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Juvenile elastic arteries after 28 years of renal replacement therapy in a patient with complete complement C4 deficiency
BACKGROUND: Complement activation products are present in atherosclerotic plaques. Recently, binding of complement to elastin and collagen in the aortic wall has been demonstrated, suggesting a role of complement in the development aortic stiffness and atherosclerosis. The definitive role of complem...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3536710/ https://www.ncbi.nlm.nih.gov/pubmed/23199021 http://dx.doi.org/10.1186/1471-2369-13-161 |
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author | Knoll, Florian Zitt, Emanuel Intemann, Denis Lhotta, Karl |
author_facet | Knoll, Florian Zitt, Emanuel Intemann, Denis Lhotta, Karl |
author_sort | Knoll, Florian |
collection | PubMed |
description | BACKGROUND: Complement activation products are present in atherosclerotic plaques. Recently, binding of complement to elastin and collagen in the aortic wall has been demonstrated, suggesting a role of complement in the development aortic stiffness and atherosclerosis. The definitive role of complement in atherosclerosis and arteriosclerosis, however, remains unclear. CASE PRESENTATION: We here describe a patient with hereditary complete deficiency of complement C4 suffering from Henoch-Schoenlein purpura and on renal replacement therapy for twenty-eight years. The patient had the full range of risk factors for vascular damage such as hypertension, volume overload, hyperphosphatemia and hyperparathyroidism. Despite that, his carotid artery intima media thickness was below the normal range and his pulse wave velocity was normal. In contrast, the patient’s coronary and peripheral muscular arteries were heavily calcified. CONCLUSION: This case supports the hypothesis that complement plays an important role in the development of stiffness of elastic arteries. We speculate that inability to activate complement by the classical or lectin pathways protected the patient from atherosclerosis, arteriosclerosis, stiffening and calcification of the aorta and carotid arteries. Inhibition of complement activation may be a potential target for prophylactic and therapeutic interventions. |
format | Online Article Text |
id | pubmed-3536710 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-35367102013-01-08 Juvenile elastic arteries after 28 years of renal replacement therapy in a patient with complete complement C4 deficiency Knoll, Florian Zitt, Emanuel Intemann, Denis Lhotta, Karl BMC Nephrol Case Report BACKGROUND: Complement activation products are present in atherosclerotic plaques. Recently, binding of complement to elastin and collagen in the aortic wall has been demonstrated, suggesting a role of complement in the development aortic stiffness and atherosclerosis. The definitive role of complement in atherosclerosis and arteriosclerosis, however, remains unclear. CASE PRESENTATION: We here describe a patient with hereditary complete deficiency of complement C4 suffering from Henoch-Schoenlein purpura and on renal replacement therapy for twenty-eight years. The patient had the full range of risk factors for vascular damage such as hypertension, volume overload, hyperphosphatemia and hyperparathyroidism. Despite that, his carotid artery intima media thickness was below the normal range and his pulse wave velocity was normal. In contrast, the patient’s coronary and peripheral muscular arteries were heavily calcified. CONCLUSION: This case supports the hypothesis that complement plays an important role in the development of stiffness of elastic arteries. We speculate that inability to activate complement by the classical or lectin pathways protected the patient from atherosclerosis, arteriosclerosis, stiffening and calcification of the aorta and carotid arteries. Inhibition of complement activation may be a potential target for prophylactic and therapeutic interventions. BioMed Central 2012-12-02 /pmc/articles/PMC3536710/ /pubmed/23199021 http://dx.doi.org/10.1186/1471-2369-13-161 Text en Copyright ©2012 Knoll et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Knoll, Florian Zitt, Emanuel Intemann, Denis Lhotta, Karl Juvenile elastic arteries after 28 years of renal replacement therapy in a patient with complete complement C4 deficiency |
title | Juvenile elastic arteries after 28 years of renal replacement therapy in a patient with complete complement C4 deficiency |
title_full | Juvenile elastic arteries after 28 years of renal replacement therapy in a patient with complete complement C4 deficiency |
title_fullStr | Juvenile elastic arteries after 28 years of renal replacement therapy in a patient with complete complement C4 deficiency |
title_full_unstemmed | Juvenile elastic arteries after 28 years of renal replacement therapy in a patient with complete complement C4 deficiency |
title_short | Juvenile elastic arteries after 28 years of renal replacement therapy in a patient with complete complement C4 deficiency |
title_sort | juvenile elastic arteries after 28 years of renal replacement therapy in a patient with complete complement c4 deficiency |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3536710/ https://www.ncbi.nlm.nih.gov/pubmed/23199021 http://dx.doi.org/10.1186/1471-2369-13-161 |
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