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Blood lipid metabolism and the risk of gallstone disease: a multi-center study and meta-analysis

BACKGROUND: Gallstone disease (GSD) is a common and costly biliary disorder. Multiple studies have investigated the associations between blood lipid metabolism and GSD risk; however, the results are inconsistent. This research aimed to comprehensively evaluate the relationships among serum total cho...

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Autores principales: Zhang, Min, Mao, Min, Zhang, Chi, Hu, Fulan, Cui, Ping, Li, Guangcan, Shi, Jia, Wang, Xin, Shan, Xuefeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8889751/
https://www.ncbi.nlm.nih.gov/pubmed/35236330
http://dx.doi.org/10.1186/s12944-022-01635-9
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author Zhang, Min
Mao, Min
Zhang, Chi
Hu, Fulan
Cui, Ping
Li, Guangcan
Shi, Jia
Wang, Xin
Shan, Xuefeng
author_facet Zhang, Min
Mao, Min
Zhang, Chi
Hu, Fulan
Cui, Ping
Li, Guangcan
Shi, Jia
Wang, Xin
Shan, Xuefeng
author_sort Zhang, Min
collection PubMed
description BACKGROUND: Gallstone disease (GSD) is a common and costly biliary disorder. Multiple studies have investigated the associations between blood lipid metabolism and GSD risk; however, the results are inconsistent. This research aimed to comprehensively evaluate the relationships among serum total cholesterol, low-density lipoprotein (LDL) cholesterol, high-density lipoprotein (HDL) cholesterol, triglycerides and GSD risk. METHODS: Firstly, a multi-center cross-sectional study was carried out. Subjects who participated in the health examination in three hospitals between January 2015 and May 2020 were recruited. Multivariable logistic regression was used to investigate blood lipid metabolism associated with GSD risk. Then, a meta-analysis was performed to verify the associations further. Medline and Embase databases were systematically searched before June 10, 2021. The DerSimonian and Laird random-effect model was utilized when the heterogeneity was high; otherwise, fixed-effect model was adopted. RESULTS: There were 548,934 eligible participants included in the multi-center study, and 45,392 of them were diagnosed with GSD. The results demonstrated that total cholesterol and HDL cholesterol were negatively associated with GSD risk in both high vs. low model and per mmol/L increase model, while triglyceride was positively associated with GSD risk in the per unit increase model. In the meta-analysis, 104 studies with approximately 3 million participants were finally included. The results verified that HDL cholesterol [odds ratio (OR) = 0.636, P = 5.97 × 10(− 16) in high vs low model; OR = 0.974, P = 6.07 × 10(− 05) in per unit model] and triglyceride (OR = 1.192, P = 3.47 × 10(− 05) in high vs. low model; OR = 1.011, P = 5.12 × 10(− 05) in per unit model) were related to GSD risk in the two models. CONCLUSIONS: The findings indicated that low HDL cholesterol levels and high triglyceride levels were risk factors for GSD. This study provides a basis for identifying the population at high risk for GSD and implementing tertiary prevention strategies for GSD, thus contributing to GSD prevention as well as disease burden relief. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12944-022-01635-9.
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spelling pubmed-88897512022-03-09 Blood lipid metabolism and the risk of gallstone disease: a multi-center study and meta-analysis Zhang, Min Mao, Min Zhang, Chi Hu, Fulan Cui, Ping Li, Guangcan Shi, Jia Wang, Xin Shan, Xuefeng Lipids Health Dis Research BACKGROUND: Gallstone disease (GSD) is a common and costly biliary disorder. Multiple studies have investigated the associations between blood lipid metabolism and GSD risk; however, the results are inconsistent. This research aimed to comprehensively evaluate the relationships among serum total cholesterol, low-density lipoprotein (LDL) cholesterol, high-density lipoprotein (HDL) cholesterol, triglycerides and GSD risk. METHODS: Firstly, a multi-center cross-sectional study was carried out. Subjects who participated in the health examination in three hospitals between January 2015 and May 2020 were recruited. Multivariable logistic regression was used to investigate blood lipid metabolism associated with GSD risk. Then, a meta-analysis was performed to verify the associations further. Medline and Embase databases were systematically searched before June 10, 2021. The DerSimonian and Laird random-effect model was utilized when the heterogeneity was high; otherwise, fixed-effect model was adopted. RESULTS: There were 548,934 eligible participants included in the multi-center study, and 45,392 of them were diagnosed with GSD. The results demonstrated that total cholesterol and HDL cholesterol were negatively associated with GSD risk in both high vs. low model and per mmol/L increase model, while triglyceride was positively associated with GSD risk in the per unit increase model. In the meta-analysis, 104 studies with approximately 3 million participants were finally included. The results verified that HDL cholesterol [odds ratio (OR) = 0.636, P = 5.97 × 10(− 16) in high vs low model; OR = 0.974, P = 6.07 × 10(− 05) in per unit model] and triglyceride (OR = 1.192, P = 3.47 × 10(− 05) in high vs. low model; OR = 1.011, P = 5.12 × 10(− 05) in per unit model) were related to GSD risk in the two models. CONCLUSIONS: The findings indicated that low HDL cholesterol levels and high triglyceride levels were risk factors for GSD. This study provides a basis for identifying the population at high risk for GSD and implementing tertiary prevention strategies for GSD, thus contributing to GSD prevention as well as disease burden relief. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12944-022-01635-9. BioMed Central 2022-03-02 /pmc/articles/PMC8889751/ /pubmed/35236330 http://dx.doi.org/10.1186/s12944-022-01635-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Zhang, Min
Mao, Min
Zhang, Chi
Hu, Fulan
Cui, Ping
Li, Guangcan
Shi, Jia
Wang, Xin
Shan, Xuefeng
Blood lipid metabolism and the risk of gallstone disease: a multi-center study and meta-analysis
title Blood lipid metabolism and the risk of gallstone disease: a multi-center study and meta-analysis
title_full Blood lipid metabolism and the risk of gallstone disease: a multi-center study and meta-analysis
title_fullStr Blood lipid metabolism and the risk of gallstone disease: a multi-center study and meta-analysis
title_full_unstemmed Blood lipid metabolism and the risk of gallstone disease: a multi-center study and meta-analysis
title_short Blood lipid metabolism and the risk of gallstone disease: a multi-center study and meta-analysis
title_sort blood lipid metabolism and the risk of gallstone disease: a multi-center study and meta-analysis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8889751/
https://www.ncbi.nlm.nih.gov/pubmed/35236330
http://dx.doi.org/10.1186/s12944-022-01635-9
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