Loading…

Clinical outcomes of patients with active rheumatoid arthritis with normal acute phase reactant values

Aim Despite high clinical disease activity, some patients with active rheumatoid arthritis (RA) have normal acute phase reactant (APR) values. This study aimed to determine the clinical outcomes of active RA patients with normal APR values. Method Of 5376 patients with RA enrolled in the Korean obse...

Full description

Saved in:
Bibliographic Details
Published in:International journal of rheumatic diseases 2019-05, Vol.22 (5), p.852-859
Main Authors: Chung, Min Kyung, Park, Bohyun, Kim, In Je, Cho, Soo‐Kyung, Kim, Dam, Sung, Yoon‐Kyoung, Choi, Chan‐Bum, Choe, Jung‐Yoon, Chung, Won Tae, Hong, Seung‐Jae, Kim, Tae‐Hwan, Koh, Eunmi, Lee, Shin‐Seok, Yoon, Bo Young, Park, Hyesook, Bae, Sang‐Cheol, Lee, Jisoo
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by
cites cdi_FETCH-LOGICAL-c3259-5e53fb72be8087daa3bd8d17bd13635e2c4d7d6d72e9ea4af925741cf3c7cfe73
container_end_page 859
container_issue 5
container_start_page 852
container_title International journal of rheumatic diseases
container_volume 22
creator Chung, Min Kyung
Park, Bohyun
Kim, In Je
Cho, Soo‐Kyung
Kim, Dam
Sung, Yoon‐Kyoung
Choi, Chan‐Bum
Choe, Jung‐Yoon
Chung, Won Tae
Hong, Seung‐Jae
Kim, Tae‐Hwan
Koh, Eunmi
Lee, Shin‐Seok
Yoon, Bo Young
Park, Hyesook
Bae, Sang‐Cheol
Lee, Jisoo
description Aim Despite high clinical disease activity, some patients with active rheumatoid arthritis (RA) have normal acute phase reactant (APR) values. This study aimed to determine the clinical outcomes of active RA patients with normal APR values. Method Of 5376 patients with RA enrolled in the Korean observational study network for arthritis (KORONA) registry, 400 patients with disease duration of 2.8 at baseline, biologic‐naïve, and erythrocyte sedimentation rate (ESR) and C‐reactive protein (CRP) drawn at both baseline and 2‐year follow‐up visits were identified. Patients were grouped according to baseline APR levels: normal APRs, one APR elevated, and both APRs elevated. Results Baseline tender and swollen joint counts, mean CDAI and Health Assessment Questionnaire‐Disability Index (HAQ‐DI) scores were significantly lower in the normal APRs group compared with APR‐elevated groups (P 
doi_str_mv 10.1111/1756-185X.13469
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2179450083</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2179450083</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3259-5e53fb72be8087daa3bd8d17bd13635e2c4d7d6d72e9ea4af925741cf3c7cfe73</originalsourceid><addsrcrecordid>eNqFkbtLBDEQh4Movms7CdjYnOax2eyWcviCAy0U7EI2meUiu5szyXr435vzzitsTJMQvvlm-A1CZ5Rc0XyuqRTlhFbi7Yryoqx30OH2Z3f7LugBOorxnZCS8lLuowNOSikZrw9RO-3c4IzusB-T8T1E7Fu80MnBkCJeujTH2iT3CTjMYex18s5iHdI8uOQ2wOBDnw3ajAnwYq5jhiFX6SHhT92NEE_QXqu7CKeb-xi93t2-TB8ms6f7x-nNbGI4E_VEgOBtI1kDFamk1Zo3trJUNjYPzgUwU1hpSysZ1KAL3dZMyIKalhtpWpD8GF2uvYvgP3LfpHoXDXSdHsCPUTEq60IQUvGMXvxB3_0YhjydYoyRsi4FJ5m6XlMm-BgDtGoRXK_Dl6JErVagViGrVeDqZwW54nzjHZse7Jb_zTwDYg0sXQdf__nUzfNsLf4G9COSeA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2220696530</pqid></control><display><type>article</type><title>Clinical outcomes of patients with active rheumatoid arthritis with normal acute phase reactant values</title><source>Wiley-Blackwell Read &amp; Publish Collection</source><creator>Chung, Min Kyung ; Park, Bohyun ; Kim, In Je ; Cho, Soo‐Kyung ; Kim, Dam ; Sung, Yoon‐Kyoung ; Choi, Chan‐Bum ; Choe, Jung‐Yoon ; Chung, Won Tae ; Hong, Seung‐Jae ; Kim, Tae‐Hwan ; Koh, Eunmi ; Lee, Shin‐Seok ; Yoon, Bo Young ; Park, Hyesook ; Bae, Sang‐Cheol ; Lee, Jisoo</creator><creatorcontrib>Chung, Min Kyung ; Park, Bohyun ; Kim, In Je ; Cho, Soo‐Kyung ; Kim, Dam ; Sung, Yoon‐Kyoung ; Choi, Chan‐Bum ; Choe, Jung‐Yoon ; Chung, Won Tae ; Hong, Seung‐Jae ; Kim, Tae‐Hwan ; Koh, Eunmi ; Lee, Shin‐Seok ; Yoon, Bo Young ; Park, Hyesook ; Bae, Sang‐Cheol ; Lee, Jisoo</creatorcontrib><description>Aim Despite high clinical disease activity, some patients with active rheumatoid arthritis (RA) have normal acute phase reactant (APR) values. This study aimed to determine the clinical outcomes of active RA patients with normal APR values. Method Of 5376 patients with RA enrolled in the Korean observational study network for arthritis (KORONA) registry, 400 patients with disease duration of &lt;2 years who had Clinical Disease Activity Index (CDAI) score of &gt;2.8 at baseline, biologic‐naïve, and erythrocyte sedimentation rate (ESR) and C‐reactive protein (CRP) drawn at both baseline and 2‐year follow‐up visits were identified. Patients were grouped according to baseline APR levels: normal APRs, one APR elevated, and both APRs elevated. Results Baseline tender and swollen joint counts, mean CDAI and Health Assessment Questionnaire‐Disability Index (HAQ‐DI) scores were significantly lower in the normal APRs group compared with APR‐elevated groups (P &lt; 0.0001). At 2‐year follow‐up, mean CDAI scores, HAQ‐DI, and percentage of the patient achieving remission were not significantly different between the normal APRs group compared with the APR‐elevated groups regardless of the baseline disease activity. However, in patients with baseline CDAI moderate to high disease activity, the normal APRs group less frequently required initiation of the biologic disease‐modifying anti‐rheumatic drugs compared with the APR‐elevated groups (P = 0.044). Conclusion Active RA patients with normal APR values have milder disease presentation, but similar clinical outcomes to those with elevated APRs.</description><identifier>ISSN: 1756-1841</identifier><identifier>EISSN: 1756-185X</identifier><identifier>DOI: 10.1111/1756-185X.13469</identifier><identifier>PMID: 30677239</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>active ; Acute-Phase Proteins - analysis ; acute‐phase protein ; Antirheumatic Agents - adverse effects ; Antirheumatic Agents - therapeutic use ; Arthritis, Rheumatoid - blood ; Arthritis, Rheumatoid - diagnosis ; Arthritis, Rheumatoid - drug therapy ; Biological Products - adverse effects ; Biological Products - therapeutic use ; Biomarkers - blood ; Clinical outcomes ; Disability Evaluation ; Erythrocyte sedimentation rate ; Female ; Health risk assessment ; Humans ; Male ; Middle Aged ; normal ; Registries ; Remission ; Republic of Korea ; Rheumatoid arthritis ; Severity of Illness Index ; Time Factors ; Treatment Outcome</subject><ispartof>International journal of rheumatic diseases, 2019-05, Vol.22 (5), p.852-859</ispartof><rights>2019 Asia Pacific League of Associations for Rheumatology and John Wiley &amp; Sons Australia, Ltd</rights><rights>2019 Asia Pacific League of Associations for Rheumatology and John Wiley &amp; Sons Australia, Ltd.