Longitudinal trajectories of albuminuria and risk of subclinical and clinical heart failure, atrial fibrillation, and coronary heart disease: the MESA study - Scorecard - MDSpire
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Longitudinal trajectories of albuminuria and risk of subclinical and clinical heart failure, atrial fibrillation, and coronary heart disease: the MESA study
Clinical Scorecard: Analysis of Albuminuria Patterns and Their Association with Subclinical and Clinical Heart Failure, Atrial Fibrillation, and Coronary Heart Disease: Insights from the MESA Study
At a Glance
Category
Detail
Condition
Albuminuria and its association with heart failure (HF), atrial fibrillation (AF), and coronary heart disease (CHD)
Key Mechanisms
Progressive increases in urine albumin-creatinine ratio (UACR) reflect glomerular injury and are linked to elevated cardiac biomarkers and interstitial myocardial fibrosis, contributing to HF and cardiovascular risk
Target Population
Adults aged approximately 62 years from a multi-ethnic cohort, including those with normoalbuminuria at baseline
Care Setting
Cardiovascular risk assessment and monitoring in outpatient and research settings
Key Highlights
Distinct UACR trajectory groups over 5 and 10 years identify subgroups at elevated risk for HF, AF, and CHD, independent of baseline UACR levels.
Sustained medium to high or rapid rise in UACR is associated with 1.5- to 3.7-fold increased risk of HF, HF subtypes, AF, and CHD.
Elevated UACR trajectories correlate with increased NT-proBNP, hs-TnT, and myocardial fibrosis measured by cardiac MRI T1 mapping, linking albuminuria to subclinical cardiac injury.
Guideline-Based Recommendations
Diagnosis
Use longitudinal monitoring of urine albumin-creatinine ratio (UACR) to identify progressive albuminuria trajectories.
Consider UACR trajectories even in individuals with normoalbuminuria at baseline for cardiovascular risk stratification.
Management
Target individuals with sustained or rapidly rising UACR for intensified cardiovascular risk management to prevent HF and related conditions.
Incorporate cardiac biomarker assessment (NT-proBNP, hs-TnT) and imaging (cardiac MRI T1 mapping) for evaluation of subclinical myocardial injury in high-risk patients.
Monitoring & Follow-up
Regularly monitor UACR over time rather than relying on single measurements to detect progressive albuminuria.
Follow cardiac biomarkers and imaging findings to assess progression of myocardial fibrosis and risk of HF.
Risks
Progressive albuminuria increases risk for heart failure, particularly HF with preserved ejection fraction (HFpEF), atrial fibrillation, and coronary heart disease.
Risk associations persist independent of baseline UACR and are not fully explained by interim AF or CHD events.
Patient & Prescribing Data
Middle-aged to older adults from a multi-ethnic cohort, including those initially normoalbuminuric
Identification of high-risk UACR trajectories may guide early intervention to prevent progression to clinical HF and cardiovascular events; monitoring cardiac biomarkers and myocardial fibrosis can inform treatment response.
Clinical Best Practices
Incorporate serial UACR measurements into routine cardiovascular risk assessments to detect progressive albuminuria.
Recognize that even low-level increases in UACR below clinical thresholds carry significant cardiovascular risk.
Use combined biomarker and imaging approaches to detect subclinical myocardial injury in patients with rising albuminuria.
Focus preventive strategies on patients with sustained medium to high or rapidly rising UACR trajectories to reduce HF and cardiovascular event incidence.
Despite major advances in guideline-directed medical therapy (GDMT), worsening heart failure continues to drive significant morbidity, repeat hospitalizations and healthcare utilization worldwide.