Related Experiment Video
Updated: Aug 12, 2026

Candidate Gene Testing in Clinical Cohort Studies with Multiplexed Genotyping and Mass Spectrometry
Published on: June 21, 2018
B‑cell activating factor gene polymorphisms rs9514828 and rs1041569 increase preeclampsia risk
Kosar Shirvani Baghbabouie1, Danial Jahantigh1, Forough Forghani2
1Department of Biology, Faculty of Science, University of Sistan and Baluchestan, Zahedan, Iran.
Insights
Specific BAFF gene variations are linked to a higher risk of preeclampsia (PE) in Iranian women. These findings suggest BAFF polymorphisms could be useful biomarkers for assessing PE risk.
Area of Science:
- Genetics
- Obstetrics
- Immunology
Background:
- Preeclampsia (PE) is a significant pregnancy complication.
- Genetic factors are implicated in PE susceptibility.
- BAFF gene polymorphisms are potential candidates for investigation.
Purpose of the Study:
- To investigate the association between BAFF gene polymorphisms (rs1041569 and rs9514828) and preeclampsia susceptibility in an Iranian population.
- To explore the relationship between these polymorphisms and PE severity and onset timing.
Main Methods:
- A case-control study involving 560 pregnant women (280 PE, 280 controls) from Zahedan, Iran.
- Genotyping using PCR-RFLP.
- Statistical analysis with logistic regression to determine odds ratios (ORs) and 95% confidence intervals (CIs).
Main Results:
- The CT and TT genotypes of rs9514828 were associated with increased PE risk (OR=1.81, p=0.011; OR=2.13, p=0.002).
- The AT and TT genotypes of rs1041569 also showed increased PE risk (OR=1.48, p=0.033; OR=1.68, p=0.037).
- Haplotype analysis indicated protective effects for C-A and T-T haplotypes (OR=0.69, p=0.003 for both).
Conclusions:
- BAFF gene polymorphisms are significantly associated with preeclampsia susceptibility in the Iranian population.
- These polymorphisms may serve as potential biomarkers for preeclampsia risk assessment.
Aims:
This study investigated the association between BAFF gene polymorphisms (rs1041569 and rs9514828) and preeclampsia (PE) susceptibility in an Iranian population, with a focus on disease severity and onset timing.
Patients And Methods:
This case-control study included 560 pregnant women (280 with PE and 280 normotensive controls) from Zahedan, southeastern Iran. Genotyping was performed using PCR-RFLP. Associations were assessed using logistic regression to calculate odds ratios (ORs) with 95% confidence intervals (CIs).
Results:
For rs9514828, the CT and TT genotypes were associated with increased PE risk (OR = 1.81, p = 0.011; OR = 2.13, p = 0.002). For rs1041569, the AT and TT genotypes were also associated with increased risk (OR = 1.48, p = 0.033; OR = 1.68, p = 0.037). Haplotype analysis revealed that the C-A haplotype was protective (OR = 0.69, p = 0.003), while the T-T haplotype showed similar protection (OR = 0.69, p = 0.003). All genotype distributions were in Hardy-Weinberg equilibrium in the control group.
Conclusion:
BAFF polymorphisms are significantly associated with PE susceptibility in the Iranian population and may serve as potential biomarkers for PE risk assessment.
More Related Videos
05:31Disruption of the Mouse Blood-Brain Barrier by Small Extracellular Vesicles from Hypoxic Human Placentas
Published on: January 26, 2024
11:35Screening for Functional Non-coding Genetic Variants Using Electrophoretic Mobility Shift Assay (EMSA) and DNA-affinity Precipitation Assay (DAPA)
Published on: August 21, 2016
Related Concept Videos
Pharmacogenetic Phenotypes: Alterations in Pharmacokinetics, Drug Targets and Biologic Milieu
Pharmacogenetics of Drug Targets: β₂-Adrenergic Receptors, Apo E, Thymidylate Synthase
Pharmacogenetics of Drug Transporters: P-Glycoprotein and Solute Carrier Transporters
Single Nucleotide Polymorphisms-SNPs
Comparing Copy Number Variations and SNPs
Copy number variations or CNVs are the structural variations that cover more than 1kb of DNA sequence. The single nucleotide polymorphism (SNP), on the other hand, is a single nucleotide change or a point mutation that is found in more than 1%...
Type II Diabetes I: Introduction