ASDAS is associated with both the extent and intensity of DW-MRI spinal inflammation in active axial spondyloarthritis

ObjectiveTo investigate the relationship between Ankylosing Spondylitis Disease Activity Score (ASDAS) and intensity of spinal inflammation measured by apparent diffusion coefficient (ADC) in MRI in participants with active axial spondyloarthritis (SpA).MethodsParticipants with axial SpA and back pa...

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Veröffentlicht in:Rheumatic & musculoskeletal diseases open 2019-08, Vol.5 (2), p.e001008-e001008
Hauptverfasser: Chung, Ho Yin, Chui, Eva Tsz Fung, Lee, Kam Ho, Tsang, Helen Hoi Lun, Chan, Shirley Chiu Wai, Lau, Chak Sing
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container_title Rheumatic & musculoskeletal diseases open
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creator Chung, Ho Yin
Chui, Eva Tsz Fung
Lee, Kam Ho
Tsang, Helen Hoi Lun
Chan, Shirley Chiu Wai
Lau, Chak Sing
description ObjectiveTo investigate the relationship between Ankylosing Spondylitis Disease Activity Score (ASDAS) and intensity of spinal inflammation measured by apparent diffusion coefficient (ADC) in MRI in participants with active axial spondyloarthritis (SpA).MethodsParticipants with axial SpA and back pain were recruited. Clinical, demographic, biochemical and imaging data were collected. ASDAS was calculated based on C reactive protein (CRP) and erythrocyte sedimentation rate (ESR). Inflammatory lesions were identified in short tau inversion recovery images and the corresponding ADC maps to determine the maximum apparent diffusion coefficient (ADCmax), normalised maximum ADC, mean apparent diffusion coefficient (ADCmean) and normalised mean ADC by two independent readers. Spondyloarthritis Research Consortium of Canada (SPARCC) spine and sacroiliac (SI) joint MRI indexes were determined. Univariate and multivariate linear regression models were used to determine the associations between of ASDAS with ADC values, SPARCC spine and SI MRI scores.ResultsEighty-two participants had identifiable ADC lesions. Multivariate analyses using ADCmax and SPARCC spine MRI as independent variables showed associations with ASDAS-CRP (ADCmax: B=0.27, p=0.02; SPARCC: B=0.32, p=0.01) and ASDAS-ESR (ADCmax: B=0.24, p=0.03; SPARCC: B=0.36, p
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Clinical, demographic, biochemical and imaging data were collected. ASDAS was calculated based on C reactive protein (CRP) and erythrocyte sedimentation rate (ESR). Inflammatory lesions were identified in short tau inversion recovery images and the corresponding ADC maps to determine the maximum apparent diffusion coefficient (ADCmax), normalised maximum ADC, mean apparent diffusion coefficient (ADCmean) and normalised mean ADC by two independent readers. Spondyloarthritis Research Consortium of Canada (SPARCC) spine and sacroiliac (SI) joint MRI indexes were determined. Univariate and multivariate linear regression models were used to determine the associations between of ASDAS with ADC values, SPARCC spine and SI MRI scores.ResultsEighty-two participants had identifiable ADC lesions. Multivariate analyses using ADCmax and SPARCC spine MRI as independent variables showed associations with ASDAS-CRP (ADCmax: B=0.27, p=0.02; SPARCC: B=0.32, p=0.01) and ASDAS-ESR (ADCmax: B=0.24, p=0.03; SPARCC: B=0.36, p&lt;0.01); using ADCmean and SPARCC spine MRI as independent variables also showed an association with ASDAS-ESR (ADCmean: B=0.22, p=0.05; SPARCC: B=0.36, p&lt;0.01) and a tendency to associate with ASDAS-CRP (ADCmean: B=0.21, p=0.07; SPARCC: B=0.34, p&lt;0.01).ConclusionASDAS is associated with both the extent and the intensity of spinal inflammation in patients with detectable inflammatory lesions. Our results showed that ASDAS is an objective disease assessment tool.Trial registration numberHKUCTR-2087.