Effects of obesity on the association between common variations in the gene and matrix metalloproteinase 9 levels in Taiwanese.

Objectives: The gene, a member of the T-box family, is associated with congenital heart disease, electrocardiographic parameters, and development of atrial fibrillation in the general population. This study aimed to elucidate the role of gene polymorphisms in metabolic and inflammatory profiles possibly linked to -related pathologies.

Materials And Methods: A sample population of 597 individuals having routine health examinations was enrolled. Five tagging single nucleotide polymorphisms (SNPs) were analyzed using polymerase chain reaction and restriction enzyme digestion or TaqMan SNP genotyping assays. Associations between genotypes/haplotypes and matrix metalloproteinase 9 (MMP9) levels were investigated using generalized linear model analysis. Interactions between each genotype/haplotype, MMP9 level, and obesity status were tested using two-way analysis of variance with Golden Helix SVS Win32 7.3.1 software.

Results: After adjusting for clinical covariates, genotypes were found to be associated with MMP9 levels ( = 0.002 and = 0.001 for rs4113925 and rs3825214, respectively) in a dominant inheritance model. Haplotype analysis using three tag SNPs (rs11067101, rs1247973, and rs3825214) revealed a significant association between haplotype GCG and MMP9 levels (uncorrected = 0.0093 and the corrected false discovery rate = 0.0435). Multivariate analysis identified that SNP rs3825214, in addition to the and genotypes, was independently associated with MMP9 levels ( < 0.001). Using a dominant inheritance model, subgroup and interaction analysis showed associations between the rs4113925, rs3825214, and MMP9 levels only in nonobese individuals ( = 1.04 × 10 and = 7.11 × 10, respectively; interaction = 0.009 and 0.018, respectively). Subgroup analysis showed a borderline significant association between haplotype GCG and MMP9 levels (uncorrected = 0.020 and corrected false discovery rate = 0.073), but with no evidence of interaction.

Conclusion: genotypes/haplotypes are independently associated with MMP9 in Taiwanese individuals and occur predominantly in nonobese people. These associations may broaden our understanding of the mechanism underlying T-box family gene activity and related cardiovascular pathologies.