Abstract | AIMS: METHODS: A total of 622 patients with type 2 diabetes mellitus (T2DM) and 293 healthy subjects were included. Determination of erythrocyte PL fatty acids composition and genotyping of single nucleotide polymorphisms were conducted by standard methods. RESULTS: A significant interaction of rs7305618 on HNFIA with C18:2n-6 and C20:4n-6 was observed: T allele carriers (TT+CT) had a higher risk of T2DM than noncarriers only when they had a higher level of C18:2n-6 or C20:4n-6, and the odds ratios ( ORs) were 2.59 (95% CI 1.58-4.24; p for interaction=0.005) and 2.49 (95% CI 1.47-4.24; p for interaction=0.021), respectively. A significant interaction of rs8078723 at the intergenic region between PSMD3 and CSF3 with C20:5n-3 was observed: C allele carriers (CC+CT) had a lower risk of T2DM than noncarriers only when they had a higher level of C20:5n-3, and the OR was 0.44 (95% CI 0.26-0.73; p for interaction=0.014). CONCLUSIONS: rs7305618 and rs8078723 were associated with the risk of T2DM in a Chinese population and were modulated by erythrocyte PL fatty acids composition.
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Authors | Kelei Li, Tao Huang, Ju-Sheng Zheng, Jianqin Sun, Yanqiu Chen, Hua Xie, Danfeng Xu, Jianbo Wan, Duo Li |
Journal | Journal of nutrigenetics and nutrigenomics
(J Nutrigenet Nutrigenomics)
Vol. 7
Issue 4-6
Pg. 252-63
( 2014)
ISSN: 1661-6758 [Electronic] Switzerland |
PMID | 25969153
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | © 2015 S. Karger AG, Basel. |
Chemical References |
- Fatty Acids
- HNF1A protein, human
- Hepatocyte Nuclear Factor 1-alpha
- Phospholipids
- Granulocyte Colony-Stimulating Factor
- Proteasome Endopeptidase Complex
- proteasome activator PA700 subunit p58, human
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Topics |
- Adult
- Aged
- Asian People
(genetics)
- Case-Control Studies
- China
- Diabetes Mellitus, Type 2
(blood, genetics)
- Erythrocytes
(metabolism)
- Fatty Acids
(blood)
- Female
- Genotype
- Granulocyte Colony-Stimulating Factor
(genetics)
- Hepatocyte Nuclear Factor 1-alpha
(genetics)
- Humans
- Male
- Middle Aged
- Nutrigenomics
- Phospholipids
(blood)
- Polymorphism, Single Nucleotide
- Proteasome Endopeptidase Complex
(genetics)
- Risk Factors
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