Outcome Measures in Large Vessel Vasculitis: Relationship Between Patient‐, Physician‐, Imaging‐, and Laboratory‐Based Assessments
Objective To assess the relationship between measures of disease assessment in patients with large vessel vasculitis. Methods Patients with giant cell arteritis (GCA) or Takayasu arteritis (TAK) were recruited into a prospective, observational cohort. Assessments within the following outcomes were i...
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creator | Rimland, Casey A. Quinn, Kaitlin A. Rosenblum, Joel S. Schwartz, Mollie N. Bates Gribbons, K. Novakovich, Elaine Sreih, Antoine G. Merkel, Peter A. Ahlman, Mark A. Grayson, Peter C. |
description | Objective
To assess the relationship between measures of disease assessment in patients with large vessel vasculitis.
Methods
Patients with giant cell arteritis (GCA) or Takayasu arteritis (TAK) were recruited into a prospective, observational cohort. Assessments within the following outcomes were independently recorded: 1) patient‐reported outcomes (Multidimensional Fatigue Inventory, patient global assessment of disease activity [PtGA], Short Form 36 health survey [SF‐36], Brief Illness Perception Questionnaire), 2) physician global assessment of disease activity (PhGA), 3) laboratory outcomes (C‐reactive protein [CRP] level, erythrocyte sedimentation rate [ESR]), and 4) imaging outcomes (PETVAS, a qualitative score of vascular 18F‐fluorodeoxyglucose–positron emission tomography activity).
Results
Analyses were performed on 112 patients (GCA = 56, TAK = 56), over 296 visits, with a median follow‐up of 6 months. Correlation network analysis revealed assessment measures clustered independently by type of outcome. PhGA was centrally linked to all other outcome types, but correlations were modest (ρ = 0.12–0.32; P < 0.05). PETVAS, CRP level, and PtGA were independently associated with clinically active disease. All 4 patient‐reported outcomes strongly correlated with each other (ρ = 0.35–0.60; P < 0.0001). Patient‐reported outcomes were not correlated with PETVAS, and only PtGA correlated with CRP level (ρ = 0.16; P < 0.01). Patients whose clinical assessment changed from active disease to remission (n = 29) had a corresponding significant decrease in ESR, CRP level, and PETVAS at the remission visit. Patients whose clinical assessment changed from remission to active disease (n = 11) had a corresponding significant increase in CRP level and PtGA at the active visit.
Conclusion
Measures of disease assessment in large vessel vasculitis consist of independent, yet complementary, outcomes, supporting the need to develop composite outcome measures or a standard set of measures covering multiple types of outcomes. |
doi_str_mv | 10.1002/acr.24117 |
format | Article |
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To assess the relationship between measures of disease assessment in patients with large vessel vasculitis.
Methods
Patients with giant cell arteritis (GCA) or Takayasu arteritis (TAK) were recruited into a prospective, observational cohort. Assessments within the following outcomes were independently recorded: 1) patient‐reported outcomes (Multidimensional Fatigue Inventory, patient global assessment of disease activity [PtGA], Short Form 36 health survey [SF‐36], Brief Illness Perception Questionnaire), 2) physician global assessment of disease activity (PhGA), 3) laboratory outcomes (C‐reactive protein [CRP] level, erythrocyte sedimentation rate [ESR]), and 4) imaging outcomes (PETVAS, a qualitative score of vascular 18F‐fluorodeoxyglucose–positron emission tomography activity).
Results
Analyses were performed on 112 patients (GCA = 56, TAK = 56), over 296 visits, with a median follow‐up of 6 months. Correlation network analysis revealed assessment measures clustered independently by type of outcome. PhGA was centrally linked to all other outcome types, but correlations were modest (ρ = 0.12–0.32; P < 0.05). PETVAS, CRP level, and PtGA were independently associated with clinically active disease. All 4 patient‐reported outcomes strongly correlated with each other (ρ = 0.35–0.60; P < 0.0001). Patient‐reported outcomes were not correlated with PETVAS, and only PtGA correlated with CRP level (ρ = 0.16; P < 0.01). Patients whose clinical assessment changed from active disease to remission (n = 29) had a corresponding significant decrease in ESR, CRP level, and PETVAS at the remission visit. Patients whose clinical assessment changed from remission to active disease (n = 11) had a corresponding significant increase in CRP level and PtGA at the active visit.
