Mutations in ENPP1 are associated with 'idiopathic' infantile arterial calcification

Frank Rutsch, Nico Ruf, Sucheta Vaingankar, Mohammad R. Toliat, Anita Suk, Wolfgang Höhne, Galen Schauer, Mandy Lehmann, Tony Roscioli, Dirk Schnabel, Jörg T. Epplen, Alex Knisely, Andrea Superti-Furga, James McGill, Marco Filippone, Alan R Sinaiko, Hillary Vallance, Bernd Hinrichs, Wendy Smith, Merry FerreRobert Terkeltaub, Peter Nürnberg

Research output: Contribution to journalArticlepeer-review

385 Scopus citations

Abstract

Idiopathic infantile arterial calcification (IIAC; OMIM 208000) is characterized by calcification of the internal elastic lamina of muscular arteries and stenosis due to myointimal proliferation. We analyzed affected individuals from 11 unrelated kindreds and found that IIAC was associated with mutations that inactivated ecto-nucleotide pyrophosphatase/phosphodiesterase I (ENPP1). This cell surface enzyme generates inorganic pyrophosphate (PPi), a solute that regulates cell differentiation and serves as an essential physiologic inhibitor of calcification.

Original languageEnglish (US)
Pages (from-to)379-381
Number of pages3
JournalNature Genetics
Volume34
Issue number4
DOIs
StatePublished - Aug 1 2003

Bibliographical note

Funding Information:
We thank H. Ritter for microsatellite analyses; I. Bäβmann for technical assistance in cell culturing and mRNA preparation; and D. Morris, N. Makhseed and E. Harps for providing material from affected individuals. This work was supported in part by grants from the Deutsche Forschungsgemeinschaft (F.R., P.N.), the German Federal Department of Education and Research (P.N.), the US National Institutes of Health and Veterans Affairs Research Service (R.T.) and the US Arthritis National Research Foundation (S.V.).

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