Oral supplementation of inorganic pyrophosphate in pseudoxanthoma elasticum

xlomafota13 shared this article with you from Inoreader Oral supplementation of inorganic pyrophosphate in pseudoxanthoma elasticum Via Experimental Dermatology ABSTRACT Pseudoxanthoma elasticum (PXE; OMIM 264800) is a rare heritable multisystem disorder, characterized by ectopic mineralization affecting elastic fibers in the skin, eyes, and the cardiovascular system. Skin findings often lead to early diagnosis of PXE, but currently no specific treatment exists to counteract the progression of symptoms. PXE belongs to a group of Mendelian calcification disorders linked to pyrophosphate metabolism, which also includes generalized arterial calcification of infancy (GACI), and arterial calcification due to CD73 deficiency (ACDC). Inactivating mutations in ABCC6, ENPP1 and NT5E are the genetic cause of these diseases, respectively, and all of them result in reduced inorganic pyrophosphate (PPi) concentration in the circulation. Although PPi is a strong inhibitor of ectopic calcification, oral supplementation therapy was initially not considered because of its low bioavailability. Our earlier work however demonstrated that orally administered pyrophosphate inhibits ectopic calcification in the animal models of PXE and GACI, and that orally given Na4P2O7 is absorbed in humans. Here we report that gelatin encapsulated Na2H2P2O7 has similar absorption properties in healthy volunteers and people affected by PXE. The sodium-free K2H2P2O7 form resulted in similar uptake in healthy volunteers, and inhibited calcification in Abcc6-/- mice as effectively as its sodium counterpart. Novel pyrophosphate compounds showing higher bioavailability in mice were also identified. Our results provide an important step toward testing oral PPi in clinical trials in PXE, or potentially any condition accompanied by ectopic calcification including diabetes, chronic kidney disease or ageing. View on the web Inoreader. Take back control of your news feed. Follow us on Twitter and Facebook.