Key result
The AGT T704C and ACE I/D polymorphisms were significantly associated with an increased risk of preeclampsia, with the AGT T704C dominant model showing an OR of 1.33.
Why the study?
Data evaluating associations between renin-angiotensin system polymorphisms (AGT T704C, ACE I/D, and AT1R A1166C) and preeclampsia risk were conflicting.
Do renin-angiotensin system polymorphisms (AGT T704C, ACE I/D, AT1R A1166C) increase the risk of preeclampsia in pregnant women?
Meta-Analysis
Do renin-angiotensin system polymorphisms (AGT T704C, ACE I/D, AT1R A1166C) increase the risk of preeclampsia in pregnant women?
Odds Ratio: 1.33 (95% CI 1.12–1.59)
p-value: p=0.001
The AGT T704C and ACE I/D polymorphisms of the renin-angiotensin system are associated with an increased risk of preeclampsia.
May inform preeclampsia risk stratification; leaves open causal validation and clinical utility before practice change.
PURPOSE: Some data suggest an association between the single nucleotide polymorphisms AGT T704C, ACE I/D, and AT1R A1166C and preeclampsia, but overall, the data are conflicting; the aim of our study was to discover a more stable and reliable association between these polymorphisms and PE risk. METHODS: A comprehensive literature search for this meta-analysis was conducted. Odds ratios (OR) and 95% confidence intervals (CIs) were calculated to evaluate the strength, and heterogeneity test was conducted. Trial sequential analysis was also performed. RESULTS: A total of forty studies were finally included in our meta-analysis. The AGT T704C polymorphism was associated with PE risk in three genetic models (dominant OR = 1.33, 95%CI = 1.12-1.59; heterozygote OR = 1.26, 95%CI = 1.05-1.52; homozygote OR = 1.44, 95%CI = 1.14-1.83). No heterogeneity was observed in the three genetic models for the ACE I/D polymorphism. For subgroup analysis by geography, no significant association was detected. Significant associations were observed in mixed race, early-onset, late-onset, and more than 200 subgroups for the AT1R A1166C polymorphism; however, only one study was analyzed in these subgroups. CONCLUSIONS: Our results indicated the AGT T704C and ACE I/D polymorphisms were associated with an increased risk of PE. Increased risks were also observed for the two polymorphisms in subgroups including Asians, Europeans, Caucasoid, and Mongoloid. Moreover, an increased PE risk with the ACE I/D polymorphism in the severe PE population was also detected. Regarding the AT1R A1166C polymorphism, weak associations were observed, but further studies are required.
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Wang et al. (2020) conducted a meta-analysis in Preeclampsia. AGT T704C and ACE I/D polymorphisms vs. Reference genotypes was evaluated on Preeclampsia risk (AGT T704C dominant model) (OR 1.33, 95% CI 1.12-1.59, p=0.001). The AGT T704C and ACE I/D polymorphisms were significantly associated with an increased risk of preeclampsia, with the AGT T704C dominant model showing an OR of 1.33.
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