Management of Primary Hyperoxaluria Type 1 in Italy

Pietro Manuel Ferraro, Giovanni Gambaro, Giorgia Mandrile, Giovanni Montini, Andrea Pasini, Licia Peruzzi

Risultato della ricerca: Contributo in rivistaArticolo in rivista


Primary hyperoxaluria type 1 is a rare genetic disease; the onset of symptoms ranges from childhood to the sixth decade of life and the disease may go unrecognized for several years. There is an urgent need for drugs able to inhibit the liver production of oxalate and to prevent the disease progression; lumasiran, an innovative molecule based on RNAi interference, is one of the most promising drugs. A group of leading Italian experts on this disease met to respond to some unmet medical needs (early diagnosis, availability of genetic tests and dosage of plasma oxalate, timing of liver transplantation, need for etiologic treatment), based on the analysis of the main scientific evidence and their personal experience. Children showing the characteristic symptoms of the disease usually undergo a metabolic screening and obtain an early diagnosis, while the experience is very limited in adults and the diagnosis difficult. It is therefore essential to increase the knowledge around this disease and the importance of metabolic and genetic screening to define a checklist of shared clinical and laboratory criteria and to establish a multidisciplinary management of potential patients. Oxalate is the cause of the disease: it is crucial to reduce both oxaluria and oxalemia through appropriate therapeutic strategies, able to prevent and/or reduce renal and systemic complications of primary type 1 hyperoxaluria. Lumasiran allows to significantly reduce the levels of oxalate both in blood and in urine, halting the course of the disease and preventing serious renal and systemic complications, if the therapy is started at an early stage of the disease.
Titolo tradotto del contributo[Autom. eng. transl.] Management of Primary Hyperoxaluria Type 1 in Italy
Lingua originaleItalian
pagine (da-a)N/A-N/A
Stato di pubblicazionePubblicato - 2021


  • hyperoxalemia
  • hyperoxaluria
  • lumasiran
  • primary hyperoxaluria type 1


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