J Am Heart Assoc. 2025 Dec 30:e043643. doi: 10.1161/JAHA.125.043643. Online ahead of print.
ABSTRACT
BACKGROUND: The subendocardial viability ratio (SEVR) reflects myocardial perfusion relative to workload. This study explored the association of SEVR with mortality and subclinical target organ damage in an older adult population.
METHODS: We analyzed the data from the Northern Shanghai Study, a community-based cohort of older adults aged over 65 years. SEVR was measured with arterial tonometry. Cross-sectional associations were assessed between SEVR levels and target organ damage (including arterial stiffness, peripheral artery disease, carotid plaque, left ventricular hypertrophy, left ventricular diastolic dysfunction, chronic kidney dysfunction, and microalbuminuria). Longitudinal associations between SEVR and mortality were evaluated using Cox and Fine-Gray models.
RESULTS: Among 3237 participants (mean age 71±6 years, 57% female), 233 deaths occurred over a median follow-up of 5.7 years, including 94 cardiovascular deaths. Participants were divided into 2 groups by the median value of SEVR (129%). The group with a lower SEVR (≤129%) was associated with higher risk of cardiovascular death (adjusted CoxHazard Ratio [HR]=1.70 [1.05-2.75]; P=0.03), but not with all-cause death (adjusted CoxHR=1.30 [0.98-1.73]; P=0.07). As for target organ damage, participants with more damaged organs had lower SEVR values (P for trend <0.001). Specifically, the occurrence of arterial stiffness and left ventricular diastolic dysfunction increased the potential of worse SEVR, with odds ratio 1.46 (1.17-1.83); P<0.001, and 1.90 (1.35-2.67); P<0.001, respectively.
CONCLUSIONS: Lower SEVR is independently associated with both increased cardiovascular mortality and organ damage, including arterial stiffness and left ventricular diastolic dysfunction in older adult populations. SEVR may be a convenient marker for early cardiovascular risk stratification in aging populations.
REGISTRATION: URL: https://ClinicalTrial.gov; Unique Identifier: NCT02368938.
PMID:41467407 | DOI:10.1161/JAHA.125.043643