A genome-wide study of panic disorder suggests the amiloride-sensitive cation channel 1 as a candidate gene

Noomi Gregersen, Hans A Dahl, Henriette Nørmølle Buttenschøn, Mette Nyegaard, Anne Hedemand, Thomas Damm Als, August G. Wang, Sofus Joensen, David Pd Woldbye, Pernille Koefoed, Ann Suhl Kristensen, Torben A Kruse, Anders Børglum, Ole Mors

Research output: Contribution to journalArticlepeer-review

38 Citations (Scopus)

Abstract

Panic disorder (PD) is a mental disorder with recurrent panic attacks that occur spontaneously and are not associated to any particular object or situation. There is no consensus on what causes PD. However, it is recognized that PD is influenced by environmental factors, as well as genetic factors. Despite a significant hereditary component, genetic studies have only been modestly successful in identifying genes of importance for the development of PD. In this study, we conducted a genome-wide scan using microsatellite markers and PD patients and control individuals from the isolated population of the Faroe Islands. Subsequently, we conducted a fine mapping, which revealed the amiloride-sensitive cation channel 1 (ACCN1) located on chromosome 17q11.2-q12 as a potential candidate gene for PD. The further analyses of the ACCN1 gene using single-nucleotide polymorphisms (SNPs) revealed significant association with PD in an extended Faroese case-control sample. However, analyses of a larger independent Danish case-control sample yielded no substantial significant association. This suggests that the possible risk alleles associated in the isolated population are not those involved in the development of PD in a larger outbred population.European Journal of Human Genetics advance online publication, 3 August 2011; doi:10.1038/ejhg.2011.148.
Original languageEnglish
Pages (from-to)84-90
Number of pages7
JournalEuropean Journal of Human Genetics
Volume20
DOIs
Publication statusPublished - 3 Aug 2011

Keywords

  • panic disorder
  • genome-wide scan
  • isolated population
  • association analysis
  • ACCN1

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