International journal of clinical and experimental medicine · 2015
Association of β-fibrinogen gene polymorphism and plasma fibrinogen and allergic purpura nephritis.
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Gong Jianhua, Xu Qian, Hu Fengqi, Yuan Hai
Аннотация
OBJECTIVE: To investigate the association of β-fibrinogen gene polymorphism with plasma fibrinogen and allergic purpura nephritis.
METHODS: We designed a case-control study (334 case and 300 control) to genotype the β-fibrinogen gene -455G/A polymorphism. The genotype and allele frequencies between the case and control group were compared. And we also compared the Fg concentration between different genotype.
RESULTS: In the case group, there were 143 cases of GA type, accounting for 42.8%; there were 168 cases of GG type, accounting for 50.3%; there were 23 cases of AA type, accounting for 6.9%. While in the control group, GG type was the most common. There were 228 cases of GG type, accounting for 76%; there were 66 cases of GA type, accounting for 22%; there was 6 case of AA type, accounting for 2%. The frequency of Fgβ-455G/A genotype between the two groups showed statistical significance (P<0.05). The levels of plasma Fg in the two groups showed statistical significance (P<0.01). In HSPN group Fgβ GA and AA-type the concentration of Fg [(4.2 ± 0.5) g/L], compared with the GG genotype [(3.1 ± 0.4) g/L], was significantly increased with statistical significance (P<0.01).
CONCLUSION: The Fgβ-455G/A polymorphism was associated with the risk for HSPN and Fg concentration.
METHODS: We designed a case-control study (334 case and 300 control) to genotype the β-fibrinogen gene -455G/A polymorphism. The genotype and allele frequencies between the case and control group were compared. And we also compared the Fg concentration between different genotype.
RESULTS: In the case group, there were 143 cases of GA type, accounting for 42.8%; there were 168 cases of GG type, accounting for 50.3%; there were 23 cases of AA type, accounting for 6.9%. While in the control group, GG type was the most common. There were 228 cases of GG type, accounting for 76%; there were 66 cases of GA type, accounting for 22%; there was 6 case of AA type, accounting for 2%. The frequency of Fgβ-455G/A genotype between the two groups showed statistical significance (P<0.05). The levels of plasma Fg in the two groups showed statistical significance (P<0.01). In HSPN group Fgβ GA and AA-type the concentration of Fg [(4.2 ± 0.5) g/L], compared with the GG genotype [(3.1 ± 0.4) g/L], was significantly increased with statistical significance (P<0.01).
CONCLUSION: The Fgβ-455G/A polymorphism was associated with the risk for HSPN and Fg concentration.