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Progression of Medial Arterial Calcification in CKD
INTRODUCTION: Medial arterial calcification is common in chronic kidney disease (CKD) and portends poor clinical outcomes, but its progression relative to the severity of CKD and the role of other risk factors is unknown because of the lack of reliable quantification. METHODS: Calcification of breas...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6224661/ https://www.ncbi.nlm.nih.gov/pubmed/30450459 http://dx.doi.org/10.1016/j.ekir.2018.07.011 |
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author | Manzoor, Shumila Ahmed, Syed Ali, Arshad Han, Kum Hyun Sechopoulos, Ioannis O’Neill, Ansley Fei, Baowei O’Neill, W. Charles |
author_facet | Manzoor, Shumila Ahmed, Syed Ali, Arshad Han, Kum Hyun Sechopoulos, Ioannis O’Neill, Ansley Fei, Baowei O’Neill, W. Charles |
author_sort | Manzoor, Shumila |
collection | PubMed |
description | INTRODUCTION: Medial arterial calcification is common in chronic kidney disease (CKD) and portends poor clinical outcomes, but its progression relative to the severity of CKD and the role of other risk factors is unknown because of the lack of reliable quantification. METHODS: Calcification of breast arteries detected by mammography, which is exclusively medial and correlates with medial calcification in peripheral arteries and with cardiovascular outcomes, was used to measure the progression of medial arterial calcification in women with CKD and end-stage renal disease (ESRD). Measurements showed intra- and interobserver correlations of 0.98, an interstudy variability of 8% to 11%, and a correlation with computed tomographic measurements of 0.92. RESULTS: Progression of calcification was measured in 60 control subjects (estimated glomerular filtration rate (eGFR) ≥ 90 ml/min per 1.73 m(2)) and 137 subjects with CKD (eGFR < 90 ml/min per 1.73 m(2)). Progression in control subjects was linear over time and independent of age. The rate of progression was increased in CKD but only at eGFR < 40 ml/min per 1.73 m(2) (median, 8.1 vs. 3.9 mm/breast/yr in controls; P = 0.006). Progression accelerated markedly in subjects with ESRD (median, 20 mm/breast/yr; n = 36), but did not differ from controls after kidney transplantation (n = 25). Diabetes significantly augmented progression in subjects with CKD and ESRD but not in controls. CONCLUSION: Mammography is a convenient and reliable method to measure the progression of medial arterial calcification. Progression does not increase until advanced stages of CKD, accelerates markedly in ESRD, and returns to control rates after kidney transplantation. Diabetes significantly increases progression in CKD and ESRD. |
format | Online Article Text |
id | pubmed-6224661 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-62246612018-11-16 Progression of Medial Arterial Calcification in CKD Manzoor, Shumila Ahmed, Syed Ali, Arshad Han, Kum Hyun Sechopoulos, Ioannis O’Neill, Ansley Fei, Baowei O’Neill, W. Charles Kidney Int Rep Clinical Research INTRODUCTION: Medial arterial calcification is common in chronic kidney disease (CKD) and portends poor clinical outcomes, but its progression relative to the severity of CKD and the role of other risk factors is unknown because of the lack of reliable quantification. METHODS: Calcification of breast arteries detected by mammography, which is exclusively medial and correlates with medial calcification in peripheral arteries and with cardiovascular outcomes, was used to measure the progression of medial arterial calcification in women with CKD and end-stage renal disease (ESRD). Measurements showed intra- and interobserver correlations of 0.98, an interstudy variability of 8% to 11%, and a correlation with computed tomographic measurements of 0.92. RESULTS: Progression of calcification was measured in 60 control subjects (estimated glomerular filtration rate (eGFR) ≥ 90 ml/min per 1.73 m(2)) and 137 subjects with CKD (eGFR < 90 ml/min per 1.73 m(2)). Progression in control subjects was linear over time and independent of age. The rate of progression was increased in CKD but only at eGFR < 40 ml/min per 1.73 m(2) (median, 8.1 vs. 3.9 mm/breast/yr in controls; P = 0.006). Progression accelerated markedly in subjects with ESRD (median, 20 mm/breast/yr; n = 36), but did not differ from controls after kidney transplantation (n = 25). Diabetes significantly augmented progression in subjects with CKD and ESRD but not in controls. CONCLUSION: Mammography is a convenient and reliable method to measure the progression of medial arterial calcification. Progression does not increase until advanced stages of CKD, accelerates markedly in ESRD, and returns to control rates after kidney transplantation. Diabetes significantly increases progression in CKD and ESRD. Elsevier 2018-07-21 /pmc/articles/PMC6224661/ /pubmed/30450459 http://dx.doi.org/10.1016/j.ekir.2018.07.011 Text en © 2018 International Society of Nephrology. Published by Elsevier Inc. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Clinical Research Manzoor, Shumila Ahmed, Syed Ali, Arshad Han, Kum Hyun Sechopoulos, Ioannis O’Neill, Ansley Fei, Baowei O’Neill, W. Charles Progression of Medial Arterial Calcification in CKD |
title | Progression of Medial Arterial Calcification in CKD |
title_full | Progression of Medial Arterial Calcification in CKD |
title_fullStr | Progression of Medial Arterial Calcification in CKD |
title_full_unstemmed | Progression of Medial Arterial Calcification in CKD |
title_short | Progression of Medial Arterial Calcification in CKD |
title_sort | progression of medial arterial calcification in ckd |
topic | Clinical Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6224661/ https://www.ncbi.nlm.nih.gov/pubmed/30450459 http://dx.doi.org/10.1016/j.ekir.2018.07.011 |
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