Why the study?
Previous studies have reported inconsistent associations between the angiotensin-converting enzyme (ACE) gene insertion/deletion (I/D) polymorphism and hypertension across different ethnicities, prompting evaluation of this relationship in Balinese patients.
Does the ACE I/D polymorphism influence hypertension staging and blood pressure levels in untreated hypertensive patients of Balinese ancestry?
Cross-Sectional (n=87)
Does the ACE I/D polymorphism influence hypertension staging and blood pressure levels in untreated hypertensive patients of Balinese ancestry?
In untreated Balinese hypertensive patients, the ACE D allele and DD genotype were unexpectedly associated with significantly lower diastolic blood pressure, highlighting how ethnic background modulates genetic associations in hypertension.
Answers are grounded in this paper and cite their sources.
Should not yet guide genetic risk stratification in hypertension; leaves open the role of ethnic-specific ACE polymorphism effects pending larger prospective validation.
Hypertension continues to pose a major public health challenge worldwide, playing a critical role in the development of cardiovascular diseases and related fatalities. Its pathogenesis is multifactorial, involving both environmental influences and genetic predispositions. Among the genetic factors, the insertion/deletion (I/D) polymorphism in the angiotensin-converting enzyme (ACE) gene has garnered widespread attention, with previous studies reporting inconsistent associations with hypertension across different ethnicities. This cross-sectional study investigated the relationship between ACE I/D polymorphism and blood pressure in 87 untreated hypertensive patients of Balinese ancestry. Genotyping revealed the II genotype as the most prevalent (63.2%), followed by ID (29.9%) and DD (6.9%). While no significant association was found between genotypes and hypertension staging (p=0.090) or systolic blood pressure (p=0.552). A statistically significant variation was observed in diastolic blood pressure (DBP), with individuals carrying the DD genotype exhibiting the lowest mean DBP (p = 0.022). Similar trends emerged in allele-based analysis, where D allele carriers had significantly lower DBP (p = 0.006). These findings demonstrate an inverse association between the D allele and diastolic blood pressure in this cohort, diverging from traditional risk patterns reported in other populations. This suggests that the ACE I/D polymorphism may act as a potential risk factor modulated by population-specific contexts, highlighting the importance of ethnic diversity in precision medicine for hypertension management.
No takes yet. Share an insight, caveat, or question.
Handani et al. (2026) conducted a cross-sectional in Untreated primary hypertension (n=87). ACE I/D gene polymorphism (DD genotype / D allele) vs. II genotype / I allele was evaluated on Mean diastolic blood pressure (mmHg) (p=0.022).
Synapse has enriched 10 related papers. Consider them for comparative context: