Long Non-coding RNAs Genes Polymorphisms and Their Expression Levels in Patients With Rheumatoid Arthritis

Long non-coding RNAs (lncRNAs) are increasingly recognized to play important roles in multiple autoimmune diseases. This study aimed to evaluate the association of four lncRNAs (ANRIL, lnc-DC, MALAT1, ZFAS1) genes single nucleotide polymorphisms (SNPs) with susceptibility to rheumatoid arthritis (RA...

Full description

Bibliographic Details
Main Authors: Tian-Ping Zhang, Bang-Qiang Zhu, Sha-Sha Tao, Yin-Guang Fan, Xiao-Mei Li, Hai-Feng Pan, Dong-Qing Ye
Format: Article
Language:English
Published: Frontiers Media S.A. 2019-10-01
Series:Frontiers in Immunology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fimmu.2019.02529/full
_version_ 1811270174516445184
author Tian-Ping Zhang
Tian-Ping Zhang
Bang-Qiang Zhu
Sha-Sha Tao
Yin-Guang Fan
Xiao-Mei Li
Hai-Feng Pan
Dong-Qing Ye
author_facet Tian-Ping Zhang
Tian-Ping Zhang
Bang-Qiang Zhu
Sha-Sha Tao
Yin-Guang Fan
Xiao-Mei Li
Hai-Feng Pan
Dong-Qing Ye
author_sort Tian-Ping Zhang
collection DOAJ
description Long non-coding RNAs (lncRNAs) are increasingly recognized to play important roles in multiple autoimmune diseases. This study aimed to evaluate the association of four lncRNAs (ANRIL, lnc-DC, MALAT1, ZFAS1) genes single nucleotide polymorphisms (SNPs) with susceptibility to rheumatoid arthritis (RA) patients, as well as their expression levels. Seventeen SNPs of the four lncRNAs were genotyped in a cohort of 660 RA patients and 710 controls using improved multiple ligase detection reaction (iMLDR). The lncRNAs expressions in peripheral blood mononuclear cells (PBMCs) from 120 RA patients and 120 controls were detected by qRT-PCR. No significant differences were found for the allele and genotype frequencies distribution of ANRIL SNPs (rs1412830, rs944796, rs61271866, rs2518723, rs3217992), lnc-DC SNPs (rs7217280, rs10515177), MALAT1 SNPs (rs619586, rs4102217, rs591291, rs11227209, rs35138901), ZFAS1 SNPs (rs237742, rs73116127, rs6125607, rs6125608) between RA patients and normal controls (all P > 0.05). The genotype effects of dominant and recessive models were also evaluated, but no significant association was found. In addition, our results demonstrated that the rs944796 G allele, rs2518723 T allele, rs3217992 T allele frequencies were significantly associated with anti-CCP in RA patients (all P < 0.05). The haplotype CGTA frequency for ZFAS1 was significantly higher in RA patients (P = 0.036). Compared with normal controls, the expression levels of ANRIL, lnc-DC, MALAT1, ZFAS1 in PBMCs were significantly reduced in RA patients (all P < 0.001). Moreover, ZFAS1 expression was negatively associated with CRP in RA patients (P = 0.002). In summary, ANRIL, lnc-DC, MALAT1, and ZFAS1 genes SNPs were not associated with RA susceptibility, while altered ANRIL, lnc-DC, MALAT1, ZFAS1 levels in RA patients suggested that these lncRNAs might play a role in RA.
first_indexed 2024-04-12T21:56:07Z
format Article
id doaj.art-4c89f6db2d414f5892eae7a940f611d6
institution Directory Open Access Journal
issn 1664-3224
language English
last_indexed 2024-04-12T21:56:07Z
publishDate 2019-10-01
publisher Frontiers Media S.A.
record_format Article
series Frontiers in Immunology
spelling doaj.art-4c89f6db2d414f5892eae7a940f611d62022-12-22T03:15:19ZengFrontiers Media S.A.Frontiers in Immunology1664-32242019-10-011010.3389/fimmu.2019.02529447661Long Non-coding RNAs Genes Polymorphisms and Their Expression Levels in Patients With Rheumatoid ArthritisTian-Ping Zhang0Tian-Ping Zhang1Bang-Qiang Zhu2Sha-Sha Tao3Yin-Guang Fan4Xiao-Mei Li5Hai-Feng Pan6Dong-Qing Ye7Anhui Province Key Laboratory of Major Autoimmune Diseases, Department of Epidemiology and Biostatistics, School of Public Health, Anhui Medical University, Hefei, ChinaDepartment of Infectious Diseases, The First Affiliated Hospital of Anhui Medical University, Hefei, ChinaAnhui Province Key Laboratory of Major Autoimmune Diseases, Department of Epidemiology and Biostatistics, School of Public Health, Anhui Medical University, Hefei, ChinaAnhui Province Key Laboratory of Major Autoimmune Diseases, Department of Epidemiology and Biostatistics, School of Public Health, Anhui Medical University, Hefei, ChinaAnhui Province Key Laboratory of Major Autoimmune Diseases, Department of Epidemiology and Biostatistics, School of Public Health, Anhui Medical University, Hefei, ChinaDepartment of Rheumatology, The First Affiliated Hospital of