Key result
Higher circulating ANG1-7 linked to ~65% lower odds of cognitive impairment per SD.
Why the study?
Dysregulation of the renin angiotensin system is linked to Alzheimer's disease pathophysiology, but few studies have assessed circulating RAS components and incident cognitive decline or impairment.
Are circulating RAS biomarkers associated with incident cognitive decline and cognitive impairment in initially cognitively healthy adults?
Cohort (n=310)
Are circulating RAS biomarkers associated with incident cognitive decline and cognitive impairment in initially cognitively healthy adults?
Higher circulating levels of angiotensin 1-7 are associated with a significantly lower risk of cognitive impairment and better global cognitive function over 15 years in initially cognitively healthy adults.
Answers are grounded in this paper and cite their sources.
May aid long-term cognitive risk stratification; leaves open whether ANG1-7 is a modifiable preventive target.
Background Evidence suggests that dysregulation of the renin angiotensin system (RAS) is associated with the pathophysiologic process of Alzheimer's disease (AD). Few studies have evaluated the relationship between circulating RAS components and incident cognitive decline or impairment. Objective Our study aims to evaluate the relationship between circulating RAS biomarkers (angiotensin II [ANGII], angiotensin 1-7 [ANG1-7], angiotensin converting enzyme-1 [ACE-1], and 2 [ACE-2]), in initially cognitively healthy adults, and incident cognitive decline and cognitive impairment. Methods In this secondary analysis, 310 community-dwelling participants from the randomized controlled Action for Health in Diabetes (Look AHEAD) study without dementia, who were not on RAS-altering medication, were included. Results Participants, compared to those excluded, were more likely to be female (65%), white (76%), overweight (34%), have lower baseline HbA1c (6.7%), lower SBP (119.7 mmHg), lower serum creatinine (0.79 mg/dL), higher total cholesterol (190.1 mg/dL) and LDL (112.5 mg/dL), and higher history of dyslipidemia (65%) at baseline. 1 SD increase of ANG1-7 measured in year 1 was associated with lower odds of cognitive impairment (OR = 0.35, 95% CI 0.16-0.77; p = 0.001), while higher ANG1-7 levels predicted better global cognitive function [β x 10 −3 = 1.03 (0.50); p = 0.039], 15 years later. Conclusions These results provide preliminary evidence that circulating RAS components are predictive of protection against cognitive impairment and decline and may serve as a marker of the early stages of dementia. Further research is warranted to fully understand the relationship between the brain and the circulatory RAS.
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Yaşar et al. (2026) conducted a cohort in Diabetes and initially cognitively healthy (n=310). Circulating RAS biomarkers (specifically ANG1-7) vs. Lower levels of ANG1-7 was evaluated on Cognitive impairment (OR 0.35, 95% CI 0.16-0.77, p=0.001). A 1 SD increase in circulating ANG1-7 was associated with significantly lower odds of cognitive impairment over 15 years (OR 0.35; 95% CI 0.16-0.77; p=0.001).
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