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Proteoglycan binding as proatherogenic function metric of apoB-containing lipoproteins and chronic kidney graft failure
Lipoprotein-proteoglycan binding is an early key event in atherosclerotic lesion formation and thus conceivably could play a major role in vasculopathy-driven chronic graft failure and cardiovascular mortality in renal transplant recipients. The present study investigated whether lipoprotein-proteog...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Biochemistry and Molecular Biology
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8173310/ https://www.ncbi.nlm.nih.gov/pubmed/33939983 http://dx.doi.org/10.1016/j.jlr.2021.100083 |
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author | Steffen, Hannah L.M. Anderson, Josephine L.C. Poot, Margot L. Lei, Yu Connelly, Margery A. Bakker, Stephan J.L. Öörni, Katariina Tietge, Uwe J.F. |
author_facet | Steffen, Hannah L.M. Anderson, Josephine L.C. Poot, Margot L. Lei, Yu Connelly, Margery A. Bakker, Stephan J.L. Öörni, Katariina Tietge, Uwe J.F. |
author_sort | Steffen, Hannah L.M. |
collection | PubMed |
description | Lipoprotein-proteoglycan binding is an early key event in atherosclerotic lesion formation and thus conceivably could play a major role in vasculopathy-driven chronic graft failure and cardiovascular mortality in renal transplant recipients. The present study investigated whether lipoprotein-proteoglycan binding susceptibility (LPBS) of apoB-containing lipoproteins and levels of the classical atherosclerosis biomarker LDL-C were associated with cardiovascular mortality (n = 130) and graft failure (n = 73) in 589 renal transplant recipients who were followed up from at least 1 year after transplantation for 9.5 years. At baseline, LPBS was significantly higher in patients who subsequently developed graft failure than in those with a surviving graft (1.68 ± 0.93 vs. 1.46 ± 0.49 nmol/mmol, P = 0.001). Cox regression analysis showed an association between LPBS and chronic graft failure in an age- and sex-adjusted model (hazard ratio: 1.45; 95% CI, 1.14–1.85; P = 0.002), but no association was observed with cardiovascular mortality. LDL-C levels were not associated with graft failure or cardiovascular mortality. This study shows that measurement of cholesterol retention outperformed the traditionally used quantitative parameter of LDL-C levels in predicting graft failure, suggesting a higher relevance of proatherogenic function than the quantity of apoB-containing lipoproteins in chronic kidney graft failure. |
format | Online Article Text |
id | pubmed-8173310 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Society for Biochemistry and Molecular Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-81733102021-06-11 Proteoglycan binding as proatherogenic function metric of apoB-containing lipoproteins and chronic kidney graft failure Steffen, Hannah L.M. Anderson, Josephine L.C. Poot, Margot L. Lei, Yu Connelly, Margery A. Bakker, Stephan J.L. Öörni, Katariina Tietge, Uwe J.F. J Lipid Res Research Article Lipoprotein-proteoglycan binding is an early key event in atherosclerotic lesion formation and thus conceivably could play a major role in vasculopathy-driven chronic graft failure and cardiovascular mortality in renal transplant recipients. The present study investigated whether lipoprotein-proteoglycan binding susceptibility (LPBS) of apoB-containing lipoproteins and levels of the classical atherosclerosis biomarker LDL-C were associated with cardiovascular mortality (n = 130) and graft failure (n = 73) in 589 renal transplant recipients who were followed up from at least 1 year after transplantation for 9.5 years. At baseline, LPBS was significantly higher in patients who subsequently developed graft failure than in those with a surviving graft (1.68 ± 0.93 vs. 1.46 ± 0.49 nmol/mmol, P = 0.001). Cox regression analysis showed an association between LPBS and chronic graft failure in an age- and sex-adjusted model (hazard ratio: 1.45; 95% CI, 1.14–1.85; P = 0.002), but no association was observed with cardiovascular mortality. LDL-C levels were not associated with graft failure or cardiovascular mortality. This study shows that measurement of cholesterol retention outperformed the traditionally used quantitative parameter of LDL-C levels in predicting graft failure, suggesting a higher relevance of proatherogenic function than the quantity of apoB-containing lipoproteins in chronic kidney graft failure. American Society for Biochemistry and Molecular Biology 2021-04-30 /pmc/articles/PMC8173310/ /pubmed/33939983 http://dx.doi.org/10.1016/j.jlr.2021.100083 Text en © 2021 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Research Article Steffen, Hannah L.M. Anderson, Josephine L.C. Poot, Margot L. Lei, Yu Connelly, Margery A. Bakker, Stephan J.L. Öörni, Katariina Tietge, Uwe J.F. Proteoglycan binding as proatherogenic function metric of apoB-containing lipoproteins and chronic kidney graft failure |
title | Proteoglycan binding as proatherogenic function metric of apoB-containing lipoproteins and chronic kidney graft failure |
title_full | Proteoglycan binding as proatherogenic function metric of apoB-containing lipoproteins and chronic kidney graft failure |
title_fullStr | Proteoglycan binding as proatherogenic function metric of apoB-containing lipoproteins and chronic kidney graft failure |
title_full_unstemmed | Proteoglycan binding as proatherogenic function metric of apoB-containing lipoproteins and chronic kidney graft failure |
title_short | Proteoglycan binding as proatherogenic function metric of apoB-containing lipoproteins and chronic kidney graft failure |
title_sort | proteoglycan binding as proatherogenic function metric of apob-containing lipoproteins and chronic kidney graft failure |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8173310/ https://www.ncbi.nlm.nih.gov/pubmed/33939983 http://dx.doi.org/10.1016/j.jlr.2021.100083 |
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