</rights><rights>International Journal of Rheumatic Diseases © 2019 Asia Pacific League of Associations for Rheumatology and John Wiley &amp; Sons Australia, Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3259-5e53fb72be8087daa3bd8d17bd13635e2c4d7d6d72e9ea4af925741cf3c7cfe73</cites><orcidid>0000-0002-1585-1022 ; 0000-0002-9635-4799 ; 0000-0001-6279-7025 ; 0000-0003-0957-0395 ; 0000-0002-5286-0593 ; 0000-0002-4691-5455 ; 0000-0002-9359-6522 ; 0000-0002-8538-9662 ; 0000-0002-3689-1226 ; 0000-0002-3542-2276 ; 0000-0001-6414-9187 ; 0000-0001-6691-8939 ; 0000-0003-4493-8837 ; 0000-0002-9803-529X ; 0000-0001-6810-7355 ; 0000-0003-4658-1093</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30677239$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chung, Min Kyung</creatorcontrib><creatorcontrib>Park, Bohyun</creatorcontrib><creatorcontrib>Kim, In Je</creatorcontrib><creatorcontrib>Cho, Soo‐Kyung</creatorcontrib><creatorcontrib>Kim, Dam</creatorcontrib><creatorcontrib>Sung, Yoon‐Kyoung</creatorcontrib><creatorcontrib>Choi, Chan‐Bum</creatorcontrib><creatorcontrib>Choe, Jung‐Yoon</creatorcontrib><creatorcontrib>Chung, Won Tae</creatorcontrib><creatorcontrib>Hong, Seung‐Jae</creatorcontrib><creatorcontrib>Kim, Tae‐Hwan</creatorcontrib><creatorcontrib>Koh, Eunmi</creatorcontrib><creatorcontrib>Lee, Shin‐Seok</creatorcontrib><creatorcontrib>Yoon, Bo Young</creatorcontrib><creatorcontrib>Park, Hyesook</creatorcontrib><creatorcontrib>Bae, Sang‐Cheol</creatorcontrib><creatorcontrib>Lee, Jisoo</creatorcontrib><title>Clinical outcomes of patients with active rheumatoid arthritis with normal acute phase reactant values</title><title>International journal of rheumatic diseases</title><addtitle>Int J Rheum Dis</addtitle><description>Aim Despite high clinical disease activity, some patients with active rheumatoid arthritis (RA) have normal acute phase reactant (APR) values. This study aimed to determine the clinical outcomes of active RA patients with normal APR values. Method Of 5376 patients with RA enrolled in the Korean observational study network for arthritis (KORONA) registry, 400 patients with disease duration of &lt;2 years who had Clinical Disease Activity Index (CDAI) score of &gt;2.8 at baseline, biologic‐naïve, and erythrocyte sedimentation rate (ESR) and C‐reactive protein (CRP) drawn at both baseline and 2‐year follow‐up visits were identified. Patients were grouped according to baseline APR levels: normal APRs, one APR elevated, and both APRs elevated. Results Baseline tender and swollen joint counts, mean CDAI and Health Assessment Questionnaire‐Disability Index (HAQ‐DI) scores were significantly lower in the normal APRs group compared with APR‐elevated groups (P &lt; 0.0001). At 2‐year follow‐up, mean CDAI scores, HAQ‐DI, and percentage of the patient achieving remission were not significantly different between the normal APRs group compared with the APR‐elevated groups regardless of the baseline disease activity. However, in patients with baseline CDAI moderate to high disease activity, the normal APRs group less frequently required initiation of the biologic disease‐modifying anti‐rheumatic drugs compared with the APR‐elevated groups (P = 0.044). Conclusion Active RA patients with normal APR values have milder disease presentation, but similar clinical outcomes to those with elevated APRs.