University of Science and Technology of China, Hefei, ChinaAnhui Province Key Laboratory of Major Autoimmune Diseases, Department of Epidemiology and Biostatistics, School of Public Health, Anhui Medical University, Hefei, ChinaAnhui Province Key Laboratory of Major Autoimmune Diseases, Department of Epidemiology and Biostatistics, School of Public Health, Anhui Medical University, Hefei, ChinaLong non-coding RNAs (lncRNAs) are increasingly recognized to play important roles in multiple autoimmune diseases. This study aimed to evaluate the association of four lncRNAs (ANRIL, lnc-DC, MALAT1, ZFAS1) genes single nucleotide polymorphisms (SNPs) with susceptibility to rheumatoid arthritis (RA) patients, as well as their expression levels. Seventeen SNPs of the four lncRNAs were genotyped in a cohort of 660 RA patients and 710 controls using improved multiple ligase detection reaction (iMLDR). The lncRNAs expressions in peripheral blood mononuclear cells (PBMCs) from 120 RA patients and 120 controls were detected by qRT-PCR. No significant differences were found for the allele and genotype frequencies distribution of ANRIL SNPs (rs1412830, rs944796, rs61271866, rs2518723, rs3217992), lnc-DC SNPs (rs7217280, rs10515177), MALAT1 SNPs (rs619586, rs4102217, rs591291, rs11227209, rs35138901), ZFAS1 SNPs (rs237742, rs73116127, rs6125607, rs6125608) between RA patients and normal controls (all P > 0.05). The genotype effects of dominant and recessive models were also evaluated, but no significant association was found. In addition, our results demonstrated that the rs944796 G allele, rs2518723 T allele, rs3217992 T allele frequencies were significantly associated with anti-CCP in RA patients (all P < 0.05). The haplotype CGTA frequency for ZFAS1 was significantly higher in RA patients (P = 0.036). Compared with normal controls, the expression levels of ANRIL, lnc-DC, MALAT1, ZFAS1 in PBMCs were significantly reduced in RA patients (all P < 0.001). Moreover, ZFAS1 expression was negatively associated with CRP in RA patients (P = 0.002). In summary, ANRIL, lnc-DC, MALAT1, and ZFAS1 genes SNPs were not associated with RA susceptibility, while altered ANRIL, lnc-DC, MALAT1, ZFAS1 levels in RA patients suggested that these lncRNAs might play a role in RA.https://www.frontiersin.org/article/10.3389/fimmu.2019.02529/fullANRILlnc-DCMALAT1ZFAS1single nucleotide polymorphismsrheumatoid arthritis
spellingShingle Tian-Ping Zhang
Tian-Ping Zhang
Bang-Qiang Zhu
Sha-Sha Tao
Yin-Guang Fan
Xiao-Mei Li
Hai-Feng Pan
Dong-Qing Ye
Long Non-coding RNAs Genes Polymorphisms and Their Expression Levels in Patients With Rheumatoid Arthritis
Frontiers in Immunology
ANRIL
lnc-DC
MALAT1
ZFAS1
single nucleotide polymorphisms
rheumatoid arthritis
title Long Non-coding RNAs Genes Polymorphisms and Their Expression Levels in Patients With Rheumatoid Arthritis
title_full Long Non-coding RNAs Genes Polymorphisms and Their Expression Levels in Patients With Rheumatoid Arthritis
title_fullStr Long Non-coding RNAs Genes Polymorphisms and Their Expression Levels in Patients With Rheumatoid Arthritis
title_full_unstemmed Long Non-coding RNAs Genes Polymorphisms and Their Expression Levels in Patients With Rheumatoid Arthritis
title_short Long Non-coding RNAs Genes Polymorphisms and Their Expression Levels in Patients With Rheumatoid Arthritis
title_sort long non coding rnas genes polymorphisms and their expression levels in patients with rheumatoid arthritis
topic ANRIL
lnc-DC
MALAT1
ZFAS1
single nucleotide polymorphisms
rheumatoid arthritis
url https://www.frontiersin.org/article/10.3389/fimmu.2019.02529/full
work_keys_str_mv AT tianpingzhang longnoncodingrnasgenespolymorphismsandtheirexpressionlevelsinpatientswithrheumatoidarthritis
AT tianpingzhang longnoncodingrnasgenespolymorphismsandtheirexpressionlevelsinpatientswithrheumatoidarthritis
AT bangqiangzhu longnoncodingrnasgenespolymorphismsandtheirexpressionlevelsinpatientswithrheumatoidarthritis
AT shashatao longnoncodingrnasgenespolymorphismsandtheirexpressionlevelsinpatientswithrheumatoidarthritis
AT yinguangfan longnoncodingrnasgenespolymorphismsandtheirexpressionlevelsinpatientswithrheumatoidarthritis
AT xiaomeili longnoncodingrnasgenespolymorphismsandtheirexpressionlevelsinpatientswithrheumatoidarthritis
AT haifengpan longnoncodingrnasgenespolymorphismsandtheirexpressionlevelsinpatientswithrheumatoidarthritis
AT dongqingye longnoncodingrnasgenespolymorphismsandtheirexpressionlevelsinpatientswithrheumatoidarthritis