Key result
Angiopoietin-2 polymorphisms evaluated for association with SLE risk in Egyptian patients.
Why the study?
Angiopoietin-2 polymorphisms have been implicated in autoimmune disorders, but their association with SLE susceptibility in Egyptian patients was unclear.
Are Angiopoietin-2 polymorphisms (rs12674822 and rs3739390) associated with systemic lupus erythematosus risk in Egyptian patients?
Case-Control (n=160)
No
Are Angiopoietin-2 polymorphisms (rs12674822 and rs3739390) associated with systemic lupus erythematosus risk in Egyptian patients?
The Ang-2 rs12674822 polymorphism may represent a potential genetic risk marker for systemic lupus erythematosus in Egyptian patients.
Answers are grounded in this paper and cite their sources.
Should not yet change SLE risk assessment; hypothesis-generating for Ang-2 polymorphisms in Egyptians and requires larger validation.
Systemic lupus erythematosus (SLE) is a multifactorial autoimmune disease influenced by genetic and environmental factors. Angiopoietin-2 (Ang-2), an angiogenesis-related gene, has been implicated in several autoimmune disorders. This study aimed to investigate whether Ang-2 polymorphisms (rs12674822 and rs3739390) are associated with SLE susceptibility in Egyptian patients. A case – control study was conducted, including 80 SLE patients and 80 age- and sex-matched healthy controls. Clinical and laboratory data were collected, and genotyping was performed using TaqMan allelic discrimination assays. Associations with SLE were assessed through logistic regression analysis. The results showed that, the rs12674822 GT and TT genotypes were significantly associated with increased SLE risk (OR = 5.15, 95% CI = 2.46–10.78, p < 0.001), and this association remained significant after multivariate adjustment (OR = 7.10, 95% CI = 2.07–24.34, p < 0.05). No significant association was observed for rs3739390. Hardy – Weinberg equilibrium analysis indicated deviation for rs12674822 in controls. The Ang-2 rs12674822 polymorphism may represent a potential genetic risk marker for SLE in Egyptians, whereas rs3739390 showed no association. These findings are preliminary and require confirmation in larger multicentre studies with functional analyses. Notably, the rs12674822 results should be interpreted cautiously due to a borderline deviation from Hardy – Weinberg Equilibrium (p = 0.070).Trial registration Not applicable (observational study).
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Fouda et al. (2026) conducted a case-control in Systemic lupus erythematosus (SLE) (n=160). Ang-2 rs12674822 GT and TT genotypes vs. Healthy controls was evaluated on Systemic lupus erythematosus risk (OR 5.15, 95% CI 2.46-10.78, p=< 0.001). The Ang-2 rs12674822 GT and TT genotypes were significantly associated with increased risk of systemic lupus erythematosus (OR 5.15; 95% CI 2.46-10.78; p<0.001).
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