Ultrasound in clinically suspect arthralgia: the role of power Doppler to predict rheumatoid arthritis development

Objective To determine the usefulness of power Doppler (PD) ultrasound (US) to predict rheumatoid arthritis (RA) development in patients with clinically suspect arthralgia (CSA). Methods Retrospective analysis of a US unit cohort over a 1-year period. Patients with CSA and no previous diagnosis of i...

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Veröffentlicht in:Arthritis research & therapy 2021-12, Vol.23 (1), p.299-299, Article 299
Hauptverfasser: Molina Collada, Juan, Lopez Gloria, Katerine, Castrejon, Isabel, Nieto-Gonzalez, Juan Carlos, Rivera, Javier, Montero, Fernando, Gonzalez, Carlos, Alvaro-Gracia, Jose Maria
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container_end_page 299
container_issue 1
container_start_page 299
container_title Arthritis research & therapy
container_volume 23
creator Molina Collada, Juan
Lopez Gloria, Katerine
Castrejon, Isabel
Nieto-Gonzalez, Juan Carlos
Rivera, Javier
Montero, Fernando
Gonzalez, Carlos
Alvaro-Gracia, Jose Maria
description Objective To determine the usefulness of power Doppler (PD) ultrasound (US) to predict rheumatoid arthritis (RA) development in patients with clinically suspect arthralgia (CSA). Methods Retrospective analysis of a US unit cohort over a 1-year period. Patients with CSA and no previous diagnosis of inflammatory arthritis (IA) were included for analysis. All underwent bilateral US examination of the hands and/or feet according to the EULAR guidelines. Active US inflammation was defined as PD synovitis and/or tenosynovitis >= 1 at any location. RA diagnosis according to clinician criteria 6 months after the US examination was checked. Univariate and multivariate logistic regression models were employed to investigate possible predictive factors of RA development. Results A total of 110 CSA patients (80 females, mean age 53.6 years) were included for analysis. After 6 months of follow-up, 14 (12.7%) developed RA and 34 (30.9%) IA. US active inflammation was present in 38 (34.5%) patients (28.2% showed PD synovitis and 18.2% PD tenosynovitis). Multivariate analysis showed that ACPA (OR 1.0003; 95% CI 1.002-1.006) and ESR (OR 1.054; 95% CI 1.016-1.094) were significantly associated with the detection of US active inflammation at baseline. Only PD tenosynovitis was found to be an independent predictive factor of an evolution towards RA (OR 6.982; 95% CI 1.106-44.057) and IA (OR 5.360; 95% CI 1.012-28.390). Conclusion US is able to detect features of subclinical inflammation in CSA patients, especially in those with higher ESR and ACPA values. Only PD tenosynovitis at baseline US assessment was found to be an independent predictor of RA and IA development in CSA patients.
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Methods Retrospective analysis of a US unit cohort over a 1-year period. Patients with CSA and no previous diagnosis of inflammatory arthritis (IA) were included for analysis. All underwent bilateral US examination of the hands and/or feet according to the EULAR guidelines. Active US inflammation was defined as PD synovitis and/or tenosynovitis &gt;= 1 at any location. RA diagnosis according to clinician criteria 6 months after the US examination was checked. Univariate and multivariate logistic regression models were employed to investigate possible predictive factors of RA development. Results A total of 110 CSA patients (80 females, mean age 53.6 years) were included for analysis. After 6 months of follow-up, 14 (12.7%) developed RA and 34 (30.9%) IA. US active inflammation was present in 38 (34.5%) patients (28.2% showed PD synovitis and 18.2% PD tenosynovitis). Multivariate analysis showed that ACPA (OR 1.0003; 95% CI 1.002-1.006) and ESR (OR 1.054; 95% CI 1.016-1.094) were significantly associated with the detection of US active inflammation at baseline. Only PD tenosynovitis was found to be an independent predictive factor of an evolution towards RA (OR 6.982; 95% CI 1.106-44.057) and IA (OR 5.360; 95% CI 1.012-28.390). Conclusion US is able to detect features of subclinical inflammation in CSA patients, especially in those with higher ESR and ACPA values. Only PD tenosynovitis at baseline US assessment was found to be an independent predictor of RA and IA development in CSA patients.</description><identifier>ISSN: 1478-6354</identifier><identifier>ISSN: 1478-6362</identifier><identifier>EISSN: 1478-6362</identifier><identifier>DOI: 10.1186/s13075-021-02685-7</identifier><identifier>PMID: 34876221</identifier><language>eng</language><publisher>LONDON: Springer Nature</publisher><subject>Antirheumatic agents ; Arthralgia ; Arthritis ; Clinically suspect arthralgia ; Complications and side effects ; Connective tissue ; Demographics ; Development and progression ; Diagnosis ; Disease ; Dosage and administration ; Inflammation ; Life Sciences &amp; Biomedicine ; Outpatient care facilities ; Power Doppler ; Rheumatoid arthritis ; Rheumatology ; Science &amp; Technology ; Tenosynovitis ; Ultrasonic imaging ; Ultrasound</subject><ispartof>Arthritis research &amp; therapy, 2021-12, Vol.23 (1), p.299-299, Article 299</ispartof><rights>2021. The Author(s).</rights><rights>COPYRIGHT 2021 BioMed Central Ltd.</rights><rights>2021. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s) 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>true</woscitedreferencessubscribed><woscitedreferencescount>9</woscitedreferencescount><woscitedreferencesoriginalsourcerecordid>wos000728329800001</woscitedreferencesoriginalsourcerecordid><citedby>FETCH-LOGICAL-c563t-a4c35a4e77d57c3c8b5c867b98e79bb255bab9c53a7d70321a281517f57719743</citedby><cites>FETCH-LOGICAL-c563t-a4c35a4e77d57c3c8b5c867b98e79bb255bab9c53a7d70321a281517f57719743</cites><orcidid>0000-0003-4594-7663 ; 0000-0001-5511-8274 ; 0000-0001-5191-7802</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8653555/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8653555/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,315,728,781,785,865,886,2103,2115,27928,27929,53795,53797</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34876221$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Molina Collada, Juan</creatorcontrib><creatorcontrib>Lopez Gloria, Katerine</creatorcontrib><creatorcontrib>Castrejon, Isabel</creatorcontrib><creatorcontrib>Nieto-Gonzalez, Juan Carlos</creatorcontrib><creatorcontrib>Rivera, Javier</creatorcontrib><creatorcontrib>Montero, Fernando</creatorcontrib><creatorcontrib>Gonzalez, Carlos</creatorcontrib><creatorcontrib>Alvaro-Gracia, Jose Maria</creatorcontrib><title>Ultrasound in clinically suspect arthralgia: the role of power Doppler to predict rheumatoid arthritis development</title><title>Arthritis research &amp; therapy</title><addtitle>ARTHRITIS RES THER</addtitle><addtitle>Arthritis Res Ther</addtitle><description>Objective To determine the usefulness of power Doppler (PD) ultrasound (US) to predict rheumatoid arthritis (RA) development in patients with clinically suspect arthralgia (CSA). Methods Retrospective analysis of a US unit cohort over a 1-year period. Patients with CSA and no previous diagnosis of inflammatory arthritis (IA) were included for analysis. All underwent bilateral US examination of the hands and/or feet according to the EULAR guidelines. Active US inflammation was defined as PD synovitis and/or tenosynovitis &gt;= 1 at any location. RA diagnosis according to clinician criteria 6 months after the US examination was checked. Univariate and multivariate logistic regression models were employed to investigate possible predictive factors of RA development. Results A total of 110 CSA patients (80 females, mean age 53.6 years) were included for analysis. After 6 months of follow-up, 14 (12.7%) developed RA and 34 (30.9%) IA. US active inflammation was present in 38 (34.5%) patients (28.2% showed PD synovitis and 18.2% PD tenosynovitis). Multivariate analysis showed that ACPA (OR 1.0003; 95% CI 1.002-1.006) and ESR (OR 1.054; 95% CI 1.016-1.094) were significantly associated with the detection of US active inflammation at baseline. Only PD tenosynovitis was found to be an independent predictive factor of an evolution towards RA (OR 6.982; 95% CI 1.106-44.057) and IA (OR 5.360; 95% CI 1.012-28.390). Conclusion US is able to detect features of subclinical inflammation in CSA patients, especially in those with higher ESR and ACPA values. 