Prevalence and significance of thyroid autoantibodies in patients with chronic hepatitis C virus infection: a prospective controlled study

OBJECTIVE To clarify controversies on the prevalence and clinical significance of thyroid autoimmunity in hepatitis C virus (HCV) infection. DESIGN A prospective controlled and follow‐up study. PATIENTS AND MEASUREMENTS Serum thyroid microsomal antibody (TMA) and thyroid stimulating hormone were ass...

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Veröffentlicht in:Clinical endocrinology (Oxford) 1999-04, Vol.50 (4), p.503-509
Hauptverfasser: Huang, Miau-Ju, Tsai, Sun-Lung, Huang, Bie-Yu, Sheen, I-Shyan, Yeh, Chau-Ting, Liaw, Yun-Fan
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container_end_page 509
container_issue 4
container_start_page 503
container_title Clinical endocrinology (Oxford)
container_volume 50
creator Huang, Miau-Ju
Tsai, Sun-Lung
Huang, Bie-Yu
Sheen, I-Shyan
Yeh, Chau-Ting
Liaw, Yun-Fan
description OBJECTIVE To clarify controversies on the prevalence and clinical significance of thyroid autoimmunity in hepatitis C virus (HCV) infection. DESIGN A prospective controlled and follow‐up study. PATIENTS AND MEASUREMENTS Serum thyroid microsomal antibody (TMA) and thyroid stimulating hormone were assayed and compared in a consecutive, unselected series of 130 patients with chronic HCV infection, 130 sex/age (± 2 years)‐matched patients with chronic hepatitis B virus (HBV) infection and 260 matched normal controls. RESULTS The prevalence of thyroid autoantibodies in male patients with chronic HCV was 
doi_str_mv 10.1046/j.1365-2265.1999.00686.x
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DESIGN A prospective controlled and follow‐up study. PATIENTS AND MEASUREMENTS Serum thyroid microsomal antibody (TMA) and thyroid stimulating hormone were assayed and compared in a consecutive, unselected series of 130 patients with chronic HCV infection, 130 sex/age (± 2 years)‐matched patients with chronic hepatitis B virus (HBV) infection and 260 matched normal controls. RESULTS The prevalence of thyroid autoantibodies in male patients with chronic HCV was &lt; 2%. The prevalence of TMA (&lt; 1 : 400) in female patients with chronic HCV infection was significantly higher than that of HBV controls (22.1 vs. 1.6%; P &lt; 0.001), and higher but not significant compared with normal controls (13.5%). However, the trend of increasing prevalence with age in normal controls was not observed in HCV patients. TMA seropositive female HCV patients were not different from seronegative counterparts in age, duration of infection, HLA haplotype, associated autoantibodies and liver histology but had a significantly higher prevalence of genotype 1b/2b mixed infection (P &lt; 0.01) and anti‐GOR (P &lt; 0.05). Of the 23 HCV patients seropositive for thyroid autoantibodies, seven had Hashimoto's thyroiditis, two had Graves' disease and three had received subtotal thyroidectomy. During follow‐up, four of 15 female patients showed a 14–16‐fold increase in TMA titre and one developed hyperthyroidism. Patients with thyroid autoantibodies did not show a propensity to develop thyroid dysfunction during interferon therapy. CONCLUSIONS These results suggest a weak association between HCV and thyroid autoimmunity in females. As in the ordinary population with thyroid autoantibodies, they should be evaluated for thyroid status and be followed‐up if thyroid autoimmunity is evident. However, seropositivity of thyroid autoantibodies is not a contraindication to interferon therapy.</description><identifier>ISSN: 0300-0664</identifier><identifier>EISSN: 1365-2265</identifier><identifier>DOI: 10.1046/j.1365-2265.1999.00686.x</identifier><identifier>PMID: 10468911</identifier><identifier>CODEN: CLECAP</identifier><language>eng</language><publisher>Oxford BSL: Blackwell Science Ltd</publisher><subject>Adult ; Aged ; Antiviral Agents - therapeutic use ; Autoantibodies - blood ; Biological and medical sciences ; Case-Control Studies ; Female ; Hepatitis B, Chronic - immunology ; Hepatitis C, Chronic - immunology ; Hepatitis C, Chronic - therapy ; Human viral diseases ; Humans ; Infectious diseases ; Interferon-alpha - therapeutic use ; Male ; Medical sciences ; Middle Aged ; Prevalence ; Thyroglobulin - immunology ; Thyrotropin - blood ; Viral diseases ; Viral hepatitis</subject><ispartof>Clinical endocrinology (Oxford), 1999-04, Vol.50 (4), p.503-509</ispartof><rights>Blackwell Science Ltd, Oxford</rights><rights>1999 INIST-CNRS</rights><rights>Copyright Blackwell Scientific Publications Ltd. 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DESIGN A prospective controlled and follow‐up study. PATIENTS AND MEASUREMENTS Serum thyroid microsomal antibody (TMA) and thyroid stimulating hormone were assayed and compared in a consecutive, unselected series of 130 patients with chronic HCV infection, 130 sex/age (± 2 years)‐matched patients with chronic hepatitis B virus (HBV) infection and 260 matched normal controls. RESULTS The prevalence of thyroid autoantibodies in male patients with chronic HCV was &lt; 2%. The prevalence of TMA (&lt; 1 : 400) in female patients with chronic HCV infection was significantly higher than that of HBV controls (22.1 vs. 1.6%; P &lt; 0.001), and higher but not significant compared with normal controls (13.5%). However, the trend of increasing prevalence with age in normal controls was not observed in HCV patients. TMA seropositive female HCV patients were not different from seronegative counterparts in age, duration of infection, HLA haplotype, associated autoantibodies and liver histology but had a significantly higher prevalence of genotype 1b/2b mixed infection (P &lt; 0.01) and anti‐GOR (P &lt; 0.05). Of the 23 HCV patients seropositive for thyroid autoantibodies, seven had Hashimoto's thyroiditis, two had Graves' disease and three had received subtotal thyroidectomy. During follow‐up, four of 15 female patients showed a 14–16‐fold increase in TMA titre and one developed hyperthyroidism. Patients with thyroid autoantibodies did not show a propensity to develop thyroid dysfunction during interferon therapy. CONCLUSIONS These results suggest a weak association between HCV and thyroid autoimmunity in females. As in the ordinary population with thyroid autoantibodies, they should be evaluated for thyroid status and be followed‐up if thyroid autoimmunity is evident. 