The effects of circulating MIR22-3p and MIR16-1-3p levels in different stages of subacute thyroiditis. (3rd June 2023)

• Record Type: Journal Article
• Authors: Karakus, Nevin; Catak, Merve; Kutluturk, Faruk; Kocak, Mustafa; Akman Ekici, Merve; Citir, Muhterem
• Is Part Of: Nucleosides, nucleotides & nucleic acids. Volume 42:Number 6(2023)
• Page Start: 436
• Page End: 447
• Publication Date: 2023-06-03
• Subjects: Subacute thyroiditis -- MIR22 -- MIR16-1 -- expression level; Nucleosides -- Periodicals; Nucleotides -- Periodicals; Nucleic acids -- Periodicals; 572.8
• DOI: 10.1080/15257770.2022.2154360
• Languages: English
• ISSNs: 1525-7770

Abstract

Abstract: Subacute thyroiditis (SAT) is an inflammatory thyroid disease with a frequency is 5% among all thyroid diseases. miRNAs are endogenous, non-coding RNAs ranging in length from 19 to 25 nucleotides. They play an important role in the posttranscriptional regulation of gene expression. In this study, we aimed to investigate whether the expression levels of two circulating miRNAs, MIR22 and MIR16-1, can be used as a parameter in the diagnosis and follow-up of SAT disease. Fifty patients diagnosed with SAT and 41 healthy controls were included in this study. Expression levels of miRNAs were determined by real time-PCR method. Expression data of miRNAs were calculated by fold change (2 -ΔΔCt ) method. The statistical significance of miRNA expression was evaluated by t-test. The expression levels of MIR22-3p and MIR16-1-3p were not found to be statistically different between SAT patients and controls and also between the patients in different stages (hyperthyroid, euthyroid, and hypothyroid) of the disease. According to correlation analyses, we observed a positive strong correlation between erythrocyte sedimentation rate (ESR) and the expression levels of MIR22-3p and MIR16-1-3p ( r = 0.960, p = 0.000 and r = 0.865, p = 0.006, respectively), and a positive strong correlation between fT4 and the expression levels of MIR22-3p in SAT patients in euthyroid stage ( r = 0.712, p = 0.047). In this study, we showed that the expression levels of MIR22-3p and MIR16-1-3p have correlation with clinical characteristics of SAT disease. Our results suggest that MIR22 and MIR16-1 may be effective in the pathogenesis of SAT.