Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 1 de 1
Filtrar
Mais filtros

Base de dados
Ano de publicação
Tipo de documento
País de afiliação
Intervalo de ano de publicação
1.
Biomol Biomed ; 24(5): 1170-1177, 2024 Sep 06.
Artigo em Inglês | MEDLINE | ID: mdl-38761409

RESUMO

Hashimoto's thyroiditis (HT) is a prevalent autoimmune disease. We investigated the relationship of peripheral blood long noncoding RNA-plasmacytoma variant translocation 1 (lncRNA-PVT1) and microRNA (miR)-146a levels with Th17/Treg-related cytokines in HT patients and their clinical significance. Correlations of PVT1 and miR-146a with Th17/Treg-related cytokines were analyzed, and its clinical value in diagnosing HT was assessed. Results showed reduced lncRNA-PVT1 and interleukin (IL)-10 levels and increased miR-146a and IL-17 levels in HT patients. lncRNA-PVT1 negatively interrelated with miR-146a, IL-17, IL-23 and IL-6, and positively interrelated with IL-10; miR-146a positively correlated with IL-17, IL-23 and IL-6, but negatively correlated with IL-10 in HT patients. The area under the curve (AUC) of lncRNA-PVT1 and miR-146a levels for diagnosing HT were 0.822 and 0.844, respectively (sensitivity 88.73% and 86.62%, specificity 67.02% and 69.15%, cut-off values 0.76 and 2.73), with their combined detections yielding a higher AUC. Patients with poorly expressed lncRNA-PVT1 and highly expressed miR-146a had elevated HT incidence. lncRNA-PVT1 and miR-146a levels were also found to be an independent influencing factor for HT occurrence. Our findings suggest that HT patients have low peripheral blood lncRNA-PVT1 expression and high miR-146a expression. lncRNA-PVT1 and miR-146a level changes were correlated with Th17/Treg cytokine imbalance and could be a potential diagnostic tool and independent influencing factor for HT.


Assuntos
Citocinas , Doença de Hashimoto , MicroRNAs , RNA Longo não Codificante , Linfócitos T Reguladores , Células Th17 , Humanos , RNA Longo não Codificante/sangue , RNA Longo não Codificante/genética , MicroRNAs/sangue , MicroRNAs/genética , Células Th17/imunologia , Feminino , Doença de Hashimoto/sangue , Doença de Hashimoto/genética , Doença de Hashimoto/imunologia , Masculino , Pessoa de Meia-Idade , Adulto , Citocinas/sangue , Linfócitos T Reguladores/imunologia , Linfócitos T Reguladores/metabolismo , Relevância Clínica
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA