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Concordance between the tuberculin skin test and interferon gamma release assay (IGRA) for diagnosing latent tuberculosis infection in patients with systemic lupus erythematosus and patient characteristics associated with an indeterminate IGRA

Objective We investigated the agreement between the tuberculin skin test (TST) and the QuantiFERON-TB gold (QFT-G) assay in the diagnosis of latent tuberculosis infection (LTBI) in patients with systemic lupus erythematosus (SLE). Furthermore, we evaluated the factors associated with indeterminate r...

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Published in:Lupus 2016-10, Vol.25 (12), p.1341-1348
Main Authors: Cho, H, Kim, Y W, Suh, C-H, Jung, J-Y, Um, Y-J, Jung, J-H, Kim, H-A
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Kim, Y W
Suh, C-H
Jung, J-Y
Um, Y-J
Jung, J-H
Kim, H-A
description Objective We investigated the agreement between the tuberculin skin test (TST) and the QuantiFERON-TB gold (QFT-G) assay in the diagnosis of latent tuberculosis infection (LTBI) in patients with systemic lupus erythematosus (SLE). Furthermore, we evaluated the factors associated with indeterminate results in the QFT-G assay in patients with SLE. Methods We enrolled 136 patients with SLE prospectively, and compared them to 66 patients with rheumatoid arthritis (RA). In addition to the TST, QFT-G assay, patients’ medications, and Bacillus Calmette-Guérin (BCG) vaccination status were also investigated. A positive TST or QFT-G assay result without an active tuberculosis lesion on chest x-ray was considered to indicate a diagnosis of LTBI. Results The prevalence of LTBI was 26.5% in patients with SLE and 30.3% in patients with RA. The agreement between the TST and QFT-G assay was fair in SLE patients, but poor in RA patients. BCG vaccination was one factor associated with discordance between TST and QFT-G. Older age and higher SLE Disease Activity Index (SLEDAI) score were associated with a negative TST/positive QFT-G result in patients with SLE. Higher SLEDAI score and increased glucocorticoid dose were associated with an indeterminate result in the QFT-G assay for patients with SLE. Conclusions Agreement between the QFT-G assay and TST in patients with SLE was found to be fair. However, BCG vaccination status, age, and SLEDAI score are all factors that could result in discordance between the two tests. Indeterminate results from the QFT-G assay may be caused by a higher SLEDAI score or increased glucocorticoid dose.
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Furthermore, we evaluated the factors associated with indeterminate results in the QFT-G assay in patients with SLE. Methods We enrolled 136 patients with SLE prospectively, and compared them to 66 patients with rheumatoid arthritis (RA). In addition to the TST, QFT-G assay, patients’ medications, and Bacillus Calmette-Guérin (BCG) vaccination status were also investigated. A positive TST or QFT-G assay result without an active tuberculosis lesion on chest x-ray was considered to indicate a diagnosis of LTBI. Results The prevalence of LTBI was 26.5% in patients with SLE and 30.3% in patients with RA. The agreement between the TST and QFT-G assay was fair in SLE patients, but poor in RA patients. BCG vaccination was one factor associated with discordance between TST and QFT-G. Older age and higher SLE Disease Activity Index (SLEDAI) score were associated with a negative TST/positive QFT-G result in patients with SLE. Higher SLEDAI score and increased glucocorticoid dose were associated with an indeterminate result in the QFT-G assay for patients with SLE. Conclusions Agreement between the QFT-G assay and TST in patients with SLE was found to be fair. However, BCG vaccination status, age, and SLEDAI score are all factors that could result in discordance between the two tests. Indeterminate results from the QFT-G assay may be caused by a higher SLEDAI score or increased glucocorticoid dose.</description><identifier>ISSN: 0961-2033</identifier><identifier>EISSN: 1477-0962</identifier><identifier>DOI: 10.1177/0961203316639381</identifier><identifier>PMID: 26985011</identifier><language>eng</language><publisher>London, England: SAGE Publications</publisher><subject>Adult ; Age Factors ; Arthritis, Rheumatoid - diagnosis ; Arthritis, Rheumatoid - immunology ; Female ; Glucocorticoids - therapeutic use ; Humans ; Interferon-gamma Release Tests - methods ; Latent Tuberculosis - diagnosis ; Latent Tuberculosis - epidemiology ; Lupus Erythematosus, Systemic - drug therapy ; Lupus Erythematosus, Systemic - immunology ; Lupus Erythematosus, Systemic - microbiology ; Middle Aged ; Mycobacterium ; Prevalence ; Prospective Studies ; Risk Factors ; Sensitivity and Specificity ; Tuberculin Test - methods</subject><ispartof>Lupus, 2016-10, Vol.25 (12), p.1341-1348</ispartof><rights>The Author(s) 2016</rights><rights>The Author(s) 2016.