Interferon-induced thyroid dysfunction in chronic hepatitis C

Background:  Treatment of chronic hepatitis C with interferon is known to be associated with thyroid dysfunction (TD) in 5–14% of patients. We studied the incidence, types, outcome and risk factors predictive of thyroid dysfunction. Methods:  A retrospective analysis was performed on all patients tr...

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Veröffentlicht in:Journal of gastroenterology and hepatology 2009-06, Vol.24 (6), p.1017-1023
Hauptverfasser: Jamil, Khaleel M, Leedman, Peter J, Kontorinis, Nickolas, Tarquinio, Lorenzo, Nazareth, Saroja, McInerney, Marion, Connelly, Crystal, Flexman, James, Burke, Valerie, Metcalf, Cecily, Cheng, Wendy
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container_end_page 1023
container_issue 6
container_start_page 1017
container_title Journal of gastroenterology and hepatology
container_volume 24
creator Jamil, Khaleel M
Leedman, Peter J
Kontorinis, Nickolas
Tarquinio, Lorenzo
Nazareth, Saroja
McInerney, Marion
Connelly, Crystal
Flexman, James
Burke, Valerie
Metcalf, Cecily
Cheng, Wendy
description Background:  Treatment of chronic hepatitis C with interferon is known to be associated with thyroid dysfunction (TD) in 5–14% of patients. We studied the incidence, types, outcome and risk factors predictive of thyroid dysfunction. Methods:  A retrospective analysis was performed on all patients treated with interferon alpha (IFN) or pegylated interferon alpha (PEG‐IFN) ± ribavirin (RBV), who developed abnormal thyroid function tests (TFTs). These cases were compared with treatment‐matched controls to identify factors predictive of thyroid dysfunction. Statistical methods consisted of: χ2 test, Fischer's exact test, Welch's t‐test, and multivariate analysis. Results:  From a total of 511 patients, 45 cases with TD were identified (8.8%). Pegylated interferon alpha was associated with higher rates of TD than IFN (14.1% vs 6.0%, P = 0.0029). Female sex (OR 5.6, 95% CI 1.1–7) and Asian ethnicity (OR 2.7, 95% CI 1.4–22) were independent predictors of developing TD. Cytology was obtained in 13 patients: benign follicular pattern (8); thyroiditis (3); and normal (2). Thyroid peroxidase (TPO) antibodies (P = 0.004) and earlier onset of dysfunction (P = 0.03) were associated with need for treatment. Sixteen patients had persistent TD by the end of the follow‐up period, predicted by female sex, non‐Asian ethnicity, prior history of TD and TPO antibodies. Conclusions:  Pegylated interferon alpha, female sex and Asian ethnicity are independent risk factors for TD. Thyroid peroxidase antibodies and earlier TD within the course of IFN are associated with the requirement for treatment. Thyroid function tests should be monitored during and after IFN‐based therapy. The most common cytological finding is a benign follicular pattern.