</description><subject>active</subject><subject>Acute-Phase Proteins - analysis</subject><subject>acute‐phase protein</subject><subject>Antirheumatic Agents - adverse effects</subject><subject>Antirheumatic Agents - therapeutic use</subject><subject>Arthritis, Rheumatoid - blood</subject><subject>Arthritis, Rheumatoid - diagnosis</subject><subject>Arthritis, Rheumatoid - drug therapy</subject><subject>Biological Products - adverse effects</subject><subject>Biological Products - therapeutic use</subject><subject>Biomarkers - blood</subject><subject>Clinical outcomes</subject><subject>Disability Evaluation</subject><subject>Erythrocyte sedimentation rate</subject><subject>Female</subject><subject>Health risk assessment</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>normal</subject><subject>Registries</subject><subject>Remission</subject><subject>Republic of Korea</subject><subject>Rheumatoid arthritis</subject><subject>Severity of Illness Index</subject><subject>Time Factors</subject><subject>Treatment Outcome</subject><issn>1756-1841</issn><issn>1756-185X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNqFkbtLBDEQh4Movms7CdjYnOax2eyWcviCAy0U7EI2meUiu5szyXr435vzzitsTJMQvvlm-A1CZ5Rc0XyuqRTlhFbi7Yryoqx30OH2Z3f7LugBOorxnZCS8lLuowNOSikZrw9RO-3c4IzusB-T8T1E7Fu80MnBkCJeujTH2iT3CTjMYex18s5iHdI8uOQ2wOBDnw3ajAnwYq5jhiFX6SHhT92NEE_QXqu7CKeb-xi93t2-TB8ms6f7x-nNbGI4E_VEgOBtI1kDFamk1Zo3trJUNjYPzgUwU1hpSysZ1KAL3dZMyIKalhtpWpD8GF2uvYvgP3LfpHoXDXSdHsCPUTEq60IQUvGMXvxB3_0YhjydYoyRsi4FJ5m6XlMm-BgDtGoRXK_Dl6JErVagViGrVeDqZwW54nzjHZse7Jb_zTwDYg0sXQdf__nUzfNsLf4G9COSeA</recordid><startdate>201905</startdate><enddate>201905</enddate><creator>Chung, Min Kyung</creator><creator>Park, Bohyun</creator><creator>Kim, In Je</creator><creator>Cho, Soo‐Kyung</creator><creator>Kim, Dam</creator><creator>Sung, Yoon‐Kyoung</creator><creator>Choi, Chan‐Bum</creator><creator>Choe, Jung‐Yoon</creator><creator>Chung, Won Tae</creator><creator>Hong, Seung‐Jae</creator><creator>Kim, Tae‐Hwan</creator><creator>Koh, Eunmi</creator><creator>Lee, Shin‐Seok</creator><creator>Yoon, Bo Young</creator><creator>Park, Hyesook</creator><creator>Bae, Sang‐Cheol</creator><creator>Lee, Jisoo</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>7T5</scope><scope>H94</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-1585-1022</orcidid><orcidid>https://orcid.org/0000-0002-9635-4799</orcidid><orcidid>https://orcid.org/0000-0001-6279-7025</orcidid><orcidid>https://orcid.org/0000-0003-0957-0395</orcidid><orcidid>https://orcid.org/0000-0002-5286-0593</orcidid><orcidid>https://orcid.org/0000-0002-4691-5455</orcidid><orcidid>https://orcid.org/0000-0002-9359-6522</orcidid><orcidid>https://orcid.org/0000-0002-8538-9662</orcidid><orcidid>https://orcid.org/0000-0002-3689-1226</orcidid><orcidid>https://orcid.org/0000-0002-3542-2276</orcidid><orcidid>https://orcid.org/0000-0001-6414-9187</orcidid><orcidid>https://orcid.org/0000-0001-6691-8939</orcidid><orcidid>https://orcid.org/0000-0003-4493-8837</orcidid><orcidid>https://orcid.org/0000-0002-9803-529X</orcidid><orcidid>https://orcid.org/0000-0001-6810-7355</orcidid><orcidid>https://orcid.org/0000-0003-4658-1093</orcidid></search><sort><creationdate>201905</creationdate><title>Clinical outcomes of patients with active rheumatoid arthritis with normal acute phase reactant values</title><author>Chung, Min Kyung ; Park, Bohyun ; Kim, In Je ; Cho, Soo‐Kyung ; Kim, Dam ; Sung, Yoon‐Kyoung ; Choi, Chan‐Bum ; Choe, Jung‐Yoon ; Chung, Won Tae ; Hong, Seung‐Jae ; Kim, Tae‐Hwan ; Koh, Eunmi ; Lee, Shin‐Seok ; Yoon, Bo Young ; Park, Hyesook ; Bae, Sang‐Cheol ; Lee, Jisoo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3259-5e53fb72be8087daa3bd8d17bd13635e2c4d7d6d72e9ea4af925741cf3c7cfe73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>active</topic><topic>Acute-Phase Proteins - analysis</topic><topic>acute‐phase protein</topic><topic>Antirheumatic