Ali Amiri , Toomaj Sabooteh , Farhad Shahsavar , Khatereh Anbari , Flora Pouremadi
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引用次数: 16
Abstract
Objective
Tuberculosis (TB) is caused by infection of Mycobacterium tuberculosis. Host genetic variability is an important determinant of the risk of developing TB in humans. Although the association between MBL polymorphisms and TB has been studied in various populations, the results are controversial. The aim of this study was to investigate mannose-binding lectin (MBL) gene polymorphisms with susceptibility to pulmonary tuberculosis (PTB) in a Lur population of Iran.
Methods
In this case-control study, four functional MBL gene polymorphisms (HL, XY, PQ and AB) were genotyped by using PCR Single Strand Conformation Polymorphism (SSCP) technique in a Lur population living in Lorestan Province, consisting of 100 patients with pulmonary tuberculosis (PTB) age and sex matched 100 healthy controls (HCs). Association analyses were performed with the SPSS 21 statistical software.
Results
We found that MBL (HH) genotype polymorphism significantly was associated with increased susceptibility to TB (35% in patients vs. 22% in controls, P = 0.0417, OR = 1.909, %95 CI = 1.020–3.573). Additionally, H allele showed a significant association with increased risk of TB (56.5% in patients vs. 46% in controls, P = 0.0357, OR = 1.525, %95 CI = 1.028–2.262). Also, the distribution of L allele in patients was significantly lower frequency in TB patients compared to controls (43.5% vs. 54%, P = 0.0357, OR = 0.656, %95 CI = 0.442–0.973). However, the allelic and genotypic frequencies of AB, XY and PQ polymorphisms were not significantly different between the patients and the controls. We couldn't detect any significant differences between haplotypes among TB patients and healthy controls.
Conclusions
Our findings demonstrated that HH genotype and H allele may increase the susceptibility to pulmonary TB in the Lur population of Iran, although L allele may decrease the susceptibility to pulmonary TB in this population. We suggest that it is necessary to further more studies with larger sample size and other ethnic population.
目的结核(TB)是由结核分枝杆菌感染引起的疾病。宿主遗传变异是人类发生结核病风险的一个重要决定因素。尽管在不同人群中研究了MBL多态性与结核病之间的关系,但结果存在争议。本研究的目的是研究甘露糖结合凝集素(MBL)基因多态性与伊朗鲁尔人群肺结核(PTB)易感性的关系。方法采用PCR单链构象多态性(SSCP)技术,对100例年龄和性别与100例健康对照(hc)相匹配的洛雷斯坦省鲁尔族肺结核(PTB)患者的4种MBL基因多态性(HL、XY、PQ和AB)进行基因分型。采用SPSS 21统计软件进行关联分析。结果MBL (HH)基因型多态性与TB易感性增加显著相关(患者35% vs对照组22%,P = 0.0417, OR = 1.909, %95 CI = 1.020-3.573)。此外,H等位基因与结核病风险增加显著相关(患者为56.5%,对照组为46%,P = 0.0357, OR = 1.525, %95 CI = 1.028-2.262)。此外,L等位基因在结核病患者中的分布频率显著低于对照组(43.5% vs. 54%, P = 0.0357, OR = 0.656, %95 CI = 0.442-0.973)。而AB、XY和PQ多态性的等位基因和基因型频率在患者和对照组之间无显著差异。我们没有发现结核病患者和健康对照之间的单倍型有任何显著差异。结论HH基因型和H等位基因可能增加伊朗鲁尔人群对肺结核的易感性,而L等位基因可能降低该人群对肺结核的易感性。我们建议有必要进一步开展更大样本量和其他民族人群的研究。