Pretražite po imenu i prezimenu autora, mentora, urednika, prevoditelja

Napredna pretraga

Pregled bibliografske jedinice broj: 551919

Genetic variation in the autophagy gene ULK1 and risk of Crohn's disease


Henckaerts, L.; Cleynen, I.; Brinar, Marko; John, J.M.; Van Steen, K.; Rutgeerts, P.; Vermeire, S.
Genetic variation in the autophagy gene ULK1 and risk of Crohn's disease // Inflammatory bowel diseases, 17 (2011), 6; 1392-1397 doi:10.1002/ibd.21486 (međunarodna recenzija, članak, znanstveni)


CROSBI ID: 551919 Za ispravke kontaktirajte CROSBI podršku putem web obrasca

Naslov
Genetic variation in the autophagy gene ULK1 and risk of Crohn's disease

Autori
Henckaerts, L. ; Cleynen, I. ; Brinar, Marko ; John, J.M. ; Van Steen, K. ; Rutgeerts, P. ; Vermeire, S.

Izvornik
Inflammatory bowel diseases (1078-0998) 17 (2011), 6; 1392-1397

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
genetic; variation; autophagy; ULK1

Sažetak
The autophagy pathway has been linked with Crohn's disease (CD) through association of the ATG16L1 and IRGM genes with susceptibility for CD, and also to the Nod2 pathway, involved in CD. Our aim was to investigate polymorphisms in selected autophagy genes for their association with susceptibility to CD. We prioritized all known human homologs of yeast autophagy (Atg) genes according to their location in a known inflammatory bowel disease (IBD) locus or in a genomic region detected in a genome-wide association study (GWAS) or GWAS-meta-analysis. A total of 70 haplotype tagging single nucleotide polymorphisms (tSNPs) in 12 genes were genotyped in a cohort of CD patients (n = 947) and controls (n = 548). Transmission disequilibrium testing (TDT) was performed in an independent cohort of 335 parent-child CD-trios. The frequency of the T-allele of tSNP rs12303764 in ULK1 was significantly higher in CD (64%) versus controls (57%, corrected P-value 0.002). TDT demonstrated overtransmission of this allele to affected offspring (P = 0.02). Model-based multifactor dimensionality reduction (MB-MDR) interaction analysis confirmed a strong main effect for rs12303764. No interaction was found between ULK1 and CARD15, or between ULK1 genotypes and CD phenotypes. We report a genetic association with a tSNP in ULK1, an interesting candidate gene for IBD, given the role of ULK1 in autophagy initiation, and the interaction between Nod2 and autophagy pathways. To further clarify the role of ULK1 in CD, an in-depth investigation of the variation in the region and possible role for copy number variation in this region should be evaluated. (Inflamm Bowel Dis 2010).

Izvorni jezik
Engleski

Znanstvena područja
Kliničke medicinske znanosti



POVEZANOST RADA


Projekti:
108-1081874-1917 - Upalne bolesti crijeva (Crohnova bolest i ulcerozni kolitis) (Vucelić, Boris, MZOS ) ( CroRIS)

Ustanove:
Medicinski fakultet, Zagreb

Profili:

Avatar Url Marko Brinar (autor)

Poveznice na cjeloviti tekst rada:

doi onlinelibrary.wiley.com

Citiraj ovu publikaciju:

Henckaerts, L.; Cleynen, I.; Brinar, Marko; John, J.M.; Van Steen, K.; Rutgeerts, P.; Vermeire, S.
Genetic variation in the autophagy gene ULK1 and risk of Crohn's disease // Inflammatory bowel diseases, 17 (2011), 6; 1392-1397 doi:10.1002/ibd.21486 (međunarodna recenzija, članak, znanstveni)
Henckaerts, L., Cleynen, I., Brinar, M., John, J., Van Steen, K., Rutgeerts, P. & Vermeire, S. (2011) Genetic variation in the autophagy gene ULK1 and risk of Crohn's disease. Inflammatory bowel diseases, 17 (6), 1392-1397 doi:10.1002/ibd.21486.
@article{article, author = {Henckaerts, L. and Cleynen, I. and Brinar, Marko and John, J.M. and Van Steen, K. and Rutgeerts, P. and Vermeire, S.}, year = {2011}, pages = {1392-1397}, DOI = {10.1002/ibd.21486}, keywords = {genetic, variation, autophagy, ULK1}, journal = {Inflammatory bowel diseases}, doi = {10.1002/ibd.21486}, volume = {17}, number = {6}, issn = {1078-0998}, title = {Genetic variation in the autophagy gene ULK1 and risk of Crohn's disease}, keyword = {genetic, variation, autophagy, ULK1} }
@article{article, author = {Henckaerts, L. and Cleynen, I. and Brinar, Marko and John, J.M. and Van Steen, K. and Rutgeerts, P. and Vermeire, S.}, year = {2011}, pages = {1392-1397}, DOI = {10.1002/ibd.21486}, keywords = {genetic, variation, autophagy, ULK1}, journal = {Inflammatory bowel diseases}, doi = {10.1002/ibd.21486}, volume = {17}, number = {6}, issn = {1078-0998}, title = {Genetic variation in the autophagy gene ULK1 and risk of Crohn's disease}, keyword = {genetic, variation, autophagy, ULK1} }

Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus
  • MEDLINE


Citati:





    Contrast
    Increase Font
    Decrease Font
    Dyslexic Font