Angiopoietin-2 is associated with metabolic syndrome in chronic kidney disease

Backgrounds: Metabolic syndrome is a subclinical status in promoting atherosclerotic cardiovascular disease and type 2 diabetes mellitus. The significance of metabolic syndrome and pathophysiology in chronic kidney disease is not investigated. Methods: We enrolled adult patients with CKD stages 3 to...

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Autores principales: Fan-Chi Chang, Ming-Ching Lee, Chih-Kang Chiang, Jia-Sin Liu, Tai-Shuan Lai, Wen-Chih Chiang, Yung-Ming Chen, Tzong-Shinn Chu
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Publicado: Elsevier 2021
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spelling oai:doaj.org-article:5d54c016601a4c5380422afd6e6fe57a2021-12-02T04:59:10ZAngiopoietin-2 is associated with metabolic syndrome in chronic kidney disease0929-664610.1016/j.jfma.2021.05.003https://doaj.org/article/5d54c016601a4c5380422afd6e6fe57a2021-12-01T00:00:00Zhttp://www.sciencedirect.com/science/article/pii/S0929664621001881https://doaj.org/toc/0929-6646Backgrounds: Metabolic syndrome is a subclinical status in promoting atherosclerotic cardiovascular disease and type 2 diabetes mellitus. The significance of metabolic syndrome and pathophysiology in chronic kidney disease is not investigated. Methods: We enrolled adult patients with CKD stages 3 to 5 from December 2006 to December 2007. Metabolic syndrome was defined by the US National Cholesterol Education Programme Adult Treatment Panel III guidelines. Plasma levels of angiogenic growth factors were measured. Univariate and multivariate logistic regression analyses were used. Results: Total 451 patients were analyzed with median estimated glomerular filtration rate of 27.0 ml/min per 1.73m2 (interquartile range 14.3–41.3). Patients with metabolic syndrome were older (P = 0.002), had higher percentage using diuretics (P = 0.002) but lower percentage using pentoxifylline (P = 0.017). Patients with metabolic syndrome had higher levels of high-sensitivity C-reactive protein (P < 0.0001), uric acid (P = 0.009) and angiopoietin-2 (P = 0.001). Multivariate logistic regression analyses revealed significant association between plasma levels of angiopoietin-2 and metabolic syndrome (P = 0.042). Conclusion: The prevalence of metabolic syndrome in advanced CKD was higher than general population. CKD patients with metabolic syndrome had higher levels of high-sensitivity C-reactive protein, uric acid and angiopoietin-2. Plasma levels of angiopoietin-2 were significantly associated with metabolic syndrome in patients with CKD. Metabolic syndrome in CKD may be not only a prognostic factor but also an interventional target, possibly through ameliorating inflammation. Prospective and interventional studies are necessary to establish the pathophysiology.Fan-Chi ChangMing-Ching LeeChih-Kang ChiangJia-Sin LiuTai-Shuan LaiWen-Chih ChiangYung-Ming ChenTzong-Shinn ChuElsevierarticleMetabolic syndromeAngiopoietin-2Chronic kidney diseaseInflammationEndothelial dysfunctionMedicine (General)R5-920ENJournal of the Formosan Medical Association, Vol 120, Iss 12, Pp 2113-2119 (2021)
institution DOAJ
collection DOAJ
language EN
topic Metabolic syndrome
Angiopoietin-2
Chronic kidney disease
Inflammation
Endothelial dysfunction
Medicine (General)
R5-920
spellingShingle Metabolic syndrome
Angiopoietin-2
Chronic kidney disease
Inflammation
Endothelial dysfunction
Medicine (General)
R5-920
Fan-Chi Chang
Ming-Ching Lee
Chih-Kang Chiang
Jia-Sin Liu
Tai-Shuan Lai
Wen-Chih Chiang
Yung-Ming Chen
Tzong-Shinn Chu
Angiopoietin-2 is associated with metabolic syndrome in chronic kidney disease
description Backgrounds: Metabolic syndrome is a subclinical status in promoting atherosclerotic cardiovascular disease and type 2 diabetes mellitus. The significance of metabolic syndrome and pathophysiology in chronic kidney disease is not investigated. Methods: We enrolled adult patients with CKD stages 3 to 5 from December 2006 to December 2007. Metabolic syndrome was defined by the US National Cholesterol Education Programme Adult Treatment Panel III guidelines. Plasma levels of angiogenic growth factors were measured. Univariate and multivariate logistic regression analyses were used. Results: Total 451 patients were analyzed with median estimated glomerular filtration rate of 27.0 ml/min per 1.73m2 (interquartile range 14.3–41.3). Patients with metabolic syndrome were older (P = 0.002), had higher percentage using diuretics (P = 0.002) but lower percentage using pentoxifylline (P = 0.017). Patients with metabolic syndrome had higher levels of high-sensitivity C-reactive protein (P < 0.0001), uric acid (P = 0.009) and angiopoietin-2 (P = 0.001). Multivariate logistic regression analyses revealed significant association between plasma levels of angiopoietin-2 and metabolic syndrome (P = 0.042). Conclusion: The prevalence of metabolic syndrome in advanced CKD was higher than general population. CKD patients with metabolic syndrome had higher levels of high-sensitivity C-reactive protein, uric acid and angiopoietin-2. Plasma levels of angiopoietin-2 were significantly associated with metabolic syndrome in patients with CKD. Metabolic syndrome in CKD may be not only a prognostic factor but also an interventional target, possibly through ameliorating inflammation. Prospective and interventional studies are necessary to establish the pathophysiology.
format article
author Fan-Chi Chang
Ming-Ching Lee
Chih-Kang Chiang
Jia-Sin Liu
Tai-Shuan Lai
Wen-Chih Chiang
Yung-Ming Chen
Tzong-Shinn Chu
author_facet Fan-Chi Chang
Ming-Ching Lee
Chih-Kang Chiang
Jia-Sin Liu
Tai-Shuan Lai
Wen-Chih Chiang
Yung-Ming Chen
Tzong-Shinn Chu
author_sort Fan-Chi Chang
title Angiopoietin-2 is associated with metabolic syndrome in chronic kidney disease
title_short Angiopoietin-2 is associated with metabolic syndrome in chronic kidney disease
title_full Angiopoietin-2 is associated with metabolic syndrome in chronic kidney disease
title_fullStr Angiopoietin-2 is associated with metabolic syndrome in chronic kidney disease
title_full_unstemmed Angiopoietin-2 is associated with metabolic syndrome in chronic kidney disease
title_sort angiopoietin-2 is associated with metabolic syndrome in chronic kidney disease
publisher Elsevier
publishDate 2021
url https://doaj.org/article/5d54c016601a4c5380422afd6e6fe57a
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