</description><identifier>ISSN: 2056-5933</identifier><identifier>EISSN: 2056-5933</identifier><identifier>DOI: 10.1136/rmdopen-2019-001008</identifier><identifier>PMID: 31452930</identifier><language>eng</language><publisher>England: BMJ Publishing Group LTD</publisher><subject>Arthritis ; Back pain ; Back Pain - diagnosis ; Back Pain - etiology ; Biomarkers ; Bone marrow ; Canada ; Diffusion Magnetic Resonance Imaging - methods ; Female ; Humans ; Image Processing, Computer-Assisted ; Inflammation ; Male ; Middle Aged ; Multivariate Analysis ; NMR ; Nuclear magnetic resonance ; Osteoporosis ; Questionnaires ; Severity of Illness Index ; Spondylarthritis - complications ; Spondylarthritis - diagnosis ; Spondylarthritis - etiology ; Spondylarthritis - metabolism ; Spondyloarthritis ; Systematic review</subject><ispartof>Rheumatic &amp; musculoskeletal diseases open, 2019-08, Vol.5 (2), p.e001008-e001008</ispartof><rights>Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.</rights><rights>2019 Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ . Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b472t-a692312e808a4b418606956ee5c476126dd3d566bbf931c12521e8ad66e045b13</citedby><cites>FETCH-LOGICAL-b472t-a692312e808a4b418606956ee5c476126dd3d566bbf931c12521e8ad66e045b13</cites><orcidid>0000-0002-0175-1346</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://rmdopen.bmj.com/content/5/2/e001008.full.pdf$$EPDF$$P50$$Gbmj$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://rmdopen.bmj.com/content/5/2/e001008.full$$EHTML$$P50$$Gbmj$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,27549,27550,27924,27925,53791,53793,77601,77632</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31452930$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chung, Ho Yin</creatorcontrib><creatorcontrib>Chui, Eva Tsz Fung</creatorcontrib><creatorcontrib>Lee, Kam Ho</creatorcontrib><creatorcontrib>Tsang, Helen Hoi Lun</creatorcontrib><creatorcontrib>Chan, Shirley Chiu Wai</creatorcontrib><creatorcontrib>Lau, Chak Sing</creatorcontrib><title>ASDAS is associated with both the extent and intensity of DW-MRI spinal inflammation in active axial spondyloarthritis</title><title>Rheumatic &amp; musculoskeletal diseases open</title><addtitle>RMD Open</addtitle><description>ObjectiveTo investigate the relationship between Ankylosing Spondylitis Disease Activity Score (ASDAS) and intensity of spinal inflammation measured by apparent diffusion coefficient (ADC) in MRI in participants with active axial spondyloarthritis (SpA).MethodsParticipants with axial SpA and back pain were recruited. Clinical, demographic, biochemical and imaging data were collected. ASDAS was calculated based on C reactive protein (CRP) and erythrocyte sedimentation rate (ESR). Inflammatory lesions were identified in short tau inversion recovery images and the corresponding ADC maps to determine the maximum apparent diffusion coefficient (ADCmax), normalised maximum ADC, mean apparent diffusion coefficient (ADCmean) and normalised mean ADC by two independent readers. Spondyloarthritis Research Consortium of Canada (SPARCC) spine and sacroiliac (SI) joint MRI indexes were determined. Univariate and multivariate linear regression models were used to determine the associations between of ASDAS with ADC values, SPARCC spine and SI MRI scores.ResultsEighty-two participants had identifiable ADC lesions. Multivariate analyses using ADCmax and SPARCC spine MRI as independent variables showed associations with ASDAS-CRP (ADCmax: B=0.27, p=0.02; SPARCC: B=0.32, p=0.01) and ASDAS-ESR (ADCmax: B=0.24, p=0.03; SPARCC: B=0.36, p&lt;0.01); using ADCmean and SPARCC spine MRI as independent variables also showed an association with ASDAS-ESR (ADCmean: B=0.22, p=0.05; SPARCC: B=0.36, p&lt;0.01) and a tendency to associate with ASDAS-CRP (ADCmean: B=0.21, p=0.07; SPARCC: B=0.34, p&lt;0.01).ConclusionASDAS is associated with both the extent and the intensity of spinal inflammation in patients with detectable inflammatory lesions. Our results showed that ASDAS is an objective disease assessment tool.Trial registration numberHKUCTR-2087.