Association of Genetic Polymorphisms of Fibrinogen, Factor XIII A-Subunit and α 2 -Antiplasmin with Fibrinogen Levels in Pregnant Women

• Published in: Life (Basel, Switzerland) Switzerland), 2021-12, Vol.11 (12)
• Main Authors: Schwedler, Christian, Heymann, Guido, Bukreeva, Larisa, Hoppe, Berthold
• Format: Article
• Language: English
• ISSN: 2075-1729; 2075-1729

Fibrinogen synthesis is stimulated by proinflammatory triggers and depends on α-, β- and γ-fibrinogen ( , , ) genotypes. Constellations of fibrinogen, factor XIII A-subunit ( ) and α -antiplasmin ( ) genotypes predisposing for dense fibrin gels with high antifibrinolytic capacity (e.g., rs1800790 A-allele carriage in 34Val/Val or 6Arg/Arg wildtypes) are related with reduced inflammation. As both relationships are likely to influence each other, we tested whether the association of fibrinogen genotypes with fibrinogen levels is influenced by and genotypes in a population under proinflammatory stress. In total, 639 women were followed during pregnancy (2218 observations). The relationship between fibrinogen genotypes and levels was statistically assessed in univariate and multivariate analyses without and with stratification for Val34Leu and Arg6Trp. Strong associations with fibrinogen levels could be found for rs1800790G > A, rs2070016T > C and rs1049636T > C. For rs1800790G > A and rs2070016T > C, this relationship significantly depended on Val34Leu and Arg6Trp genotypes. Specifically, in 34Val/Val wildtypes, carriage of rs1800790A was related to significantly lower fibrinogen levels compared with rs1800790GG wildtypes ( < 0.01). For 6Arg/Arg wildtypes, a comparable relationship could be found ( < 0.04). As these genotype constellations related to lower fibrinogen levels have previously been shown to be associated with reduced inflammatory activity, these findings suggest that the influence of fibrinogen, and genotypes on inflammation could affect the control of fibrinogen levels and vice versa.