doi_str_mv 10.1111/j.1440-1746.2008.05690.x
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We studied the incidence, types, outcome and risk factors predictive of thyroid dysfunction. Methods:  A retrospective analysis was performed on all patients treated with interferon alpha (IFN) or pegylated interferon alpha (PEG‐IFN) ± ribavirin (RBV), who developed abnormal thyroid function tests (TFTs). These cases were compared with treatment‐matched controls to identify factors predictive of thyroid dysfunction. Statistical methods consisted of: χ2 test, Fischer's exact test, Welch's t‐test, and multivariate analysis. Results:  From a total of 511 patients, 45 cases with TD were identified (8.8%). Pegylated interferon alpha was associated with higher rates of TD than IFN (14.1% vs 6.0%, P = 0.0029). Female sex (OR 5.6, 95% CI 1.1–7) and Asian ethnicity (OR 2.7, 95% CI 1.4–22) were independent predictors of developing TD. Cytology was obtained in 13 patients: benign follicular pattern (8); thyroiditis (3); and normal (2). Thyroid peroxidase (TPO) antibodies (P = 0.004) and earlier onset of dysfunction (P = 0.03) were associated with need for treatment. Sixteen patients had persistent TD by the end of the follow‐up period, predicted by female sex, non‐Asian ethnicity, prior history of TD and TPO antibodies. Conclusions:  Pegylated interferon alpha, female sex and Asian ethnicity are independent risk factors for TD. Thyroid peroxidase antibodies and earlier TD within the course of IFN are associated with the requirement for treatment. Thyroid function tests should be monitored during and after IFN‐based therapy. The most common cytological finding is a benign follicular pattern.</description><identifier>ISSN: 0815-9319</identifier><identifier>EISSN: 1440-1746</identifier><identifier>DOI: 10.1111/j.1440-1746.2008.05690.x</identifier><identifier>PMID: 19054259</identifier><language>eng</language><publisher>Melbourne, Australia: Blackwell Publishing Asia</publisher><subject>Adult ; autoimmune thyroid disease ; Biological and medical sciences ; Case-Control Studies ; Chi-Square Distribution ; Drug Therapy, Combination ; Endocrinopathies ; Female ; Gastroenterology. Liver. Pancreas. Abdomen ; Hepatitis C, Chronic - drug therapy ; hepatitis-C ; Human viral diseases ; Humans ; Infectious diseases ; interferon ; Interferon-alpha - adverse effects ; Interferon-alpha - therapeutic use ; Male ; Medical sciences ; Middle Aged ; Non tumoral diseases. Target tissue resistance. Benign neoplasms ; Recombinant Proteins ; Retrospective Studies ; Ribavirin - adverse effects ; Ribavirin - therapeutic use ; Risk Factors ; Sex Factors ; Thyroid Diseases - chemically induced ; Thyroid Function Tests ; Thyroid. Thyroid axis (diseases) ; TPO antibodies ; Viral diseases ; Viral hepatitis ; Western Australia</subject><ispartof>Journal of gastroenterology and hepatology, 2009-06, Vol.24 (6), p.1017-1023</ispartof><rights>2008 The Authors. 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We studied the incidence, types, outcome and risk factors predictive of thyroid dysfunction. Methods:  A retrospective analysis was performed on all patients treated with interferon alpha (IFN) or pegylated interferon alpha (PEG‐IFN) ± ribavirin (RBV), who developed abnormal thyroid function tests (TFTs). These cases were compared with treatment‐matched controls to identify factors predictive of thyroid dysfunction. Statistical methods consisted of: χ2 test, Fischer's exact test, Welch's t‐test, and multivariate analysis. Results:  From a total of 511 patients, 45 cases with TD were identified (8.8%). Pegylated interferon alpha was associated with higher rates of TD than IFN (14.1% vs 6.0%, P = 0.0029). Female sex (OR 5.6, 95% CI 1.1–7) and Asian ethnicity (OR 2.7, 95% CI 1.4–22) were independent predictors of developing TD. Cytology was obtained in 13 patients: benign follicular