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A genome wide association study of pulmonary tuberculosis susceptibility in Indonesians
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A genome wide association study of pulmonary tuberculosis susceptibility in Indonesians..pdf | Published version | 247.17 kB | Adobe PDF | View/Open |
Title: | A genome wide association study of pulmonary tuberculosis susceptibility in Indonesians |
Authors: | Png, E Alisjahbana, B Sahiratmadja, E Marzuki, S Nelwan, RHH Balabanova, YM Nikolayevskyy, VN Drobniewski, FA Nejentsev, S Adnan, I Van De Vosse, E Hibberd, ML Van Crevel, R Ottenhoff, THM Seielstad, M |
Item Type: | Journal Article |
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. © 2012 Png et al; licensee BioMed Central Ltd. |
Issue Date: | 13-Jan-2012 |
Date of Acceptance: | 13-Jan-2012 |
URI: | http://hdl.handle.net/10044/1/23747 |
DOI: | https://dx.doi.org/10.1186/1471-2350-13-5 |
ISSN: | 1471-2350 |
Publisher: | BioMed Central |
Journal / Book Title: | BMC Medical Genetics |
Volume: | 13 |
Copyright Statement: | © 2012 Png et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
Publication Status: | Published |
Appears in Collections: | Department of Medicine (up to 2019) |
This item is licensed under a Creative Commons License