</description><subject>Arthritis</subject><subject>Back pain</subject><subject>Back Pain - diagnosis</subject><subject>Back Pain - etiology</subject><subject>Biomarkers</subject><subject>Bone marrow</subject><subject>Canada</subject><subject>Diffusion Magnetic Resonance Imaging - methods</subject><subject>Female</subject><subject>Humans</subject><subject>Image Processing, Computer-Assisted</subject><subject>Inflammation</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Multivariate Analysis</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>Osteoporosis</subject><subject>Questionnaires</subject><subject>Severity of Illness Index</subject><subject>Spondylarthritis - complications</subject><subject>Spondylarthritis - diagnosis</subject><subject>Spondylarthritis - etiology</subject><subject>Spondylarthritis - metabolism</subject><subject>Spondyloarthritis</subject><subject>Systematic review</subject><issn>2056-5933</issn><issn>2056-5933</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>9YT</sourceid><sourceid>ACMMV</sourceid><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNqNkVFLHDEUhYNYqmz9BQUJ-OLL2Nxkkpl5KSxaW8EiqKWPITPJdLPMJNMku3X_vbG7Fe2TL8kN57uH3HsQ-gjkDICJT2HUfjKuoASaghAgpN5Dh5RwUfCGsf0X9QE6inFJMlQyVgF7jw4YlJw2jByi9fzuYn6HbcQqRt9ZlYzGf2xa4NbnIy0MNg_JuISV09i6XEabNtj3-OJn8f32CsfJOjVkqR_UOKpkvcsPrLpk1warB5vFOHmnN4NXIS2CTTZ-QO96NURztLtn6Mfll_vzb8X1zder8_l10ZYVTYUSDWVATU1qVbYl1IKIhgtjeFdWAqjQmmkuRNv2DYMOKKdgaqWFMKTkLbAZ-rz1nVbtaHSXBwlqkFOwowob6ZWVrxVnF_KXX0shGuB5YTN0ujMI_vfKxCRHGzszDMoZv4qS0hqAVqTiGT35D136Vci7-UvVFQCvaabYluqCjzGY_vkzQORTtHIXrXyKVm6jzV3HL-d47vkXZAbOtkA7Lt_k-AhuJLA5</recordid><startdate>20190801</startdate><enddate>20190801</enddate><creator>Chung, Ho Yin</creator><creator>Chui, Eva Tsz Fung</creator><creator>Lee, Kam Ho</creator><creator>Tsang, Helen Hoi Lun</creator><creator>Chan, Shirley Chiu Wai</creator><creator>Lau, Chak Sing</creator><general>BMJ Publishing Group LTD</general><general>BMJ Publishing Group</general><scope>9YT</scope><scope>ACMMV</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-0175-1346</orcidid></search><sort><creationdate>20190801</creationdate><title>ASDAS is associated with both the extent and intensity of DW-MRI spinal inflammation in active axial spondyloarthritis</title><author>Chung, Ho Yin ; Chui, Eva Tsz Fung ; Lee, Kam Ho ; Tsang, Helen Hoi Lun ; Chan, Shirley Chiu Wai ; Lau, Chak Sing</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b472t-a692312e808a4b418606956ee5c476126dd3d566bbf931c12521e8ad66e045b13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Arthritis</topic><topic>Back pain</topic><topic>Back Pain - diagnosis</topic><topic>Back Pain - etiology</topic><topic>Biomarkers</topic><topic>Bone marrow</topic><topic>Canada</topic><topic>Diffusion Magnetic Resonance Imaging - methods</topic><topic>Female</topic><topic>Humans</topic><topic>Image Processing, Computer-Assisted</topic><topic>Inflammation</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Multivariate Analysis</topic><topic>NMR</topic><topic>Nuclear magnetic resonance</topic><topic>Osteoporosis</topic><topic>Questionnaires</topic><topic>Severity of Illness Index</topic><topic>Spondylarthritis - complications</topic><topic>Spondylarthritis - diagnosis</topic><topic>Spondylarthritis - etiology</topic><topic>Spondylarthritis - metabolism</topic><topic>Spondyloarthritis</topic><topic>Systematic review</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chung, Ho Yin</creatorcontrib><creatorcontrib>Chui, Eva Tsz Fung</creatorcontrib><creatorcontrib>Lee, Kam