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. 2023 Apr;24(2):108-115.
doi: 10.1038/s41435-023-00200-3. Epub 2023 Apr 12.

Long non-coding RNA maternally expressed gene 3, miR-125a-5p, CXCL13, and NF-kB in patients with immune thrombocytopenia

Affiliations

Long non-coding RNA maternally expressed gene 3, miR-125a-5p, CXCL13, and NF-kB in patients with immune thrombocytopenia

Mervat Naguib et al. Genes Immun. 2023 Apr.

Abstract

The main aim of this study was to assess the expression level of circulating long non-coding RNA maternally expressed gene 3 (lncRNA-MEG3), microRNA (miR-125a-5P), the chemokine C-X-C motif ligand13 (CXCL13), and the nuclear factor kappa-light-chain-enhancer of activated B cells (NF-kB) in immune thrombocytopenia (ITP) cases and to study its relation to the disease severity and treatment response. This case-control study included 45 patients newly diagnosed as ITP and 45 healthy subjects. We assessed complete blood count, antinuclear antibodies, hepatitis B and C virus serology, lncRNA-MEG3, miR-125a-5P, and CXCL13 expression in serum by real-time PCR and NF-kb protein by ELISA. In ITP patients compared to control, lncRNA-MEG3 was significantly increased, and miRNA-125a-5P was decreased, and this was associated with higher CXCL13 and NF-kB levels (P < 0.001, for all).There was a significant negative correlation between platelet count and lncRNA-MEG3, CXCL13, and NF-kb, while a positive correlation with miR-125a-5p in ITP patients. Patients who responded to steroids had significantly higher miR-125a-5p (P = 0.016) and significantly lower lncRNA-MEG3 (P < 0.001), CXCL13 (P = 0.005), and NF-kb (p = 0.002). Based on the ROC curves, lncRNA-MEG3 displayed the highest area under the curve (AUC) in the identification of organ bleeding (AUC = 0.805), the response to steroids (AUC = 0.853), and the need for splenectomy (AUC = 0.75).

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Conflict of interest statement

The authors declare no competing interests.

Figures

Fig. 1
Fig. 1. ROC curve diagnostic test accuracy of Lng- MEG3, miR125a-5P, CXCL13 and NF-kB for response to steroids in patients with ITP.
ROC curve diagnostic test accuracy for response to steroids in patients with ITP showed lncRNA-MEG3 (AUC = 0.853), miR-125a-5p (AUC = 0.716), CXCL13 (AUC = 0.749) and NF-kB (AUC = 0.780).
Fig. 2
Fig. 2. ROC curve diagnostic test accuracy of Lng- MEG3, miR125a-5P, CXCL13 and NF-kB for need to splenectomy in patients with ITP.
ROC curve diagnostic test accuracy for need to splenectomy in patients with ITP showed lncRNA-MEG3 (AUC = 0.750), miR-125a-5p (AUC = 0.603), CXCL13 (AUC = 0.564) and NF-kB (AUC = 0.639).

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References

    1. Neunert CE. Management of newly diagnosed immune thrombocytopenia: can we change outcomes? Blood Adv. 2017;1:2295–301. doi: 10.1182/bloodadvances.2017009860. - DOI - PMC - PubMed
    1. Song I, Kim J, Kwon K, Koo S, Jo D. Expression of CD154 (CD40L) on stimulated T lymphocytes in patients with idopathic thrombocytopenic purpura. Hematology. 2016;21:187–92. doi: 10.1179/1607845415Y.0000000032. - DOI - PubMed
    1. Raphael I, Joern RR, Forsthuber TG. Memory CD4+ T Cells in Immunity and Autoimmune Diseases. Cells. 2020;9:531. doi: 10.3390/cells9030531. - DOI - PMC - PubMed
    1. Kostic M, Zivkovic N, Cvetanovic A, Marjanović G. CD4+ T cell phenotypes in the pathogenesis of immune thrombocytopenia. Cell Immunol. 2020;351:104096. doi: 10.1016/j.cellimm.2020.104096. - DOI - PubMed
    1. Ko NY, Chen LR, Chen KH. The Role of Micro RNA and Long-Non-Coding RNA in Osteoporosis. Int J Mol Sci. 2020;21:4886. doi: 10.3390/ijms21144886. - DOI - PMC - PubMed