Rheumatoid factor and immunoglobulin M mark hepatitis C-associated mixed cryoglobulinaemia: an 8-year prospective study

The prevalence and factors of hepatitis C virus (HCV) -associated mixed cryoglobulinaemia in Asia remain elusive, and we aimed to investigate these topics. An 8-year prospective cohort study was conducted in 678 consecutive Taiwanese individuals with chronic HCV infection (438 completed an anti-HCV...

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Veröffentlicht in:Clinical microbiology and infection 2020-03, Vol.26 (3), p.366-372
Hauptverfasser: Cheng, Y.-T., Cheng, J.-S., Lin, C.-H., Chen, T.-H., Lee, K.-C., Chang, M.-L.
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container_end_page 372
container_issue 3
container_start_page 366
container_title Clinical microbiology and infection
container_volume 26
creator Cheng, Y.-T.
Cheng, J.-S.
Lin, C.-H.
Chen, T.-H.
Lee, K.-C.
Chang, M.-L.
description The prevalence and factors of hepatitis C virus (HCV) -associated mixed cryoglobulinaemia in Asia remain elusive, and we aimed to investigate these topics. An 8-year prospective cohort study was conducted in 678 consecutive Taiwanese individuals with chronic HCV infection (438 completed an anti-HCV therapy course). Of 678 individuals, 437 (64.5%) had mixed cryoglobulinaemia and 20 (2.9%) had mixed cryoglobulinaemic syndrome. At baseline, IgM (cut-off >122 mg/dL), triglycerides and IgG levels, and HCV genotype 3 were independently associated with mixed cryoglobulinaemia. Rheumatoid factor (RF) levels were associated with mixed cryoglobulinaemic syndrome (cut-off >12.2 IU/mL). At 24 weeks post-therapy, the 362 individuals with a sustained virological response (SVR) had higher cured (106/362 (29.3%) versus 10/76 (13.2%), p = 0.003) and lower persistent (100/362 (27.6%) versus 33/76 (43.4%), p = 0.003) mixed cryoglobulinaemia rates than non-SVR patients. Among SVR patients, compared with baseline levels, RF, IgG and IgM levels decreased, except in individuals with new mixed cryoglobulinaemia. Pre-therapy IgM levels were associated with 24-week post-therapy new (95% CI of OR 1.002–1.023) and persistent (95% CI of OR 1.004–1.015) mixed cryoglobulinaemia in SVR patients. After up to 8 years, 24-week post-therapy IgM levels were associated with mixed cryoglobulinaemia in SVR patients (9/51; 17.64%; 95% CI of HR 1.004–1.011). Among 17 SVR patients with pre-therapy mixed cryoglobulinaemic syndrome, 5 (29.4%) had long-term mixed cryoglobulinaemia and 4 (23.5%) had mixed cryoglobulinaemic syndrome. Over 60% of chronic HCV-infected individuals had mixed cryoglobulinaemia, and 17.64% of SVR patients had mixed cryoglobulinaemia 8 years post-therapy. Pre-therapy RF and IgM levels marked HCV-associated mixed cryoglobulinaemic syndrome and mixed cryoglobulinaemia, respectively.
