Genetic polymorphisms of MBL2 and tuberculosis susceptibility: a meta-analysis of 22 case-control studies
The association of mannose-binding lectin gene ( ) polymorphisms with tuberculosis susceptibility was inconclusive. In this study, a meta-analysis of 22 case-control studies was carried out to assess the effect of polymorphisms on tuberculosis risk. A search was performed in Embase, PubMed and Web o...
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Veröffentlicht in: | Archives of medical science 2018-10, Vol.14 (6), p.1212-1232 |
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Sprache: | eng |
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Zusammenfassung: | The association of mannose-binding lectin gene (
) polymorphisms with tuberculosis susceptibility was inconclusive. In this study, a meta-analysis of 22 case-control studies was carried out to assess the effect of
polymorphisms on tuberculosis risk.
A search was performed in Embase, PubMed and Web of Science up to Sep 30, 2015. Odds ratio (OR) and 95% confidence interval (95% CI) were used to assess the association. Statistical analyses were performed using STATA 12.0 software.
rs1800451 was associated with a decreased tuberculosis risk in the allele model (C vs. A: OR = 0.93, 95% CI: 0.86-1.00,
= 0.050). In analyses stratified by ethnicity, rs7096206 (C/G: OR = 1.31, 95% CI: 1.10-1.57,
= 0.003; GG vs. GC + CC: OR = 0.69, 95% CI: 0.56-0.85,
< 0.001) and A/O (O/A: OR = 1.34, 95% CI: 1.10-1.64,
= 0.004) were associated with tuberculosis risk in Asians, A/O (AA vs. AO + OO: OR = 0.71, 95% CI: 0.51-0.99,
= 0.041) and rs1800451 (AC vs. AA + CC: OR = 2.70, 95% CI: 1.27-5.74,
= 0.010) were associated with tuberculosis risk in Americans, and rs1800451 (C/A: OR = 0.92, 95% CI: 0.86-0.99,
= 0.035) was associated with tuberculosis risk in Africans. Additionally, rs1800450 (B/A: OR = 0.42, 95% CI: 0.25-0.72,
= 0.001) was associated with tuberculosis risk in Europeans.
The
rs1800451 polymorphism is associated with decreased TB risk in the general population, and A/O, rs7096206, rs1800450 and rs1800451 are likely to be associated with the risk for some specific ethnic groups. |
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ISSN: | 1734-1922 1896-9151 |
DOI: | 10.5114/aoms.2017.65319 |