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Lopez Gloria, Katerine ; Castrejon, Isabel ; Nieto-Gonzalez, Juan Carlos ; Rivera, Javier ; Montero, Fernando ; Gonzalez, Carlos ; Alvaro-Gracia, Jose Maria</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c563t-a4c35a4e77d57c3c8b5c867b98e79bb255bab9c53a7d70321a281517f57719743</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Antirheumatic agents</topic><topic>Arthralgia</topic><topic>Arthritis</topic><topic>Clinically suspect arthralgia</topic><topic>Complications and side effects</topic><topic>Connective tissue</topic><topic>Demographics</topic><topic>Development and progression</topic><topic>Diagnosis</topic><topic>Disease</topic><topic>Dosage and administration</topic><topic>Inflammation</topic><topic>Life Sciences &amp; Biomedicine</topic><topic>Outpatient care facilities</topic><topic>Power Doppler</topic><topic>Rheumatoid arthritis</topic><topic>Rheumatology</topic><topic>Science &amp; 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Medical Complete (Alumni)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Access via ProQuest (Open Access)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Arthritis research &amp; therapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Molina Collada, Juan</au><au>Lopez Gloria, Katerine</au><au>Castrejon, Isabel</au><au>Nieto-Gonzalez, Juan Carlos</au><au>Rivera, Javier</au><au>Montero, Fernando</au><au>Gonzalez, Carlos</au><au>Alvaro-Gracia, Jose Maria</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ultrasound in clinically suspect arthralgia: the role of power Doppler to predict rheumatoid arthritis development</atitle><jtitle>Arthritis research &amp; therapy</jtitle><stitle>ARTHRITIS RES THER</stitle><addtitle>Arthritis Res Ther</addtitle><date>2021-12-08</date><risdate>2021</risdate><volume>23</volume><issue>1</issue><spage>299</spage><epage>299</epage><pages>299-299</pages><artnum>299</artnum><issn>1478-6354</issn><issn>1478-6362</issn><eissn>1478-6362</eissn><abstract>Objective To determine the usefulness of power Doppler (PD) ultrasound (US) to predict rheumatoid arthritis (RA) development in patients with clinically suspect arthralgia (CSA). Methods Retrospective analysis of a US unit cohort over a 1-year period. Patients with CSA and no previous diagnosis of inflammatory arthritis (IA) were included for analysis. All underwent bilateral US examination of the hands and/or feet according to the EULAR guidelines. Active US inflammation was defined as PD synovitis and/or tenosynovitis &gt;= 1 at any location. RA diagnosis according to clinician criteria 6 months after the US examination was checked. Univariate and multivariate logistic regression models were employed to investigate possible predictive factors of RA development. Results A total of 110 CSA patients (80 females, mean age 53.6 years) were included for analysis. After 6 months of follow-up, 14 (12.7%) developed RA and 34 (30.9%) IA. US active inflammation was present in 38 (34.5%) patients (28.2% showed PD synovitis and 18.2% PD tenosynovitis). Multivariate analysis showed that ACPA (OR 1.0003; 95% CI 1.002-1.006) and ESR (OR 1.054; 95% CI 1.016-1.094) were significantly associated with the detection of US active inflammation at baseline. Only PD tenosynovitis was found to be an independent predictive factor of an evolution towards RA (OR 6.982; 95% CI 1.106-44.057) and IA (OR 5.360; 95% CI 1.012-28.390). Conclusion US is able to detect features of subclinical inflammation in CSA patients, especially in those with higher ESR and ACPA values. Only PD tenosynovitis at baseline US assessment was found to be an independent predictor of RA and IA development in CSA patients.</abstract><cop>LONDON</cop><pub>Springer Nature</pub><pmid>34876221</pmid><doi>10.1186/s13075-021-02685-7</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0003-4594-7663</orcidid><orcidid>https://orcid.org/0000-0001-5511-8274</orcidid><orcidid>https://orcid.org/0000-0001-5191-7802</orcidid><oa>free_for_read</oa></addata></record>
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subjects Antirheumatic agents
Arthralgia
Arthritis
Clinically suspect arthralgia
Complications and side effects
Connective tissue
Demographics
Development and progression
Diagnosis
Disease
Dosage and administration
Inflammation
Life Sciences & Biomedicine
Outpatient care facilities
Power Doppler
Rheumatoid arthritis
Rheumatology
Science & Technology
Tenosynovitis
Ultrasonic imaging
Ultrasound
title Ultrasound in clinically suspect arthralgia: the role of power Doppler to predict rheumatoid arthritis development
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