Why the study?
Emerging data indicate potential involvement of the Renin-Angiotensin System in neurodegenerative diseases including Alzheimer's dementia, leading to investigation of the therapeutic implications of RAS modulators.
Do Renin-Angiotensin System modulators reduce cognitive decline and neurodegeneration in Alzheimer's dementia?
Do Renin-Angiotensin System modulators reduce cognitive decline and neurodegeneration in Alzheimer's dementia?
RAS modulators, particularly ARBs, show promise as therapeutic interventions for Alzheimer's dementia by mitigating neuroinflammation and cognitive decline.
The Renin-Angiotensin System (RAS) has attracted considerable interest beyond its traditional cardiovascular role due to emerging data indicating its potential involvement in neurodegenerative diseases, including Alzheimer's dementia (AD). This review investigates the therapeutic implications of RAS modulators, specifically focusing on angiotensin-converting enzyme inhibitors (ACEIs), angiotensin receptor blockers (ARBs), and renin inhibitors in AD. ACEIs, commonly used for hypertension, show promise in AD by reducing angiotensin (Ang) II levels. This reduction is significant as Ang II contributes to neuroinflammation, oxidative stress, and β-amyloid (Aβ) accumulation, all implicated in AD pathogenesis. ARBs, known for vasodilation, exhibit neuroprotection by blocking Ang II receptors, improving cerebral blood flow and cognitive decline in AD models. Renin inhibitors offer a novel approach by targeting the initial RAS step, displaying anti-inflammatory and antioxidant effects that mitigate AD degeneration. Preclinical studies demonstrate RAS regulation's favorable impact on neuroinflammation, neuronal damage, cognitive function, and Aβ metabolism. Clinical trials on RAS modulators in AD are limited, but with promising results, ARBs being more effective that ACEIs in reducing cognitive decline. The varied roles of ACEIs, ARBs, and renin inhibitors in RAS modulation present a promising avenue for AD therapeutic intervention, requiring further research to potentially transform AD treatment strategies.
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Ababei et al. (2023) studied this question.
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