Chen Wei-Wei, Wan Baoshan, Zhang Ranran, Cao Wen, Liang Li, Zhao Yan-Lin, Chen Jin, Yue Jun
1 Department of Clinical Laboratory Medicine, Shanghai Pulmonary Hospital Affiliated to Tongji University School of Medicine, Shanghai, P.R. China.
2 National Center for Tuberculosis Control and Prevention, Chinese Center for Disease Control and Prevention, Beijing, P.R. China.
Genet Test Mol Biomarkers. 2019 Jul;23(7):442-447. doi: 10.1089/gtmb.2019.0003. Epub 2019 Jun 20.
Single nucleotide polymorphisms (SNPs) within precursor microRNAs (miRNAs) can affect the expression of the miRNAs and may be involved in the pathogenesis of pulmonary tuberculosis (PTB) and extrapulmonary tuberculosis (EPTB). We investigated the potential associations among four precursor miRNA SNPs (miR-149 A>G, C>T; miR-196a2 C>T; miR-499 C>T) and both PTB and EPTB. The study included 380 PTB patients, 242 EPTB patients, and 606 healthy control (HC) subjects from a Chinese Han population. We determined the miRNA relative expression levels from 10 HCs and 10 tuberculosis (TB) patients by quantitative PCR. We found that the PTB group had a significantly lower miR-149 level ( < 0.05) versus the HCs. The allele and genotype frequencies of the miR-149 SNPs were significantly different between the TB patients and the HC group. The C allele at the rs2292832 and the A allele at the rs71428439 locus were associated with susceptibility to EPTB. The C allele of rs2292832 was associated with an increased risk of EPTB compared with that of HCs ( < 0.01), and the A allele of rs71428439 was protective against EPTB ( < 0.01) and PTB ( < 0.01). We identified genetic polymorphisms in miR-149 that appear to be associated with susceptibility to both PTB and EPTB within a Chinese population.
前体微小RNA(miRNA)中的单核苷酸多态性(SNP)可影响miRNA的表达,并可能参与肺结核(PTB)和肺外结核(EPTB)的发病机制。我们研究了4个前体miRNA SNP(miR-149 A>G、C>T;miR-196a2 C>T;miR-499 C>T)与PTB和EPTB之间的潜在关联。该研究纳入了来自中国汉族人群的380例PTB患者、242例EPTB患者和606名健康对照(HC)受试者。我们通过定量PCR测定了10名HC受试者和10名结核病(TB)患者的miRNA相对表达水平。我们发现,与HC组相比,PTB组的miR-149水平显著更低(<0.05)。TB患者与HC组之间miR-149 SNP的等位基因和基因型频率存在显著差异。rs2292832位点的C等位基因和rs71428439位点的A等位基因与EPTB易感性相关。与HC组相比,rs2292832的C等位基因与EPTB风险增加相关(<0.01),rs71428439的A等位基因对EPTB(<0.01)和PTB(<0.01)具有保护作用。我们在中国人群中鉴定出miR-149的基因多态性,其似乎与PTB和EPTB的易感性均相关。