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The Reduced Predictive Value of Interleukin 28b Gene Polymorphisms in a Cohort of Patients With Thyroiditis Developed During Antiviral Therapy for Chronic Hepatitis C: A Preliminary Study

Author(s):
Huy A TranHuy A Tran1,*, Tracey L JonesTracey L Jones2, Elizabeth A IannaElizabeth A Ianna2, Robert A GibsonRobert A Gibson2, Glenn E M ReevesGlenn E M Reeves1
1Hunter Area Pathology Service, John Hunter Hospital, [email protected], New South Wales 2310, Australia
2Hepatitis C Service, Gastroenterology Department, John Hunter Hospital, Australia

Hepatitis Monthly:Vol. 12, issue 8; 6036
Published online:Aug 30, 2012
Article type:Research Article
Received:May 01, 2012
Accepted:May 22, 2012
How to Cite:Huy A Tran, Tracey L Jones, Elizabeth A Ianna, Robert A Gibson, Glenn E M Reeves, The Reduced Predictive Value of Interleukin 28b Gene Polymorphisms in a Cohort of Patients With Thyroiditis Developed During Antiviral Therapy for Chronic Hepatitis C: A Preliminary Study.Hepat Mon.2012;12(8):6036.https://doi.org/10.5812/hepatmon.6036 .

Abstract

Background:

Single nucleotide polymorphism in the interleukin28B (IL28B) gene was recently shown to be associated with a significant increase in response to interferon-? and ribavirin treatment in patients with chronic hepatitis C. Similarly, thyroid disease (TD) occurring during treatment confer an improved sustained virologic response (SVR).

Objectives:

To determine the role of IL28B genotypes in a cohort of hepatitis C patients who develop TD during treatment and its relationship to SVR.

Patients and Methods:

IL28B gene profiles including rs12979860, rs12980275 and rs 8099917 and their genotypes were determined in a cohort of 23 hepatitis C patients who developed TD during treatment and their relationship to SVR.

Results:

Out of 23 studies cases, 19 has one or more favorable genotypes, of which 15 (78.9%) achieved SVR. Eleven has all three unfavorable genotypes and yet achieved 72.7 % SVR. The presence of more than one favorable genotype only correctly predicts SVR vs. non- SVR in ~50 % of cases, i.e. by chance.

Conclusions:

Despite the small number of subjects, the presence of one or more unfavorable IL28B genotype does not portend a poor SVR prognostic outcome. This suggests that TD in this clinical context may be a critical factor in the achievement of SVR, probably above that of the genetic predisposition.

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