Why the study?
Are ACE I/D and AT1R A1166C polymorphisms associated with an increased risk of preeclampsia and altered lipid peroxidation in pregnant women?
Are ACE I/D and AT1R A1166C polymorphisms associated with an increased risk of preeclampsia and altered lipid peroxidation in pregnant women?
The ACE D allele is associated with an increased risk of preeclampsia, and RAAS polymorphisms may influence lipid peroxidation and oxidative stress in this condition.
ACE D allele may flag preeclampsia risk in case-control data; leaves open utility for prediction or prevention pending prospective validation.
BACKGROUND: The aim of the present study was to investigate the association between angiotensin converting enzyme (ACE) insertion/deletion (I/D) and angiotensin II type-1 receptor (AT1R) A1166C polymorphisms with the risk of preeclampsia and lipid peroxidation in preeclamptic women from Western Iran. METHODS: One hundred and ninety-eight preeclamptic women (128 women with mild and 70 with severe forms) and 100 age- and parity-matched controls were enrolled in this case-control study. RESULTS: The presence of D allele of ACE was associated with a 1.8-fold increased risk of preeclampsia (p=0.002) in total preeclamptic patients. The frequency of AT1R AC+CC genotypes was higher in mild preeclamptic women (32%) compared to controls (27.2%) (p>0.05). In mild preeclamptic women with ID genotype, the level of total antioxidant capacity (TAC) was significantly decreased compared to those with II genotype. Also, there was a trend toward increasing malondialdehyde (MDA) and decreasing TAC levels in mild and severe preeclamptic women with AT1R AA through CC genotypes. CONCLUSIONS: Our study indicates that lipid peroxidation and oxidative stress are involved in the development of preeclampsia that might be influenced by polymorphism in the renin-angiotensin-aldosterone system genes.
No takes yet. Share an insight, caveat, or question.
Rahimi et al. (2012) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: