ArticleCureus2025
Influence of Factor V Leiden Mutation and Protein C and Protein S Deficiencies on Preeclampsia Among Sudanese Women.
Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
Background Preeclampsia (PE) is a serious pregnancy complication that can endanger the health of both mothers and fetuses. Genetic factors, such as mutations in thrombophilia and deficiencies in natural anticoagulants, could contribute to its development, but their exact roles are not well-understood, especially among Sudanese women. Objective To assess the relationship between the Factor V Leiden (FVL) thrombophilic mutation and reduced levels of the natural anticoagulants Protein C (PC) and Protein S (PS) with the occurrence of PE among Sudanese women. Methods and materials A case-control study included 300 women, divided equally into three groups: 100 with PE, 100 healthy normotensive pregnant women, and 100 healthy non-pregnant women. Polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) was used to detect FVL mutations. PC and PS levels were measured using colorimetric assays. Logistic regression analysis assessed the relationships between these variables and the risk of developing PE. Results Our findings showed no significant link between FVL mutations and PE (p=.390). PC levels alone did not emerge as significant independent predictors of PE (OR 1.01, 95% CI 0.99-1.02, p=.419). However, women with low PC and S levels were strongly associated with PE in univariate and multivariate analyses (OR 77.67, 95% CI 8.97-672.5, p<.001). This combination was significantly more common in the PE group than in the control group (p<.001). Additionally, reduced PS levels were significantly associated with an increased risk of PE. Conclusion Combined PC/PS deficiencies are strongly associated with PE among Sudanese women, indicating a significant role for these natural anticoagulants in the pathogenesis of the disease. An FVL mutation was not significantly associated with PE in this Sudanese population.
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