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FUT2: filling the gap between genes and environment in Behçet's disease?
  1. Joana M Xavier1,2,
  2. Farhad Shahram3,
  3. Inês Sousa1,2,
  4. Fereydoun Davatchi3,
  5. Mafalda Matos1,2,
  6. Bahar Sadeghi Abdollahi3,
  7. João Sobral1,2,
  8. Abdolhadi Nadji3,
  9. Manuela Oliveira4,
  10. Fahmida Ghaderibarim3,
  11. Niloofar Mojarad Shafiee3,
  12. Sofia A Oliveira1,2
  1. 1Instituto de Medicina Molecular, Faculdade de Medicina da Universidade de Lisboa, Lisboa, Portugal
  2. 2Instituto Gulbenkian de Ciência, Oeiras, Portugal
  3. 3Rheumatology Research Center, Shariati Hospital, Tehran University of Medical Sciences, Tehran, Iran
  4. 4Centro de Investigação Matemática e Aplicaçóes – CIMA, Universidade de Évora, Évora, Portugal
  1. Correspondence to Dr Sofia A Oliveira, Instituto de Medicina Molecular, Faculdade de Medicina da Universidade de Lisboa, Av Prof Egas Moniz, Edifício Egas Moniz, Lisboa 1649-028, Portugal; aaoliveira{at}


Objectives To identify new susceptibility loci for Behçet's disease (BD), we performed a genome-wide association study (GWAS) using DNA pooling.

Methods Two replicate pools of 292 Iranian BD cases and of 294 age- and sex-matched controls were allelotyped in quadruplicate on the Affymetrix Genome-Wide Human SNP Array 6.0. Of the 51 top markers, 47 were technically validated through individually genotyping. Replication of validated single nucleotide polymorphisms (SNPs) was performed in an independent Iranian dataset (684 cases and 532 controls).

Results In addition to the well-established HLA-B locus, rs7528842 in a gene desert on chromosome 1p21.2, and rs632111 at the 3′UTR of FUT2 were associated in both the discovery and replication datasets (individually and in combination). However, only the FUT2 SNP was associated in a previous GWAS for BD in Turkish people. Fine-mapping of FUT2 in the full Iranian dataset showed additional associations in five coding SNPs (2.97E-06<pcombined<1.34E-04), including the rs601338 nonsense (W143X) variant which, in Caucasians, determines the secretion of the H antigen (precursor of the ABO blood group antigens) in body fluids and on the intestinal mucosa. Meta-analysis with the published Turkish GWAS data strengthened the FUT2 associations (4.78E-09<pmeta<1.66E-07).

Conclusions This study suggests for the first time a putative link between a specific gene and environment in the aetiopathogenesis of BD. The non-secretor phenotype affects mucosal glycosylation, which may explain its known association with dysbiosis and altered susceptibility to infections. A different antigenic stimulation in early life and consequent increased propensity for autoimmunity and inflammation may contribute to BD development.

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