NR3C1 rs6198 Variant May Be Involved in the Relationship of Graves' Disease with Stressful Events

Although stressful events are known to trigger Graves' disease (GD), the mechanisms involved in this process are not well understood. The gene, encoding for the glucocorticoid receptor (GR), presents single nucleotide polymorphisms (SNPs) that are associated with stress-related diseases. To inv...

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Veröffentlicht in:Biomedicines 2023-04, Vol.11 (4), p.1155
Hauptverfasser: Nascimento, Matheus, Teixeira, Elisângela Souza, Dal' Bó, Izabela Fernanda, Peres, Karina Colombera, Rabi, Larissa Teodoro, Cury, Adriano Namo, Cançado, Natália Amaral, Miklos, Ana Beatriz Pinotti Pedro, Schwengber, Fernando, Bufalo, Natássia Elena, Ward, Laura Sterian
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Sprache:eng
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Zusammenfassung:Although stressful events are known to trigger Graves' disease (GD), the mechanisms involved in this process are not well understood. The gene, encoding for the glucocorticoid receptor (GR), presents single nucleotide polymorphisms (SNPs) that are associated with stress-related diseases. To investigate the relationship between SNPs, GD susceptibility, and clinical features, we studied 792 individuals, including 384 patients, among which 209 presented with Graves' orbitopathy (GO), and 408 paired healthy controls. Stressful life events were evaluated in a subset of 59 patients and 66 controls using the IES-R self-report questionnaire. SNPs rs104893913, rs104893909, and rs104893911 appeared at low frequencies and presented similar profiles in patients and controls. However, variant forms of rs6198 were rarer in GD patients, suggesting a protective effect. Stressful events were more common in patients than controls, and were reported to have clearly occurred immediately before the onset of GD symptoms in 23 cases. However, no association was found between these events and rs6198 genotypes or GD/GO characteristics. We suggest that the rs6198 polymorphism may be an important protective factor against GD, but its relationship with stressful events needs further investigation.
ISSN:2227-9059
2227-9059
DOI:10.3390/biomedicines11041155