doi_str_mv 10.1016/j.cmi.2019.06.018
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An 8-year prospective cohort study was conducted in 678 consecutive Taiwanese individuals with chronic HCV infection (438 completed an anti-HCV therapy course). Of 678 individuals, 437 (64.5%) had mixed cryoglobulinaemia and 20 (2.9%) had mixed cryoglobulinaemic syndrome. At baseline, IgM (cut-off &gt;122 mg/dL), triglycerides and IgG levels, and HCV genotype 3 were independently associated with mixed cryoglobulinaemia. Rheumatoid factor (RF) levels were associated with mixed cryoglobulinaemic syndrome (cut-off &gt;12.2 IU/mL). At 24 weeks post-therapy, the 362 individuals with a sustained virological response (SVR) had higher cured (106/362 (29.3%) versus 10/76 (13.2%), p = 0.003) and lower persistent (100/362 (27.6%) versus 33/76 (43.4%), p = 0.003) mixed cryoglobulinaemia rates than non-SVR patients. Among SVR patients, compared with baseline levels, RF, IgG and IgM levels decreased, except in individuals with new mixed cryoglobulinaemia. Pre-therapy IgM levels were associated with 24-week post-therapy new (95% CI of OR 1.002–1.023) and persistent (95% CI of OR 1.004–1.015) mixed cryoglobulinaemia in SVR patients. After up to 8 years, 24-week post-therapy IgM levels were associated with mixed cryoglobulinaemia in SVR patients (9/51; 17.64%; 95% CI of HR 1.004–1.011). Among 17 SVR patients with pre-therapy mixed cryoglobulinaemic syndrome, 5 (29.4%) had long-term mixed cryoglobulinaemia and 4 (23.5%) had mixed cryoglobulinaemic syndrome. Over 60% of chronic HCV-infected individuals had mixed cryoglobulinaemia, and 17.64% of SVR patients had mixed cryoglobulinaemia 8 years post-therapy. 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Pre-therapy IgM levels were associated with 24-week post-therapy new (95% CI of OR 1.002–1.023) and persistent (95% CI of OR 1.004–1.015) mixed cryoglobulinaemia in SVR patients. After up to 8 years, 24-week post-therapy IgM levels were associated with mixed cryoglobulinaemia in SVR patients (9/51; 17.64%; 95% CI of HR 1.004–1.011). Among 17 SVR patients with pre-therapy mixed cryoglobulinaemic syndrome, 5 (29.4%) had long-term mixed cryoglobulinaemia and 4 (23.5%) had mixed cryoglobulinaemic syndrome. Over 60% of chronic HCV-infected individuals had mixed cryoglobulinaemia, and 17.64% of SVR patients had mixed cryoglobulinaemia 8 years post-therapy. Pre-therapy RF and IgM levels marked HCV-associated mixed cryoglobulinaemic syndrome and mixed cryoglobulinaemia, respectively.</description><subject>Hepatitis C virus</subject><subject>IgM</subject><subject>Mixed cryoglobulinaemia</subject><subject>Mixed cryoglobulinaemic syndrome</subject><subject>Rheumatoid factor</subject><subject>Sustained virological response</subject><issn>1198-743X</issn><issn>1469-0691</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp9kE9v1DAQxS0EoqXwAbggH7kkeJysHcMJrcofqQgJgcTNmtiz1EucLLZT2G-Pqy09cpmZw3tP836MPQfRggD1at-6GFopwLRCtQKGB-wcemUaoQw8rDeYodF99_2MPcl5L4SQXdc_ZmcdSGk2Rp2z31-uaY1YluD5Dl1ZEsfZ8xDjOi8_pmVcpzDzTzxi-smv6YAllJD5tsGcFxewkOcx_KnTpeO9ASkGfF2T-NAcCRM_pCUfyJVwQzyX1R-fskc7nDI9u9sX7Nu7y6_bD83V5_cft2-vGtcZVRrQ5MRObwaJmgBIaC9VjzSikFpKPw5SjUYYMYwbg6Brv0ETojBm433fdRfs5Sm3fvBrpVxsDNnRNOFMy5qtlL2S_QAaqhROUlefzYl29pBC7X20IOwtb7u3lbe95W2FspV39by4i1_HSP7e8Q9wFbw5CaiWvAmUbHaBZkc-pMrD-iX8J_4v0GGSEQ</recordid><startdate>202003</startdate><enddate>202003</enddate><creator>Cheng, Y.-T.</creator><creator>Cheng, J.-S.</creator><creator>Lin, C.-H.</creator><creator>Chen, T.-H.</creator><creator>Lee, K.-C.</creator><creator>Chang, M.-L.</creator><general>Elsevier Ltd</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>202003</creationdate><title>Rheumatoid factor and immunoglobulin M mark hepatitis C-associated mixed cryoglobulinaemia: an 8-year prospective study</title><author>Cheng, Y.-T. ; Cheng, J.