pattern (8); thyroiditis (3); and normal (2). Thyroid peroxidase (TPO) antibodies (P = 0.004) and earlier onset of dysfunction (P = 0.03) were associated with need for treatment. Sixteen patients had persistent TD by the end of the follow‐up period, predicted by female sex, non‐Asian ethnicity, prior history of TD and TPO antibodies. Conclusions:  Pegylated interferon alpha, female sex and Asian ethnicity are independent risk factors for TD. Thyroid peroxidase antibodies and earlier TD within the course of IFN are associated with the requirement for treatment. Thyroid function tests should be monitored during and after IFN‐based therapy. 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Benign neoplasms</subject><subject>Recombinant Proteins</subject><subject>Retrospective Studies</subject><subject>Ribavirin - adverse effects</subject><subject>Ribavirin - therapeutic use</subject><subject>Risk Factors</subject><subject>Sex Factors</subject><subject>Thyroid Diseases - chemically induced</subject><subject>Thyroid Function Tests</subject><subject>Thyroid. Thyroid axis (diseases)</subject><subject>TPO antibodies</subject><subject>Viral diseases</subject><subject>Viral hepatitis</subject><subject>Western Australia</subject><issn>0815-9319</issn><issn>1440-1746</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkEGPEyEYQInRuHX1L5i5qKcZPwYY4LAH02i72mhiNnoklPlIqe1MhZnY_nsZ29SbkQsE3gPyCCkoVDSPt9uKcg4llbypagBVgWg0VMdHZHY9eExmoKgoNaP6hjxLaQsAHKR4Sm6oBsFroWfk7r4bMHqMfVeGrh0dtsWwOcU-tEV7Sn7s3BD6rghd4TYZCq7Y4MEOYQipmD8nT7zdJXxxmW_Jw4f3D_NlufqyuJ-_W5VOMAYl1rWwTa2Vdq5pGNIWtOeISqDU3HLt_Vp4hVTlbS2h9bVjTLdrhWvOJLslb87XHmL_c8Q0mH1IDnc722E_JiMZE5IBY5l8_U8yx2qU4DSD6gy62KcU0ZtDDHsbT4aCmRqbrZlSminlpCnzp7E5ZvXl5Y1xvcf2r3iJmoFXF8AmZ3c-2s6FdOVqKqjQss7c3Zn7FXZ4-u8PmI-L5bTKfnn2QxrwePVt_GEayaQw3z8vzJJ_BaFW38wn9htJ16W1</recordid><startdate>200906</startdate><enddate>200906</enddate><creator>Jamil, Khaleel M</creator><creator>Leedman, Peter J</creator><creator>Kontorinis, Nickolas</creator><creator>Tarquinio, Lorenzo</creator><creator>Nazareth, Saroja</creator><creator>McInerney, Marion</creator><creator>Connelly, Crystal</creator><creator>Flexman, James</creator><creator>Burke, Valerie</creator><creator>Metcalf, Cecily</creator><creator>Cheng, Wendy</creator><general>Blackwell Publishing Asia</general><general>Wiley-Blackwell</general><scope>BSCLL</scope><scope>IQODW</scope><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>7T5</scope><scope>7U9</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>200906</creationdate><title>Interferon-induced thyroid dysfunction in chronic hepatitis C</title><author>Jamil, Khaleel M ; Leedman, Peter J ; Kontorinis, Nickolas ; Tarquinio, Lorenzo ; Nazareth, Saroja ; McInerney, Marion ; Connelly, Crystal ; Flexman, James ; Burke, Valerie ; Metcalf, Cecily ; Cheng, Wendy</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5330-e225a62989cc663e1d09f4ee85e794a49ffb5f8e189f4970df2c339db8eb4373</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Adult</topic><topic>autoimmune thyroid disease</topic><topic>Biological and medical sciences</topic><topic>Case-Control Studies</topic><topic>Chi-Square Distribution</topic><topic>Drug Therapy, Combination</topic><topic>Endocrinopathies</topic><topic>Female</topic><topic>Gastroenterology. 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Thyroid axis (diseases)</topic><topic>TPO antibodies</topic><topic>Viral diseases</topic><topic>Viral hepatitis</topic><topic>Western Australia</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jamil, Khaleel M</creatorcontrib><creatorcontrib>Leedman, Peter J</creatorcontrib><creatorcontrib>Kontorinis, Nickolas</creatorcontrib><creatorcontrib>Tarquinio, Lorenzo</creatorcontrib><creatorcontrib>Nazareth, Saroja</creatorcontrib><creatorcontrib>McInerney, Marion</creatorcontrib><creatorcontrib>Connelly, Crystal</creatorcontrib><creatorcontrib>Flexman, James</creatorcontrib><creatorcontrib>Burke, Valerie</creatorcontrib><creatorcontrib>Metcalf, Cecily</creatorcontrib><creatorcontrib>Cheng, Wendy</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>Immunology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of