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Tsai, Sun-Lung ; Huang, Bie-Yu ; Sheen, I-Shyan ; Yeh, Chau-Ting ; Liaw, Yun-Fan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4586-52ed6225ea269346e05a7146f5ba1fd27dba06bc62740274763e6b2259aa71143</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Antiviral Agents - therapeutic use</topic><topic>Autoantibodies - blood</topic><topic>Biological and medical sciences</topic><topic>Case-Control Studies</topic><topic>Female</topic><topic>Hepatitis B, Chronic - immunology</topic><topic>Hepatitis C, Chronic - immunology</topic><topic>Hepatitis C, Chronic - therapy</topic><topic>Human viral diseases</topic><topic>Humans</topic><topic>Infectious diseases</topic><topic>Interferon-alpha - therapeutic use</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Prevalence</topic><topic>Thyroglobulin - immunology</topic><topic>Thyrotropin - blood</topic><topic>Viral diseases</topic><topic>Viral hepatitis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Huang, Miau-Ju</creatorcontrib><creatorcontrib>Tsai, Sun-Lung</creatorcontrib><creatorcontrib>Huang, Bie-Yu</creatorcontrib><creatorcontrib>Sheen, I-Shyan</creatorcontrib><creatorcontrib>Yeh, Chau-Ting</creatorcontrib><creatorcontrib>Liaw, Yun-Fan</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><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>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical endocrinology (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Huang, Miau-Ju</au><au>Tsai, Sun-Lung</au><au>Huang, Bie-Yu</au><au>Sheen, I-Shyan</au><au>Yeh, Chau-Ting</au><au>Liaw, Yun-Fan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prevalence and significance of thyroid autoantibodies in patients with chronic hepatitis C virus infection: a prospective controlled study</atitle><jtitle>Clinical endocrinology (Oxford)</jtitle><addtitle>Clinical Endocrinology</addtitle><date>1999-04</date><risdate>1999</risdate><volume>50</volume><issue>4</issue><spage>503</spage><epage>509</epage><pages>503-509</pages><issn>0300-0664</issn><eissn>1365-2265</eissn><coden>CLECAP</coden><abstract>OBJECTIVE To clarify controversies on the prevalence and clinical significance of thyroid autoimmunity in hepatitis C virus (HCV) infection. DESIGN A prospective controlled and follow‐up study. PATIENTS AND MEASUREMENTS Serum thyroid microsomal antibody (TMA) and thyroid stimulating hormone were assayed and compared in a consecutive, unselected series of 130 patients with chronic HCV infection, 130 sex/age (± 2 years)‐matched patients with chronic hepatitis B virus (HBV) infection and 260 matched normal controls. RESULTS The prevalence of thyroid autoantibodies in male patients with chronic HCV was &lt; 2%. The prevalence of TMA (&lt; 1 : 400) in female patients with chronic HCV infection was significantly higher than that of HBV controls (22.1 vs. 1.6%; P &lt; 0.001), and higher but not significant compared with normal controls (13.5%). However, the trend of increasing prevalence with age in normal controls was not observed in HCV patients. TMA seropositive female HCV patients were not different from seronegative counterparts in age, duration of infection, HLA haplotype, associated autoantibodies and liver histology but had a significantly higher prevalence of genotype 1b/2b mixed infection (P &lt; 0.01) and anti‐GOR (P &lt; 0.05). Of the 23 HCV patients seropositive for thyroid autoantibodies, seven had Hashimoto's thyroiditis, two had Graves' disease and three had received subtotal thyroidectomy. During follow‐up, four of 15 female patients showed a 14–16‐fold increase in TMA titre and one developed hyperthyroidism. Patients with thyroid autoantibodies did not show a propensity to develop thyroid dysfunction during interferon therapy. CONCLUSIONS These results suggest a weak association between HCV and thyroid autoimmunity in females. As in the ordinary population with thyroid autoantibodies, they should be evaluated for thyroid status and be followed‐up if thyroid autoimmunity is evident. However, seropositivity of thyroid autoantibodies is not a contraindication to interferon therapy.</abstract><cop>Oxford BSL</cop><pub>Blackwell Science Ltd</pub><pmid>10468911</pmid><doi>10.1046/j.1365-2265.1999.00686.x</doi><tpages>7</tpages></addata></record>
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subjects Adult
Aged
Antiviral Agents - therapeutic use
Autoantibodies - blood
Biological and medical sciences
Case-Control Studies
Female
Hepatitis B, Chronic - immunology
Hepatitis C, Chronic - immunology
Hepatitis C, Chronic - therapy
Human viral diseases
Humans
Infectious diseases
Interferon-alpha - therapeutic use
Male
Medical sciences
Middle Aged
Prevalence
Thyroglobulin - immunology
Thyrotropin - blood
Viral diseases
Viral hepatitis
title Prevalence and significance of thyroid autoantibodies in patients with chronic hepatitis C virus infection: a prospective controlled study
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