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Biomarkers of cardiovascular risk across phenotypes of osteoarthritis

BACKGROUND: The objective of this study was to explore the associations between ultrasonographic and radiographic joint scores and levels of arterial CVD risk markers in patients with osteoarthritis (OA). Secondly, to compare the levels of arterial CVD risk markers between OA phenotypes and controls...

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Autores principales: Provan, S. A., Rollefstad, S., Ikdahl, E., Mathiessen, A., Berg, I. J., Eeg, I., Wilkinson, I. B., McEniery, C. M., Kvien, T. K., Hammer, H. B., Østerås, N., Haugen, I. K., Semb, A. G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6686275/
https://www.ncbi.nlm.nih.gov/pubmed/31410391
http://dx.doi.org/10.1186/s41927-019-0081-8
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author Provan, S. A.
Rollefstad, S.
Ikdahl, E.
Mathiessen, A.
Berg, I. J.
Eeg, I.
Wilkinson, I. B.
McEniery, C. M.
Kvien, T. K.
Hammer, H. B.
Østerås, N.
Haugen, I. K.
Semb, A. G.
author_facet Provan, S. A.
Rollefstad, S.
Ikdahl, E.
Mathiessen, A.
Berg, I. J.
Eeg, I.
Wilkinson, I. B.
McEniery, C. M.
Kvien, T. K.
Hammer, H. B.
Østerås, N.
Haugen, I. K.
Semb, A. G.
author_sort Provan, S. A.
collection PubMed
description BACKGROUND: The objective of this study was to explore the associations between ultrasonographic and radiographic joint scores and levels of arterial CVD risk markers in patients with osteoarthritis (OA). Secondly, to compare the levels of arterial CVD risk markers between OA phenotypes and controls. METHOD: The “Musculoskeletal pain in Ullensaker” Study (MUST) invited residents of Ullensaker municipality with self-reported OA to a medical examination. OA was defined according to the American College of Rheumatology (ACR) criteria and phenotyped based on joint distribution. Joints of the hands, hips and knees were examined by ultrasonography and conventional radiography, and scored for osteosteophytes. Hands were also scored for inflammation by grey scale (GS) synovitis and power Doppler (PD) signal. Control populations were a cohort of inhabitants of Oslo (OCP), and for external validation, a UK community-based register (UKPC). Pulse pressure augmentation index (AIx) and pulse wave velocity (PWV) were measured using the Sphygmocor apparatus (Atcor®). Ankel-brachial index (ABI) was estimated in a subset of patients. In separate adjusted regression models we explored the associations between ultrasonography and radiograph joint scores and AIx, PWV and ABI. CVD risk markers were also compared between phenotypes of OA and controls in adjusted analyses. RESULTS: Three hundred and sixty six persons with OA were included (mean age (range); 63.0 (42.0–75.0)), (females (%); 264 (72)). Of these, 155 (42.3%) had isolated hand OA, 111 (30.3%) had isolated lower limb OA and 100 (27.3%) had generalized OA. 108 persons were included in the OCP and 963 persons in the UKPC; (mean age (range); OCP: 57.2 (40.4–70.4), UKPC: 63.9 (40.0–75.0), females (%); OCP: 47 (43.5), UKPC: 543 (56.4%). Hand osteophytes were associated with AIx while GS and PD scores were not related to CVD risk markers. All OA phenotypes had higher levels of AIx compared to OCP in adjusted analyses. External validation against UKPC confirmed these findings. CONCLUSIONS: Hand osteophytes might be related to higher risk of CVD. People with OA had higher augmented central pressure compared to controls. Words 330. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s41927-019-0081-8) contains supplementary material, which is available to authorized users.
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spelling pubmed-66862752019-08-13 Biomarkers of cardiovascular risk across phenotypes of osteoarthritis Provan, S. A. Rollefstad, S. Ikdahl, E. Mathiessen, A. Berg, I. J. Eeg, I. Wilkinson, I. B. McEniery, C. M. Kvien, T. K. Hammer, H. B. Østerås, N. Haugen, I. K. Semb, A. G. BMC Rheumatol Research Article BACKGROUND: The objective of this study was to explore the associations between ultrasonographic and radiographic joint scores and levels of arterial CVD risk markers in patients with osteoarthritis (OA). Secondly, to compare the levels of arterial CVD risk markers between OA phenotypes and controls. METHOD: The “Musculoskeletal pain in Ullensaker” Study (MUST) invited residents of Ullensaker municipality with self-reported OA to a medical examination. OA was defined according to the American College of Rheumatology (ACR) criteria and phenotyped based on joint distribution. Joints of the hands, hips and knees were examined by ultrasonography and conventional radiography, and scored for osteosteophytes. Hands were also scored for inflammation by grey scale (GS) synovitis and power Doppler (PD) signal. Control populations were a cohort of inhabitants of Oslo (OCP), and for external validation, a UK community-based register (UKPC). Pulse pressure augmentation index (AIx) and pulse wave velocity (PWV) were measured using the Sphygmocor apparatus (Atcor®). Ankel-brachial index (ABI) was estimated in a subset of patients. In separate adjusted regression models we explored the associations between ultrasonography and radiograph joint scores and AIx, PWV and ABI. CVD risk markers were also compared between phenotypes of OA and controls in adjusted analyses. RESULTS: Three hundred and sixty six persons with OA were included (mean age (range); 63.0 (42.0–75.0)), (females (%); 264 (72)). Of these, 155 (42.3%) had isolated hand OA, 111 (30.3%) had isolated lower limb OA and 100 (27.3%) had generalized OA. 108 persons were included in the OCP and 963 persons in the UKPC; (mean age (range); OCP: 57.2 (40.4–70.4), UKPC: 63.9 (40.0–75.0), females (%); OCP: 47 (43.5), UKPC: 543 (56.4%). Hand osteophytes were associated with AIx while GS and PD scores were not related to CVD risk markers. All OA phenotypes had higher levels of AIx compared to OCP in adjusted analyses. External validation against UKPC confirmed these findings. CONCLUSIONS: Hand osteophytes might be related to higher risk of CVD. People with OA had higher augmented central pressure compared to controls. Words 330. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s41927-019-0081-8) contains supplementary material, which is available to authorized users. BioMed Central 2019-08-08 /pmc/articles/PMC6686275/ /pubmed/31410391 http://dx.doi.org/10.1186/s41927-019-0081-8 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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
Provan, S. A.
Rollefstad, S.
Ikdahl, E.
Mathiessen, A.
Berg, I. J.
Eeg, I.
Wilkinson, I. B.
McEniery, C. M.
Kvien, T. K.
Hammer, H. B.
Østerås, N.
Haugen, I. K.
Semb, A. G.
Biomarkers of cardiovascular risk across phenotypes of osteoarthritis
title Biomarkers of cardiovascular risk across phenotypes of osteoarthritis
title_full Biomarkers of cardiovascular risk across phenotypes of osteoarthritis
title_fullStr Biomarkers of cardiovascular risk across phenotypes of osteoarthritis
title_full_unstemmed Biomarkers of cardiovascular risk across phenotypes of osteoarthritis
title_short Biomarkers of cardiovascular risk across phenotypes of osteoarthritis
title_sort biomarkers of cardiovascular risk across phenotypes of osteoarthritis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6686275/
https://www.ncbi.nlm.nih.gov/pubmed/31410391
http://dx.doi.org/10.1186/s41927-019-0081-8
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