Common nonsynonymous variants in PCSK1 confer risk of obesity.

Research output: Contribution to journalJournal articleResearchpeer-review

  • Michael Benzinou
  • John W M Creemers
  • Helene Choquet
  • Stephane Lobbens
  • Christian Dina
  • Emmanuelle Durand
  • Audrey Guerardel
  • Philippe Boutin
  • Beatrice Jouret
  • Barbara Heude
  • Beverley Balkau
  • Jean Tichet
  • Michel Marre
  • Natascha Potoczna
  • Fritz Horber
  • Catherine Le Stunff
  • Sebastien Czernichow
  • Annelli Sandbæk
  • Torsten Lauritzen
  • Knut Borch-Johnsen
  • Gitte Andersen
  • Wieland Kiess
  • Antje Körner
  • Peter Kovacs
  • Peter Jacobson
  • Lena M S Carlsson
  • Andrew J Walley
  • Torben Jørgensen
  • David Meyre
  • Philippe Froguel
Mutations in PCSK1 cause monogenic obesity. To assess the contribution of PCSK1 to polygenic obesity risk, we genotyped tag SNPs in a total of 13,659 individuals of European ancestry from eight independent case-control or family-based cohorts. The nonsynonymous variants rs6232, encoding N221D, and rs6234-rs6235, encoding the Q665E-S690T pair, were consistently associated with obesity in adults and children (P = 7.27 x 10(-8) and P = 2.31 x 10(-12), respectively). Functional analysis showed a significant impairment of the N221D-mutant PC1/3 protein catalytic activity.
Original languageEnglish
JournalNature Genetics
Volume40
Issue number8
Pages (from-to)943-5
Number of pages2
ISSN1061-4036
DOIs
Publication statusPublished - 2008

Bibliographical note

Keywords: Adult; Case-Control Studies; Child; European Continental Ancestry Group; Genetic Predisposition to Disease; Humans; Obesity; Polymorphism, Single Nucleotide; Proprotein Convertase 1

ID: 8466806