MMP2 and triple-A syndrome: As a hallmark of pathological remodeling in AAA, we observed the strongest interaction between TGFB1 with the TGFB1 receptor family and notably strong co-localization with MMP2 and MMP9, suggesting the role of TGFB1 pathway as one of the reminiscent factors that could link the presence of SNPs to the development of AAA.