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c370t-a7715b95c00f256e9a7f5a0eab81ba07d20cdd25a98cbe22644ad4c56d5ce293</citedby><cites>FETCH-LOGICAL-c370t-a7715b95c00f256e9a7f5a0eab81ba07d20cdd25a98cbe22644ad4c56d5ce293</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925,79364</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26985011$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cho, H</creatorcontrib><creatorcontrib>Kim, Y W</creatorcontrib><creatorcontrib>Suh, C-H</creatorcontrib><creatorcontrib>Jung, J-Y</creatorcontrib><creatorcontrib>Um, Y-J</creatorcontrib><creatorcontrib>Jung, J-H</creatorcontrib><creatorcontrib>Kim, H-A</creatorcontrib><title>Concordance between the tuberculin skin test and interferon gamma release assay (IGRA) for diagnosing latent tuberculosis infection in patients with systemic lupus erythematosus and patient characteristics associated with an indeterminate IGRA</title><title>Lupus</title><addtitle>Lupus</addtitle><description>Objective We investigated the agreement between the tuberculin skin test (TST) and the QuantiFERON-TB gold (QFT-G) assay in the diagnosis of latent tuberculosis infection (LTBI) in patients with systemic lupus erythematosus (SLE). Furthermore, we evaluated the factors associated with indeterminate results in the QFT-G assay in patients with SLE. Methods We enrolled 136 patients with SLE prospectively, and compared them to 66 patients with rheumatoid arthritis (RA). In addition to the TST, QFT-G assay, patients’ medications, and Bacillus Calmette-Guérin (BCG) vaccination status were also investigated. A positive TST or QFT-G assay result without an active tuberculosis lesion on chest x-ray was considered to indicate a diagnosis of LTBI. Results The prevalence of LTBI was 26.5% in patients with SLE and 30.3% in patients with RA. The agreement between the TST and QFT-G assay was fair in SLE patients, but poor in RA patients. BCG vaccination was one factor associated with discordance between TST and QFT-G. Older age and higher SLE Disease Activity Index (SLEDAI) score were associated with a negative TST/positive QFT-G result in patients with SLE. Higher SLEDAI score and increased glucocorticoid dose were associated with an indeterminate result in the QFT-G assay for patients with SLE. Conclusions Agreement between the QFT-G assay and TST in patients with SLE was found to be fair. However, BCG vaccination status, age, and SLEDAI score are all factors that could result in discordance between the two tests. Indeterminate results from the QFT-G assay may be caused by a higher SLEDAI score or increased glucocorticoid dose.</description><subject>Adult</subject><subject>Age Factors</subject><subject>Arthritis, Rheumatoid - diagnosis</subject><subject>Arthritis, Rheumatoid - immunology</subject><subject>Female</subject><subject>Glucocorticoids - therapeutic use</subject><subject>Humans</subject><subject>Interferon-gamma Release Tests - methods</subject><subject>Latent Tuberculosis - diagnosis</subject><subject>Latent Tuberculosis - epidemiology</subject><subject>Lupus Erythematosus, Systemic - drug therapy</subject><subject>Lupus Erythematosus, Systemic - immunology</subject><subject>Lupus Erythematosus, Systemic - microbiology</subject><subject>Middle Aged</subject><subject>Mycobacterium</subject><subject>Prevalence</subject><subject>Prospective Studies</subject><subject>Risk Factors</subject><subject>Sensitivity and Specificity</subject><subject>Tuberculin Test - methods</subject><issn>0961-2033</issn><issn>1477-0962</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNqNkk2LFDEQhoMo7rh69yQ5rofWJP2R7uMy6LqwIMjem-qkeiZrdzKm0izzu_cPmGbGPQiCl4RUPXnyEoqx91J8klLrz6JrpBJlKZum7MpWvmAbWWld5Lp6yTZru1j7F-wN0YMQopRd85pdqKZrayHlhj1tgzchWvAG-YDpEdHztEeelgGjWSbnOf3MS0JKHLzlzieMI8bg-Q7mGXjECYGQAxEc-dXtzY_rj3wMkVsHOx_I-R2fIKFPz9JcpCwa0SSXPVl_gOQyQfzRpT2nIyWcneHTcliIYzzmSDOkQPm0hjjj3OwhgsmBHCVnaM0QjMuP2ZMIVrnFDMzO5zJf071lr0aYCN-d90t2__XL_fZbcff95nZ7fVeYUotUgNayHrraCDGqusEO9FiDQBhaOYDQVgljraqha82ASjVVBbYydWNrg6orL9nVSXuI4deSv6-fHRmcJvAYFuplq3TbyqaS_4OWnWhboTIqTqiJgSji2B-imyEeeyn6dSj6v4ciX_lwti_DjPb5wp8pyEBxAgh22D-EJfr8L_8W_gZoFMYy</recordid><startdate>201610</startdate><enddate>201610</enddate><creator>Cho, H</creator><creator>Kim, Y W</creator><creator>Suh, C-H</creator><creator>Jung, J-Y</creator><creator>Um, Y-J</creator><creator>Jung, J-H</creator><creator>Kim, H-A</creator><general>SAGE Publications</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>7X8</scope><scope>7QL</scope><scope>7T5</scope><scope>C1K</scope><scope>H94</scope></search><sort><creationdate>201610</creationdate><title>Concordance between the tuberculin skin test and interferon gamma release assay (IGRA) for diagnosing latent tuberculosis infection in patients with systemic lupus erythematosus and patient