Hashemi Mohammad, Sharifi-Mood Batool, Rasouli Azam, Amininia Shadi, Naderi Mohammad, Taheri Mohsen
Cellular and Molecular Research Center, Zahedan University of Medical Sciences, Zahedan, Iran; Department of Clinical Biochemistry, School of Medicine, Zahedan University of Medical Sciences, Zahedan, Iran.
Research Center for Infectious Diseases and Tropical Medicine, Zahedan University of Medical Sciences, Zahedan, Iran.
EXCLI J. 2015 Jan 21;14:117-22. doi: 10.17179/excli2014-636. eCollection 2015.
Macrophage migration inhibitory factor (MIF) has an important role in controlling infection. The aim of this study was to evaluate the possible association between MIF -173 G/C functional polymorphism and pulmonary tuberculosis (PTB) in an Iranian population from Zahedan Southeast Iran. This case-control study was done on 161 PTB and 142 healthy subjects. Genomic DNA was extracted from all participants by salting out method. The MIF -173 G/C variant was genotyped using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). The finding showed that the MIF -173 G/C polymorphism increased the risk of PTB in codominant (OR=1.76, 95 % CI=1.05-2.95, p=0.038, GC vs GG) and dominant (OR=1.78, 95 % CI=1.09-2.91, p=0.027, GC+CC vs GG) tested inheritance models. Furthermore, the minor allele frequency (MAF) increased the risk of PTB in comparison with G allele (OR=1.63, 95 % CI=1.07-2.48, p=0.028). In conclusion, the present study provides evidence that -173 G/C polymorphism may increase the risk of PTB.
巨噬细胞移动抑制因子(MIF)在控制感染方面发挥着重要作用。本研究旨在评估伊朗东南部扎黑丹地区人群中MIF -173 G/C功能多态性与肺结核(PTB)之间可能存在的关联。这项病例对照研究对161例肺结核患者和142名健康受试者进行。采用盐析法从所有参与者中提取基因组DNA。使用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)对MIF -173 G/C变异进行基因分型。研究结果表明,在共显性(OR=1.76,95%可信区间=1.05 - 2.95,p=0.038,GC与GG相比)和显性(OR=1.78,95%可信区间=1.09 - 2.91,p=0.027,GC + CC与GG相比)遗传模型中,MIF -173 G/C多态性增加了患肺结核的风险。此外,与G等位基因相比,次要等位基因频率(MAF)增加了患肺结核的风险(OR=1.63,95%可信区间=1.07 - 2.48,p=0.028)。总之,本研究提供了证据表明-173 G/C多态性可能增加患肺结核的风险。