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Expression analysis of Treg-related lncRNAs in neuromyelitis optica spectrum disorder
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作者:

Harsij, Atefeh
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Shahid Beheshti Univ Med Sci, Dept Med Genet, Tehran, Iran Shahid Beheshti Univ Med Sci, Dept Med Genet, Tehran, Iran

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Ghiasian, Masoud
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Hamadan Univ Med Sci, Dept Neurol, Hamadan, Iran Shahid Beheshti Univ Med Sci, Dept Med Genet, Tehran, Iran

Eslami, Solat
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Alborz Univ Med Sci, Sch Med, Dept Med Biotechnol, Karaj, Iran Shahid Beheshti Univ Med Sci, Dept Med Genet, Tehran, Iran

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Taheri, Mohammad
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Jena Univ Hosp, Inst Human Genet, Jena, Germany
Shahid Beheshti Univ Med Sci, Urol & Nephrol Res Ctr, Tehran, Iran Shahid Beheshti Univ Med Sci, Dept Med Genet, Tehran, Iran

Sayad, Arezou
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Shahid Beheshti Univ Med Sci, Dept Med Genet, Tehran, Iran Shahid Beheshti Univ Med Sci, Dept Med Genet, Tehran, Iran
机构:
[1] Shahid Beheshti Univ Med Sci, Dept Med Genet, Tehran, Iran
[2] Hamadan Univ Med Sci, Neurophysiol Res Ctr, Hamadan, Iran
[3] Hamadan Univ Med Sci, Dept Neurol, Hamadan, Iran
[4] Alborz Univ Med Sci, Sch Med, Dept Med Biotechnol, Karaj, Iran
[5] Jena Univ Hosp, Inst Human Genet, Jena, Germany
[6] Shahid Beheshti Univ Med Sci, Urol & Nephrol Res Ctr, Tehran, Iran
关键词:
Neuromyelitis optica spectrum disorder;
T cells;
lncRNAs;
Expression;
LONG NONCODING RNAS;
REGULATORY T-CELLS;
CHEMOKINE PROFILES;
CYTOKINE;
DIFFERENTIATION;
AQUAPORIN-4;
ACTIVATION;
MARKER;
D O I:
10.1016/j.msard.2023.105350
中图分类号:
R74 [神经病学与精神病学];
学科分类号:
摘要:
Neuromyelitis Optica Spectrum Disorder (NMOSD) is an autoimmune condition affecting the central nervous system, in which various kinds of immune cells, including T and B cells, and numerous cytokines and chemokines are implicated. LncRNAs modulating the function or differentiation of regulatory T cells (Tregs) may be involved in the pathoetiology of NMO. To assess the involvement of these lncRNAs in this disease, we studied the expression levels of TH2-LCR, MAFTRR, NEST, RMRP, and FLICR in NMO patients and healthy subjects. All of the lncRNAs listed were up-regulated in NMO patients compared with healthy controls. Although the interaction of group and gender factors significantly affected the expression of NEST, RMRP, and TH2-LCR genes, we detected no effect of gender factor on the expression of the examined genes. The highest expression correlation was found between RMRP and TH2-LCR among cases with correlation coefficient 0.73. ROC curve analysis indicated that TH2-LCR, MAFTRR, RMRP, and FLICR had significant prospective diagnostic power (AUC +/- SD = 0.99 +/- 0.002, 0.97 +/- 0.01, 0.91 +/- 0.01 and 0.84 +/- 0.04, respectively). Best of these genes was TH2-LCR with AUC +/- SD = 0.99 +/- 0.002, sensitivity= 0.97, specificity= 1, P-value= <0.0001. RMRP and TH2-LCR had a positive correlation with age and age at onset and a negative correlation with EDSS. Cumulatively, TH2-LCR, MAFTRR, RMRP, and FLICR lncRNAs, particularly TH2-LCR, could be considered as potential contributors to the pathogenesis of NMO disease.
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