis. Results from FinnGen and UKB were combined using the fixed‐effect model. In FinnGen, the odds of cholelithiasis increased per 1‐SD increase of body mass index (BMI) (OR = 1.631, p = 2.16 × 10(−7)), together with body fat percentage (OR = 2.108, p = 4.56 × 10(−3)) and fasting insulin (OR = 2.340, p = 9.09 × 10(−3)). The odds of cholelithiasis would also increase with lowering of total cholesterol (OR = 0.789, p = 8.34 × 10(−5)) and low‐density lipoprotein–cholesterol (LDL‐C) (OR = 0.792, p = 2.45 × 10(−4)). However, LDL‐C was not significant in multivariable MR. In UKB, the results of BMI, body fat percentage, total cholesterol, and LDL‐C were replicated. In meta‐analysis, the liability to type 2 diabetes mellitus and smoking could also increase the risk of cholelithiasis. Moreover, there were no associations with other predominant risk factors. CONCLUSIONS: Our MR study corroborated the risk factors of cholelithiasis from previous MR studies. Furthermore, lower total cholesterol level could be an independent risk factor. John Wiley and Sons Inc. 2021-12-13 2022-04 /pmc/articles/PMC9300195/ /pubmed/34624136 http://dx.doi.org/10.1002/hep.32183 Text en © 2021 The Authors. Hepatology published by Wiley Periodicals LLC on behalf of American Association for the Study of Liver Diseases. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Chen, Lanlan Yang, Hongqun Li, Haitao He, Chang Yang, Liu Lv, Guoyue Insights into modifiable risk factors of cholelithiasis: A Mendelian randomization study |
title | Insights into modifiable risk factors of cholelithiasis: A Mendelian randomization study |
title_full | Insights into modifiable risk factors of cholelithiasis: A Mendelian randomization study |
title_fullStr | Insights into modifiable risk factors of cholelithiasis: A Mendelian randomization study |
title_full_unstemmed | Insights into modifiable risk factors of cholelithiasis: A Mendelian randomization study |
title_short | Insights into modifiable risk factors of cholelithiasis: A Mendelian randomization study |
title_sort | insights into modifiable risk factors of cholelithiasis: a mendelian randomization study |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9300195/ https://www.ncbi.nlm.nih.gov/pubmed/34624136 http://dx.doi.org/10.1002/hep.32183 |
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