Key result
Higher urinary 2,3-dinor-8-F2-isoprostane linked to ~96% higher incident thoracic aortic calcium risk per SD.
Why the study?
Urinary isoprostanes are markers of systemic oxidative stress implicated in ASCVD pathogenesis, but their associations with subclinical atherosclerosis measures are unclear.
Are urinary isoprostane levels associated with measures of subclinical atherosclerosis?
Cohort (n=1,089)
Yes
Are urinary isoprostane levels associated with measures of subclinical atherosclerosis?
Higher urinary isoprostanes are inconsistently associated with subclinical atherosclerosis imaging measures, suggesting limited prognostic utility for ASCVD development.
Isoprostane associations with plaque and TAC suggest limited prognostic utility; hypothesis-generating without supporting clinical adoption.
Background: Urinary isoprostanes are markers of systemic oxidative stress, which is implicated in the pathogenesis of atherosclerotic cardiovascular disease (ASCVD). Coronary artery calcium (CAC), thoracic aortic calcium (TAC) and carotid plaque are measure subclinical atherosclerosis and prognosticate ASCVD risk. We examined the associations between urinary isoprostane levels and measures of plaque prevalence, burden, incidence and progression across three vascular beds in a cohort from the Multi-Ethnic Study of Atherosclerosis. Participants underwent computed tomography for CAC and TAC, and duplex ultrasound for carotid plaque. TAC and CAC were reassessed at 2.4 and 10 years, respectively. Regression models were adjusted for CVD risk factors. Highest versus lowest tertile of isoprostane measures were associated with 22% higher prevalence of carotid plaque [(PR 1.22 (1.04, 1.45)] and 14% difference [3,26] in greater extent of carotid plaque at baseline. Conclusions: Higher urinary isoprostanes were inconsistently associated with some measures of subclinical atherosclerosis by imaging. This suggests a limited role of urinary isoprostane levels as a prognostic marker for the development of ASCVD. Trial registration: The MESA cohort design is registered at clinicaltrials.gov as follows: https://clinicaltrials.gov/ct2/show/NCT00005487.
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Wallace et al. (2022) conducted a cohort in Subclinical atherosclerosis (n=1,089). Urinary isoprostanes (8-isoprostane and 2,3-dinor-8-F2-isoprostane) vs. Lowest tertile of isoprostanes or per 1-SD increment was evaluated on Incident ascending thoracic aortic calcium (ATAC) at follow-up (RR 1.96, 95% CI 1.24, 3.09). A 1-SD higher level of urinary 2,3-dinor-8-F2-isoprostane was associated with a 96% higher risk of incident ascending thoracic aortic calcium at follow-up (RR 1.96).
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