Aug 2026· Personalized Medicine· pp.
1-10
· 0 citations· 27 references
Medicine
TL;DR
BAFF polymorphisms are significantly associated with PE susceptibility in the Iranian population and may serve as potential biomarkers for PE risk assessment.
Abstract
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.
Abstract Aim To evaluate six VEGFA polymorphisms (rs1570360, rs699947, rs3025033, rs2146323, rs1413711 and rs833061) and serum VEGFA concentrations in 270 Lithuanian patients with multiple sclerosis (MS) and 270 matched healthy controls. Methods Genotyping was performed using real-time PCR, and serum VEGFA levels were...
The SDC1 rs2230924 C/T genotype and T allele may increase PE risk in pregnant women and validation in larger and multi-ethnic cohorts is necessary before clinical application.
Tzu-Yang Chang, Yi-Yung Chen, Yi-Hsiu Kuo et al.· Placenta· 0 citations
OLR1 rs11053646 SNP does not appear to be associated with T2D risk in Saudi adults, and small sample size may have limited statistical power to detect potential associations.
V. Vennu· Endocrine, Metabolic & Immun...· 0 citations
BACKGROUND
This study investigated associations between MSH5 polymorphisms and autoimmune thyroid disease (AITD) susceptibility.
METHODS
We genotyped rs409558 and rs707939 in 943 patients with AITD, including 591 with Graves' disease (GD) and 352 with Hashimoto's thyroiditis (HT), and 488 controls. Genetic associatio...
The g-allele of MDM2-snp309 exhibited a stronger capacity than the t-allele to drive the full-length p2 promoter of the MDM2 gene in several human cell lines, suggesting that the association between MDM2-snp309 and breast cancer is likely multifactorial rather than due to inconsistent gene expression in different cance...
Unknown authors· 0 citations
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