A multicentre study on high-frequency ultrasound evaluation of the skin and joints in patients with psoriatic arthritis treated with infliximab

Our objective was to describe the ultrasound features of patients with PsA in joints and skin and their changes after treatment with infliximab. Eight hospitals recruited PsA active patients. Clinical (joint count for pain, TJC, and swelling, SJC, pain VAS, ESR, C-reactive protein and PASI) and US v...

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Veröffentlicht in:Clinical and experimental rheumatology 2012-11, Vol.30 (6), p.879-885
Hauptverfasser: DE AGUSTIN, J. J, MORAGUES, C, DE MIGUEL, E, MÖLLER, I, ACEBES, C, NAREDO, E, USON, J, REJON, E, MAYORDOMO, L, GARRIDO, J
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container_issue 6
container_start_page 879
container_title Clinical and experimental rheumatology
container_volume 30
creator DE AGUSTIN, J. J
MORAGUES, C
DE MIGUEL, E
MÖLLER, I
ACEBES, C
NAREDO, E
USON, J
REJON, E
MAYORDOMO, L
GARRIDO, J
description Our objective was to describe the ultrasound features of patients with PsA in joints and skin and their changes after treatment with infliximab. Eight hospitals recruited PsA active patients. Clinical (joint count for pain, TJC, and swelling, SJC, pain VAS, ESR, C-reactive protein and PASI) and US variables (plaque thickness, PD signal of dermal lesions, synovitis, erosions, and PD signal, assessed by 4-category ordinal scales) were independently recorded at baseline and 4, 12 and 24-week after starting treatment with infliximab. The results were analysed with paired T, Wilcoxon test, ANOVA and marginal homogeneity test. Changes in 24 patients from baseline to last available data were significant for clinical variables, pain VAS, TJC and SJC as well as for ESR, CRP (all p
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J ; MORAGUES, C ; DE MIGUEL, E ; MÖLLER, I ; ACEBES, C ; NAREDO, E ; USON, J ; REJON, E ; MAYORDOMO, L ; GARRIDO, J</creator><creatorcontrib>DE AGUSTIN, J. J ; MORAGUES, C ; DE MIGUEL, E ; MÖLLER, I ; ACEBES, C ; NAREDO, E ; USON, J ; REJON, E ; MAYORDOMO, L ; GARRIDO, J</creatorcontrib><description>Our objective was to describe the ultrasound features of patients with PsA in joints and skin and their changes after treatment with infliximab. Eight hospitals recruited PsA active patients. Clinical (joint count for pain, TJC, and swelling, SJC, pain VAS, ESR, C-reactive protein and PASI) and US variables (plaque thickness, PD signal of dermal lesions, synovitis, erosions, and PD signal, assessed by 4-category ordinal scales) were independently recorded at baseline and 4, 12 and 24-week after starting treatment with infliximab. The results were analysed with paired T, Wilcoxon test, ANOVA and marginal homogeneity test. Changes in 24 patients from baseline to last available data were significant for clinical variables, pain VAS, TJC and SJC as well as for ESR, CRP (all p&lt;0.0005). Dermatological PASI changed from 14.6±14.9 to 2.1±4.1 and plaque thickness from 3.34±1.75 mm to 1.74±0.96 mm (both p&lt;0.0005); synovitis and PD signal improved (both p&lt;0.0005). Psoriatic plaque PD improved across the study (p&lt;0.0005) with no signal increasing from 36.4% to 88.9% and positive PD signal decreasing from 63.6% to 11.1% of the plaques. Treatment with anti-TNF-α infliximab improves the symptoms of patients with PsA at joint and psoriatic skin levels from a clinical and ultrasonographic perspective.</description><identifier>ISSN: 0392-856X</identifier><identifier>EISSN: 1593-098X</identifier><identifier>PMID: 23020866</identifier><language>eng</language><publisher>Pisa: Clinical and Experimental Rheumatology</publisher><subject>Adult ; Anti-Inflammatory Agents - therapeutic use ; Antibodies, Monoclonal - therapeutic use ; Arthritis, Psoriatic - diagnostic imaging ; Arthritis, Psoriatic - drug therapy ; Arthritis, Psoriatic - pathology ; Biological and medical sciences ; Dermatology ; Diseases of the osteoarticular system ; Diseases of the spine ; Female ; Humans ; Inflammatory joint diseases ; Infliximab ; Joints - diagnostic imaging ; Joints - drug effects ; Joints - pathology ; Male ; Medical sciences ; Middle Aged ; Multivariate Analysis ; Observer Variation ; Predictive Value of Tests ; Prospective Studies ; Psoriasis. 