gastroenterology and hepatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jamil, Khaleel M</au><au>Leedman, Peter J</au><au>Kontorinis, Nickolas</au><au>Tarquinio, Lorenzo</au><au>Nazareth, Saroja</au><au>McInerney, Marion</au><au>Connelly, Crystal</au><au>Flexman, James</au><au>Burke, Valerie</au><au>Metcalf, Cecily</au><au>Cheng, Wendy</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Interferon-induced thyroid dysfunction in chronic hepatitis C</atitle><jtitle>Journal of gastroenterology and hepatology</jtitle><addtitle>J Gastroenterol Hepatol</addtitle><date>2009-06</date><risdate>2009</risdate><volume>24</volume><issue>6</issue><spage>1017</spage><epage>1023</epage><pages>1017-1023</pages><issn>0815-9319</issn><eissn>1440-1746</eissn><abstract>Background:  Treatment of chronic hepatitis C with interferon is known to be associated with thyroid dysfunction (TD) in 5–14% of patients. We studied the incidence, types, outcome and risk factors predictive of thyroid dysfunction. Methods:  A retrospective analysis was performed on all patients treated with interferon alpha (IFN) or pegylated interferon alpha (PEG‐IFN) ± ribavirin (RBV), who developed abnormal thyroid function tests (TFTs). These cases were compared with treatment‐matched controls to identify factors predictive of thyroid dysfunction. Statistical methods consisted of: χ2 test, Fischer's exact test, Welch's t‐test, and multivariate analysis. Results:  From a total of 511 patients, 45 cases with TD were identified (8.8%). Pegylated interferon alpha was associated with higher rates of TD than IFN (14.1% vs 6.0%, P = 0.0029). Female sex (OR 5.6, 95% CI 1.1–7) and Asian ethnicity (OR 2.7, 95% CI 1.4–22) were independent predictors of developing TD. Cytology was obtained in 13 patients: benign follicular pattern (8); thyroiditis (3); and normal (2). Thyroid peroxidase (TPO) antibodies (P = 0.004) and earlier onset of dysfunction (P = 0.03) were associated with need for treatment. Sixteen patients had persistent TD by the end of the follow‐up period, predicted by female sex, non‐Asian ethnicity, prior history of TD and TPO antibodies. Conclusions:  Pegylated interferon alpha, female sex and Asian ethnicity are independent risk factors for TD. Thyroid peroxidase antibodies and earlier TD within the course of IFN are associated with the requirement for treatment. Thyroid function tests should be monitored during and after IFN‐based therapy. The most common cytological finding is a benign follicular pattern.</abstract><cop>Melbourne, Australia</cop><pub>Blackwell Publishing Asia</pub><pmid>19054259</pmid><doi>10.1111/j.1440-1746.2008.05690.x</doi><tpages>7</tpages></addata></record>
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subjects Adult
autoimmune thyroid disease
Biological and medical sciences
Case-Control Studies
Chi-Square Distribution
Drug Therapy, Combination
Endocrinopathies
Female
Gastroenterology. Liver. Pancreas. Abdomen
Hepatitis C, Chronic - drug therapy
hepatitis-C
Human viral diseases
Humans
Infectious diseases
interferon
Interferon-alpha - adverse effects
Interferon-alpha - therapeutic use
Male
Medical sciences
Middle Aged
Non tumoral diseases. Target tissue resistance. Benign neoplasms
Recombinant Proteins
Retrospective Studies
Ribavirin - adverse effects
Ribavirin - therapeutic use
Risk Factors
Sex Factors
Thyroid Diseases - chemically induced
Thyroid Function Tests
Thyroid. Thyroid axis (diseases)
TPO antibodies
Viral diseases
Viral hepatitis
Western Australia
title Interferon-induced thyroid dysfunction in chronic hepatitis C
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