characteristics associated with an indeterminate IGRA</title><author>Cho, H ; Kim, Y W ; Suh, C-H ; Jung, J-Y ; Um, Y-J ; Jung, J-H ; Kim, H-A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c370t-a7715b95c00f256e9a7f5a0eab81ba07d20cdd25a98cbe22644ad4c56d5ce293</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Adult</topic><topic>Age Factors</topic><topic>Arthritis, Rheumatoid - diagnosis</topic><topic>Arthritis, Rheumatoid - immunology</topic><topic>Female</topic><topic>Glucocorticoids - therapeutic use</topic><topic>Humans</topic><topic>Interferon-gamma Release Tests - methods</topic><topic>Latent Tuberculosis - diagnosis</topic><topic>Latent Tuberculosis - epidemiology</topic><topic>Lupus Erythematosus, Systemic - drug therapy</topic><topic>Lupus Erythematosus, Systemic - immunology</topic><topic>Lupus Erythematosus, Systemic - microbiology</topic><topic>Middle Aged</topic><topic>Mycobacterium</topic><topic>Prevalence</topic><topic>Prospective Studies</topic><topic>Risk Factors</topic><topic>Sensitivity and Specificity</topic><topic>Tuberculin Test - methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cho, H</creatorcontrib><creatorcontrib>Kim, Y W</creatorcontrib><creatorcontrib>Suh, C-H</creatorcontrib><creatorcontrib>Jung, J-Y</creatorcontrib><creatorcontrib>Um, Y-J</creatorcontrib><creatorcontrib>Jung, J-H</creatorcontrib><creatorcontrib>Kim, H-A</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Immunology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>Lupus</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cho, H</au><au>Kim, Y W</au><au>Suh, C-H</au><au>Jung, J-Y</au><au>Um, Y-J</au><au>Jung, J-H</au><au>Kim, H-A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Concordance between the tuberculin skin test and interferon gamma release assay (IGRA) for diagnosing latent tuberculosis infection in patients with systemic lupus erythematosus and patient characteristics associated with an indeterminate IGRA</atitle><jtitle>Lupus</jtitle><addtitle>Lupus</addtitle><date>2016-10</date><risdate>2016</risdate><volume>25</volume><issue>12</issue><spage>1341</spage><epage>1348</epage><pages>1341-1348</pages><issn>0961-2033</issn><eissn>1477-0962</eissn><abstract>Objective We investigated the agreement between the tuberculin skin test (TST) and the QuantiFERON-TB gold (QFT-G) assay in the diagnosis of latent tuberculosis infection (LTBI) in patients with systemic lupus erythematosus (SLE). Furthermore, we evaluated the factors associated with indeterminate results in the QFT-G assay in patients with SLE. Methods We enrolled 136 patients with SLE prospectively, and compared them to 66 patients with rheumatoid arthritis (RA). In addition to the TST, QFT-G assay, patients’ medications, and Bacillus Calmette-Guérin (BCG) vaccination status were also investigated. A positive TST or QFT-G assay result without an active tuberculosis lesion on chest x-ray was considered to indicate a diagnosis of LTBI. Results The prevalence of LTBI was 26.5% in patients with SLE and 30.3% in patients with RA. The agreement between the TST and QFT-G assay was fair in SLE patients, but poor in RA patients. BCG vaccination was one factor associated with discordance between TST and QFT-G. Older age and higher SLE Disease Activity Index (SLEDAI) score were associated with a negative TST/positive QFT-G result in patients with SLE. Higher SLEDAI score and increased glucocorticoid dose were associated with an indeterminate result in the QFT-G assay for patients with SLE. Conclusions Agreement between the QFT-G assay and TST in patients with SLE was found to be fair. However, BCG vaccination status, age, and SLEDAI score are all factors that could result in discordance between the two tests. Indeterminate results from the QFT-G assay may be caused by a higher SLEDAI score or increased glucocorticoid dose.</abstract><cop>London, England</cop><pub>SAGE Publications</pub><pmid>26985011</pmid><doi>10.1177/0961203316639381</doi><tpages>8</tpages></addata></record>
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subjects Adult
Age Factors
Arthritis, Rheumatoid - diagnosis
Arthritis, Rheumatoid - immunology
Female
Glucocorticoids - therapeutic use
Humans
Interferon-gamma Release Tests - methods
Latent Tuberculosis - diagnosis
Latent Tuberculosis - epidemiology
Lupus Erythematosus, Systemic - drug therapy
Lupus Erythematosus, Systemic - immunology
Lupus Erythematosus, Systemic - microbiology
Middle Aged
Mycobacterium
Prevalence
Prospective Studies
Risk Factors
Sensitivity and Specificity
Tuberculin Test - methods
title Concordance between the tuberculin skin test and interferon gamma release assay (IGRA) for diagnosing latent tuberculosis infection in patients with systemic lupus erythematosus and patient characteristics associated with an indeterminate IGRA
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