Conclusion
Measures of disease assessment in large vessel vasculitis consist of independent, yet complementary, outcomes, supporting the need to develop composite outcome measures or a standard set of measures covering multiple types of outcomes.</description><identifier>ISSN: 2151-464X</identifier><identifier>EISSN: 2151-4658</identifier><identifier>DOI: 10.1002/acr.24117</identifier><identifier>PMID: 31785185</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>Adult ; Aged ; Arteritis ; Disease Progression ; Erythrocyte sedimentation rate ; Female ; Giant Cell Arteritis - diagnostic imaging ; Humans ; Laboratories ; Male ; Middle Aged ; Outcome Assessment, Health Care ; Patients ; Positron emission tomography ; Prospective Studies ; Remission ; Severity of Illness Index ; Takayasu Arteritis - diagnostic imaging ; Takayasu's disease ; Vasculitis ; Vein & artery diseases ; Young Adult</subject><ispartof>Arthritis care & research (2010), 2020-09, Vol.72 (9), p.1296-1304</ispartof><rights>2019, American College of Rheumatology. This article has been contributed to by US Government employees and their work is in the public domain in the USA.</rights><rights>2020 American College of Rheumatology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5097-751a7317d6c8a89c9d979cd7443ae1af8f4272ee4d7dd958b019ea8ce74e57b33</citedby><cites>FETCH-LOGICAL-c5097-751a7317d6c8a89c9d979cd7443ae1af8f4272ee4d7dd958b019ea8ce74e57b33</cites><orcidid>0000-0002-7864-0185 ; 0000-0002-5187-6921 ; 0000-0002-8269-9438</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Facr.24117$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Facr.24117$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,780,784,885,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31785185$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rimland, Casey A.</creatorcontrib><creatorcontrib>Quinn, Kaitlin A.</creatorcontrib><creatorcontrib>Rosenblum, Joel S.</creatorcontrib><creatorcontrib>Schwartz, Mollie N.</creatorcontrib><creatorcontrib>Bates Gribbons, K.</creatorcontrib><creatorcontrib>Novakovich, Elaine</creatorcontrib><creatorcontrib>Sreih, Antoine G.</creatorcontrib><creatorcontrib>Merkel, Peter A.</creatorcontrib><creatorcontrib>Ahlman, Mark A.</creatorcontrib><creatorcontrib>Grayson, Peter C.</creatorcontrib><title>Outcome Measures in Large Vessel Vasculitis: Relationship Between Patient‐, Physician‐, Imaging‐, and Laboratory‐Based Assessments</title><title>Arthritis care & research (2010)</title><addtitle>Arthritis Care Res (Hoboken)</addtitle><description>Objective
To assess the relationship between measures of disease assessment in patients with large vessel vasculitis.
Methods
Patients with giant cell arteritis (GCA) or Takayasu arteritis (TAK) were recruited into a prospective, observational cohort. Assessments within the following outcomes were independently recorded: 1) patient‐reported outcomes (Multidimensional Fatigue Inventory, patient global assessment of disease activity [PtGA], Short Form 36 health survey [SF‐36], Brief Illness Perception Questionnaire), 2) physician global assessment of disease activity (PhGA), 3) laboratory outcomes (C‐reactive protein [CRP] level, erythrocyte sedimentation rate [ESR]), and 4) imaging outcomes (PETVAS, a qualitative score of vascular 18F‐fluorodeoxyglucose–positron emission tomography activity).
Results
Analyses were performed on 112 patients (GCA = 56, TAK = 56), over 296 visits, with a median follow‐up of 6 months. Correlation network analysis revealed assessment measures clustered independently by type of outcome. PhGA was centrally linked to all other outcome types, but correlations were modest (ρ = 0.12–0.32; P < 0.05). PETVAS, CRP level, and PtGA were independently associated with clinically active disease. All 4 patient‐reported outcomes strongly correlated with each other (ρ = 0.35–0.60; P < 0.0001). Patient‐reported outcomes were not correlated with PETVAS, and only PtGA correlated with CRP level (ρ = 0.16; P < 0.01). Patients whose clinical assessment changed from active disease to remission (n = 29) had a corresponding significant decrease in ESR, CRP level, and PETVAS at the remission visit. Patients whose clinical assessment changed from remission to active disease (n = 11) had a corresponding significant increase in CRP level and PtGA at the active visit.
