Key result
The interaction between the ACE ID+II genotype and daily salt intake was significantly associated with an increased risk of hypertension (adjusted OR 3.6), an effect that was more prominent in overweight individuals.
Why the study?
Does the interaction between ACE I/D genotype and daily salt intake influence hypertension in Japanese men?
Cross-Sectional (n=284)
Does the interaction between ACE I/D genotype and daily salt intake influence hypertension in Japanese men?
Odds Ratio: 3.6 (95% CI 1–12.5)
p-value: p=0.047
The ACE I/D polymorphism interacts with daily salt intake to influence hypertension risk in Japanese men, an effect that is further exacerbated by being overweight.
ACE I/D-salt interaction was associated with hypertension in Japanese men; leaves open genotype-guided dietary advice pending prospective trials.
The contribution of angiotensin I-converting enzyme insertion-deletion polymorphism (ACE I/D) to salt-sensitivity hypertension has been extensively studied by means of salt-loading tests, but whether or not the interaction with daily salt intake affects blood pressure still remains to be clarified. We therefore conducted a cross-sectional study of 284 Japanese male workers (age range, 20-64 years) to examine the effect of ACE I/D genotype and daily salt intake on hypertension. Blood pressure was measured and the ACE I/D was identified by polymerase chain reaction (PCR). Daily salt intake was calculated from a food frequency questionnaire (FFQ). In multivariate analyses, we explored the interaction of ACE I/D and salt intake by means of logistic regression analysis and multiple linear regression analysis. ACE I/D per se was not associated with blood pressure levels or hypertension. ACE I/D interacted with daily salt intake and correlated with hypertension (p for interaction = 0.047). In the ID+II genotype, hypertension was increased by high salt intake (p = 0.005), while in the DD genotype it was not (p = 0.257). The interaction was more prominent in the overweight group (p = 0.039) than in non-overweight group. In the overweight group, high salt intake induced a 10.5 mmHg higher diastolic blood pressure in the ID+II genotype than in the DD genotype (p = 0.042). Our results suggest that ACE I/D and daily salt intake constitute a gene-environment interaction, which may be further modulated by overweight.
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Zhang et al. (2006) conducted a cross-sectional in Hypertension (n=284). ACE I/D polymorphism (ID+II genotype) and daily salt intake vs. DD genotype and daily salt intake was evaluated on Hypertension (SBP ≥ 160 mmHg and/or DBP ≥ 95 mmHg and/or current treatment) (OR 3.6, 95% CI 1.0-12.5, p=0.047). The interaction between the ACE ID+II genotype and daily salt intake was significantly associated with an increased risk of hypertension (adjusted OR 3.6), an effect that was more prominent in overweight individuals.
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