Ho</creatorcontrib><creatorcontrib>Tsang, Helen Hoi Lun</creatorcontrib><creatorcontrib>Chan, Shirley Chiu Wai</creatorcontrib><creatorcontrib>Lau, Chak Sing</creatorcontrib><collection>BMJ Open Access Journals</collection><collection>BMJ Journals:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health &amp; 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musculoskeletal diseases open</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chung, Ho Yin</au><au>Chui, Eva Tsz Fung</au><au>Lee, Kam Ho</au><au>Tsang, Helen Hoi Lun</au><au>Chan, Shirley Chiu Wai</au><au>Lau, Chak Sing</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>ASDAS is associated with both the extent and intensity of DW-MRI spinal inflammation in active axial spondyloarthritis</atitle><jtitle>Rheumatic &amp; musculoskeletal diseases open</jtitle><addtitle>RMD Open</addtitle><date>2019-08-01</date><risdate>2019</risdate><volume>5</volume><issue>2</issue><spage>e001008</spage><epage>e001008</epage><pages>e001008-e001008</pages><issn>2056-5933</issn><eissn>2056-5933</eissn><abstract>ObjectiveTo investigate the relationship between Ankylosing Spondylitis Disease Activity Score (ASDAS) and intensity of spinal inflammation measured by apparent diffusion coefficient (ADC) in MRI in participants with active axial spondyloarthritis (SpA).MethodsParticipants with axial SpA and back pain were recruited. Clinical, demographic, biochemical and imaging data were collected. ASDAS was calculated based on C reactive protein (CRP) and erythrocyte sedimentation rate (ESR). Inflammatory lesions were identified in short tau inversion recovery images and the corresponding ADC maps to determine the maximum apparent diffusion coefficient (ADCmax), normalised maximum ADC, mean apparent diffusion coefficient (ADCmean) and normalised mean ADC by two independent readers. Spondyloarthritis Research Consortium of Canada (SPARCC) spine and sacroiliac (SI) joint MRI indexes were determined. Univariate and multivariate linear regression models were used to determine the associations between of ASDAS with ADC values, SPARCC spine and SI MRI scores.ResultsEighty-two participants had identifiable ADC lesions. Multivariate analyses using ADCmax and SPARCC spine MRI as independent variables showed associations with ASDAS-CRP (ADCmax: B=0.27, p=0.02; SPARCC: B=0.32, p=0.01) and ASDAS-ESR (ADCmax: B=0.24, p=0.03; SPARCC: B=0.36, p&lt;0.01); using ADCmean and SPARCC spine MRI as independent variables also showed an association with ASDAS-ESR (ADCmean: B=0.22, p=0.05; SPARCC: B=0.36, p&lt;0.01) and a tendency to associate with ASDAS-CRP (ADCmean: B=0.21, p=0.07; SPARCC: B=0.34, p&lt;0.01).ConclusionASDAS is associated with both the extent and the intensity of spinal inflammation in patients with detectable inflammatory lesions. Our results showed that ASDAS is an objective disease assessment tool.Trial registration numberHKUCTR-2087.</abstract><cop>England</cop><pub>BMJ Publishing Group LTD</pub><pmid>31452930</pmid><doi>10.1136/rmdopen-2019-001008</doi><orcidid>https://orcid.org/0000-0002-0175-1346</orcidid><oa>free_for_read</oa></addata></record>
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subjects Arthritis
Back pain
Back Pain - diagnosis
Back Pain - etiology
Biomarkers
Bone marrow
Canada
Diffusion Magnetic Resonance Imaging - methods
Female
Humans
Image Processing, Computer-Assisted
Inflammation
Male
Middle Aged
Multivariate Analysis
NMR
Nuclear magnetic resonance
Osteoporosis
Questionnaires
Severity of Illness Index
Spondylarthritis - complications
Spondylarthritis - diagnosis
Spondylarthritis - etiology
Spondylarthritis - metabolism
Spondyloarthritis
Systematic review
title ASDAS is associated with both the extent and intensity of DW-MRI spinal inflammation in active axial spondyloarthritis
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