Conclusion
Measures of disease assessment in large vessel vasculitis consist of independent, yet complementary, outcomes, supporting the need to develop composite outcome measures or a standard set of measures covering multiple types of outcomes.</description><subject>Adult</subject><subject>Aged</subject><subject>Arteritis</subject><subject>Disease Progression</subject><subject>Erythrocyte sedimentation rate</subject><subject>Female</subject><subject>Giant Cell Arteritis - diagnostic imaging</subject><subject>Humans</subject><subject>Laboratories</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Outcome Assessment, Health Care</subject><subject>Patients</subject><subject>Positron emission tomography</subject><subject>Prospective Studies</subject><subject>Remission</subject><subject>Severity of Illness Index</subject><subject>Takayasu Arteritis - diagnostic imaging</subject><subject>Takayasu's disease</subject><subject>Vasculitis</subject><subject>Vein & artery diseases</subject><subject>Young Adult</subject><issn>2151-464X</issn><issn>2151-4658</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kc9uEzEQxlcIRKvSAy-ALHEBibS21469HJDSiD-VglpVUHGzJt5J4mp3HTy7VLlx5sQz8iSYpESAhC8ej3_zzYy-ongs-IngXJ6CTydSCWHuFYdSaDFSY23v72P16aA4Jrrh-ZTS2rJ6WByUwlgtrD4svl0MvY8tsvcINCQkFjo2g7REdo1E2LBrID80oQ_0kl1hA32IHa3Cmp1hf4vYscucwq7_8fX7C3a52lDwAbrt67yFZeiW2xi6OuvOY4I-pk1OnQFhzSa5B1Gb6-lR8WABDeHx3X1UfHzz-sP03Wh28fZ8OpmNvOaVGRktwOQF6rG3YCtf1ZWpfG2UKgEFLOxCSSMRVW3qutJ2zkWFYD0ahdrMy_KoeLXTXQ_zFmufeydo3DqFFtLGRQju758urNwyfnFGjjm3Mgs8uxNI8fOA1Ls2kMemgQ7jQE6WkpdWaW0z-vQf9CYOqcvrOalKq6txdilTz3eUT5Eo4WI_jODul8kum-y2Jmf2yZ_T78nflmbgdAfchgY3_1dyk-nVTvInASW2ag</recordid><startdate>202009</startdate><enddate>202009</enddate><creator>Rimland, Casey A.</creator><creator>Quinn, Kaitlin A.</creator><creator>Rosenblum, Joel S.</creator><creator>Schwartz, Mollie N.</creator><creator>Bates Gribbons, K.</creator><creator>Novakovich, Elaine</creator><creator>Sreih, Antoine G.</creator><creator>Merkel, Peter A.</creator><creator>Ahlman, Mark A.</creator><creator>Grayson, Peter C.</creator><general>Wiley Subscription Services, Inc</general><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>7QP</scope><scope>NAPCQ</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-7864-0185</orcidid><orcidid>https://orcid.org/0000-0002-5187-6921</orcidid><orcidid>https://orcid.org/0000-0002-8269-9438</orcidid></search><sort><creationdate>202009</creationdate><title>Outcome Measures in Large Vessel Vasculitis: Relationship Between Patient‐, Physician‐, Imaging‐, and Laboratory‐Based Assessments</title><author>Rimland, Casey A. ; Quinn, Kaitlin A. ; Rosenblum, Joel S. ; Schwartz, Mollie N. ; Bates Gribbons, K. ; Novakovich, Elaine ; Sreih, Antoine G. ; Merkel, Peter A. ; Ahlman, Mark A. ; Grayson, Peter C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5097-751a7317d6c8a89c9d979cd7443ae1af8f4272ee4d7dd958b019ea8ce74e57b33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Arteritis</topic><topic>Disease Progression</topic><topic>Erythrocyte sedimentation rate</topic><topic>Female</topic><topic>Giant Cell Arteritis - diagnostic imaging</topic><topic>Humans</topic><topic>Laboratories</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Outcome Assessment, Health Care</topic><topic>Patients</topic><topic>Positron emission tomography</topic><topic>Prospective Studies</topic><topic>Remission</topic><topic>Severity of Illness Index</topic><topic>Takayasu Arteritis - diagnostic imaging</topic><topic>Takayasu's disease</topic><topic>Vasculitis</topic><topic>Vein & artery diseases</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rimland, Casey A.</creatorcontrib><creatorcontrib>Quinn, Kaitlin A.</creatorcontrib><creatorcontrib>Rosenblum, Joel S.</creatorcontrib><creatorcontrib>Schwartz, Mollie N.</creatorcontrib><creatorcontrib>Bates Gribbons, K.</creatorcontrib><creatorcontrib>Novakovich, Elaine</creatorcontrib><creatorcontrib>Sreih, Antoine G.</creatorcontrib><creatorcontrib>Merkel, Peter A.