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Bone mineral density and carotid atherosclerosis in systemic lupus erythematosus: a controlled cross-sectional study

INTRODUCTION: As osteoporosis is reported to be associated with atherosclerosis in the general population we examined the relationship between bone mass and carotid measurements in patients with systemic lupus erythematosus (SLE) and controls, and possible links between them in SLE. METHODS: In a cr...

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Autores principales: Ajeganova, Sofia, Gustafsson, Thomas, Jogestrand, Tomas, Frostegård, Johan, Hafström, Ingiäld
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4407386/
https://www.ncbi.nlm.nih.gov/pubmed/25885788
http://dx.doi.org/10.1186/s13075-015-0595-4
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author Ajeganova, Sofia
Gustafsson, Thomas
Jogestrand, Tomas
Frostegård, Johan
Hafström, Ingiäld
author_facet Ajeganova, Sofia
Gustafsson, Thomas
Jogestrand, Tomas
Frostegård, Johan
Hafström, Ingiäld
author_sort Ajeganova, Sofia
collection PubMed
description INTRODUCTION: As osteoporosis is reported to be associated with atherosclerosis in the general population we examined the relationship between bone mass and carotid measurements in patients with systemic lupus erythematosus (SLE) and controls, and possible links between them in SLE. METHODS: In a cross-sectional study, 111 SLE-patient were compared with 111 age- and sex-matched controls, mean age 48.7(12.9) years, 89% were women, of which 51% postmenopausal. Carotid intima media thickness (cIMT), carotid plaque occurrence and echogenicity were determined by B-mode ultrasound and bone mineral density (BMD) by dual-energy X-ray absorptiometry (DXA). RESULTS: BMD and cIMT were inversely associated both in patients and controls. Patients, but not controls, with carotid plaque had higher cIMT at low BMD than at normal BMD, p = 0.010. Logistic regression indicated more than doubled odds ratio (OR) of carotid plaque in patients, particularly in post-menopausal women, than in controls in relation to all BMD measurements. For low BMD at hip, significant increased OR for echolucent plaque was shown for patients compared with controls. In patients, significant impact of age, body mass index, smoking, systolic blood pressure, blood lipids, diabetes mellitus, impaired renal function, low levels of complement C3 and C4, history of nephritis, SLE-damage index and ever use of antimalarial was found for association between BMD and higher cIMT and carotid plaque. In multivariate regression, low C4 was independent contributor to association between total BMD and upper cIMT tertile, accounted for OR (95% confidence interval) of 3.2 (1.03-10.01), and also for association with bilateral carotid plaque, OR of 4.8 (1.03-22.66). The contribution of low C4 for the association between BMD and carotid atherosclerosis was enhanced within the second and third tertiles of total BMD. CONCLUSION: This study is the first to demonstrate inverse association between BMD and carotid measurements in both SLE-patients and controls. Our results suggest that SLE-patients may suffer higher burden of (sub)clinical atherosclerotic disease, especially presence of both echolucent and echogenic plaque, than controls with the same bone mineral status. Low complement C4 seems to play an important role in earlier development of carotid atherosclerosis already within (sub)normal ranges of total BMD in patients. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13075-015-0595-4) contains supplementary material, which is available to authorized users.
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spelling pubmed-44073862015-04-24 Bone mineral density and carotid atherosclerosis in systemic lupus erythematosus: a controlled cross-sectional study Ajeganova, Sofia Gustafsson, Thomas Jogestrand, Tomas Frostegård, Johan Hafström, Ingiäld Arthritis Res Ther Research Article INTRODUCTION: As osteoporosis is reported to be associated with atherosclerosis in the general population we examined the relationship between bone mass and carotid measurements in patients with systemic lupus erythematosus (SLE) and controls, and possible links between them in SLE. METHODS: In a cross-sectional study, 111 SLE-patient were compared with 111 age- and sex-matched controls, mean age 48.7(12.9) years, 89% were women, of which 51% postmenopausal. Carotid intima media thickness (cIMT), carotid plaque occurrence and echogenicity were determined by B-mode ultrasound and bone mineral density (BMD) by dual-energy X-ray absorptiometry (DXA). RESULTS: BMD and cIMT were inversely associated both in patients and controls. Patients, but not controls, with carotid plaque had higher cIMT at low BMD than at normal BMD, p = 0.010. Logistic regression indicated more than doubled odds ratio (OR) of carotid plaque in patients, particularly in post-menopausal women, than in controls in relation to all BMD measurements. For low BMD at hip, significant increased OR for echolucent plaque was shown for patients compared with controls. In patients, significant impact of age, body mass index, smoking, systolic blood pressure, blood lipids, diabetes mellitus, impaired renal function, low levels of complement C3 and C4, history of nephritis, SLE-damage index and ever use of antimalarial was found for association between BMD and higher cIMT and carotid plaque. In multivariate regression, low C4 was independent contributor to association between total BMD and upper cIMT tertile, accounted for OR (95% confidence interval) of 3.2 (1.03-10.01), and also for association with bilateral carotid plaque, OR of 4.8 (1.03-22.66). The contribution of low C4 for the association between BMD and carotid atherosclerosis was enhanced within the second and third tertiles of total BMD. CONCLUSION: This study is the first to demonstrate inverse association between BMD and carotid measurements in both SLE-patients and controls. Our results suggest that SLE-patients may suffer higher burden of (sub)clinical atherosclerotic disease, especially presence of both echolucent and echogenic plaque, than controls with the same bone mineral status. Low complement C4 seems to play an important role in earlier development of carotid atherosclerosis already within (sub)normal ranges of total BMD in patients. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13075-015-0595-4) contains supplementary material, which is available to authorized users. BioMed Central 2015-03-25 2015 /pmc/articles/PMC4407386/ /pubmed/25885788 http://dx.doi.org/10.1186/s13075-015-0595-4 Text en © Ajeganova et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Ajeganova, Sofia
Gustafsson, Thomas
Jogestrand, Tomas
Frostegård, Johan
Hafström, Ingiäld
Bone mineral density and carotid atherosclerosis in systemic lupus erythematosus: a controlled cross-sectional study
title Bone mineral density and carotid atherosclerosis in systemic lupus erythematosus: a controlled cross-sectional study
title_full Bone mineral density and carotid atherosclerosis in systemic lupus erythematosus: a controlled cross-sectional study
title_fullStr Bone mineral density and carotid atherosclerosis in systemic lupus erythematosus: a controlled cross-sectional study
title_full_unstemmed Bone mineral density and carotid atherosclerosis in systemic lupus erythematosus: a controlled cross-sectional study
title_short Bone mineral density and carotid atherosclerosis in systemic lupus erythematosus: a controlled cross-sectional study
title_sort bone mineral density and carotid atherosclerosis in systemic lupus erythematosus: a controlled cross-sectional study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4407386/
https://www.ncbi.nlm.nih.gov/pubmed/25885788
http://dx.doi.org/10.1186/s13075-015-0595-4
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