Association of Single-Nucleotide Polymorphisms in the VDR Gene with Tuberculosis and Infection of Beijing Genotype Mycobacterium tuberculosis

被引:6
作者
Yu, Jinjie [1 ,2 ]
Liu, Mengwen [3 ]
Mijiti, Xiaokaiti [4 ]
Liu, Haican [2 ]
Wang, Quan [4 ]
Yin, Chunjie [3 ]
Anwaierjiang, Aiketaguli [5 ]
Xu, Miao [4 ]
Li, Machao [3 ]
Deng, Lele [2 ,6 ]
Xiao, Hui [3 ]
Zhao, Xiuqin [2 ]
Wan, Kanglin [2 ]
Li, Guilian [2 ]
Yuan, Xiuqin [1 ]
机构
[1] Univ South China, Sch Publ Hlth, Hengyang 421001, Peoples R China
[2] Natl Inst Communicable Dis Control & Prevent, Collaborat Innovat Ctr Diag & Treatment Infect Dis, Chinese Ctr Dis Control & Prevent, State Key Lab Infect Dis Prevent & Control, Beijing 102206, Peoples R China
[3] Xinjiang Med Univ, Sch Publ Hlth, Urumqi 830011, Xinjiang, Peoples R China
[4] Xinjiang Med Univ, Affiliated Hosp 8, Urumqi 830049, Xinjiang, Peoples R China
[5] Coll Xinjiang Uyghur Med, Hetian 848000, Peoples R China
[6] Natl Inst Viral Dis Control & Prevent, Chinese Ctr Dis Control & Prevent, Beijing, Peoples R China
关键词
vitamin D receptor; VDR; polymorphism; tuberculosis; Mycobacterium tuberculosis; Beijing lineage; GENOME-WIDE ASSOCIATION; SUSCEPTIBILITY; POPULATION; PULMONARY; STRAINS;
D O I
10.2147/IDR.S407595
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background: The aim of the present study was to investigate the association between vitamin D receptor (VDR) gene polymorphism and tuberculosis susceptibility, as well as the potential interaction of host genetic factors with the heterogeneity of Mycobacterium tuberculosis in the population from Xinjiang, China.Methods: From January 2019 to January 2020, we enrolled 221 tuberculosis patients as the case group and 363 staff with no clinical symptoms as the control group from four designated tuberculosis hospitals in southern Xinjiang, China. The polymorphisms of Fok I, Taq I, Apa I, Bsm I, rs3847987 and rs739837 in the VDR were detected by sequencing. M. tuberculosis isolates were collected from the case group and identified as Beijing or non-Beijing lineage by multiplex PCR. Propensity score (PS), univariate analysis and multivariable logistic regression models were used to perform the analysis.Results: Our results showed that the allele and genotype frequencies of Fok I, Taq I, Apa I, Bsm I, rs3847987 and rs739837 in VDR were not correlated with tuberculosis susceptibility or lineages of M. tuberculosis. Two out of six loci of the VDR gene formed one haplotype block, and none of the haplotypes was found to correlate with tuberculosis susceptibility or lineages of M. tuberculosis infected.Conclusion: Polymorphisms in the VDR gene may not indicate susceptibility to tuberculosis. There was also no evidence on the interaction between the VDR gene of host and the lineages of M. tuberculosis in the population from Xinjiang, China. Further studies are nonetheless required to prove our conclusions.
引用
收藏
页码:3157 / 3169
页数:13
相关论文
共 48 条
[31]   Vitamin D: Immuno-modulation and tuberculosis treatment [J].
Selvaraj, Paramasivam ;
Harishankar, Murugesan ;
Afsal, Kolloli .
CANADIAN JOURNAL OF PHYSIOLOGY AND PHARMACOLOGY, 2015, 93 (05) :377-384
[32]  
Sha YX, 2020, J ANHUI MED U, V55, P1588
[33]   Coding and non-coding polymorphisms in VDR gene and susceptibility to pulmonary tuberculosis in tribes, castes and Muslims of Central India [J].
