Systemic Assessment of Solute Carrier Family 11-member A1 (rs17235409) Gene Polymorphism and Mycobacterium Tuberculosis Risk in Asian and Caucasian Population: A Comprehensive Updated Meta-analysis

被引:1
|
作者
Pauline, Rashmi [1 ]
Devaraj, Danis Vijay [2 ]
Sivasubramanian, Jayanthi [3 ]
Velmurugan, Saranya [1 ]
Stephen, Sharon Benita [1 ]
Yasam, Santhosh Kumar [1 ]
Kulanthaivel, Langeswaran [1 ]
Subbaraj, Gowtham Kumar [1 ]
机构
[1] Chettinad Acad Res & Educ, Chettinad Hosp & Res Inst, Fac Allied Hlth Sci, Kelambakkam 603103, Tamil Nadu, India
[2] Karpaga Vinayaga Inst Med Sci & Res Ctr, Dept Microbiol, Mathuranthagam, Tamil Nadu, India
[3] Panimalar Med Coll Hosp & Res Inst, Dept Microbiol, Chennai, Tamil Nadu, India
关键词
Gene polymorphism; genetic susceptibility; microbial infections; solute carrier family 11-member a1; tuberculosis; NRAMP1; POLYMORPHISMS; SUSCEPTIBILITY; ASSOCIATION; D543N; INFECTION; FORMS; VDR;
D O I
10.4103/ijmy.ijmy_180_23
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background: The present meta-analysis was assessed to confirm the association between solute carrier family 11-member A1 (SLC11A1) gene (rs17235409) polymorphism with the Mycobacterium tuberculosis infection in the Asian and Caucasian populations. Methods: A search was conducted using the databases including Google Scholar, Science Direct, Embase, and PubMed to find the case-control studies related to SLC11A1 gene polymorphism and tuberculosis (TB) infection. The MetaGenyo programme was used to perform statistical analyses of the data. The odds ratio and 95% confidence interval were calculated based on genetic models such as allelic model, dominant model, recessive model, and overdominant. The heterogeneity and publication bias for the present study were examined to assess its quality. The study was registered in PROSPERO (ID Number: 461434). Results: This current study revealed the association between the SLC11A1 gene polymorphism with TB. The statistical value obtained at P < 0.05 was deemed to be statistically significant. The meta-analysis results revealed that allele contrast and recessive models are significant association between SLC11A1 gene polymorphism with risk of TB infections, and dominant and overdominant models have no significant association with TB risk. In addition, the subgroup analysis based on the ethnicity dominant revealed a significant association with the risk of TB. Therefore, this results that the gene SLC11A1 has a significant association for allelic and recessive and has no significant association for dominant and overdominant with the risk of TB. Conclusion: According to the data retrieved from the database with respect to the present study revealed that SLC11A1 gene polymorphism rs17235409 for allelic, recessive models have been associated with TB infections, but dominant and overdominant models have not been associated with TB infections.
引用
收藏
页码:467 / 477
页数:11
相关论文
共 8 条
  • [1] Solute carrier family 11 member 1 genetic polymorphisms rs17235409 and rs3731865 associate with susceptibility to extremity post-traumatic osteomyelitis in a Chinese Han population
    Jiang, Nan
    Zhong, Yong-Cong
    Lin, Qing-Rong
    Song, Chen-Sheng
    Yu, Bin
    Hu, Yan-Jun
    INTERNATIONAL JOURNAL OF IMMUNOGENETICS, 2023, 50 (03) : 127 - 133
  • [2] The Bridging Integrator 1 Gene Polymorphism rs744373 and the Risk of Alzheimer’s Disease in Caucasian and Asian Populations: An Updated Meta-Analysis
    Ruixia Zhu
    Xu Liu
    Zhiyi He
    Molecular Neurobiology, 2017, 54 : 1419 - 1428
  • [3] The Bridging Integrator 1 Gene Polymorphism rs744373 and the Risk of Alzheimer's Disease in Caucasian and Asian Populations: An Updated Meta-Analysis
    Zhu, Ruixia
    Liu, Xu
    He, Zhiyi
    MOLECULAR NEUROBIOLOGY, 2017, 54 (02) : 1419 - 1428
  • [4] The ALDH2 gene rs671 polymorphism is associated with cardiometabolic risk factors in East Asian population: an updated meta-analysis
    Liu, Ruikang
    Peng, Miaomiao
    Zhang, Jiaoyue
    Qiu, Kangli
    Zeng, Tianshu
    Chen, Lulu
    FRONTIERS IN ENDOCRINOLOGY, 2024, 15
  • [5] Meta-analysis of BACE1 gene rs638405 polymorphism and the risk of Alzheimer's disease in Caucasion and Asian population
    Yu, Minhua
    Liu, Yue
    Shen, Jun
    Lv, Dongwei
    Zhang, Junjian
    NEUROSCIENCE LETTERS, 2016, 616 : 189 - 196
  • [6] The Relationship between Solute Carrier Family 1 Member 1 Polymorphisms (rs301430 and rs301434) and the Risk of Obsessive-Compulsive Disorders: A Meta-Analysis and Trial Sequential Analysis
    Wu, Bingjie
    Hu, Handan
    Liu, Lanxiao
    Huang, Peng
    JOURNAL OF BIOLOGICAL REGULATORS AND HOMEOSTATIC AGENTS, 2023, 37 (09): : 4623 - 4633
  • [7] Association between "solute carrier family 30 member 8" (SLC30A8) gene polymorphism and susceptibility to type 2 diabetes mellitus in Chinese Han and minority populations: an updated meta-analysis
    Wang, Yan
    Duan, Leizhen
    Yu, Songcheng
    Liu, Xinxin
    Han, Han
    Wang, Jun
    Li, Wenjie
    ASIA PACIFIC JOURNAL OF CLINICAL NUTRITION, 2018, 27 (06) : 1374 - 1390
  • [8] Solute Carrier Family 30 Member 8 Gene 807c/T Polymorphism and Type 2 Diabetes Mellitus in the Chinese Population: a Meta-Analysis Including 6,942 Subjects
    Li, Yan-Yan
    Lu, Xin-Zheng
    Wang, Hui
    Yang, Xin-Xing
    Geng, Hong-Yu
    Gong, Ge
    Zhan, Yi-Yang
    Kim, Hyun Jun
    Yang, Zhi-Jian
    FRONTIERS IN ENDOCRINOLOGY, 2018, 9