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Chorioretinal thinning in chronic kidney disease links to inflammation and endothelial dysfunction
BACKGROUND. Chronic kidney disease (CKD) is strongly associated with cardiovascular disease and there is an established association between vasculopathy affecting the kidney and eye. Optical coherence tomography (OCT) is a novel, rapid method for high-definition imaging of the retina and choroid. It...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Clinical Investigation
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5135281/ https://www.ncbi.nlm.nih.gov/pubmed/27942587 http://dx.doi.org/10.1172/jci.insight.89173 |
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author | Balmforth, Craig van Bragt, Job J.M.H. Ruijs, Titia Cameron, James R. Kimmitt, Robert Moorhouse, Rebecca Czopek, Alicja Hu, May Khei Gallacher, Peter J. Dear, James W. Borooah, Shyamanga MacIntyre, Iain M. Pearson, Tom M.C. Willox, Laura Talwar, Dinesh Tafflet, Muriel Roubeix, Christophe Sennlaub, Florian Chandran, Siddharthan Dhillon, Baljean Webb, David J. Dhaun, Neeraj |
author_facet | Balmforth, Craig van Bragt, Job J.M.H. Ruijs, Titia Cameron, James R. Kimmitt, Robert Moorhouse, Rebecca Czopek, Alicja Hu, May Khei Gallacher, Peter J. Dear, James W. Borooah, Shyamanga MacIntyre, Iain M. Pearson, Tom M.C. Willox, Laura Talwar, Dinesh Tafflet, Muriel Roubeix, Christophe Sennlaub, Florian Chandran, Siddharthan Dhillon, Baljean Webb, David J. Dhaun, Neeraj |
author_sort | Balmforth, Craig |
collection | PubMed |
description | BACKGROUND. Chronic kidney disease (CKD) is strongly associated with cardiovascular disease and there is an established association between vasculopathy affecting the kidney and eye. Optical coherence tomography (OCT) is a novel, rapid method for high-definition imaging of the retina and choroid. Its use in patients at high cardiovascular disease risk remains unexplored. METHODS. We used the new SPECTRALIS OCT machine to examine retinal and retinal nerve fiber layer (RNFL) thickness, macular volume, and choroidal thickness in a prospective cross-sectional study in 150 subjects: 50 patients with hypertension (defined as a documented clinic BP greater than or equal to 140/90 mmHg (prior to starting any treatment) with no underlying cause identified); 50 with CKD (estimated glomerular filtration rate (eGFR) 8–125 ml/min/1.73 m(2)); and 50 matched healthy controls. We excluded those with diabetes. The same, masked ophthalmologist carried out each study. Plasma IL-6, TNF-α , asymmetric dimethylarginine (ADMA), and endothelin-1 (ET-1), as measures of inflammation and endothelial function, were also assessed. RESULTS. Retinal thickness, macular volume, and choroidal thickness were all reduced in CKD compared with hypertensive and healthy subjects (for retinal thickness and macular volume P < 0.0001 for CKD vs. healthy and for CKD vs. hypertensive subjects; for choroidal thickness P < 0.001 for CKD vs. healthy and for CKD vs. hypertensive subjects). RNFL thickness did not differ between groups. Interestingly, a thinner choroid was associated with a lower eGFR (r = 0.35, P <0.0001) and, in CKD, with proteinuria (r = –0.58, P < 0.001) as well as increased circulating C-reactive protein (r = –0.57, P = 0.0002), IL-6 (r = –0.40, P < 0.01), ADMA (r = –0.37, P = 0.02), and ET-1 (r = –0.44, P < 0.01). Finally, choroidal thinning was associated with renal histological inflammation and arterial stiffness. In a model of hypertension, choroidal thinning was seen only in the presence of renal injury. CONCLUSIONS. Chorioretinal thinning in CKD is associated with lower eGFR and greater proteinuria, but not BP. Larger studies, in more targeted groups of patients, are now needed to clarify whether these eye changes reflect the natural history of CKD. Similarly, the associations with arterial stiffness, inflammation, and endothelial dysfunction warrant further examination. TRIAL REGISTRATION. Registration number at www.clinicalTrials.gov: NCT02132741. SOURCE OF FUNDING. TR was supported by a bursary from the Erasmus Medical Centre, Rotterdam. JJMHvB was supported by a bursary from the Utrecht University. JRC is supported by a Rowling Scholarship. SB was supported by a Wellcome Trust funded clinical research fellowship from the Scottish Translational Medicine and Therapeutics Initiative, and by a Rowling Scholarship, at the time of this work. ND is supported by a British Heart Foundation Intermediate Clinical Research Fellowship (FS/13/30/29994). |
format | Online Article Text |
id | pubmed-5135281 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | American Society for Clinical Investigation |
record_format | MEDLINE/PubMed |
