Article

European Journal of Human Genetics (2009) 17, 213–218; doi:10.1038/ejhg.2008.194; published online 5 November 2008

Screening for replication of genome-wide SNP associations in sporadic ALS

Simon Cronin1,2, Barbara Tomik3, Daniel G Bradley4, Agnieszka Slowik3 and Orla Hardiman2,5

  1. 1Department of Clinical Neurological Sciences, Royal College of Surgeons in Ireland, Dublin 2, Ireland
  2. 2Department of Neurology, Beaumont Hospital, Dublin 9, Ireland
  3. 3Department of Neurology, Jagiellonian University, Krakow, Poland
  4. 4Smurfit Institute of Genetics, Trinity College, Dublin 2, Ireland
  5. 5Trinity College Institute of Neuroscience, Trinity College, Dublin 2, Ireland

Correspondence: Dr S Cronin, The Irish ALS Research Group, Department of Neurology, Beaumont Hospital, Dublin 9, Ireland. Tel: +353 1 8092174; Fax: +353 1 8092302; E-mail: scronin@rcsi.ie

Received 21 May 2008; Revised 18 August 2008; Accepted 12 September 2008; Published online 5 November 2008.

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Abstract

We recently reported a joint analysis of genome-wide association (GWA) data on 958 sporadic amyotrophic lateral sclerosis (ALS) cases and 932 controls from Ireland and the publicly available data sets from the United States and the Netherlands. The strongest pooled association was rs10260404 in the dipeptidyl-peptidase 6 (DPP6) gene. Here, we sought confirmation of joint analysis signals in both an expanded Irish and a Polish ALS cohort. Among 287 522 autosomal single-nucleotide polymorphisms (SNPs), 27 were commonly associated on joint analysis of the Irish, US and Dutch GWAs. These 27 SNPs were genotyped in an expanded Irish cohort (312 patients with SALS; 259 controls) and an additional Polish cohort (218 patients; 356 controls). Eleven SNPs, including rs10260404, reached a final P-value below 0.05 in the Irish cohort. In the Polish cohort, only one SNP, rs6299711, showed nominal association with ALS. Pooling of data for 1267 patients with ALS and 1336 control subjects did not identify any association reaching Bonferroni significance (P<1.74 times 10-7). The present strategy did not reveal any consistently associated SNP across four populations. The result for DPP6 is surprising, as it has been replicated elsewhere. We discuss the possible interpretations and implications of these findings for future ALS GWA studies both within and between populations.

Keywords:

amyotrophic lateral sclerosis, genome-wide study, DPP6, genetics

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