-S. ; Lin, C.-H. ; Chen, T.-H. ; Lee, K.-C. ; Chang, M.-L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c396t-17ec0f7582a7e11e07d264aeba02722db826b90908b59a1723387eaa0995dd433</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Hepatitis C virus</topic><topic>IgM</topic><topic>Mixed cryoglobulinaemia</topic><topic>Mixed cryoglobulinaemic syndrome</topic><topic>Rheumatoid factor</topic><topic>Sustained virological response</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cheng, Y.-T.</creatorcontrib><creatorcontrib>Cheng, J.-S.</creatorcontrib><creatorcontrib>Lin, C.-H.</creatorcontrib><creatorcontrib>Chen, T.-H.</creatorcontrib><creatorcontrib>Lee, K.-C.</creatorcontrib><creatorcontrib>Chang, M.-L.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical microbiology and infection</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cheng, Y.-T.</au><au>Cheng, J.-S.</au><au>Lin, C.-H.</au><au>Chen, T.-H.</au><au>Lee, K.-C.</au><au>Chang, M.-L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Rheumatoid factor and immunoglobulin M mark hepatitis C-associated mixed cryoglobulinaemia: an 8-year prospective study</atitle><jtitle>Clinical microbiology and infection</jtitle><addtitle>Clin Microbiol Infect</addtitle><date>2020-03</date><risdate>2020</risdate><volume>26</volume><issue>3</issue><spage>366</spage><epage>372</epage><pages>366-372</pages><issn>1198-743X</issn><eissn>1469-0691</eissn><abstract>The prevalence and factors of hepatitis C virus (HCV) -associated mixed cryoglobulinaemia in Asia remain elusive, and we aimed to investigate these topics. An 8-year prospective cohort study was conducted in 678 consecutive Taiwanese individuals with chronic HCV infection (438 completed an anti-HCV therapy course). Of 678 individuals, 437 (64.5%) had mixed cryoglobulinaemia and 20 (2.9%) had mixed cryoglobulinaemic syndrome. At baseline, IgM (cut-off &gt;122 mg/dL), triglycerides and IgG levels, and HCV genotype 3 were independently associated with mixed cryoglobulinaemia. Rheumatoid factor (RF) levels were associated with mixed cryoglobulinaemic syndrome (cut-off &gt;12.2 IU/mL). At 24 weeks post-therapy, the 362 individuals with a sustained virological response (SVR) had higher cured (106/362 (29.3%) versus 10/76 (13.2%), p = 0.003) and lower persistent (100/362 (27.6%) versus 33/76 (43.4%), p = 0.003) mixed cryoglobulinaemia rates than non-SVR patients. Among SVR patients, compared with baseline levels, RF, IgG and IgM levels decreased, except in individuals with new mixed cryoglobulinaemia. Pre-therapy IgM levels were associated with 24-week post-therapy new (95% CI of OR 1.002–1.023) and persistent (95% CI of OR 1.004–1.015) mixed cryoglobulinaemia in SVR patients. After up to 8 years, 24-week post-therapy IgM levels were associated with mixed cryoglobulinaemia in SVR patients (9/51; 17.64%; 95% CI of HR 1.004–1.011). Among 17 SVR patients with pre-therapy mixed cryoglobulinaemic syndrome, 5 (29.4%) had long-term mixed cryoglobulinaemia and 4 (23.5%) had mixed cryoglobulinaemic syndrome. Over 60% of chronic HCV-infected individuals had mixed cryoglobulinaemia, and 17.64% of SVR patients had mixed cryoglobulinaemia 8 years post-therapy. Pre-therapy RF and IgM levels marked HCV-associated mixed cryoglobulinaemic syndrome and mixed cryoglobulinaemia, respectively.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>31229596</pmid><doi>10.1016/j.cmi.2019.06.018</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
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subjects Hepatitis C virus
IgM
Mixed cryoglobulinaemia
Mixed cryoglobulinaemic syndrome
Rheumatoid factor
Sustained virological response
title Rheumatoid factor and immunoglobulin M mark hepatitis C-associated mixed cryoglobulinaemia: an 8-year prospective study
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