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J</creatorcontrib><creatorcontrib>MORAGUES, C</creatorcontrib><creatorcontrib>DE MIGUEL, E</creatorcontrib><creatorcontrib>MÖLLER, I</creatorcontrib><creatorcontrib>ACEBES, C</creatorcontrib><creatorcontrib>NAREDO, E</creatorcontrib><creatorcontrib>USON, J</creatorcontrib><creatorcontrib>REJON, E</creatorcontrib><creatorcontrib>MAYORDOMO, L</creatorcontrib><creatorcontrib>GARRIDO, J</creatorcontrib><title>A multicentre study on high-frequency ultrasound evaluation of the skin and joints in patients with psoriatic arthritis treated with infliximab</title><title>Clinical and experimental rheumatology</title><addtitle>Clin Exp Rheumatol</addtitle><description>Our objective was to describe the ultrasound features of patients with PsA in joints and skin and their changes after treatment with infliximab. Eight hospitals recruited PsA active patients. Clinical (joint count for pain, TJC, and swelling, SJC, pain VAS, ESR, C-reactive protein and PASI) and US variables (plaque thickness, PD signal of dermal lesions, synovitis, erosions, and PD signal, assessed by 4-category ordinal scales) were independently recorded at baseline and 4, 12 and 24-week after starting treatment with infliximab. The results were analysed with paired T, Wilcoxon test, ANOVA and marginal homogeneity test. Changes in 24 patients from baseline to last available data were significant for clinical variables, pain VAS, TJC and SJC as well as for ESR, CRP (all p&lt;0.0005). Dermatological PASI changed from 14.6±14.9 to 2.1±4.1 and plaque thickness from 3.34±1.75 mm to 1.74±0.96 mm (both p&lt;0.0005); synovitis and PD signal improved (both p&lt;0.0005). Psoriatic plaque PD improved across the study (p&lt;0.0005) with no signal increasing from 36.4% to 88.9% and positive PD signal decreasing from 63.6% to 11.1% of the plaques. Treatment with anti-TNF-α infliximab improves the symptoms of patients with PsA at joint and psoriatic skin levels from a clinical and ultrasonographic perspective.</description><subject>Adult</subject><subject>Anti-Inflammatory Agents - therapeutic use</subject><subject>Antibodies, Monoclonal - therapeutic use</subject><subject>Arthritis, Psoriatic - diagnostic imaging</subject><subject>Arthritis, Psoriatic - drug therapy</subject><subject>Arthritis, Psoriatic - pathology</subject><subject>Biological and medical sciences</subject><subject>Dermatology</subject><subject>Diseases of the osteoarticular system</subject><subject>Diseases of the spine</subject><subject>Female</subject><subject>Humans</subject><subject>Inflammatory joint diseases</subject><subject>Infliximab</subject><subject>Joints - diagnostic imaging</subject><subject>Joints - drug effects</subject><subject>Joints - pathology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Multivariate Analysis</subject><subject>Observer Variation</subject><subject>Predictive Value of Tests</subject><subject>Prospective Studies</subject><subject>Psoriasis. Parapsoriasis. Lichen</subject><subject>Reproducibility of Results</subject><subject>Severity of Illness Index</subject><subject>Skin - diagnostic imaging</subject><subject>Skin - drug effects</subject><subject>Skin - pathology</subject><subject>Spain</subject><subject>Time Factors</subject><subject>Treatment Outcome</subject><subject>Ultrasonography, Doppler</subject><subject>Young Adult</subject><issn>0392-856X</issn><issn>1593-098X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpF0MlOwzAQAFALgWhZfgH5gsQlkpc4jo9VxSZV4gJSb9HEcYhL6gTbAfoV_DJGLeLkZZ7HM3OE5lQonhFVro_RnHDFslIU6xk6C2FDCCtEIU_RjHHCSFkUc_S9wNupj1YbF73BIU7NDg8Od_a1y1pv3ifj9A4n4iEMk2uw-YB-gmgTGlocu_TozToMKbQZrIsBp9OYgPndf9rY4TEM3qYbjcHHzttoA06_QTTNHljX9vbLbqG-QCct9MFcHtZz9HJ3-7x8yFZP94_LxSobWU5jprWkQkDOQJqiLg0HRimRWmlVcCGZNCrNAGgKtDUtpa5l3lJQtciVULnk5-hmn3f0Q-oxxGprgzZ9D84MU6gok5xRJQlP9OpAp3prmmr0qVC_q_6GmMD1AUDQ0LcenLbh3xWlSLkI_wEQdn8M</recordid><startdate>20121101</startdate><enddate>20121101</enddate><creator>DE AGUSTIN, J. 