</creatorcontrib><creatorcontrib>Ahlman, Mark A.</creatorcontrib><creatorcontrib>Grayson, Peter C.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Nursing & Allied Health Premium</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Arthritis care & research (2010)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rimland, Casey A.</au><au>Quinn, Kaitlin A.</au><au>Rosenblum, Joel S.</au><au>Schwartz, Mollie N.</au><au>Bates Gribbons, K.</au><au>Novakovich, Elaine</au><au>Sreih, Antoine G.</au><au>Merkel, Peter A.</au><au>Ahlman, Mark A.</au><au>Grayson, Peter C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Outcome Measures in Large Vessel Vasculitis: Relationship Between Patient‐, Physician‐, Imaging‐, and Laboratory‐Based Assessments</atitle><jtitle>Arthritis care & research (2010)</jtitle><addtitle>Arthritis Care Res (Hoboken)</addtitle><date>2020-09</date><risdate>2020</risdate><volume>72</volume><issue>9</issue><spage>1296</spage><epage>1304</epage><pages>1296-1304</pages><issn>2151-464X</issn><eissn>2151-4658</eissn><abstract>Objective
To assess the relationship between measures of disease assessment in patients with large vessel vasculitis.
Methods
Patients with giant cell arteritis (GCA) or Takayasu arteritis (TAK) were recruited into a prospective, observational cohort. Assessments within the following outcomes were independently recorded: 1) patient‐reported outcomes (Multidimensional Fatigue Inventory, patient global assessment of disease activity [PtGA], Short Form 36 health survey [SF‐36], Brief Illness Perception Questionnaire), 2) physician global assessment of disease activity (PhGA), 3) laboratory outcomes (C‐reactive protein [CRP] level, erythrocyte sedimentation rate [ESR]), and 4) imaging outcomes (PETVAS, a qualitative score of vascular 18F‐fluorodeoxyglucose–positron emission tomography activity).
Results
Analyses were performed on 112 patients (GCA = 56, TAK = 56), over 296 visits, with a median follow‐up of 6 months. Correlation network analysis revealed assessment measures clustered independently by type of outcome. PhGA was centrally linked to all other outcome types, but correlations were modest (ρ = 0.12–0.32; P < 0.05). PETVAS, CRP level, and PtGA were independently associated with clinically active disease. All 4 patient‐reported outcomes strongly correlated with each other (ρ = 0.35–0.60; P < 0.0001). Patient‐reported outcomes were not correlated with PETVAS, and only PtGA correlated with CRP level (ρ = 0.16; P < 0.01). Patients whose clinical assessment changed from active disease to remission (n = 29) had a corresponding significant decrease in ESR, CRP level, and PETVAS at the remission visit. Patients whose clinical assessment changed from remission to active disease (n = 11) had a corresponding significant increase in CRP level and PtGA at the active visit.
Conclusion
Measures of disease assessment in large vessel vasculitis consist of independent, yet complementary, outcomes, supporting the need to develop composite outcome measures or a standard set of measures covering multiple types of outcomes.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>31785185</pmid><doi>10.1002/acr.24117</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-7864-0185</orcidid><orcidid>https://orcid.org/0000-0002-5187-6921</orcidid><orcidid>https://orcid.org/0000-0002-8269-9438</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adult Aged Arteritis Disease Progression Erythrocyte sedimentation rate Female Giant Cell Arteritis - diagnostic imaging Humans Laboratories Male Middle Aged Outcome Assessment, Health Care Patients Positron emission tomography Prospective Studies Remission Severity of Illness Index Takayasu Arteritis - diagnostic imaging Takayasu's disease Vasculitis Vein & artery diseases Young Adult |
title | Outcome Measures in Large Vessel Vasculitis: Relationship Between Patient‐, Physician‐, Imaging‐, and Laboratory‐Based Assessments |
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