Why the study?
Does the distribution of ACE I/D genotypes differ between Alzheimer's disease patients with and without hypertension?
Does the distribution of ACE I/D genotypes differ between Alzheimer's disease patients with and without hypertension?
The contribution of the ACE gene to the development of Alzheimer's disease appears to be independent of hypertension.
Objective Angiotensin-converting enzyme (ACE) insertion/deletion (I/D) polymorphisms are considered biomarkers of late-onset Alzheimer's disease (AD). However, the results of studies of these polymorphisms have been inconsistent. The ACE protein directly degrades beta-amyloid and thereby slows the progression of AD and its onset. However, it also activates the renin–angiotensin–aldosterone system, which can contribute to hypertension and/or cardiovascular events that increase the risk for developing AD. Methods In this study, we examined the bidirectional association of the ACE gene and AD in patients with AD with and without hypertension. Results Patients who were clinically diagnosed with AD (n = 983) underwent ACE I/D genotyping. The distribution of the ACE I/D genotypes (P = 0.355 for I/I vs. D/D; P = 0.888 for I/D vs. D/D) and I alleles (P = 0.895) did not significantly differ between hypertensive patients with AD and patients with AD without hypertension. Conclusions In contrast to traditional theories, the results of this study suggested that the contribution of the ACE gene to the development of AD was not associated with hypertension and similar cardiovascular effects.
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Yang et al. (2017) studied this question.
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