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J ; MORAGUES, C ; DE MIGUEL, E ; MÖLLER, I ; ACEBES, C ; NAREDO, E ; USON, J ; REJON, E ; MAYORDOMO, L ; GARRIDO, J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p241t-cc7155a42a7e6b8e3a21107c9c9635727e9098a1e3afb187cb74f1a9b54959473</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Adult</topic><topic>Anti-Inflammatory Agents - therapeutic use</topic><topic>Antibodies, Monoclonal - therapeutic use</topic><topic>Arthritis, Psoriatic - diagnostic imaging</topic><topic>Arthritis, Psoriatic - drug therapy</topic><topic>Arthritis, Psoriatic - pathology</topic><topic>Biological and medical sciences</topic><topic>Dermatology</topic><topic>Diseases of the osteoarticular system</topic><topic>Diseases of the spine</topic><topic>Female</topic><topic>Humans</topic><topic>Inflammatory joint diseases</topic><topic>Infliximab</topic><topic>Joints - diagnostic imaging</topic><topic>Joints - drug effects</topic><topic>Joints - pathology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Multivariate Analysis</topic><topic>Observer Variation</topic><topic>Predictive Value of Tests</topic><topic>Prospective Studies</topic><topic>Psoriasis. 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J</creatorcontrib><creatorcontrib>MORAGUES, C</creatorcontrib><creatorcontrib>DE MIGUEL, E</creatorcontrib><creatorcontrib>MÖLLER, I</creatorcontrib><creatorcontrib>ACEBES, C</creatorcontrib><creatorcontrib>NAREDO, E</creatorcontrib><creatorcontrib>USON, J</creatorcontrib><creatorcontrib>REJON, E</creatorcontrib><creatorcontrib>MAYORDOMO, L</creatorcontrib><creatorcontrib>GARRIDO, J</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical and experimental rheumatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>DE AGUSTIN, J. J</au><au>MORAGUES, C</au><au>DE MIGUEL, E</au><au>MÖLLER, I</au><au>ACEBES, C</au><au>NAREDO, E</au><au>USON, J</au><au>REJON, E</au><au>MAYORDOMO, L</au><au>GARRIDO, J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A multicentre study on high-frequency ultrasound evaluation of the skin and joints in patients with psoriatic arthritis treated with infliximab</atitle><jtitle>Clinical and experimental rheumatology</jtitle><addtitle>Clin Exp Rheumatol</addtitle><date>2012-11-01</date><risdate>2012</risdate><volume>30</volume><issue>6</issue><spage>879</spage><epage>885</epage><pages>879-885</pages><issn>0392-856X</issn><eissn>1593-098X</eissn><abstract>Our objective was to describe the ultrasound features of patients with PsA in joints and skin and their changes after treatment with infliximab. Eight hospitals recruited PsA active patients. Clinical (joint count for pain, TJC, and swelling, SJC, pain VAS, ESR, C-reactive protein and PASI) and US variables (plaque thickness, PD signal of dermal lesions, synovitis, erosions, and PD signal, assessed by 4-category ordinal scales) were independently recorded at baseline and 4, 12 and 24-week after starting treatment with infliximab. The results were analysed with paired T, Wilcoxon test, ANOVA and marginal homogeneity test. Changes in 24 patients from baseline to last available data were significant for clinical variables, pain VAS, TJC and SJC as well as for ESR, CRP (all p&lt;0.0005). Dermatological PASI changed from 14.6±14.9 to 2.1±4.1 and plaque thickness from 3.34±1.75 mm to 1.74±0.96 mm (both p&lt;0.0005); synovitis and PD signal improved (both p&lt;0.0005). Psoriatic plaque PD improved across the study (p&lt;0.0005) with no signal increasing from 36.4% to 88.9% and positive PD signal decreasing from 63.6% to 11.1% of the plaques. Treatment with anti-TNF-α infliximab improves the symptoms of patients with PsA at joint and psoriatic skin levels from a clinical and ultrasonographic perspective.</abstract><cop>Pisa</cop><pub>Clinical and Experimental Rheumatology</pub><pmid>23020866</pmid><tpages>7</tpages></addata></record>
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subjects Adult
Anti-Inflammatory Agents - therapeutic use
Antibodies, Monoclonal - therapeutic use
Arthritis, Psoriatic - diagnostic imaging
Arthritis, Psoriatic - drug therapy
Arthritis, Psoriatic - pathology
Biological and medical sciences
Dermatology
Diseases of the osteoarticular system
Diseases of the spine
Female
Humans
Inflammatory joint diseases
Infliximab
Joints - diagnostic imaging
Joints - drug effects
Joints - pathology
Male
Medical sciences
Middle Aged
Multivariate Analysis
Observer Variation
Predictive Value of Tests
Prospective Studies
Psoriasis. Parapsoriasis. Lichen
Reproducibility of Results
Severity of Illness Index
Skin - diagnostic imaging
Skin - drug effects
Skin - pathology
Spain
Time Factors
Treatment Outcome
Ultrasonography, Doppler
Young Adult
title A multicentre study on high-frequency ultrasound evaluation of the skin and joints in patients with psoriatic arthritis treated with infliximab
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