spelling | pubmed-51352812016-12-10 Chorioretinal thinning in chronic kidney disease links to inflammation and endothelial dysfunction Balmforth, Craig van Bragt, Job J.M.H. Ruijs, Titia Cameron, James R. Kimmitt, Robert Moorhouse, Rebecca Czopek, Alicja Hu, May Khei Gallacher, Peter J. Dear, James W. Borooah, Shyamanga MacIntyre, Iain M. Pearson, Tom M.C. Willox, Laura Talwar, Dinesh Tafflet, Muriel Roubeix, Christophe Sennlaub, Florian Chandran, Siddharthan Dhillon, Baljean Webb, David J. Dhaun, Neeraj JCI Insight Clinical Medicine BACKGROUND. Chronic kidney disease (CKD) is strongly associated with cardiovascular disease and there is an established association between vasculopathy affecting the kidney and eye. Optical coherence tomography (OCT) is a novel, rapid method for high-definition imaging of the retina and choroid. Its use in patients at high cardiovascular disease risk remains unexplored. METHODS. We used the new SPECTRALIS OCT machine to examine retinal and retinal nerve fiber layer (RNFL) thickness, macular volume, and choroidal thickness in a prospective cross-sectional study in 150 subjects: 50 patients with hypertension (defined as a documented clinic BP greater than or equal to 140/90 mmHg (prior to starting any treatment) with no underlying cause identified); 50 with CKD (estimated glomerular filtration rate (eGFR) 8–125 ml/min/1.73 m(2)); and 50 matched healthy controls. We excluded those with diabetes. The same, masked ophthalmologist carried out each study. Plasma IL-6, TNF-α , asymmetric dimethylarginine (ADMA), and endothelin-1 (ET-1), as measures of inflammation and endothelial function, were also assessed. RESULTS. Retinal thickness, macular volume, and choroidal thickness were all reduced in CKD compared with hypertensive and healthy subjects (for retinal thickness and macular volume P < 0.0001 for CKD vs. healthy and for CKD vs. hypertensive subjects; for choroidal thickness P < 0.001 for CKD vs. healthy and for CKD vs. hypertensive subjects). RNFL thickness did not differ between groups. Interestingly, a thinner choroid was associated with a lower eGFR (r = 0.35, P <0.0001) and, in CKD, with proteinuria (r = –0.58, P < 0.001) as well as increased circulating C-reactive protein (r = –0.57, P = 0.0002), IL-6 (r = –0.40, P < 0.01), ADMA (r = –0.37, P = 0.02), and ET-1 (r = –0.44, P < 0.01). Finally, choroidal thinning was associated with renal histological inflammation and arterial stiffness. In a model of hypertension, choroidal thinning was seen only in the presence of renal injury. CONCLUSIONS. Chorioretinal thinning in CKD is associated with lower eGFR and greater proteinuria, but not BP. Larger studies, in more targeted groups of patients, are now needed to clarify whether these eye changes reflect the natural history of CKD. Similarly, the associations with arterial stiffness, inflammation, and endothelial dysfunction warrant further examination. TRIAL REGISTRATION. Registration number at www.clinicalTrials.gov: NCT02132741. SOURCE OF FUNDING. TR was supported by a bursary from the Erasmus Medical Centre, Rotterdam. JJMHvB was supported by a bursary from the Utrecht University. JRC is supported by a Rowling Scholarship. SB was supported by a Wellcome Trust funded clinical research fellowship from the Scottish Translational Medicine and Therapeutics Initiative, and by a Rowling Scholarship, at the time of this work. ND is supported by a British Heart Foundation Intermediate Clinical Research Fellowship (FS/13/30/29994). American Society for Clinical Investigation 2016-12-08 /pmc/articles/PMC5135281/ /pubmed/27942587 http://dx.doi.org/10.1172/jci.insight.89173 Text en Copyright © 2016 Balmforth et al. http://creativecommons.org/licenses/by/4.0/ This work is licensed under the Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Clinical Medicine Balmforth, Craig van Bragt, Job J.M.H. Ruijs, Titia Cameron, James R. Kimmitt, Robert Moorhouse, Rebecca Czopek, Alicja Hu, May Khei Gallacher, Peter J. Dear, James W. Borooah, Shyamanga MacIntyre, Iain M. Pearson, Tom M.C. Willox, Laura Talwar, Dinesh Tafflet, Muriel Roubeix, Christophe Sennlaub, Florian Chandran, Siddharthan Dhillon, Baljean Webb, David J. Dhaun, Neeraj Chorioretinal thinning in chronic kidney disease links to inflammation and endothelial dysfunction |
title | Chorioretinal thinning in chronic kidney disease links to inflammation and endothelial dysfunction |
title_full | Chorioretinal thinning in chronic kidney disease links to inflammation and endothelial dysfunction |
title_fullStr | Chorioretinal thinning in chronic kidney disease links to inflammation and endothelial dysfunction |
title_full_unstemmed | Chorioretinal thinning in chronic kidney disease links to inflammation and endothelial dysfunction |
title_short | Chorioretinal thinning in chronic kidney disease links to inflammation and endothelial dysfunction |
title_sort | chorioretinal thinning in chronic kidney disease links to inflammation and endothelial dysfunction |
topic | Clinical Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5135281/ https://www.ncbi.nlm.nih.gov/pubmed/27942587 http://dx.doi.org/10.1172/jci.insight.89173 |
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