Both transient (physical exertion, fainting, DDAVP) and chronic (thyroid, oestrogen and corticosteroid hormone influences and

ageing) acquired effects can alter the levels of plasma VWF and need to be taken into account when considering the diagnosis of type 1 VWD. Family linkage and twin studies suggest that approximately 70% of the variability in VWF levels can be explained by genetic influences [39]. Recent genetic studies [35, 40-42] of approximately 500 index cases of type 1 VWD indicate that about 65% of cases have plausible VWF gene mutations that might explain their low levels of VWF. However, the primary pathogenic nature of these variations R788 solubility dmso remains to be proven in many cases and recent studies in different ethnic populations suggest that the distinction between neutral and pathogenic variants may be challenging [42].

In addition to single nucleotide variants (SNVs) being the primary cause of low VWF this website levels, there is also evidence that VWF gene polymorphic haplotypes may influence this phenotype. In particular, SNV haplotypes in the region of the gene encoding the D2/D′/D3 regions of VWF appear to be especially influential in this regard [43], Fig. 5 [43]. In addition to genetic variation within the VWF locus, there is also evidence that variability outside of the VWF gene contributes to the levels of plasma VWF. There are already reports of proximal VWF promoter polymorphisms being associated with VWF levels [44]. Furthermore, the VWF locus has been shown to be shear-responsive and the mechanisms responsible for this reactivity again demonstrate genetic variability [45]. Finally, very little is known about the genetic regulation of VWF expression mediated by more distant elements,

although in silico analysis suggests the presence of several upstream regions that are likely to contribute to this function. There is already strong evidence that the ABO blood group locus acts as a genetic modifier of the type 1 VWD phenotype [46]. This effect appears to account for approximately 30% of the genetic influence on VWF levels. The recent CHARGE meta-analysis has now identified several new genes that appear to be associated with VWF plasma levels [47]. Several of 上海皓元 these loci encode proteins that are involved in vesicular trafficking and exocytosis, and protein clearance and thus have plausible biological associations with VWF plasma levels. In addition, a search for VWF modifier genes in inbred mouse models has also identified seven loci (only two of which map to the mouse VWF gene) that influence this phenotype [48-50]. Of further interest, these mouse loci have previously been highlighted by genetic linkage studies in a large human study addressing inherited thrombophilia [51].