Prostaglandin transporter mutations cause pachydermoperiostosis with myelofibrosis

Christine P. Diggle, David A. Parry, Clare V. Logan, Paul Laissue, Carolina Rivera, Carlos Martín Restrepo, Dora J. Fonseca, Joanne E. Morgan, Yannick Allanore, Michaela Fontenay, Julien Wipff, Mathilde Varret, Laure Gibault, Nadezhda Dalantaeva, Márta Korbonits, Bowen Zhou, Gang Yuan, Ghita Harifi, Kivanc Cefle, Sukru PalanduzHadim Akoglu, Petra J. Zwijnenburg, Klaske D. Lichtenbelt, Bérengère Aubry-Rozier, Andrea Superti-Furga, Bruno Dallapiccola, Maria Accadia, Francesco Brancati, Eamonn G. Sheridan, Graham R. Taylor, Ian M. Carr, Colin A. Johnson, Alexander F. Markham, David T. Bonthron

Research output: Contribution to journalArticlepeer-review

Abstract

Pachydermoperiostosis, or primary hypertrophic osteoarthropathy (PHO), is an inherited multisystem disorder, whose features closely mimic the reactive osteoarthropathy that commonly accompanies neoplastic and inflammatory pathologies. We previously described deficiency of the prostaglandin-degrading enzyme 15-hydroxyprostaglandin dehydrogenase (HPGD) as a cause of this condition, implicating elevated circulating prostaglandin E2 (PGE2) as causative of PHO, and perhaps also as the principal mediator of secondary HO. However, PHO is genetically heterogeneous. Here, we use whole-exome sequencing to identify recessive mutations of the prostaglandin transporter SLCO2A1, in individuals lacking HPGD mutations. We performed exome sequencing of four probands with severe PHO, followed by conventional mutation analysis of SLCO2A1 in nine others. Biallelic SLCO2A1 mutations were identified in 12 of the 13 families. Affected individuals had elevated urinary PGE2, but unlike HPGD-deficient patients, also excreted considerable quantities of the PGE2 metabolite, PGE-M. Clinical differences between the two groups were also identified, notably that SLCO2A1-deficient individuals have a high frequency of severe anemia due to myelofibrosis. These findings reinforce the key role of systemic or local prostaglandin excess as the stimulus to HO. They also suggest that the induction or maintenance of hematopoietic stem cells by prostaglandin may depend upon transporter activity.

Original languageEnglish
Pages (from-to)1175-1181
Number of pages7
JournalHuman Mutation
Volume33
Issue number8
DOIs
Publication statusPublished - Aug 2012

Keywords

  • Genetics
  • Myelofibrosis
  • Osteoarthropathy
  • Prostaglandin
  • SLC02A1

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Fingerprint Dive into the research topics of 'Prostaglandin transporter mutations cause pachydermoperiostosis with myelofibrosis'. Together they form a unique fingerprint.

Cite this