scholarly journals Genome-Wide Association Study Identifies Novel Loci Associated With Concentrations of Four Plasma Phospholipid Fatty Acids in the De Novo Lipogenesis Pathway

2013 ◽  
Vol 6 (2) ◽  
pp. 171-183 ◽  
Author(s):  
Jason H.Y. Wu ◽  
Rozenn N. Lemaitre ◽  
Ani Manichaikul ◽  
Weihua Guan ◽  
Toshiko Tanaka ◽  
...  
PLoS Genetics ◽  
2009 ◽  
Vol 5 (1) ◽  
pp. e1000338 ◽  
Author(s):  
Toshiko Tanaka ◽  
Jian Shen ◽  
Gonçalo R. Abecasis ◽  
Aliaksei Kisialiou ◽  
Jose M. Ordovas ◽  
...  

BMC Genomics ◽  
2018 ◽  
Vol 19 (1) ◽  
Author(s):  
G. A. Rovadoscki ◽  
S. F. N. Pertile ◽  
A. B. Alvarenga ◽  
A. S. M. Cesar ◽  
F. Pértille ◽  
...  

Circulation ◽  
2012 ◽  
Vol 125 (suppl_10) ◽  
Author(s):  
Jason H Wu ◽  
Rozenn N Lemaitre ◽  
Toshiko Tanaka ◽  
Weihua Guan ◽  
Ani Manichaikul ◽  
...  

Background Palmitic acid (16:0), stearic acid (18:0), palmitoleic acid (16:1n-7), and oleic acid (18:1n-9) are major saturated and mono-unsaturated fatty acids that are synthesized via de novo lipogenesis (DNL) or obtained from the diet. Circulating levels of these fatty acids are linked to several diseases including diabetes and heart disease. Prior family and twin studies suggest high heritability of circulating levels, but potential genes involved are unknown. Objective To carry out a Genome-Wide Association Study (GWAS) to investigate genetic determinants of circulating levels of these fatty acids. Methods GWAS in 5 population-based cohorts (n=8,961) of European ancestry. Each study conducted linear regression analysis using an additive genetic model. All analyses were adjusted for age, sex, site of recruitment, and principal components to account for possible population genetic substructure where appropriate. Study-specific results were combined using inverse-variance weighted meta-analysis. Results We found SNPs at 7 novel loci linked at GWA significance to levels of one or more of these fatty acids ( Figure ). Directionality is reported for minor alleles. SNPs in ALG14 were associated with higher levels of 16:0 ( P =2.7x10 -11 ) and lower levels of 18:0 ( P =2.7x10 -11 ). SNPs in FADS1 /2 were associated with higher 18:1n-9 ( P =2.2x10 -32 ) and 16:1n-7 ( P =6.6x10 -13 ), and lower 18:0 ( P =1.3x10 -20 ). SNPs in LPGAT1 were associated with lower 18:0 ( P =2.8x10 -9 ). SNPs in GCKR ( P =9.8x10 -10 ) and HIF1AN ( P =5.7x10 -9 ) were associated with higher 16:1n-7, whereas those in PKD2L1 ( P =5.7x10 -15 ) and another locus on chromosome 2 (not near known genes) were associated with lower 16:1n-7. Conclusion Our findings provide novel evidence that common variations in genes with diverse functions, including protein glycosylation, polyunsaturated fatty acid metabolism, phospholipid modeling, and glucose- and oxygen-sensing pathways, are associated with circulating levels of fatty acids in the DNL pathway.


Author(s):  
М. Халюзова ◽  
M. Khalyuzova ◽  
М. Цыганов ◽  
M. Tsyganov ◽  
Д. Исубакова ◽  
...  

Purpose: To conduct genome wide association study of the association of 750,000 SNPs and an increased frequency of different types of chromosomal aberrations, induced by chronic irradiation in the dose range of 100–300 mSv. Material and methods: The study was conducted among Siberian Group of Chemical Enterprises healthy employees (n = 37) exposed to professional external γ-radiation in a dose range of 100–300 mSv. The de novo induced CNVs were previously detected in these persons. Mean dose – 188.8 ± 8.3 mSv, median – 185 mSv, interquartile range – 147.8–218.7 mSv, min – 103.4 mSv, max – 295.8 mSv. Genotyping of DNA samples from 37 employees was carried out by microarray CytoScan™ HD Array (Affymetrix, USA), containing 750,000 SNP-markers of 36,000 genes. The standard cytogenetic analysis was performed in the entire examined group. Results: We analyzed the association of these SNPs with the frequencies of aberrant cells and following chromosomal aberrations: single chromatid fragments, chromatid exchanges, paired fragments, dicentrics, rings, and translocations. We have found that 8 SNPs (rs10779468, rs158735, rs158710, rs158712, rs11131536, rs528170, rs9533572, rs10512439) are associated with the frequency of aberrant cells. Conclusion: We have discovered polymorphic variants that are associated with an increased frequency of aberrant cells in workers of Siberian Group of Chemical Enterprises exposed to irradiation at a dose of 100–300 mSv. This polymorphic variants can be considered as potential markers of individual radiosensitivity. To confirm identified associations, further validation studies on an extended sample of people exposed to radiation are needed.


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