Agents - adverse effects</topic><topic>Antirheumatic Agents - therapeutic use</topic><topic>Arthritis, Rheumatoid - blood</topic><topic>Arthritis, Rheumatoid - diagnosis</topic><topic>Arthritis, Rheumatoid - drug therapy</topic><topic>Biological Products - adverse effects</topic><topic>Biological Products - therapeutic use</topic><topic>Biomarkers - blood</topic><topic>Clinical outcomes</topic><topic>Disability Evaluation</topic><topic>Erythrocyte sedimentation rate</topic><topic>Female</topic><topic>Health risk assessment</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>normal</topic><topic>Registries</topic><topic>Remission</topic><topic>Republic of Korea</topic><topic>Rheumatoid arthritis</topic><topic>Severity of Illness Index</topic><topic>Time Factors</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chung, Min Kyung</creatorcontrib><creatorcontrib>Park, Bohyun</creatorcontrib><creatorcontrib>Kim, In Je</creatorcontrib><creatorcontrib>Cho, Soo‐Kyung</creatorcontrib><creatorcontrib>Kim, Dam</creatorcontrib><creatorcontrib>Sung, Yoon‐Kyoung</creatorcontrib><creatorcontrib>Choi, Chan‐Bum</creatorcontrib><creatorcontrib>Choe, Jung‐Yoon</creatorcontrib><creatorcontrib>Chung, Won Tae</creatorcontrib><creatorcontrib>Hong, Seung‐Jae</creatorcontrib><creatorcontrib>Kim, Tae‐Hwan</creatorcontrib><creatorcontrib>Koh, Eunmi</creatorcontrib><creatorcontrib>Lee, Shin‐Seok</creatorcontrib><creatorcontrib>Yoon, Bo Young</creatorcontrib><creatorcontrib>Park, Hyesook</creatorcontrib><creatorcontrib>Bae, Sang‐Cheol</creatorcontrib><creatorcontrib>Lee, Jisoo</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 &amp; Calcified Tissue Abstracts</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>International journal of rheumatic diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chung, Min Kyung</au><au>Park, Bohyun</au><au>Kim, In Je</au><au>Cho, Soo‐Kyung</au><au>Kim, Dam</au><au>Sung, Yoon‐Kyoung</au><au>Choi, Chan‐Bum</au><au>Choe, Jung‐Yoon</au><au>Chung, Won Tae</au><au>Hong, Seung‐Jae</au><au>Kim, Tae‐Hwan</au><au>Koh, Eunmi</au><au>Lee, Shin‐Seok</au><au>Yoon, Bo Young</au><au>Park, Hyesook</au><au>Bae, Sang‐Cheol</au><au>Lee, Jisoo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Clinical outcomes of patients with active rheumatoid arthritis with normal acute phase reactant values</atitle><jtitle>International journal of rheumatic diseases</jtitle><addtitle>Int J Rheum Dis</addtitle><date>2019-05</date><risdate>2019</risdate><volume>22</volume><issue>5</issue><spage>852</spage><epage>859</epage><pages>852-859</pages><issn>1756-1841</issn><eissn>1756-185X</eissn><abstract>Aim Despite high clinical disease activity, some patients with active rheumatoid arthritis (RA) have normal acute phase reactant (APR) values. This study aimed to determine the clinical outcomes of active RA patients with normal APR values. Method Of 5376 patients with RA enrolled in the Korean observational study network for arthritis (KORONA) registry, 400 patients with disease duration of &lt;2 years who had Clinical Disease Activity Index (CDAI) score of &gt;2.8 at baseline, biologic‐naïve, and erythrocyte sedimentation rate (ESR) and C‐reactive protein (CRP) drawn at both baseline and 2‐year follow‐up visits were identified. Patients were grouped according to baseline APR levels: normal APRs, one APR elevated, and both APRs elevated. Results Baseline tender and swollen joint counts, mean CDAI and Health Assessment Questionnaire‐Disability Index (HAQ‐DI) scores were significantly lower in the normal APRs group compared with APR‐elevated groups (P &lt; 0.0001). At 2‐year follow‐up, mean CDAI scores, HAQ‐DI, and percentage of the patient achieving remission were not significantly different between the normal APRs group compared with the APR‐elevated groups regardless of the baseline disease activity. However, in patients with baseline CDAI moderate to high disease activity, the normal APRs group less frequently required initiation of the biologic disease‐modifying anti‐rheumatic drugs compared with the APR‐elevated groups (P = 0.044). Conclusion Active RA patients with normal APR values have milder disease presentation, but similar clinical outcomes to those with elevated APRs.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>30677239</pmid><doi>10.1111/1756-185X.13469</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-1585-1022</orcidid><orcidid>https://orcid.org/0000-0002-9635-4799</orcidid><orcidid>https://orcid.org/0000-0001-6279-7025</orcidid><orcidid>https://orcid.org/0000-0003-0957-0395</orcidid><orcidid>https://orcid.org/0000-0002-5286-0593</orcidid><orcidid>https://orcid.org/0000-0002-4691-5455</orcidid><orcidid>https://orcid.org/0000-0002-9359-6522</orcidid><orcidid>https://orcid.org/0000-0002-8538-9662</orcidid><orcidid>https://orcid.org/0000-0002-3689-1226</orcidid><orcidid>https://orcid.org/0000-0002-3542-2276</orcidid><orcidid>https://orcid.org/0000-0001-6414-9187</orcidid><orcidid>https://orcid.org/0000-0001-6691-8939</orcidid><orcidid>https://orcid.org/0000-0003-4493-8837</orcidid><orcidid>https://orcid.org/0000-0002-9803-529X</orcidid><orcidid>https://orcid.org/0000-0001-6810-7355</orcidid><orcidid>https://orcid.org/0000-0003-4658-1093</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 1756-1841
ispartof International journal of rheumatic diseases, 2019-05, Vol.22 (5), p.852-859
issn 1756-1841
1756-185X
language eng
recordid cdi_proquest_miscellaneous_2179450083
source Wiley-Blackwell Read & Publish Collection
subjects active
Acute-Phase Proteins - analysis
acute‐phase protein
Antirheumatic Agents - adverse effects
Antirheumatic Agents - therapeutic use
Arthritis, Rheumatoid - blood
Arthritis, Rheumatoid - diagnosis
Arthritis, Rheumatoid - drug therapy
Biological Products - adverse effects
Biological Products - therapeutic use
Biomarkers - blood
Clinical outcomes
Disability Evaluation
Erythrocyte sedimentation rate
Female
Health risk assessment
Humans
Male
Middle Aged
normal
Registries
Remission
Republic of Korea
Rheumatoid arthritis
Severity of Illness Index
Time Factors
Treatment Outcome
title Clinical outcomes of patients with active rheumatoid arthritis with normal acute phase reactant values
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-01T06%3A19%3A57IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Clinical%20outcomes%20of%20patients%20with%20active%20rheumatoid%20arthritis%20with%20normal%20acute%20phase%20reactant%20values&rft.jtitle=International%20journal%20of%20rheumatic%20diseases&rft.au=Chung,%20Min%20Kyung&rft.date=2019-05&rft.volume=22&rft.issue=5&rft.spage=852&rft.epage=859&rft.pages=852-859&rft.issn=1756-1841&rft.eissn=1756-185X&rft_id=info:doi/10.1111/1756-185X.13469&rft_dat=%3Cproquest_cross%3E2179450083%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c3259-5e53fb72be8087daa3bd8d17bd13635e2c4d7d6d72e9ea4af925741cf3c7cfe73%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2220696530&rft_id=info:pmid/30677239&rfr_iscdi=true