Table 1.
Genes involved | Implication in lymphatic function | Implication in cardiovascular disease |
---|---|---|
GATA2 | Linked with primary (hereditary) lymphedema in Emberger syndrome [41] | Linked with familial early- onset of coronary artery disease [40] Linked with hematological diseases characterized by altered myeloid cell differentiation [41] |
VEGF-C and its receptor, VEGFR-3 | Mutation of the VEGFR-3 gene causes primary lymphedema [8] | A polymorphism in the gene encoding VEGF-C, causing lower levels of circulating VEGF-C, is associated with CAD [48] VEGF-C levels in plasma correlate with plasma mass of Lp-PLA2 [49] VEGF-C levels in plasma correlate with metabolic parameters and dyslipidemia [50] |
FOXC2/PROX-1 | Key genes involved in the process of lymphatic vessel formation [53] Transcription factors highly expressed from the onset of valve formation and collecting vessel maturation [43] |
Familial combined hyperlipidaemia (FCHL) is associated with decreased PROX-1 and / or FOXC2 expression in adipose tissue [44] Genetic linkage shows an association between FOXC2 and FCHL [45] |