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Reduced progression of bone erosion in cytomegalovirus seropositive rheumatoid arthritis patients

BACKGROUND: Human cytomegalovirus (HCMV) seropositivity has been associated with higher inflammation during rheumatoid arthritis (RA). However, no data are available on the impact of HCMV seropositivity on bone erosion progression during RA. METHODS: We selected 487 individuals of ESPOIR cohort who...

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Autores principales: Rauwel, B., Degboé, Y., Nigon, D., Boyer, J.-F., Abravanel, F., Izopet, J., Combe, B., Ruyssen-Witrand, A., Constantin, A., Cantagrel, A., Davignon, J.-L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6971916/
https://www.ncbi.nlm.nih.gov/pubmed/31959222
http://dx.doi.org/10.1186/s13075-020-2098-1
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author Rauwel, B.
Degboé, Y.
Nigon, D.
Boyer, J.-F.
Abravanel, F.
Izopet, J.
Combe, B.
Ruyssen-Witrand, A.
Constantin, A.
Cantagrel, A.
Davignon, J.-L.
author_facet Rauwel, B.
Degboé, Y.
Nigon, D.
Boyer, J.-F.
Abravanel, F.
Izopet, J.
Combe, B.
Ruyssen-Witrand, A.
Constantin, A.
Cantagrel, A.
Davignon, J.-L.
author_sort Rauwel, B.
collection PubMed
description BACKGROUND: Human cytomegalovirus (HCMV) seropositivity has been associated with higher inflammation during rheumatoid arthritis (RA). However, no data are available on the impact of HCMV seropositivity on bone erosion progression during RA. METHODS: We selected 487 individuals of ESPOIR cohort who fulfilled the 2010 ACR/EULAR criteria for RA. HCMV serology for these patients was determined using Architect CMV IgG assay. Baseline and 1-year central X-ray reading using modified Total Sharp Score (mTSS), Erosion Sharp Score, and joint space narrowing Sharp score were used to quantify structural damage progression. We performed univariate and multivariate analyses to investigate the association between HCMV status and bone erosion progression. RESULTS: We analyzed 273 HCMV seropositive (HCMV+) and 214 HCMV seronegative (HCMV−) RA patients. At inclusion, HCMV+ patients were less frequently ACPA+ (49.8% versus 58.9%, p < 0.0465) and had a higher DAS28-ESR (5.55 ± 1.24 versus 5.20 ± 1.14, p < 0.0013) in comparison with HCMV−. At 1 year, bone erosion progression (delta erosion Sharp score > 1 point) was lower in HCMV+ patients (16.1% versus 25.2%, p = 0.0128) in comparison with HCMV−. HCMV+ status remained independently associated with lower bone erosion progression in multivariate analysis. CONCLUSIONS: Our findings suggest that, independently of other confounding factors, HCMV seropositivity is associated with a lower progression of bone erosion during RA.
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spelling pubmed-69719162020-01-27 Reduced progression of bone erosion in cytomegalovirus seropositive rheumatoid arthritis patients Rauwel, B. Degboé, Y. Nigon, D. Boyer, J.-F. Abravanel, F. Izopet, J. Combe, B. Ruyssen-Witrand, A. Constantin, A. Cantagrel, A. Davignon, J.-L. Arthritis Res Ther Research Article BACKGROUND: Human cytomegalovirus (HCMV) seropositivity has been associated with higher inflammation during rheumatoid arthritis (RA). However, no data are available on the impact of HCMV seropositivity on bone erosion progression during RA. METHODS: We selected 487 individuals of ESPOIR cohort who fulfilled the 2010 ACR/EULAR criteria for RA. HCMV serology for these patients was determined using Architect CMV IgG assay. Baseline and 1-year central X-ray reading using modified Total Sharp Score (mTSS), Erosion Sharp Score, and joint space narrowing Sharp score were used to quantify structural damage progression. We performed univariate and multivariate analyses to investigate the association between HCMV status and bone erosion progression. RESULTS: We analyzed 273 HCMV seropositive (HCMV+) and 214 HCMV seronegative (HCMV−) RA patients. At inclusion, HCMV+ patients were less frequently ACPA+ (49.8% versus 58.9%, p < 0.0465) and had a higher DAS28-ESR (5.55 ± 1.24 versus 5.20 ± 1.14, p < 0.0013) in comparison with HCMV−. At 1 year, bone erosion progression (delta erosion Sharp score > 1 point) was lower in HCMV+ patients (16.1% versus 25.2%, p = 0.0128) in comparison with HCMV−. HCMV+ status remained independently associated with lower bone erosion progression in multivariate analysis. CONCLUSIONS: Our findings suggest that, independently of other confounding factors, HCMV seropositivity is associated with a lower progression of bone erosion during RA. BioMed Central 2020-01-20 2020 /pmc/articles/PMC6971916/ /pubmed/31959222 http://dx.doi.org/10.1186/s13075-020-2098-1 Text en © The Author(s). 2020 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
Rauwel, B.
Degboé, Y.
Nigon, D.
Boyer, J.-F.
Abravanel, F.
Izopet, J.
Combe, B.
Ruyssen-Witrand, A.
Constantin, A.
Cantagrel, A.
Davignon, J.-L.
Reduced progression of bone erosion in cytomegalovirus seropositive rheumatoid arthritis patients
title Reduced progression of bone erosion in cytomegalovirus seropositive rheumatoid arthritis patients
title_full Reduced progression of bone erosion in cytomegalovirus seropositive rheumatoid arthritis patients
title_fullStr Reduced progression of bone erosion in cytomegalovirus seropositive rheumatoid arthritis patients
title_full_unstemmed Reduced progression of bone erosion in cytomegalovirus seropositive rheumatoid arthritis patients
title_short Reduced progression of bone erosion in cytomegalovirus seropositive rheumatoid arthritis patients
title_sort reduced progression of bone erosion in cytomegalovirus seropositive rheumatoid arthritis patients
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6971916/
https://www.ncbi.nlm.nih.gov/pubmed/31959222
http://dx.doi.org/10.1186/s13075-020-2098-1
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