Key result
Higher urinary sodium excretion was independently associated with hypertension (OR 1.715) and elevated blood pressure only in carriers of the p22-phox 242T allele, suggesting a genetic susceptibility to salt-induced hypertension.
Why the study?
Does the p22-phox C242T polymorphism influence the relationship between urinary sodium excretion and blood pressure in an urban Brazilian population?
Cross-Sectional (n=1,298)
Does the p22-phox C242T polymorphism influence the relationship between urinary sodium excretion and blood pressure in an urban Brazilian population?
The p22-phox 242T allele is associated with higher blood pressure levels among subjects with higher urinary sodium excretion, suggesting a genetic susceptibility to salt-induced hypertension.
Supports p22-phox 242T as salt-sensitivity marker; hypothesis-generating and should not yet change practice.
BACKGROUND: Reactive oxygen species are implicated in the physiopathogenesis of salt-induced hypertension and the C242T polymorphism of the p22-phox gene has been associated with higher superoxide production. This study investigated the impact of this polymorphism on the relationship between urinary sodium excretion (USE) and blood pressure levels in an urban Brazilian population. METHODS: We cross-sectionally evaluated 1,298 subjects from the city of Vitoria-ES, located in the Southeast region of Brazil, by clinical history, physical examination, anthropometry, analysis of laboratory parameters, USE measurement and p22-phox C242T polymorphism genotyping. RESULTS: No significant differences in studied parameters were detected between the studied genotype groups (CC vs. CT+TT). Systolic blood pressure exhibited significant correlation with USE only in T allele carriers (r = 0.166; p<0.001), while diastolic blood pressure and hypertension status correlated with USE in both genotypes albeit more weakly in subjects with CC genotype (r = 0.098; p = 0.021 and r = 0.105; p = 0.013, respectively) than in T carriers (r = 0.236; p<0.001 and r = 0.213; p<0.001, respectively). Regression analyses adjusted for confounding factors showed that USE remained independently associated with systolic (p<0.001) and diastolic blood pressure (p<0.001) and hypertension status (p = 0.004) only in T allele carriers. Finally, higher diastolic and systolic blood pressure levels were detected in T allele carriers than in CC genotype individuals in the highest tertile of USE. CONCLUSIONS: The p22-phox 242T allele is associated with higher blood pressure levels among subjects with higher USE in an urban Brazilian population.
No takes yet. Share an insight, caveat, or question.
Schreiber et al. (2013) conducted a cross-sectional in Hypertension / Blood Pressure (n=1,298). High urinary sodium excretion in p22-phox 242T allele carriers vs. Low urinary sodium excretion / CC genotype was evaluated on Hypertension status associated with high urinary sodium excretion (>86.5 mEq/12 h) in T allele carriers (OR 1.715, 95% CI 1.191-2.469, p=0.004). Higher urinary sodium excretion was independently associated with hypertension (OR 1.715) and elevated blood pressure only in carriers of the p22-phox 242T allele, suggesting a genetic susceptibility to salt-induced hypertension.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: