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Quantification of joint blood flow by dynamic contrast-enhanced near-infrared spectroscopy: application to monitoring disease activity in a rat model of rheumatoid arthritis

Significance: Current guidelines for rheumatoid arthritis (RA) management recommend early treatment with disease modifying antirheumatic drugs (DMARDs). However, DMARD treatment fails in 30% of patients and current monitoring methods can only detect failure after 3 to 6 months of therapy. Aim: We in...

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Autores principales: Ioussoufovitch, Seva, Morrison, Laura B., Desjardins, Lise, Hadway, Jennifer A., Lawrence, Keith St., Lee, Ting-Yim, Beier, Frank, Diop, Mamadou
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society of Photo-Optical Instrumentation Engineers 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6983648/
https://www.ncbi.nlm.nih.gov/pubmed/31939225
http://dx.doi.org/10.1117/1.JBO.25.1.015003
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author Ioussoufovitch, Seva
Morrison, Laura B.
Desjardins, Lise
Hadway, Jennifer A.
Lawrence, Keith St.
Lee, Ting-Yim
Beier, Frank
Diop, Mamadou
author_facet Ioussoufovitch, Seva
Morrison, Laura B.
Desjardins, Lise
Hadway, Jennifer A.
Lawrence, Keith St.
Lee, Ting-Yim
Beier, Frank
Diop, Mamadou
author_sort Ioussoufovitch, Seva
collection PubMed
description Significance: Current guidelines for rheumatoid arthritis (RA) management recommend early treatment with disease modifying antirheumatic drugs (DMARDs). However, DMARD treatment fails in 30% of patients and current monitoring methods can only detect failure after 3 to 6 months of therapy. Aim: We investigated whether joint blood flow (BF), quantified using dynamic contrast-enhanced time-resolved near-infrared spectroscopy, can monitor disease activity and treatment response in a rat model of RA. Approach: Ankle joint BF was measured every 5 days in eight rats with adjuvant-induced arthritis (AIA) and four healthy controls. Arthritis was allowed to progress for 20 days before rats with AIA were treated with a DMARD once every 5 days until day 40. Results: Time and group had separate significant main effects on joint BF; however, there was no significant interaction between time and group despite a notable difference in average joint BF on day 5. Comparison of individual blood flow measures between rats with AIA and control group animals did not reveal a clear response to treatment. Conclusions: Joint BF time courses could not distinguish between rats with AIA and study controls. Heterogeneous disease response and low temporal frequency of BF measurements may have been important study limitations.
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spelling pubmed-69836482020-02-03 Quantification of joint blood flow by dynamic contrast-enhanced near-infrared spectroscopy: application to monitoring disease activity in a rat model of rheumatoid arthritis Ioussoufovitch, Seva Morrison, Laura B. Desjardins, Lise Hadway, Jennifer A. Lawrence, Keith St. Lee, Ting-Yim Beier, Frank Diop, Mamadou J Biomed Opt General Significance: Current guidelines for rheumatoid arthritis (RA) management recommend early treatment with disease modifying antirheumatic drugs (DMARDs). However, DMARD treatment fails in 30% of patients and current monitoring methods can only detect failure after 3 to 6 months of therapy. Aim: We investigated whether joint blood flow (BF), quantified using dynamic contrast-enhanced time-resolved near-infrared spectroscopy, can monitor disease activity and treatment response in a rat model of RA. Approach: Ankle joint BF was measured every 5 days in eight rats with adjuvant-induced arthritis (AIA) and four healthy controls. Arthritis was allowed to progress for 20 days before rats with AIA were treated with a DMARD once every 5 days until day 40. Results: Time and group had separate significant main effects on joint BF; however, there was no significant interaction between time and group despite a notable difference in average joint BF on day 5. Comparison of individual blood flow measures between rats with AIA and control group animals did not reveal a clear response to treatment. Conclusions: Joint BF time courses could not distinguish between rats with AIA and study controls. Heterogeneous disease response and low temporal frequency of BF measurements may have been important study limitations. Society of Photo-Optical Instrumentation Engineers 2020-01-14 2020-01 /pmc/articles/PMC6983648/ /pubmed/31939225 http://dx.doi.org/10.1117/1.JBO.25.1.015003 Text en © 2020 The Authors https://creativecommons.org/licenses/by/4.0/ Published by SPIE under a Creative Commons Attribution 4.0 Unported License. Distribution or reproduction of this work in whole or in part requires full attribution of the original publication, including its DOI.
spellingShingle General
Ioussoufovitch, Seva
Morrison, Laura B.
Desjardins, Lise
Hadway, Jennifer A.
Lawrence, Keith St.
Lee, Ting-Yim
Beier, Frank
Diop, Mamadou
Quantification of joint blood flow by dynamic contrast-enhanced near-infrared spectroscopy: application to monitoring disease activity in a rat model of rheumatoid arthritis
title Quantification of joint blood flow by dynamic contrast-enhanced near-infrared spectroscopy: application to monitoring disease activity in a rat model of rheumatoid arthritis
title_full Quantification of joint blood flow by dynamic contrast-enhanced near-infrared spectroscopy: application to monitoring disease activity in a rat model of rheumatoid arthritis
title_fullStr Quantification of joint blood flow by dynamic contrast-enhanced near-infrared spectroscopy: application to monitoring disease activity in a rat model of rheumatoid arthritis
title_full_unstemmed Quantification of joint blood flow by dynamic contrast-enhanced near-infrared spectroscopy: application to monitoring disease activity in a rat model of rheumatoid arthritis
title_short Quantification of joint blood flow by dynamic contrast-enhanced near-infrared spectroscopy: application to monitoring disease activity in a rat model of rheumatoid arthritis
title_sort quantification of joint blood flow by dynamic contrast-enhanced near-infrared spectroscopy: application to monitoring disease activity in a rat model of rheumatoid arthritis
topic General
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6983648/
https://www.ncbi.nlm.nih.gov/pubmed/31939225
http://dx.doi.org/10.1117/1.JBO.25.1.015003
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