Sharma, Prithvi R. ;
Singh, Shweta ;
Jena, Mamta ;
Mishra, Gunja ;
Prakash, Ravi ;
Das, P. K. ;
Bamezai, R. N. K. ;
Tiwari, P. K. .
INFECTION GENETICS AND EVOLUTION, 2011, 11 (06) :1456-1461
[34]   Investigation of genetic susceptibility to Mycobacterium tuberculosis (VDR and IL10 genes) in a population with a high level of substructure in the Brazilian Amazon region [J].
Silva, C. A. ;
Fernandes, D. C. R. O. ;
Braga, A. C. O. ;
Cavalcante, G. C. ;
Sortica, V. A. ;
Hutz, M. H. ;
Leal, D. F. V. B. ;
Fernades, M. R. ;
Santana-da-Silva, M. N. ;
Lopes Valente, S. E. ;
Pastana, L. F. ;
Pinto, P. D. C. ;
Costa, G. E. ;
Ribeiro-dos-Santos, A. ;
Santos, S. ;
Santos, N. P. C. .
INTERNATIONAL JOURNAL OF INFECTIOUS DISEASES, 2020, 98 :447-453
[35]   Polymorphisms in Autophagy Genes and Susceptibility to Tuberculosis [J].
Songane, Mario ;
Kleinnijenhuis, Johanneke ;
Alisjahbana, Bachti ;
Sahiratmadja, Edhyana ;
Parwati, Ida ;
Oosting, Marije ;
Plantinga, Theo S. ;
Joosten, Leo A. B. ;
Netea, Mihai G. ;
Ottenhoff, Tom H. M. ;
van de Vosse, Esther ;
van Crevel, Reinout .
PLOS ONE, 2012, 7 (08)
[36]   Vitamin D status, receptor gene polymorphisms, and supplementation on tuberculosis: A systematic review of case-control studies and randomized controlled trials [J].
Sutaria, Nilay ;
Liu, Ching-Ti ;
Chen, Tai C. .
JOURNAL OF CLINICAL AND TRANSLATIONAL ENDOCRINOLOGY, 2014, 1 (04) :151-160
[37]   A method for meta-analysis of molecular association studies [J].
Thakkinstian, A ;
McElduff, P ;
D'Este, C ;
Duffy, D ;
Attia, J .
STATISTICS IN MEDICINE, 2005, 24 (09) :1291-1306
[38]   Influence of Single Nucleotide Polymorphisms on Rifampin Pharmacokinetics in Tuberculosis Patients [J].
Thomas, Levin ;
Miraj, Sonal Sekhar ;
Surulivelrajan, Mallayasamy ;
Varma, Muralidhar ;
Sanju, Chidananda S., V ;
Rao, Mahadev .
ANTIBIOTICS-BASEL, 2020, 9 (06) :1-15
[39]   Variant G57E of Mannose Binding Lectin Associated with Protection against Tuberculosis Caused by Mycobacterium africanum but not by M. tuberculosis [J].
Thye, Thorsten ;
Niemann, Stefan ;
Walter, Kerstin ;
Homolka, Susanne ;
Intemann, Christopher D. ;
Chinbuah, Margaret Amanua ;
Enimil, Anthony ;
Gyapong, John ;
Osei, Ivy ;
Owusu-Dabo, Ellis ;
Ruesch-Gerdes, Sabine ;
Horstmann, Rolf D. ;
Ehlers, Stefan ;
Meyer, Christian G. .
PLOS ONE, 2011, 6 (06)
[40]   Mycobacterium tuberculosis complex and human coadaptation: a two-way street complicating host susceptibility to TB [J].
Uren, Caitlin ;
Hoal, Eileen G. ;
Moller, Marlo .
HUMAN MOLECULAR GENETICS, 2021, 30 (R1) :R146-R153