Key result
ApoE epsilon2 and epsilon4 carrier status were not associated with prevalent hypertension compared to epsilon3 homozygotes (PR 0.94, 95% CI 0.83-1.07 and PR 0.98, 95% CI 0.89-1.07, respectively).
Why the study?
Does ApoE polymorphism affect prevalent hypertension in older adults?
Cross-Sectional (n=1,406)
No
Does ApoE polymorphism affect prevalent hypertension in older adults?
ApoE genotype is not associated with prevalent hypertension in older adults, despite its known effects on LDL cholesterol levels.
ApoE genotyping does not inform hypertension risk assessment in older adults; leaves open longitudinal or subgroup effects.
Apolipoprotein E (ApoE) polymorphism influences lipid metabolism, but its association with arterial hypertension is controversial. The objective of this study was to examine the association between ApoE polymorphism and prevalent hypertension in a large unselected population of older adults. Participants from the baseline of the Bambuí Health Aging Study whose ApoE genes had been genotyped were selected for this study (N = 1406, aged 60-95 years). These subjects represented 80.7% of the total elderly residents in Bambuí city, MG, Brazil. Hypertension was defined as a systolic blood pressure > or =140 mmHg and/or a diastolic blood pressure > or =90 mmHg, or the use of anti-hypertensive medication. The exposure variable was the ApoE genotype as follows: epsilon3 carriers, epsilon3epsilon3; epsilon2 carriers, epsilon2epsilon2 or epsilon2epsilon3, and epsilon4 carriers, epsilon3epsilon4 or epsilon4epsilon4. Potential confounding variables were age, gender, traditional cardiovascular risk factors, uric acid, and creatinine levels. The prevalence of hypertension was 61.3%. Compared with the epsilon3 homozygotes, neither the epsilon2 nor the epsilon4 carrier status was associated with hypertension (adjusted prevalence ratios = 0.94, 95%CI = 0.83-1.07 and 0.98, 0.89-1.07, respectively). On the other hand, the epsilon2 allele carriers had lower LDL cholesterol levels (P < 0.001) and the epsilon4 carriers had higher LDL cholesterol levels (P = 0.036). This study provides epidemiologic evidence that the ApoE genotype is not associated with prevalent hypertension in old age.
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Fuzikawa et al. (2008) conducted a cross-sectional in Hypertension (n=1,406). ApoE epsilon2 and epsilon4 carrier status vs. ApoE epsilon3 homozygotes was evaluated on Prevalent hypertension (PR 0.94, 95% CI 0.83-1.07). ApoE epsilon2 and epsilon4 carrier status were not associated with prevalent hypertension compared to epsilon3 homozygotes (PR 0.94, 95% CI 0.83-1.07 and PR 0.98, 95% CI 0.89-1.07, respectively).
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