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Clinical and Community Factors' Correlation With NT-proBNP in First Nations: A Cross-sectional Analysis of the
Miles Marchand1, Zayeeda Shahreen Labiba2, Karleen Schulze2
1Division of Cardiology, University of British Columbia, Vancouver, British Columbia, Canada; Dilawri Cardiovascular Institute, Vancouver, British Columbia, Canada; Syilx Okanagan First Nation, British Columbia, Canada.
Background:
In Canada, Indigenous populations face inequities in cardiovascular care, and have disparate heart failure (HF) outcomes. N-terminal pro-B-type natriuretic peptide (NT-proBNP) is a biomarker that has been reported to predict subclinical left ventricular (LV) dysfunction, clinical HF, and cardiovascular events. Because of disparities in HF outcomes and care between Indigenous and non-Indigenous people in Canada, in this study we sought to understand the unique sociocultural, clinical, and community factors that are associated with circulating NT-proBNP levels.
Methods:
We conducted a cross-sectional analysis of 579 First Nations adults from the Canadian Alliance for Healthy Hearts and Minds First Nations (CAHHM-FN) study, who completed detailed questionnaires, physical measures, community audits, cardiac magnetic resonance imaging, and biomarker testing. We examined associations between NT-proBNP levels and clinical, sociocultural, and community factors, and subsequently evaluated the association between NT-proBNP and LV size, mass, and function on cardiac magnetic resonance imaging.
Results:
Increased access to primary care and cardiovascular risk factor screening were associated with lower NT-proBNP levels. Higher NT-proBNP levels were associated with older age, female sex, cardiovascular disease, and secondhand smoke exposure. Participants in the highest NT-proBNP tertile were more likely to have increased LV dimensions and mass and reduced ejection fraction.
Conclusions:
In this unique Indigenous cohort, several clinical, community, and sociocultural factors were associated with NT-proBNP elevation, which was also associated with subclinical LV abnormalities. These findings might explain some of the disparities in HF outcomes faced by Indigenous populations. Longitudinal follow-up is needed to assess these factors' predictive value on the development of incident clinical HF.
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