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Predictive values of ANGPTL8 on risk of all-cause mortality in diabetic patients: results from the REACTION Study
BACKGROUND: Angiopoietin-like protein 8 (ANGPTL8), an important regulator of lipid metabolism, is increased in diabetes and is associated with insulin resistance. However, the role of ANGPTL8 in the outcomes of diabetic patients remains unclear. This study aimed to investigate circulating levels of...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7398345/ https://www.ncbi.nlm.nih.gov/pubmed/32746907 http://dx.doi.org/10.1186/s12933-020-01103-7 |
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author | Zou, Huajie Xu, Yongping Chen, Xi Yin, Ping Li, Danpei Li, Wenjun Xie, Junhui Shao, Shiying Liu, Liegang Yu, Xuefeng |
author_facet | Zou, Huajie Xu, Yongping Chen, Xi Yin, Ping Li, Danpei Li, Wenjun Xie, Junhui Shao, Shiying Liu, Liegang Yu, Xuefeng |
author_sort | Zou, Huajie |
collection | PubMed |
description | BACKGROUND: Angiopoietin-like protein 8 (ANGPTL8), an important regulator of lipid metabolism, is increased in diabetes and is associated with insulin resistance. However, the role of ANGPTL8 in the outcomes of diabetic patients remains unclear. This study aimed to investigate circulating levels of ANGPTL8 in participants with and without diabetes and its potential associations with clinical outcomes in a 5 year cohort study. METHODS: Propensity-matched cohorts of subjects with and without diabetes from the Risk Evaluation of Cancers in Chinese Diabetic Individuals: A longitudinal (REACTION) study were generated on the basis of age, sex and body mass index at baseline. The primary outcome was all-cause mortality. The secondary outcomes were a composite of new-onset major adverse cardiovascular events, hospitalization for heart failure, and renal dysfunction (eGFR < 60/min/1.73 m(2)). RESULTS: We identified 769 matched pairs of diabetic patients and control subjects. Serum ANGPTL8 levels were elevated in patients with diabetes compared to control subjects (618.82 [Formula: see text] 318.08 vs 581.20 [Formula: see text] 299.54 pg/mL, p = 0.03). Binary logistic regression analysis showed that elevated ANGPTL8 levels were associated with greater risk ratios (RRs) of death (RR in quartile 4 vs. quartile 1, 3.54; 95% CI 1.32–9.50) and renal dysfunction (RR in quartile 4 vs. quartile 1, 12.43; 95% CI 1.48–104.81) only in diabetic patients. Multivariable-adjusted restricted cubic spline analyses revealed a significant, linear relationship between ANGPTL8 and all-cause mortality in diabetic patients (p for nonlinear trend = 0.99, p for linear trend = 0.01) but not in control subjects (p for nonlinear trend = 0.26, p for linear trend = 0.80). According to ROC curve analysis, the inclusion of ANGPTL8 in QFrailty score significantly improved its predictive performance for mortality in patients with diabetes. CONCLUSION: Serum ANGPTL8 levels were associated with an increased risk of all-cause mortality and could be used as a potential biomarker for the prediction of death in patients with diabetes. |
format | Online Article Text |
id | pubmed-7398345 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-73983452020-08-06 Predictive values of ANGPTL8 on risk of all-cause mortality in diabetic patients: results from the REACTION Study Zou, Huajie Xu, Yongping Chen, Xi Yin, Ping Li, Danpei Li, Wenjun Xie, Junhui Shao, Shiying Liu, Liegang Yu, Xuefeng Cardiovasc Diabetol Original Investigation BACKGROUND: Angiopoietin-like protein 8 (ANGPTL8), an important regulator of lipid metabolism, is increased in diabetes and is associated with insulin resistance. However, the role of ANGPTL8 in the outcomes of diabetic patients remains unclear. This study aimed to investigate circulating levels of ANGPTL8 in participants with and without diabetes and its potential associations with clinical outcomes in a 5 year cohort study. METHODS: Propensity-matched cohorts of subjects with and without diabetes from the Risk Evaluation of Cancers in Chinese Diabetic Individuals: A longitudinal (REACTION) study were generated on the basis of age, sex and body mass index at baseline. The primary outcome was all-cause mortality. The secondary outcomes were a composite of new-onset major adverse cardiovascular events, hospitalization for heart failure, and renal dysfunction (eGFR < 60/min/1.73 m(2)). RESULTS: We identified 769 matched pairs of diabetic patients and control subjects. Serum ANGPTL8 levels were elevated in patients with diabetes compared to control subjects (618.82 [Formula: see text] 318.08 vs 581.20 [Formula: see text] 299.54 pg/mL, p = 0.03). Binary logistic regression analysis showed that elevated ANGPTL8 levels were associated with greater risk ratios (RRs) of death (RR in quartile 4 vs. quartile 1, 3.54; 95% CI 1.32–9.50) and renal dysfunction (RR in quartile 4 vs. quartile 1, 12.43; 95% CI 1.48–104.81) only in diabetic patients. Multivariable-adjusted restricted cubic spline analyses revealed a significant, linear relationship between ANGPTL8 and all-cause mortality in diabetic patients (p for nonlinear trend = 0.99, p for linear trend = 0.01) but not in control subjects (p for nonlinear trend = 0.26, p for linear trend = 0.80). According to ROC curve analysis, the inclusion of ANGPTL8 in QFrailty score significantly improved its predictive performance for mortality in patients with diabetes. CONCLUSION: Serum ANGPTL8 levels were associated with an increased risk of all-cause mortality and could be used as a potential biomarker for the prediction of death in patients with diabetes. BioMed Central 2020-08-03 /pmc/articles/PMC7398345/ /pubmed/32746907 http://dx.doi.org/10.1186/s12933-020-01103-7 Text en © The Author(s) 2020 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/. The Creative Commons Public Domain Dedication waiver (http://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 | Original Investigation Zou, Huajie Xu, Yongping Chen, Xi Yin, Ping Li, Danpei Li, Wenjun Xie, Junhui Shao, Shiying Liu, Liegang Yu, Xuefeng Predictive values of ANGPTL8 on risk of all-cause mortality in diabetic patients: results from the REACTION Study |
title | Predictive values of ANGPTL8 on risk of all-cause mortality in diabetic patients: results from the REACTION Study |
title_full | Predictive values of ANGPTL8 on risk of all-cause mortality in diabetic patients: results from the REACTION Study |
title_fullStr | Predictive values of ANGPTL8 on risk of all-cause mortality in diabetic patients: results from the REACTION Study |
title_full_unstemmed | Predictive values of ANGPTL8 on risk of all-cause mortality in diabetic patients: results from the REACTION Study |
title_short | Predictive values of ANGPTL8 on risk of all-cause mortality in diabetic patients: results from the REACTION Study |
title_sort | predictive values of angptl8 on risk of all-cause mortality in diabetic patients: results from the reaction study |
topic | Original Investigation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7398345/ https://www.ncbi.nlm.nih.gov/pubmed/32746907 http://dx.doi.org/10.1186/s12933-020-01103-7 |
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