Why the study?
The correlation between ACE2 gene polymorphisms and congenital heart disease-related pulmonary arterial hypertension risk in neonates had not been reported.
Do ACE2 gene polymorphisms associate with the risk of pulmonary arterial hypertension in neonates with congenital heart disease?
Case-Control (n=321)
Yes
Do ACE2 gene polymorphisms associate with the risk of pulmonary arterial hypertension in neonates with congenital heart disease?
Odds Ratio: 0.187 (95% CI 0.039–0.67)
p-value: p=0.018
There is no significant association between ACE2 SNPs (rs2074192, rs2285666, rs2106809) or haplotypes and the risk of CHD-related pulmonary arterial hypertension in Han Chinese neonates.
No association supports ACE2 genotyping for CHD-PAH risk in neonates; leaves open sex-specific haplotype effects for validation in larger studies.
Studies have confirmed a correlation between angiotensin-converting enzyme 2 (ACE2 ) gene polymorphisms and the risk of hypertension; however, its correlation with congenital heart disease (CHD)-related-pulmonary arterial hypertension (PAH) risk in neonates has not been reported. The study enrolled 321 Han Chinese neonates, comprising 113 healthy controls and 208 patients with left-to-right shunt CHD. Among the CHD patients, 98 cases were classified as the PAH subtype [CHD PAH (+)]. Tag SNP genotyping was performed using Sanger sequencing. Associations between three ACE2 SNPs (rs2074192, rs2285666, and rs2106809) and CHD PAH (+) neonates were assessed via sex-stratified logistic regression. Differences in circulating ACE2 and angiotensin1-7 [Ang(1–7)] levels across ACE2 haplotypes were compared using analysis of variance (ANOVA). No significant associations were observed between the three ACE2 SNPs and susceptibility to CHD or the risk of PAH in either univariable or multivariable analyses. In females, the CCT haplotype showed a nominally suggestive association with CHD-PAH in both the univariable model (OR = 0.216, 95% CI: 0.047–0.740; P = 0.025; FDR_ P = 0.074) and the multivariable model (OR = 0.187, 95% CI: 0.039–0.670; P = 0.018; FDR_ P = 0.053). A nominal difference in circulating Ang-(1–7) levels was also observed across haplotypes among females, with higher levels in CCT haplotype carriers than in those carrying the CTC or TCT haplotypes (160.16 ± 19.24 pg/mL vs. 140.54 ± 28.40 pg/mL and 139.77 ± 29.85 pg/mL, respectively; P = 0.037). However, this difference did not survive FDR correction (FDR_ P = 0.074). Our study showed that there was no significant association between ACE2 SNPs or haplotypes and the risk of CHD-PAH in neonates. Our study is an observational study. According to the International Committee of Medical Journal Editors (ICMJE), purely observational studies (in which the allocation of medical interventions is not under the investigator’s discretion) do not require registration.
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Chen et al. (2026) conducted a case-control in Congenital heart disease-related pulmonary arterial hypertension (n=321). ACE2 gene polymorphisms (rs2074192, rs2285666, rs2106809 and haplotypes) vs. Non-carriers or different genotypes/haplotypes was evaluated on Risk of CHD-PAH in females carrying the CCT haplotype (multivariable model) (OR 0.187, 95% CI 0.039-0.670, p=0.018).
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