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Candidate Gene Testing in Clinical Cohort Studies with Multiplexed Genotyping and Mass Spectrometry
Published on: June 21, 2018
Association of IL-35 Subunits, IL-12A rs568408 and EBI3 rs4740, Gene Polymorphisms With Preeclampsia Risk
Mohammad Darvishzadeh1, Danial Jahantigh1, Forough Forghani2
1Department of Biology, Faculty of Science, University of Sistan and Baluchestan, Zahedan, Iran.
Genetic variations in IL-35 components are linked to preeclampsia (PE) risk. Specific IL-12A and EBI3 polymorphisms may serve as genetic markers for assessing PE susceptibility, particularly in severe cases.
Area of Science:
- Immunogenetics
- Reproductive Medicine
- Human Genetics
Background:
- Preeclampsia (PE) is a significant pregnancy complication with severe maternal and fetal health consequences.
- Emerging evidence highlights the crucial role of immunological factors in the pathogenesis of PE.
- Understanding the genetic underpinnings of PE is vital for improving risk assessment and management.
Purpose of the Study:
- To investigate the association between genetic variations in Interleukin-35 (IL-35) components, specifically IL-12A (rs568408) and EBI3 (rs4740) polymorphisms, and the susceptibility to PE.
- To analyze these associations in an Iranian population.
- To identify potential genetic markers for PE risk stratification.
Main Methods:
- A case-control study involving 470 participants was conducted.
- Genotyping of IL-12A (rs568408) and EBI3 (rs4740) polymorphisms was performed using the Polymerase Chain Reaction-Restriction Fragment Length Polymorphism (PCR-RFLP) technique.
- Statistical analysis was employed to determine the odds ratios (OR) and p-values for genotype and allele associations with PE risk.
Main Results:
- The IL-12A rs568408 AA genotype was significantly associated with increased PE susceptibility (OR = 3.350, p = 0.007), especially in severe PE cases (OR = 5.048, p < 0.001).
- The EBI3 rs4740 AA genotype demonstrated a protective effect against PE (OR = 0.495, p = 0.036), particularly in severe cases (OR = 0.409, p = 0.037).
- Combined analysis revealed that IL-12A AA/EBI3 GA genotypes conferred the highest risk for severe, early-onset PE (OR = 5.280, p = 0.046).
Conclusions:
- Genetic variations in IL-35 components, IL-12A and EBI3, are significantly associated with PE susceptibility in the studied population.
- Specific genotypes of IL-12A and EBI3 polymorphisms may serve as valuable genetic markers for predicting PE risk.
- Further research can explore these genetic markers for enhanced clinical risk assessment of preeclampsia.
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