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Outcome of Graves' Disease and Associated Genetic Predisposition: A Systematic Review of Literature

Mokoagow, I.; Manthovani, A. Z.; Epriliawati, M.

2024-09-28 endocrinology
10.1101/2024.09.27.24314519 medRxiv
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BackgroundGraves disease (GD) is an autoimmune hyperthyroidism that primarily affects the thyroid gland. The susceptibility, activity, and risk of recurrence of GD may be influenced by various genetic factors, which can interact with environmental triggers to precipitate disease relapse. This review examines the literature on the genetic predisposition to GD recurrence. MethodsLiterature from PubMed, EBSCOhost, and SCOPUS were searched. Three reviewers performed study selection and critical appraisal. ResultFive studies were selected. The literature indicates a risk of relapse in PTPN22, CTLA-4, TSH-R, IL-21, KREC, and HLA gene abnormalities. ConclusionSeveral genes are associated with GD relapse. However, predicting relapse risk requires consideration of multiple factors beyond genetic predisposition.

Published in Next Research · not in our set (fewer than 10 published preprints to learn from) · training set

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