Title: A genome wide association study of pulmonary tuberculosis susceptibility in Indonesians
Authors: Png, Eileen
Alisjahbana, Bachti
Sahiratmadja, Edhyana
Marzuki, Sangkot
Nelwan, Ron
Balabanova, Yanina
Nikolayevskyy, Vladyslav
Drobniewski, Francis
Nejentsev, Sergey
Adnan, Iskandar
van de Vosse, Esther
Hibberd, Martin L
van Crevel, Reinout
Ottenhoff, Tom HM
Seielstad, Mark
Issue Date: 13-Jan-2012
Abstract: Abstract Background There is reason to expect strong genetic influences on the risk of developing active pulmonary tuberculosis (TB) among latently infected individuals. Many of the genome wide linkage and association studies (GWAS) to date have been conducted on African populations. In order to identify additional targets in genetically dissimilar populations, and to enhance our understanding of this disease, we performed a multi-stage GWAS in a Southeast Asian cohort from Indonesia. Methods In stage 1, we used the Affymetrix 100 K SNP GeneChip marker set to genotype 259 Indonesian samples. After quality control filtering, 108 cases and 115 controls were analyzed for association of 95,207 SNPs. In stage 2, we attempted validation of 2,453 SNPs with promising associations from the first stage, in 1,189 individuals from the same Indonesian cohort, and finally in stage 3 we selected 251 SNPs from this stage to test TB association in an independent Caucasian cohort (n = 3,760) from Russia. Results Our study suggests evidence of association (P = 0.0004-0.0067) for 8 independent loci (nominal significance P < 0.05), which are located within or near the following genes involved in immune signaling: JAG1, DYNLRB2, EBF1, TMEFF2, CCL17, HAUS6, PENK and TXNDC4. Conclusions Mechanisms of immune defense suggested by some of the identified genes exhibit biological plausibility and may suggest novel pathways involved in the host containment of infection with TB.
Description: RIGHTS : This article is licensed under the BioMed Central licence at http://www.biomedcentral.com/about/license which is similar to the 'Creative Commons Attribution Licence'. In brief you may : copy, distribute, and display the work; make derivative works; or make commercial use of the work - under the following conditions: the original author must be given credit; for any reuse or distribution, it must be made clear to others what the license terms of this work are.
URI: http://www.dspace.cam.ac.uk/handle/1810/241667
Other Identifiers: http://dx.doi.org/10.1186/1471-2350-13-5
Appears in Collections:Scholarly works - Medicine

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