Literature DB >> 17949264

Susceptible alleles of the CD40 and CTLA-4 genes are not associated with the relapse after antithyroid withdrawal in Graves' disease.

Kyung Won Kim1, Young Joo Park, Tae Yong Kim, Do Joon Park, Kyong Soo Park, Bo Youn Cho.   

Abstract

In this study, we investigated whether the CD40 or cytotoxic T lymphocyte-associated molecules-4 (CTLA-4) polymorphisms, which are associated with the susceptibility of Graves' disease (GD), can predict the clinical outcome after antithyroid drug (ATD) withdrawal. All patients with GD were treated with ATD. GD patients were divided into two groups: remission or failure. The remission group was defined as patients who maintained a euthyroid state for 1 year after ATD withdrawal. The failure group was defined as patients who relapsed within 1 year after the discontinuation of ATD or who could not discontinue their ATD treatment within 24 months. The rate of treatment failure after ATD withdrawal was 72.2%. For the susceptible genes, the CC genotype in the CD40, the GG genotype in the CTLA-4 exon 1, and the CC genotype in the CTLA-4 promoter region have shown no significant association with a clinical outcome after ATD withdrawal. However, clinical parameters, such as male gender, severe thyrotoxicosis, high thyroid-stimulating hormone-binding inhibitory immunoglobulin value, and a large goiter, were related to treatment failure. These findings suggest that the genetic markers associated with the development of GD cannot be used to predict the relapse of GD patients in place of clinical parameters.

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Year:  2007        PMID: 17949264     DOI: 10.1089/thy.2007.0011

Source DB:  PubMed          Journal:  Thyroid        ISSN: 1050-7256            Impact factor:   6.568


  5 in total

1.  Genotype and phenotype predictors of relapse of graves' disease after antithyroid drug withdrawal.

Authors:  Pei-Wen Wang; I-Ya Chen; Suh-Hang Hank Juo; Edward Hsi; Rue-Tsuan Liu; Ching-Jung Hsieh
Journal:  Eur Thyroid J       Date:  2012-10-12

2.  The genetic basis of graves' disease.

Authors:  Rafał Płoski; Konrad Szymański; Tomasz Bednarczuk
Journal:  Curr Genomics       Date:  2011-12       Impact factor: 2.236

3.  CD28/CTLA-4/ICOS haplotypes confers susceptibility to Graves' disease and modulates clinical phenotype of disease.

Authors:  Edyta Pawlak-Adamska; Irena Frydecka; Marek Bolanowski; Anna Tomkiewicz; Anna Jonkisz; Lidia Karabon; Anna Partyka; Oskar Nowak; Marek Szalinski; Jacek Daroszewski
Journal:  Endocrine       Date:  2016-09-16       Impact factor: 3.633

Review 4.  Antithyroid Drug Therapy for Graves' Disease and Implications for Recurrence.

Authors:  Jia Liu; Jing Fu; Yuan Xu; Guang Wang
Journal:  Int J Endocrinol       Date:  2017-04-25       Impact factor: 3.257

5.  Benign Thyroid Diseases: Are There Gender-Specific Differences for Diagnosis and Treatment of Nontoxic Thyroid Nodules? Results from a 4-Year Retrospective Analysis of an Endocrine Tumor Board.

Authors:  Jasmin Mettler; Stella Armefti; Matthias Schmidt; Michael Faust; Marianne Engels; Costanza Chiapponi
Journal:  Visc Med       Date:  2020-01-21
  5 in total

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