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Association between lipid variability and the risk of mortality in cancer patients not receiving lipid-lowering agents
AIM: We investigated the association between total cholesterol (TC), low-density lipoprotein (LDL) cholesterol, high-density lipoprotein (HDL) cholesterol, and triglyceride (TG) variability and cancer patient mortality risk. METHODS: We retrospectively analyzed 42,539 cancer patients who were not re...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10586791/ https://www.ncbi.nlm.nih.gov/pubmed/37869078 http://dx.doi.org/10.3389/fonc.2023.1254339 |
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author | Kim, Seohyun Kim, Gyuri Cho, So Hyun Oh, Rosa Kim, Ji Yoon Lee, You-Bin Jin, Sang-Man Hur, Kyu Yeon Kim, Jae Hyeon |
author_facet | Kim, Seohyun Kim, Gyuri Cho, So Hyun Oh, Rosa Kim, Ji Yoon Lee, You-Bin Jin, Sang-Man Hur, Kyu Yeon Kim, Jae Hyeon |
author_sort | Kim, Seohyun |
collection | PubMed |
description | AIM: We investigated the association between total cholesterol (TC), low-density lipoprotein (LDL) cholesterol, high-density lipoprotein (HDL) cholesterol, and triglyceride (TG) variability and cancer patient mortality risk. METHODS: We retrospectively analyzed 42,539 cancer patients who were not receiving lipid-lowering agents and who had at least three TC measurements within 2 years of their initial cancer diagnosis. Using a multivariable Cox regression model, the risk of mortality was evaluated. RESULTS: In multivariable analysis, Q2 (adjusted hazard ratio [aHR]: 1.32, 95% confidence interval (CI): 1.24–1.41), Q3 (aHR: 1.66, 95% CI: 1.56–1.76), and Q4 (aHR: 1.96, 95% CI: 1.84–2.08) of coefficient of variation (CV) in TC were significantly associated with mortality risk compared to Q1, showing a linear association between higher TC variability and mortality (P for trend<0.001). Q2 (aHR: 1.34, 95% CI: 1.06–1.77), Q3 (aHR: 1.40, 95% CI: 1.06–1.85), and Q4 (aHR: 1.50, 95% CI: 1.14–1.97) were all significantly associated with a higher risk of death compared to Q1 in multivariable Cox regression for the association between CV in LDL and all-cause mortality (P for trend=0.005). CONCLUSION: In cancer patients who do not receive lipid-lowering agents, high variability in total cholesterol and LDL cholesterol levels was found to pose significant role in mortality risk. |
format | Online Article Text |
id | pubmed-10586791 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-105867912023-10-20 Association between lipid variability and the risk of mortality in cancer patients not receiving lipid-lowering agents Kim, Seohyun Kim, Gyuri Cho, So Hyun Oh, Rosa Kim, Ji Yoon Lee, You-Bin Jin, Sang-Man Hur, Kyu Yeon Kim, Jae Hyeon Front Oncol Oncology AIM: We investigated the association between total cholesterol (TC), low-density lipoprotein (LDL) cholesterol, high-density lipoprotein (HDL) cholesterol, and triglyceride (TG) variability and cancer patient mortality risk. METHODS: We retrospectively analyzed 42,539 cancer patients who were not receiving lipid-lowering agents and who had at least three TC measurements within 2 years of their initial cancer diagnosis. Using a multivariable Cox regression model, the risk of mortality was evaluated. RESULTS: In multivariable analysis, Q2 (adjusted hazard ratio [aHR]: 1.32, 95% confidence interval (CI): 1.24–1.41), Q3 (aHR: 1.66, 95% CI: 1.56–1.76), and Q4 (aHR: 1.96, 95% CI: 1.84–2.08) of coefficient of variation (CV) in TC were significantly associated with mortality risk compared to Q1, showing a linear association between higher TC variability and mortality (P for trend<0.001). Q2 (aHR: 1.34, 95% CI: 1.06–1.77), Q3 (aHR: 1.40, 95% CI: 1.06–1.85), and Q4 (aHR: 1.50, 95% CI: 1.14–1.97) were all significantly associated with a higher risk of death compared to Q1 in multivariable Cox regression for the association between CV in LDL and all-cause mortality (P for trend=0.005). CONCLUSION: In cancer patients who do not receive lipid-lowering agents, high variability in total cholesterol and LDL cholesterol levels was found to pose significant role in mortality risk. Frontiers Media S.A. 2023-10-05 /pmc/articles/PMC10586791/ /pubmed/37869078 http://dx.doi.org/10.3389/fonc.2023.1254339 Text en Copyright © 2023 Kim, Kim, Cho, Oh, Kim, Lee, Jin, Hur and Kim 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 Kim, Seohyun Kim, Gyuri Cho, So Hyun Oh, Rosa Kim, Ji Yoon Lee, You-Bin Jin, Sang-Man Hur, Kyu Yeon Kim, Jae Hyeon Association between lipid variability and the risk of mortality in cancer patients not receiving lipid-lowering agents |
title | Association between lipid variability and the risk of mortality in cancer patients not receiving lipid-lowering agents |
title_full | Association between lipid variability and the risk of mortality in cancer patients not receiving lipid-lowering agents |
title_fullStr | Association between lipid variability and the risk of mortality in cancer patients not receiving lipid-lowering agents |
title_full_unstemmed | Association between lipid variability and the risk of mortality in cancer patients not receiving lipid-lowering agents |
title_short | Association between lipid variability and the risk of mortality in cancer patients not receiving lipid-lowering agents |
title_sort | association between lipid variability and the risk of mortality in cancer patients not receiving lipid-lowering agents |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10586791/ https://www.ncbi.nlm.nih.gov/pubmed/37869078 http://dx.doi.org/10.3389/fonc.2023.1254339 |
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