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Lipids, cholesterols, statins and liver cancer: a Mendelian randomization study

AIM: To investigate the causal relationship of serum lipid indicators and lipid-lowering drugs with the risk of liver cancer using Mendelian randomization study. METHODS: A two-sample Mendelian randomization (TSMR) study was performed to investigate the causal relationship between serum levels of li...

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Autores principales: Liang, Zicheng, Zhang, Zhen, Tan, Xiaoning, Zeng, Puhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10516570/
https://www.ncbi.nlm.nih.gov/pubmed/37746259
http://dx.doi.org/10.3389/fonc.2023.1251873
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author Liang, Zicheng
Zhang, Zhen
Tan, Xiaoning
Zeng, Puhua
author_facet Liang, Zicheng
Zhang, Zhen
Tan, Xiaoning
Zeng, Puhua
author_sort Liang, Zicheng
collection PubMed
description AIM: To investigate the causal relationship of serum lipid indicators and lipid-lowering drugs with the risk of liver cancer using Mendelian randomization study. METHODS: A two-sample Mendelian randomization (TSMR) study was performed to investigate the causal relationship between serum levels of lipid indicators and liver cancer, including low-density lipoprotein cholesterol (LDL-c), high-density lipoprotein cholesterol (HDL-c), triglycerides (TG), total cholesterol (TC), Apolipoprotein B (ApoB), and Apolipoprotein A1 (ApoA1).Furthermore, instrumental variable weighted regression (IVW) and summary data-based MR (SMR) analyses were performed to investigate the causal effects of lipid-lowering drugs, including statins and PCSK9 inhibitors, on the risk of liver cancer. RESULTS: Serum LDL-c and serum TC levels showed negatively associated with liver cancer (n = 22 SNPs, OR = 0.363, 95% CI = 0.231 - 0.570; p = 1.070E-5) (n = 83 SNPs; OR = 0.627, 95% CI = 0.413-0.952; p = 0.028). However, serum levels of TG, HDL-c, and ApoA1 did not show any significant correlation with liver cancer. In the drug target MR (DMR) analyses, HMGCR–mediated level of LDL-c showed an inverse relationship with the risk of liver cancer in the IVW-MR analysis (n = 5 SNPs, OR = 0.201, 95% CI = 0.064 - 0.631; p = 5.95E-03) and SMR analysis (n = 20 SNPs, OR = 0.245, 95% CI = 0.065 - 0.926; p = 0.038) However, PCSK9 did not show any significant association with liver cancer based on both the IVW-MR and SMR analyses. CONCLUSION: Our results demonstrated that reduced levels of LDL-c and TC were associated with an increased risk of liver cancer. Furthermore, lipid-lowering drugs targeting HMGCR such as statins were associated with increased risk of liver cancer.
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spelling pubmed-105165702023-09-23 Lipids, cholesterols, statins and liver cancer: a Mendelian randomization study Liang, Zicheng Zhang, Zhen Tan, Xiaoning Zeng, Puhua Front Oncol Oncology AIM: To investigate the causal relationship of serum lipid indicators and lipid-lowering drugs with the risk of liver cancer using Mendelian randomization study. METHODS: A two-sample Mendelian randomization (TSMR) study was performed to investigate the causal relationship between serum levels of lipid indicators and liver cancer, including low-density lipoprotein cholesterol (LDL-c), high-density lipoprotein cholesterol (HDL-c), triglycerides (TG), total cholesterol (TC), Apolipoprotein B (ApoB), and Apolipoprotein A1 (ApoA1).Furthermore, instrumental variable weighted regression (IVW) and summary data-based MR (SMR) analyses were performed to investigate the causal effects of lipid-lowering drugs, including statins and PCSK9 inhibitors, on the risk of liver cancer. RESULTS: Serum LDL-c and serum TC levels showed negatively associated with liver cancer (n = 22 SNPs, OR = 0.363, 95% CI = 0.231 - 0.570; p = 1.070E-5) (n = 83 SNPs; OR = 0.627, 95% CI = 0.413-0.952; p = 0.028). However, serum levels of TG, HDL-c, and ApoA1 did not show any significant correlation with liver cancer. In the drug target MR (DMR) analyses, HMGCR–mediated level of LDL-c showed an inverse relationship with the risk of liver cancer in the IVW-MR analysis (n = 5 SNPs, OR = 0.201, 95% CI = 0.064 - 0.631; p = 5.95E-03) and SMR analysis (n = 20 SNPs, OR = 0.245, 95% CI = 0.065 - 0.926; p = 0.038) However, PCSK9 did not show any significant association with liver cancer based on both the IVW-MR and SMR analyses. CONCLUSION: Our results demonstrated that reduced levels of LDL-c and TC were associated with an increased risk of liver cancer. Furthermore, lipid-lowering drugs targeting HMGCR such as statins were associated with increased risk of liver cancer. Frontiers Media S.A. 2023-09-06 /pmc/articles/PMC10516570/ /pubmed/37746259 http://dx.doi.org/10.3389/fonc.2023.1251873 Text en Copyright © 2023 Liang, Zhang, Tan and Zeng https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Liang, Zicheng
Zhang, Zhen
Tan, Xiaoning
Zeng, Puhua
Lipids, cholesterols, statins and liver cancer: a Mendelian randomization study
title Lipids, cholesterols, statins and liver cancer: a Mendelian randomization study
title_full Lipids, cholesterols, statins and liver cancer: a Mendelian randomization study
title_fullStr Lipids, cholesterols, statins and liver cancer: a Mendelian randomization study
title_full_unstemmed Lipids, cholesterols, statins and liver cancer: a Mendelian randomization study
title_short Lipids, cholesterols, statins and liver cancer: a Mendelian randomization study
title_sort lipids, cholesterols, statins and liver cancer: a mendelian randomization study
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10516570/
https://www.ncbi.nlm.nih.gov/pubmed/37746259
http://dx.doi.org/10.3389/fonc.2023.1251873
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