Abstract
Fibrinogen, an acute phase protein, is an important inflammatory marker that is associated with cardiovascular diseases. We studied the association of three common human fibrinogen-β gene (FGB) variants, -455G>A, -249C>T, and -148C>T with glycemic parameters in 265 non-diabetic Hong Kong Chinese subjects. Both FGB variants, -455G>A and -148C>T were in complete linkage disequilibrium and were associated with higher levels of plasma fibrinogen and 2-h glucose after a 75-g oral glucose load (p<0.01). Carriers of FGB AC-haplotype, comprising the two nucleotide variants at positions -455 and -249, had higher fibrinogen level (2.64 ± 0.65 vs 2.42 ± 0.52 g/L, p=0.002) and 2-h glucose after a 75-g oral glucose load (5.87 ± 1.14 vs 5.47 ± 1.22 g/L, p=0.006). The associations were significant in men, but not women. In stepwise multiple regression analysis, AC-haplotype was independently associated with plasma fibrinogen level and 2-h glucose (p=0.002 and 0.010 respectively). This suggests that fibrinogen may play a role in the development of impaired glucose tolerance.
Original language | English |
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Pages (from-to) | 167-173 |
Number of pages | 7 |
Journal | Disease Markers |
Volume | 24 |
Issue number | 3 |
DOIs | |
Publication status | Published - 2008 |
Externally published | Yes |
ASJC Scopus Subject Areas
- Molecular Biology
- Genetics
- Clinical Biochemistry
- Biochemistry, medical
Keywords
- Fibrinogen
- Haplotype
- Impaired glucose tolerance
- Polymorphism